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Annual Report FY2018

Full Year Results14 June 2018AFTHealthcare

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Annual Report 2018

This Annual Report is dated 15 June 2018.
Signed on behalf of the Board of AFT Pharmaceuticals Limited by:

Hartley Atkinson

Chief Executive Officer

David Flacks

Chairman

Contents

2 AFT at a Glance

4 Key Highlights

6 Chairman and CEO’s Report

10 Full year financial results summary

14 Codeine rescheduling in Australia

16 New markets new opportunities

20 Directors and management team

24 Corporate Governance

25 Sustainability

27 Financial statements

58 Statutory disclosures

67 Directory

Full report available online at investors.aftpharm.com

Note: $ in this report are NZ$ unless otherwise stated.

Clinical development

programmes substantially

completed

Gross profit

growth 32%

–– MAXIGESIC NOW LICENSED

IN 125 COUNTRIES.

–– MAXIGESIC IV PIVOTAL STUDY

SUCCESSFULLY COMPLETED

IN THE USA.

–– MAXIGESIC PE LAUNCHED

IN NEW ZEALAND.

–– NASOSURF CLASS 1

REGISTRATION COMPLETED

ON SCHEDULE IN USA.

AND THERE’S MORE TO COME.

Achieving

AFT at a glance
REST OF WORLD

Operating revenue

$2.5m

Number of products

5

Growth drivers

Further increase sales of

Maxigesic through growth in

existing markets, additional

registrations followed by new

launches during FY2019 and

following financial years.

Additional regulatory filings

during FY2019 of new dose

forms of Maxigesic, registrations

and then additional sales.

Sales of Maxigesic are expected

to grow significantly over the

next few years driven by new

launches, but it is important

to note that there is a lag in

these sales from the time of an

out-licensing agreement due

to registration timelines which

vary widely country to country

and are difficult to estimate

with accuracy.

NEW ZEALAND

Operating revenue

$ 27.1 m

Number of products

104

Growth drivers

Ongoing growth of higher

margin OTC products to reduce

reliance of sales from lower

margin tender products.

Gross profit increased by 19%

with the gross profit margin

improving to 37%.

It is anticipated that sales will

be flat in New Zealand during

FY2019, with the divestment

of some non-core hospital

products, which will result

in improving margins as we

continue to grow the OTC

business.

AUSTRALIA

Operating revenue

$49.2m

Number of products

60

Growth drivers

Over the counter (OTC)

products: Maxigesic, Eyecare

Range, Ferro Range and Other

Pain Products Range. Additional

OTC launches to extend Ferro

Range such as Ferro Sachets

and selected new products such

as PipTaz in our hospital range.

The significant opportunity

for increased Maxigesic sales

offered by the rescheduling of

codeine on 1 February 2018 was

a key project with Maxigesic

achieving the largest market

share for Paracetamol-Ibuprofen

combination products in

the period immediately post

rescheduling. This will continue

to be an ongoing focus during

the FY2019 period and onwards.

Significant sales growth was

seen for the Eyecare range

with increased focus on the

optometry channel to drive sales

across all channels.

Margins grew as OTC product

sales increased and we expect

continued significant sales

growth and growth in profit

in Australia in FY2019 and

onwards.

SOUTHEAST ASIA

Operating revenue

$1.3m

Number of products

8

Growth drivers

Continued growth from

products launched during

FY2018.

Launch Maxigesic in Malaysia

and grow sales in Singapore and

Malaysia during FY2019.

Total operating revenue

$80.1m

Total operating revenue

(NZ$m)

FY17FY18FY16FY15FY14FY13FY12FY11FY10FY09FY08FY07FY06FY05FY04FY03FY02FY01FY00

0

10

20

30

40

50

60

70

80

90

0

10

20

30

40

50

60

70

80

Operating revenue growth

+16%

Australia revenue

+33%

our largest market

Gross profit

+32%

Gross profit margin up to

43%

OUR KEY PRODUCTS

Maxigesic

Successfully completed the

developments of existing dose forms

and additionally significantly advanced

formulation developments for the two

new formulations: dry powder sachet

and a novel proprietary fast acting

formulation which we believe will

result in additional clinical benefits.

Additional studies are underway this

FY2019 period to validate the clinical

benefits. The large pivotal Maxigesic

IV Phase 3 study in 276 bunionectomy

patients was successfully completed in

Baltimore, Maryland and Austin, Texas

which has allowed the first regulatory

filings to be completed and further

filings are underway. Regulatory

filings for both the existing tablet

formulation and new dose forms across

a significant number of countries to

complete registrations and start sales

in more territories is well underway.

NasoSURF

Initial Class I registration completed

on schedule Dec 2016 in USA. First

clinical studies are underway in

Australia and New Zealand and a

pre-IND (Investigational New Drug)

application has been made to the FDA

(Food and Drug Administration) in USA

with the intention of opening the IND

during FY2019 and then commencing

larger clinical studies. Filing of Class II

registration in USA is targeted for this

calendar year.

Maxigesic PE / Maxiclear PE

Development work is concluding and

we have recently made the first launch

for Maxigesic PE in New Zealand.

Further regulatory filings will be made

in selected territories.


Australia


New Zealand


Rest of World


Southeast Asia

Overall revenue by market

(Percentage)

33.8%

1.6%

3.1%

61.4%

AFT PHARMACEUTICALS LIMITED

Annual Report 2018

23AFT AT A GLANCE

125 countries
Maxigesic currently licensed in or distributed.

10 countries

Maxigesic sold and launched in Australia, Brunei, Israel, Italy,

Malta, New Zealand, Serbia, Singapore, United Arab Emirates,

and United Kingdom.

MAXIGESIC

CLINICAL TRIAL PROGRAMME FY2018

FINANCIAL HIGHLIGHTS (NZ$)

Operating revenue

$80.1m

Licensing income

$1.8m

Operating loss

($10.1m)

Cash available at 31 March 2018

$6.8m

7 studies

900+ patients

7 countries

Australia, Jordan, Mexico, New Zealand,

Russia, United Kingdom, United States.

Total income

$81.9m

KEY HIGHLIGHTS54AFT PHARMACEUTICALS LIMITED

Annual Report 2018

Delivering

Maxigesic licensed in 125 countries

Global Maxigesic clinical


trial substantially completed

We remain highly
committed to

commercialising our

Key Innovative Products.

David Flacks

CHAIRMAN

Our key efforts are

now shifting towards

product launches in the

out-licensed territories.

Hartley Atkinson

FOUNDER AND CEO

Chairman and CEO’s Report.

CHAIRMAN AND CEO’S REPORT76AFT PHARMACEUTICALS LIMITED

Annual Report 2018

Maximising

Our Pascomer (previously Pascoderm) Key Innovative Product
project is progressing with initial development work and

pre-IND FDA meeting completed and we are now seeking to

open an IND with FDA in order to commence clinical studies.

A detailed market study with payors has refined a target

market of around $400-450m sales in USA/EU. Out-licensing

discussions with interested parties are underway although

timing remains difficult to predict with any degree of certainty.

In our combined local markets of Australia and New Zealand,

we have continued to improve sales of higher margin OTC

products. In the New Zealand market the top-line sales

declined due to the loss in sales of some lower margin tender

products such as metoprolol. However the gross profit in

New Zealand grew by 19% despite the decline in top-line

revenue. Furthermore we divested some lower margin hospital

products to Baxter in New Zealand and expect to complete the

same deal for Australia by June this current FY2019 year which

overall will contribute positively to our financial position.

Maxigesic sales have grown significantly in Australia following

the rescheduling of codeine which occurred on 1 February 2018.

The sales uplift was somewhat delayed as consumers had

stock-piled codeine ahead of the switch date. However sales

still lifted significantly and despite competitor Paracetamol-

Ibuprofen products spending very significantly on product

promotion, we achieved a market leading sales position in the

period following 1 February 2018 rescheduling. Although we

still have ongoing work to consolidate our position and further

expand sales, the initial progress has been pleasing and our

salesforce in Australia has worked with great passion to deliver

this result against large multinational competitors.

We have maintained continuing tight overhead control on fixed

costs such as staff numbers and completed the year with a

cash balance of around $7m and with many of our expensive

Research and Development (R&D) projects such as the

Maxigesic IV study completed.

Our R&D costs are now able to be significantly reduced given

that we have concluded much of the development work

outlined in our IPO documents. We will look to moderate our

R&D spend in order to achieve a clear path to profitability.

We had always targeted break-even in either the FY2018 or

FY2019 time periods with the former target dependent upon

a significant licensing agreement. The timing of licensing

agreements is always difficult to forecast with certainty.

Finalising with a suitable partner is paramount rather than

completing an agreement with an unsuitable partner in

order to make a pre-announced deadline. However with

the increasing sales, increasing gross profit and lower R&D

spend, we are confident of break-even in the FY2019 year

independent of licensing income from additional agreements.

We highly value the support of our shareholders, many of

whom we know personally or who are AFT customers that

we are able to speak with at the various trade displays in

Australasia. It is worthwhile to note that our main shareholders

(Atkinson Family Trust and CRG) and directors all maintain

significant exposure to AFT which we believe indicates

confidence in the Company’s prospects.

We remain highly committed to commercialising our

Key Innovative Products which, once achieved, will create

significant sales and profits and additionally improve healthcare

outcomes for patients around the globe. As with all

pharmaceutical development projects, there is a development

and regulatory phase prior to sales starting and then growing.

We would like to thank all stakeholders in our business and

reconfirm again that our company directors and staff are

working very hard to achieve our potential.

We are pleased to have completed our second full financial

year as a listed company and to have made further significant

progress on development and commercialisation of our

key innovative products in addition to expanding our

Australasian business.

Our operating revenues grew 16% to $80.1m, with our largest

market Australia growing at a significant 33%. Importantly,

our overall company gross profit grew by 32% as our margins

expanded from 38% in the prior year to 43% this financial year.

This has been driven by increases in sales of over the counter

(OTC) products consistent with our strategy.

Further important advancements in product development

and registrations were made during the year. While these

are not immediately apparent in FY2018 income, again

they are important building blocks for future sales growth

and profitability.

Additional out-licensing agreements were finalised for Maxigesic

during the year such that there are now 125 countries licensed

– a significant number for any pharmaceutical company.

Progress has been made on additional out-licensing

agreements for larger markets with discussions and diligence

underway, but these were not finalised during FY2018 which in

turn has impacted licensing income during this time period.

However, we are confident that additional deals will be closed

during the FY2019 time period.

Our key efforts are now shifting towards product launches in

the out-licensed territories. We have reorganised our internal

regulatory and development teams around this key task in

order to focus upon delivering these required results.

The timing of these product launches are dictated by

registration timelines and these vary considerably country by

country. Many are also dependent upon registering first in key

EU territories which creates an additional time lag. As a result,

the income flow from out-licensing deals is not immediate,

which has significantly impacted the international sales growth

(27%) during the FY2018 time period. Although we successfully

achieved registration across almost all of Europe, the process

was significantly delayed by referral to a committee of the

European Medicine Agency (EMA) called CHMP (Committee

for Medical Products in Humans). However we are now able

to get licences granted across Europe and further launches

will occur during FY2019 which will in turn drive more

significant growth in International sales.

Additionally, the granted Maxigesic registrations in Germany

and UK will allow filings in a significant number of secondary

markets such as Africa, CIS and Middle East which are also

underway during the FY2019 time period. The new market

launches are expected to continue and roll out over the next

four to five years which is important to drive a significant

increase in International sales.

Maxigesic IV development in adults has essentially been

completed with successful conclusion of the pivotal large

clinical study in USA. The first filings have already been made

as previously targeted and further filings will be completed

over this coming FY2019 year. Licensing agreements for this

product have the potential to deliver more significant licensing

payments and discussions and diligence now are underway

in order to achieve these goals.

Development has continued successfully for further dose

forms of Maxigesic. The Maxigesic Oral Suspension large clinical

study has been completed and further regulatory filings will be

made during this FY2019 year. Further work continues on

Maxigesic Sachets and Maxigesic PE formulations which will

be concluded in the FY2019 time period. Additionally,

technology has been licensed from a USA company to develop

a faster acting version of Maxigesic with the initial development

work concluded. Additional Intellectual Property (IP) has been

also developed around the new dose forms which will be useful

in protecting the overall Maxigesic brand.

Overall we have made significant progress with Maxigesic

but the contribution to sales will only become apparent as

launches are increased from the current 10 countries to at least

125 countries. Additionally the new dose forms will then further

drive sales growth.

Development work with other Key Innovative Products has

proceeded well with our NasoSURF pre-IND meeting held

with FDA for the first major indication. Following the FDA

meeting feedback which clarifies the development process,

we are targeting filing of an application for type IIa medical

device registration towards the end of this calendar year.

Once achieved, this allows initiation of formal out-licensing

negotiations. Market research in USA and UK identified

that our first targeted indication has a significant potential

income stream.

David Flacks

CHAIRMAN

Hartley Atkinson

FOUNDER AND CEO

Maxigesic IV

development in

adults has essentially

been completed with

successful conclusion of

the pivotal large clinical

study in USA.

Gross profit up

32%

AFT PHARMACEUTICALS LIMITED

Annual Report 2018

89CHAIRMAN AND CEO’S REPORT

Full year financial
results summary

The FY2018 results reflect the ongoing strategy

of expanding our presence in our home markets of

Australia, New Zealand and Southeast Asia, while

succeeding in our key Research and Development

programmes for our innovative products to also

grow our international revenues.

Operating revenues grew 16% to $80.1m. Australia, our

largest market, grew by 33%. New Zealand declined by

7%. Southeast Asia grew 28% and Rest of World grew 27%.

Gross margin improved by 5% to 43%. The main driver was

from the growth in over the counter (OTC) revenues in

Australia and New Zealand.

Licensing income comprises the milestone payments received

from out licensing arrangements we have in our Rest of World

markets and the fees we have received from the divestment

of non-core hospital products. It is classified in the financial

statements as other income. This remained in the same range

as prior year at $1.8m (PCP $1.6m), with a combination of new

out licensing agreements commencing and milestone payments

on existing agreements, together with the divestment fees.

Research and development declined to 10% of revenues

as we completed the significant proportion of our current

development programme of our key products. Selling and

distribution declined to 36% of revenue supporting the

OTC products in Australia, New Zealand and Southeast Asia.

In total, operating expenses represented 58% of revenue

(PCP 63%).

These factors culminated in the reduction in the operating

loss for the year to $10.1m.

Operating revenue

Operating revenue grew 16% to $80.1m for the year

ended 31 March 2018 from $69.2m for the year ended

31 March 2017 due primarily to the growth in our

primary Australian market.

The following tables set out the revenues from our

four markets:

0

10

20

30

40

50

Rest of

World

South

East Asia

New

Zealand

Australia

Net revenue FY2017

(NZ$m)

Net revenue FY2018

(NZ$m)

0

10

20

30

40

50

Rest of

World

South

East Asia

New

Zealand

Australia

SUMMARY FINANCIAL RESULTS

(For the year ended 31 March 2018)

$NZ000’s 20182017

Revenue80,07169,205

Cost of sales(4 5,8 8 0)(4 3, 2 07 )


Gross profit34,19125,998

Other income2,235 2,659

Selling and distribution expenses(28,533)(25,964)

General and administrative expenses(8,308)(5,851)

Research and development expenses(8,230)(11,227)

Equity accounted loss of joint venture entity(1,494)(414)

Operating loss(10,139)(14,799)


Australia


New Zealand


Rest of World


Southeast Asia

33.8%

1.6%

3.1%

61.4%

42.1%

1.5%

2.8%

53.6%

Operating revenues

FY2018

$80.1m

16%

Overall revenue by market FY2017

(Percentage)

Overall revenue by market FY2018

(Percentage)

AFT PHARMACEUTICALS LIMITED

Annual Report 2018

1011FULL YEAR FINANCIAL RESULTS SUMMARY

Australia revenue grew by 33% to $49.2m (PCP $37.1m) and
this market now makes up 61% of group operating revenue.

With strong growth in its main OTC channel, Maxigesic

revenues grew by 65% with significant growth from 1 February

2018 following the regulatory shift of codeine based painkillers

from OTC to prescription only. Other core products such as the

Ferro range, Eyecare range and other pain range also grew

well. The hospital channel again had strong growth and these

two channels drove the growth.

New Zealand revenue declined 7% down to $27.1m (PCP

$29.2m) and now represents 34% of the group operating

revenue. The decline was due to AFT ceasing the sole supply

tender product Metoprolol in FY2018. OTC sales recovered this

year following the small decline in the Pharmacy channel in the

previous year, which is pleasing given the higher margins in

OTC products. This assisted an increase of 19% in gross profit

compared with prior year. The hospital channel had good

growth over a wide range of products.

Southeast Asia revenue grew by 28% to $1.3m (PCP $1.0m) and

this market stays steady at 1.6% of group operating revenue.

Sales were predominantly in the Singapore market where

product registration is generally quicker to obtain. The hospital

channel still accounts for most of the revenue from this market.

That said, OTC grew at 48% and we expect more of the growth

to come from this channel going forward.

Rest of World revenue grew by 27% to $2.5m (PCP $2.0m)

and this market now makes up 3.1% of the group operating

revenue. Most of the revenues are from sales and royalties

of Maxigesic. For example, sales to the United Arab Emirates

have grown by 30%, while in Italy in market sales made by

the licensee have grown well. Launches are also dictated by

regulatory timelines which influence the new market timelines.

These were negatively impacted by slower than expected

registrations in the EU. However these registrations have now

been achieved and launches are anticipated to get back on

track this current financial year.

Gross margin

Gross margin of 43% for FY2018 improved by 5% from 38%

for FY2017. The main drivers for the improvement were from

the growth in OTC revenues primarily in Australia and to a

lesser extent by the OTC revenue recovery in New Zealand.

The OTC channel has the highest gross margin. The growth

in gross margin is expected to continue as the Australian and

Rest of World OTC revenues grow.

Other income

Licensing income comprises the milestone payments received

from out licensing arrangements we have in our Rest of World

markets and the fees we have received from the divestment

of non-core hospital products. It is classified in the financial

statements as other income. This remained in the same range

at $1.8m (PCP $1.6m), with a combination of new out licensing

agreements commencing and milestone payments on existing

agreements, together with the divestment fees.

Operating overheads

Total research and development investment reduced to

$9.7m (PCP $11.6m). This includes the $1.5m spend on

Pascomer which under IFRS accounting standards we are

required to record as joint venture equity accounted loss in

the consolidated income statement. A large portion of total

research and development spend was on the Maxigesic IV

clinical trial in the United States which has now concluded

with strongly positive results.

Selling and distribution expenses increased to $28.5m

(PCP $25.9m). However, these expenses declined as a

percentage of operating revenue to 36% (PCP 38%).

They comprise primarily the support of OTC products in

the Australia, New Zealand and Southeast Asia markets.

General and administration expenses increased to $8.3m

(PCP $5.9m) primarily due to one off legal costs incurred

relating to competitor legal action challenging certain

Maxigesic claims. AFT remains confident of its legal position

with the outcome of the claims due during FY2019.

Balance sheet

Total assets of $56.6m (PCP $58.3m) have reduced primarily

due to the investment made into research and development.

Working Capital requirements remained the same at $22.9m

with close management of inventory levels and debtor

management.

The cash position of $6.8m at 31 March 2018 (PCP $15.9m)

reflects primarily the $12.7m loss due to investment into

research and development, the US$5m drawdown under

the debt facility and the $1.1m equity raise from the share

placement in May 2017.

The balance sheet is primarily working capital driven.

Intangible assets are growing and are now $5.1m (PCP $2.5m).

This year, we have capitalised $2.5m of development costs

which relate to the new delivery forms of Maxigesic.

The balance of intangible assets comprise capitalised

patents and trademarks. The investment in the Pascomer

joint venture entity has increased to $2.1m (PCP $0.6m)

with spend of $3.0m on product development.

The Company is pleased to note that, given their satisfaction

with the progress of the company, CRG the holder of the

long term loan to AFT has removed the requirement for any

repayment of the loan prior to its maturity in March 2020

and has made available a further US$5m draw down at the

Company’s option prior to 30 September 2018.

OTC products already launched in FY2017 will continue to

drive sales growth in Australia. The codeine opportunity,

whilst being difficult to accurately forecast, is significant given

that 750 million tablets of codeine-based OTC products were

sold in Australia every year. In New Zealand, Medsafe have

announced a similar codeine rescheduling which will occur

in the 2020 year. This will again offer a further opportunity

to expand Maxigesic sales in our New Zealand market.

Australia revenue

grew by 33% to $49.2m

(PCP $37.1m) and this

market now makes

up 61% of Group

Operating Revenue.

Rest of World revenue

grew by 27% to $2.5m

(PCP $2.0m) and

this market now makes

up 3.1% of Group

Operating Revenue.

AFT PHARMACEUTICALS LIMITED

Annual Report 2018

1213FULL YEAR FINANCIAL RESULTS SUMMARY

Australia’s Therapeutic Goods Association (TGA) confirmed
an interim decision that shifted codeine based painkillers

from being an over the counter (OTC) product in Australia

to a prescription only product. This change consequently

commenced on 1 February 2018 despite opposition from

incumbents and vested interest groups. We have also now

seen in New Zealand an announcement that Medsafe has a

similar codeine rescheduling which will occur in the 2020 year.

The switch in Australia offered a significant sales upside for

Maxigesic as consumers sought an alternative OTC analgesic

after the rescheduling of OTC codeine. Evidence of consumers

stock-piling codeine ahead of 1 February emerged which

delayed the uptake of alternatives such as Maxigesic. We

undertook careful evaluation of the market switch potential

and increased significantly our stockholdings of Maxigesic

which proved to be very important as sales increased

significantly around 1 February and have held up subsequently.

Our sales force in Australia has worked very hard and with

great passion to outline the benefits of Maxigesic to pharmacy

in Australia. This has resulted in great support at pharmacy

which translated to Maxigesic being the leading Paracetamol-

Ibuprofen combination after the switch date. Although there

is another combination of Paracetamol-Ibuprofen in the

market the Maxigesic combination cannot be copied as it

is patent protected in Australia until around mid-2028.

Consequently a number of different brands of the alternative

combination are available. However Maxigesic delivers a

greater maximum daily dose of active ingredients than

alternatives: Paracetamol 4000mg+ Ibuprofen 1200mg/day

compared with Paracetamol 1500mg+ Ibuprofen 600mg/day.

Promotion of our points of differentiation has and continues

to be important given that we do not have the promotional

budgets of some of our large multinational competitors.

However extensive work in pharmacy from our sales force

together with a different style of advertising featuring the

inventor of Maxigesic has helped us achieve significant

market share and sales on a limited budget. In fact even an

ex Australian Prime Minister was spotted purchasing a pack

of Maxigesic recently in a Melbourne pharmacy.

Growing OTC sales

AFT PHARMACEUTICALS LIMITED

Annual Report 2018

1415

Codeine rescheduling switch in Australia

significantly lifts sales

AUSTRALIA

REVENUE

CODEINE RESCHEDULING IN AUSTRALIA

$31.2m

FY2016

$ 37.1 m

FY2017

$49.2m

FY2018

NEW MARKETS. NEW OPPORTUNITIES1716AFT PHARMACEUTICALS LIMITED
Annual Report 2018

Multiple

launches in

new markets

Europe and

Asia focus

Significant progress was made during
FY2018 in completing the Maxigesic

clinical trial programme with studies

around the world: Maxigesic IV in Austin,

Texas and Baltimore, Maryland USA;

Maxigesic Junior in Hamilton and Auckland

New Zealand, Melbourne, Australia and

Guadalajara and Morelia, Mexico.

These studies require extensive

collaboration and are all managed by

AFT from New Zealand and our study

monitors visit the trial sites to ensure that

the study protocols are being followed

by the medical staff at the trial sites. Our

lead clinical trial monitor, Irenee Stewart,

has been with AFT for more than five

years and enjoys the challenge of

travelling to remote sites and interacting

with the site staff to ensure that all

aspects of the study are completed

according to tight regulatory rules of

Good Clinical Practice (GCP). Irenee was

previously an experienced nurse working

in ICU and Cardiac Care Departments at

Waikato Hospital. The importance of this

was recently emphasized when the

pivotal Maxigesic tablet study site in USA

at Austin Texas was audited by USA FDA

who unexpectedly arrived to conduct a

week long audit process reviewing all the

documentation. As expected the study

passed the audit procedure without any

major data queries but again this

emphasises the importance of good

GCP procedures.

On the formulation side, we are

collaborating with a French company

to develop a dry powder version of

Maxigesic that can be taken without

water. This is technically challenging

since the Paracetamol in Maxigesic

naturally has a bitter aftertaste and the

Ibuprofen component will result in an

irritating feeling to the throat.

Many different versions of coating have

been used and taste tested. The final

formulation has been chosen and

optimisation work is underway which has

also resulted in additional intellectual

property patent filings which is

important to protect the final product

from competitor copycat versions.

A similar approach was used for

Maxigesic IV where we partnered with a

European company to develop a stable

IV liquid formulation of Maxigesic.

Technically this was challenging as

Paracetamol tends to degrade in

solution and turns a bright yellow colour

with the formation of potentially toxic

oxidative by-products. The collaboration

was able to develop a stable Maxigesic

IV formulation which has resulted in a

further generation of IP to protect the

Maxigesic IV formulation in addition to

patents around Maxigesic IV.

A significant amount of development

work has been concluded and a key

requirement is now to complete

registration of both Maxigesic and the

line extensions globally, which is a

significant exercise. We have reorganised

our internal approach to this with the

creation of specialist regulatory

managers to drive this process.

Additionally a new Project Manager and

International QA Manager position has

been created and the position filled

through an internal promotion. Ongoing

evaluation of business requirements and

structure is of prime importance as the

process of registering and launching in

some 125 countries around the globe,

albeit with local licensees, is a significant

quantum shift for our business which has

traditionally been focused upon Australia

and New Zealand.

REGISTRATION

IN 23 EUROPEAN

COUNTRIES

ACHIEVED.

20+ PRODUCT

LAUNCHES IN

CENTRAL AMERICA

AND EUROPE.

NEW MARKET

LAUNCHES

WILL DRIVE

INTERNATIONAL

SALES OVER THE

NEXT THREE TO

FIVE YEARS.

FY2018 SAW

THE SUBSTANTIAL

COMPLETION OF

THE GLOBAL

MAXIGESIC IV

CLINICAL TRIAL

PROGRAMME.

A DRY POWDER

VERSION OF

MAXIGESIC BEING

FORMULATED.

A GLOBAL LINE

EXTENSION

FOR MAXIGESIC

PRODUCTS IS

UNDERWAY.

Development of AFT’s new nasal

delivery system, NasoSURF, is well under

way and on track for FDA and EU filings

for a Class II medical device registration

in this coming financial year.

Currently there are other ultrasonic and

mechanical nebulisers used in hospitals

but these are typically large, bulky,

requiring an external power source and

a pump or a fan to deliver generated

aerosols over a number of minutes.

The NasoSURF nebulizer in contrast

is a highly compact, efficient and

portable device driven by a cell phone

sized battery. It is used to deliver

medication to the patient via the

nose in literally a few breaths by virtue

of its patented ultrasonic transducer

and mesh technology.

Recently a Human Factor Evaluation

(HFE) study was performed in

Minneapolis (USA) involving healthcare

professionals and potential users.

The outcome of this study showed that

the general design and device

functionality was on track but a few

design enhancements were identified

that could both increase the user

experience and the clinical applicability

of the device. With this in mind, the AFT

design and technical team have used this

knowledge combined with feedback

from the FDA to further improve the

device and user experience as well as

ways to reduce the ongoing

manufacturing costs. Device

enhancement prototyping is well

underway and the manufacturing

development/commercialisation is on

schedule for the regulatory filings in the

USA and EU as planned.

We have also initiated a development

programme with a French company for a

specific formulation and dosage delivery

system that can be used together with

NasoSURF. This system will be used with

NasoSURF in the clinical development

studies for FDA which are expected to

occur this financial year.

Progressing Key

Innovative Products

NasoSURF nebuliser

An improved approach to

medicine delivery

Maxigesic development

and progress

The commercial realisation of our

licensing agreements in over 125

countries is a key focus for us in FY2019.

Registration progress was slower than

originally expected as the Maxigesic

regulatory application was considered

by CHMP, the European medicine

agency committee which resulted in a

delay of approximately nine months.

However we have achieved registration in

23 European countries with the goal to

achieve registrations in a further 12

countries this FY2019 year. This is an

important step towards achieving

revenue goals over the coming years as

Maxigesic registration must precede

product launches.

Attaining these registrations and

executing successful launches in core

markets, whilst maintaining growth in

established markets such as Italy and the

UAE will drive growth.

A key focus in FY2019 is Europe and Asia

where launches are confirmed for the

first half of this year in Malaysia,

Singapore (OTC Launch post re-

classification), and Ireland. Further

launches are planned in at least 20

countries in the Central American region

and multiple European countries.

Registration is imminent in Mexico with

our licensee partner Expanscience. We

aim to launch in the second half of this

financial year in this strong emerging

market where fast acting analgesic

combinations form a growing segment*

for the 123 million population.

Our German license has been granted

which aids registration submissions into

regions throughout CIS, MENA and

Africa as those countries rely upon this

license for the registration process.

Over the next year AFT will submit

Maxigesic line extensions for registration

with our key licensee partners to further

expand the product range and drive the

long term growth worldwide.

We expect a number of additional

licensing deals to be announced over

this FY2019 year which together with

growing Maxigesic tablet sales from

existing markets, new market launches

from existing licensees, new market

launches from new licensees and then

launches of additional dose forms, will

drive significant sales in the International

division over the next three to five years.

*Nicholas Hall report Nov 2017

International growth

for Maxigesic

AFT PHARMACEUTICALS LIMITED

Annual Report 2018

1819NEW MARKETS. NEW OPPORTUNITIES

David Flacks
CHAIRMAN AND

INDEPENDENT DIRECTOR

Appointed 22 June 2015

David has a number of

governance roles and is also a

corporate lawyer with boutique

corporate law firm Flacks &

Wong. David is chair of the

NZX Regulatory Governance

Committee, Harmoney Corp

and biotech start up Upside

Biotechnologies, and is a

director of the Vero NZ group

of companies and NZ Venture

Investment Fund.

David was chair of the NZX

Markets Disciplinary Tribunal until

June 2017 and was previously a

member of the Takeovers Panel.

He also holds a number of pro

bono directorships.

David was for many years a

senior corporate partner at Bell

Gully and was general counsel

and company secretary of

Carter Holt Harvey during the

1990’s. He is a law graduate from

Cambridge University.

Dr Hartley Atkinson

FOUNDER, EXECUTIVE DIRECTOR

AND CHIEF EXECUTIVE OFFICER

Appointed 4 September 1997

Hartley founded AFT in 1997.

Before founding AFT, Hartley

worked at Swiss multinational

pharmaceutical company, Roche,

for eight years where he held

positions as Sales & Marketing

Director, Medical Director,

Product Manager and Medical

Manager. Prior to his work at

Roche, Hartley was a Drug

Information Pharmacist and

Researcher at the Department

of Clinical Pharmacology,

Christchurch Hospital. Hartley

is the author of a number of

scientific publications. Hartley’s

work has been published in the

prestigious The New England

Journal of Medicine.

Hartley holds a Doctorate in

Pharmacology, a Masters in

Pharmaceutical Chemistry with

distinction, and a Degree in

Pharmacy, all from the University

of Otago.

Marree Atkinson

EXECUTIVE DIRECTOR

AND CHIEF OF STAFF

Appointed 4 September 2012

Marree has been involved in

all aspects of AFT’s business

since its establishment in

1997, including roles in sales,

regulatory affairs, customer

services and logistics. Marree’s

role as Chief of Staff sees her

involved in the day-to-day

running of AFT’s head office

including managing staffing

requirements and special

projects involving AFT’s head

and affiliate offices.

Marree is a registered nurse

previously practising at

Waikato Hospital.

Nathan (Nate) Hukill

NON-EXECUTIVE DIRECTOR

Appointed 14 May 2014

Nate is the President and

Chairman of CRG, a US-based

investment management firm

focused on the healthcare

industry. Mr. Hukill oversees

all aspects of the investment

process, including investment

sourcing, due diligence, portfolio

construction and portfolio

management. Mr. Hukill also

oversees the investor relations

process, including fund raising,

reporting and limited partner

relationship management.

Nate joined CRG in 2009,

bringing more than 16 years of

investing experience. Prior to

joining CRG, he was a Portfolio

Manager at Highland Capital,

where he invested and managed

approximately $4.5b in the

healthcare, consumer products,

and technology sectors.

Before Highland Capital, Nate

co-founded a pharmaceutical-

focused enterprise software

company called OpenQ, Inc.

He started his career as a credit

investor at Salomon Smith

Barney where he managed a

portfolio of approximately

$800m.

Nate holds a Bachelor of Science

in business administration from

the University of Colorado and

an M.B.A. from the Darden

Graduate School of Business at

the University of Virginia.

Jon Lamb

INDEPENDENT DIRECTOR

Appointed 4 September 2012

Jon has led the strategic

planning, marketing and

restructuring of various

companies throughout his

career. He has held various roles

at Beecham (a multinational

pharmaceutical company

that would later merge with

a predecessor company to

GlaxoSmithKline) including CEO

in New Zealand and Marketing

Manager in both Australia

and South Africa. He has also

held roles as CEO of Nylex in

New Zealand, Managing Director

within the Rural Division of

Fletcher Challenge, Director

of Southland Frozen Meats

and Marketing Director of the

New Zealand Kiwifruit Marketing

Board (where he was responsible

for creating the Zespri brand of

kiwifruit, and restructuring Zespri

into a retail focussed operation).

More recently, Jon was a Director

of Virionyx, a New Zealand

company that developed an

antiviral drug designed to

combat AIDS. He was Deputy

Chair of Australian diagnostic

company ATF Group that

developed a real time tool for

measuring the Hepatitis B virus in

individual patients.

Jon has been involved with

AFT since 2004, firstly as a

consultant, and then in his

current capacity as a director.

Jon is a Member of the Institute

of Directors and has a Diploma

from the Marketing Institute

of the UK (now the Chartered

Institute of Marketing).

Dr John Douglas (Doug) Wilson

INDEPENDENT DIRECTOR

Appointed 4 September 2012

Doug was an Associate Professor

at the Auckland Medical School

before taking a role as Senior

Vice President and Head of

Medicine and Regulatory Affairs

in the US for German drug

company Boehringer Ingelheim

Pharmaceuticals. He then carried

these same responsibilities to

Boehringer’s worldwide medical

research group in Germany,

overseeing all research and drug

development programmes. He

supervised sixteen drugs to

the US market through FDA

and many others into global

markets. Since his return to

New Zealand, Doug has been

a consultant to pharmaceutical

and biotech companies in New

Zealand, Australia, Italy, the

UK, Ireland and New York. He

has been a director of Neuren

Pharmaceuticals, of a drug

discovery company Phylogica

in Perth Australia, and until last

year a director of Adherium –

a medical device company.

He is currently Chief Medical

Officer of Ferghana Partners,

an investment bank in the

health care space in New York

and London.

Doug has a medical degree

from New Zealand, is a Fellow

of the Royal Australian College

of Physicians, a Fellow of the

College of Pathologists of

Australia and has a PhD from the

University of London.

Dr James (Jim) Burns

INDEPENDENT DIRECTOR

Appointed 17 September 2015

Jim has extensive executive

experience in pharmaceuticals,

biotechnology, medical devices,

and diagnostics. Jim has served

in leadership roles at large

multinational corporations,

early-stage companies, venture

capital funds and private equity.

From 2009-2016, Jim served

as Chairman of the Board,

Executive Chairman and

Chief Executive Officer of

Assurex Health, a precision

medicine company focused

on neuropsychiatric and pain

disorders. Previous roles include

President and CEO of cancer

drug development company

CASI Pharmaceuticals; President

of MedPointe Pharmaceuticals,

a specialty pharmaceutical

company; President and CEO of

biotechnology company Osiris

Therapeutics; General Partner

of Healthcare Ventures; Group

President of Becton Dickinson, a

global medical device company;

and Partner at Booz & Company,

an international strategy

consulting firm.

Jim is a Board Leadership Fellow

of the National Association of

Corporate Directors (NACD), a

Director of Vermillion (NASDAQ),

and a Director of Precera

Bioscience. Jim earned B.S.

and M.S. degrees in biological

sciences from the University of

Illinois, an M.B.A. from DePaul

University, and a D.L.S. from

Georgetown University.

Governance

Directors and management team

AFT has an experienced and balanced Board with a diverse range of skills.

The Board comprises an independent Chairman, three other independent

directors, one non-executive director and two executive directors. Their

names and information about their skills, experience and background,

together with information about AFT’s management team, are set out below.

Board of Directors

21AFT PHARMACEUTICALS LIMITED

Annual Report 2018

20DIRECTORS AND MANAGEMENT TEAM

Malcolm Tubby
CHIEF FINANCIAL OFFICER

Malcolm is a qualified Chartered

Accountant in the United

Kingdom and New Zealand with

a wealth of senior corporate

governance expertise in the

commerce sector including roles

in significant public companies

as Chief Financial Officer. He has

experience in senior positions

in public and private companies

in pharmaceuticals, beverages,

insurance and aged care facilities

in Australia and New Zealand.

Malcolm has been involved in the

AFT board since its foundation.

Malcolm is also the CFO for

AFT Pharmaceuticals.

Ioana Stanescu

HEAD OF DRUG DEVELOPMENT

Ioana has overall responsibility

for the research and development

functions of the Company.

She has more than 20 years’

experience in the pharmaceutical

industry with previous positions,

including VP QA & Regulatory

Affairs, Head of Vaccine Business

Area at FIT Biotech Ltd, and

a World Health Organisation

adviser performing institutional

assessments of National

Regulatory Authorities within

Central and Eastern Europe.

She has coordinated a variety of

European FP6 and FP7 funded

research grants. In 1999 she was

selected as an Expert by the

European Health Committee –

Council of Europe to participate

in the coordinated research

study of viral inactivation of

labile blood products. She is

also a Member of the European

QP Association.

Vladimir Ilievski

REGULATORY AFFAIRS MANAGER

Vladimir was born and raised in

Macedonia. He holds a master’s

degree in Pharmacy from the

University of Ljubljana, Slovenia,

where he started his career as

a pre-clinical researcher before

moving to New Zealand. Prior

to joining AFT Pharmaceuticals,

Vladimir worked for Douglas

Pharmaceuticals in various

roles including as QC and QA

analyst and regulatory/senior

regulatory associate. He joined

AFT Pharmaceuticals in 2006

as Regulatory Affairs Manager.

Vladimir has responsibility for

product registrations in various

countries such as New Zealand,

Australia, South-East Asia

(Malaysia, Singapore, Hong

Kong, Philippines) as well as the

European Union and USA.

Louise Clayton

DIRECTOR INTERNATIONAL

BUSINESS

Louise has worked with brands

within the supplement, OTC,

Health, and Beauty Channels.

Her experience has given

her the opportunity to drive

international brands through a

variety of management roles

encompassing sales, brand

marketing, product sourcing/new

product development, and new

market expansion. She has over

20 years’ functional experience

with International business, key

accounts, sales and marketing

teams, with a core focus on

brand growth and development

within local and International

markets such as Australia, US,

Asia, UK, and ROW.

Calvin Mackenzie

GENERAL MANAGER AUSTRALIA

Calvin joined AFT in February

2010 and has since led

AFT’s Australian team and is

responsible for AFT’s business

in Australia. Calvin has over

20 years’ experience in the

pharmaceutical industry in a

diverse range of roles with a

pharmacy, medical and specialist

focus for brand originator and

generic companies including

Johnson & Johnson, Janssen

Cilag, Arrow and Sigma. Calvin

has significant experience in

building high-performing sales

teams.

Scott Crawford

GENERAL MANAGER –

PROMOTED PRODUCTS

AUSTRALASIA & SOUTHEAST ASIA

Scott joined AFT in March 2013

and is responsible for the OTC

sales in New Zealand across

all retail channels including

pharmacy, supermarkets

and petrol & convenience.

His role involves the account

management, field supervision

and trade marketing. Scott has

over 20 years’ experience in

fast-moving consumer goods in

both Australia and New Zealand

and has previously held roles with

Red Bull and Ferrero Rocher.

Murray Keith

GROUP MARKETING MANAGER

Murray joined AFT in October

2011 and has since been

responsible for managing the

marketing function of AFT, with

a primary focus on the Australian

and New Zealand markets.

His extensive marketing career

prior to joining AFT includes

roles within Nestlé, Lion Nathan,

Bay of Plenty Rugby, Nestlé

Purina, New Zealand Lotteries

and Fonterra Brands (Tip Top).

Management team

23AFT PHARMACEUTICALS LIMITED

Annual Report 2018

22DIRECTORS AND MANAGEMENT TEAM

Corporate GovernanceSustainability
CORPORATE GOVERNANCE2524AFT PHARMACEUTICALS LIMITED

Annual Report 2018

The Board and management of AFT Pharmaceuticals Limited

(AFT or the Company) are committed to ensuring that AFT

maintains corporate governance practices in line with best

practice and adheres to the highest ethical standards.

The Board has had regard to the NZX Listing Rules and a

number of corporate governance recommendations when

establishing its governance framework, including the latest

Australian Securities Exchange (ASX) Corporate Governance

Council Principles and Recommendations (notwithstanding

AFT is not required to follow these recommendations due to

its ASX Foreign Exempt Listing) and the revised NZX

Corporate Governance Code 2017 (NZX Code).

The NZX Listing Rules require AFT to formally report its

compliance against the recommendations contained in the

NZX Code. How AFT has implemented these recommendations

is set out in AFT’s Corporate Governance Statement.

The Board considers that AFT’s corporate governance

structures, practices and processes have followed all of the

recommendations in the NZX Code in the financial year to

31 March 2018.

AFT’s Corporate Governance Statement and governance

charters and policies can be found on the investor centre of

the Company’s website – investors.aftpharm.com/Investors/.

AFT’s corporate governance charters and policies have been

approved by the Board and are regularly reviewed by the

Board and amended (as appropriate) to reflect developments

in corporate governance practices.

STOCK EXCHANGE LISTINGS

AFT is listed on the New Zealand Stock Exchange (NZX Main

Board) and on the Australian Securities Exchange (ASX) as an

ASX Foreign Exempt Listing. As an ASX Foreign Exempt

Listing, AFT needs to comply with the NZX Listing Rules

(other than as waived by NZX) but does not need to comply

with the vast majority of the ASX Listing Rule obligations.

AFT is incorporated in New Zealand.

For us, sustainability means aligning our goals with the

interests of society. We believe that by acting sustainably we

contribute positively towards the development of the world.

The Sustainable Development Goals (SDGs) are a set of global

initiatives set up by the United Nations for everyone to

contribute to. For AFT, the SDGs are a way to see which areas

of sustainability we are directly contributing to and how our

community initiatives relate to a larger vision for positive

change. AFT’s Environmental, Social and Corporate

Governance (ESG) framework remains under development and

will continue to be progressed over time.

OVERVIEW OF AFT’S

GOVERNANCE STRUCTURE

The AFT Board of Directors has been appointed by

shareholders to protect and enhance the long-term value

of AFT and to act in the best interests of AFT and all of its

shareholders. The Board is the ultimate decision-making

body of the Company and is responsible for the corporate

governance of the Company. The role and responsibilities

of the Board are set out in the Board Charter, which can be

found on the investor centre of the Company’s website.

The Board currently comprises an independent non-executive

chair, three other independent non-executive directors, one

non-executive director and two executive directors, as detailed

on pages 20 and 21 of this Annual Report.

The Board has established three standing Board Committees

to assist in the execution of its responsibilities:

• an Audit and Risk Committee;

• a Remuneration and Nominations Committee; and

• a Regulatory and Product Development Oversight

Committee.

Details of the roles and responsibilities of these committees

are described in their respective charters, which can be found

on the investor centre of the Company’s website.

AFT has been committed to sustainability for many years and

contributes to a number of the 17 SDG’s identified by the United Nations.

Providing medicines

for a diverse range

of patients

• 29 AFT products on the World Health Organisation Model

list of essential medicines

• Products range from juvenile- to aged-specific

• Products distributed for use in hospitals, prescription and

general medicines

Innovating

medicines to

improve the

health of our

end customers

• Developing products that we genuinely believe will improve

the health of our end customers.

• Repurposing existing approved pharmaceuticals to minimise

risk to user of our products

• Innovating new delivery methods for improved delivery of

medication. For example, via the development of the NasoSURF.

Providing medicines

solutions for

under-privileged or

under-represented

groups

• Making medicines available for rare diseases, designated with

orphan status under the US Food and Drug Administration.

• Donate medicines to under-privileged groups, such as patients

in the Pacific Islands.

• Work with government agencies to make specific medicines

available to under-privileged groups.

Being a

trustworthy

partner

• All of our critical product suppliers have been risk assessed.

• 20 or so partnerships in Pharmaceuticals

Protecting the

environment

• Donating product that would otherwise be wasted to

charity organisations

• Working with suppliers (within regulatory guidelines) to

reduce packaging or use eco-packaging, wherever possible

while preserving the integrity of the product

Delivering

continued

growth

• 16% growth in operating revenues

• Significant reduction in operating losses

Providing a

great work

place

• Diversity in the workplace with 22 cultures represented

amongst the staff of 88

• 61% of staff are female with 40% of senior executives female

Enhancing lives in Fiji
An ESG case study

FINANCIAL STATEMENTS2726AFT PHARMACEUTICALS LIMITED

Annual Report 2018

June 2017, the New Zealand pharmacy sales team

went to Suva Fiji to assist our local Fiji distributor to

utilise some of our excess inventory from New Zealand

to enhance the lives of the less fortunate in Fiji.

Lice is a major issue in Fiji so we distributed lice

treatments to Fiji schools through the federal

government body. We also provided this to other

Fiji government institutions such as hospitals,

prisons and the military barracks.

The New Zealand sales team donated their time

to help educate healthcare professionals in Suva.

Tina Boyes, Jamie Lee Rummins

and Rebecca Rodonich with

women and children from the

poverty campaign.

Financial

Statements.

Contents

28 Independent Auditor’s Report

31 Consolidated Income Statement

32 Consolidated Statement

of Comprehensive Income

33 Consolidated Statement

of Changes in Equity

34 Consolidated Balance Sheet

35 Consolidated Statement

of Cash Flows

36 Notes to the Financial Statements

58 Statutory Disclosures

67 Directory

FY18

Independent Auditor’s Report
To the Shareholders of AFT Pharmaceuticals Limited

OpinionWe have audited the consolidatedfinancial statementsof AFT Pharmaceuticals Limitedand

its subsidiaries (the ‘Group’), which comprise the consolidated balance sheet as at 31

March 2018, and the consolidatedincome statement, statement of comprehensive income,

statement of changes in equity and statement of cash flows for the year then ended, and

notes to theconsolidatedfinancial statements, including a summary of significant

accounting policies.

In our opinion, the accompanying consolidated financial statements, on pages 31to 57,

present fairly, in all material respects, theconsolidatedfinancial position of the Group as

at 31 March 2018, and itsconsolidatedfinancial performance and cash flows for the year

then ended in accordance with New Zealand Equivalents toInternational Financial

Reporting Standards (‘NZ IFRS’) and International Financial Reporting Standards (‘IFRS’).

Basis for opinionWe conducted our audit in accordance with International Standards on Auditing (‘ISAs’)

and International Standards on Auditing (New Zealand) (‘ISAs (NZ)’). Our responsibilities

under those standards are further described in the Auditor’s Responsibilities for the Audit

of the Consolidated Financial Statements section of our report.

We believe that the audit evidence we have obtained is sufficient and appropriate to

provide a basis for our opinion.

We are independent of the Group in accordance with Professional and Ethical Standard 1

(Revised) Code of Ethics for Assurance Practitioners issued by the New Zealand Auditing

and Assurance Standards Boardand the International Ethics Standards Board for

Accountants’ Code of Ethics for Professional Accountants, and we have fulfilled our other

ethical responsibilities in accordance with these requirements.

Other than in our capacity as auditor and the provision of taxation advice, we have no

relationship with or interests in the Company or any of its subsidiaries. These services

have not impaired our independence as auditor of the Company and Group.

Audit materialityWe consider materiality primarily in terms of the magnitude of misstatement in the

financial statements of the Groupthat in our judgement would make it probable that the

economic decisions of a reasonably knowledgeable person would be changed or influenced

(the ‘quantitative’ materiality). In addition, we also assess whether other matters that

come to our attention during the audit would in our judgement change or influence the

decisions of such a person (the ‘qualitative’ materiality). We use materiality both in

planning the scope of our audit work and in evaluating the results of our work.

We determined materiality for the Group financial statements as a whole to be $1 million.

Key audit mattersKey audit matters are those matters that, in our professional judgement, were of most

significance in our audit of the consolidated financial statements of the current period.

These matters were addressed in the context of our audit of the consolidated financial

statements as a whole, and in forming our opinion thereon, and we do not provide a

separate opinion on these matters.

2829AFT PHARMACEUTICALS LIMITED

Annual Report 2018

INDEPENDENT AUDITOR’S REPORT

Key audit matterHow our audit addressed the key audit matterand

the results of our work

Research and development costs

As disclosed in note 6 and note 12, the Group is involved in

the research and development of new products and variants of

existing products.

During the year ended31 March 2018, research and

development costs of $8,986million were incurred. Of this

total, $6,521million was expensed through profit or loss and

$2,465million has beencapitalised as intangible assets.

Judgement is required in assessing whether research and

development costs for each project should be capitalised or

expensed in accordance with the relevant financial reporting

framework.

A key consideration that impacts whether costs should be

capitalised is the technical feasibility of completing the

development of a new product, which generally includes

demonstrating approval of the product by the relevant market

regulatory authority.

In performing our procedures we:

a)understoodmanagement’s processes and controls

to assess the appropriate accounting treatment for

each project;

b)determined

whether the Group’s accounting policies

are consistent with requirements of the relevant

accounting standards;

c)obtainedan analysis from management as to the

status of each individual project and corroborated

with operational management;

d)testeda sample of costs expensed to supporting

documentation to verify the amounts being

expensed and the status of the project;

e)determined whetherthe coststested as part of our

samplein (d) should have been capitalised;

f)testeda sample of costs capitalised to supporting

documentation to verify the amounts being

capitalised and the status of the project;

g)determined whetherthe expenses tested as part of

our sample in (f) should have been expensed;

h)challenged whether management’s

treatment of the

costs is appropriate.

Other informationThe directors are responsibleon behalf of the Groupfor the other information. The other

information comprises the information in the Annual Report that accompanies the

consolidated financial statements and the audit report.

Our opinion on the consolidated financial statements does not cover the other information

and we do not express any form of assurance conclusion thereon.

Our responsibility is to read the other information and consider whether it is materially

inconsistent with the consolidated financial statements or our knowledge obtained in the

audit or otherwise appears to be materially misstated. If so, we are required to report that

fact. We have nothing to report in this regard.

Directors’ responsibilities for

the consolidated financial

statements

The directors are responsible on behalf of the Group for the preparation and fair

presentation of the consolidatedfinancial statements in accordance with NZ IFRSand

IFRS, and for such internal control as the directors determine is necessary to enable the

preparation of consolidatedfinancial statements that are free from material misstatement,

whether due to fraud or error.

In preparing the consolidatedfinancial statements, the directors are responsible on behalf

of the Group for assessing the Group’s ability to continue as a going concern, disclosing, as

applicable, matters related to going concern and using the going concern basis of

accounting unless the directors either intend to liquidate the Group or to cease operations,

or have no realistic alternative but to do so.

3031AFT PHARMACEUTICALS LIMITED
Annual Report 2018

FINANCIAL STATEMENTS

Consolidated Income Statement

For the year ended 31 March 2018

$NZ000’s Note 20182017

Revenue480,07169,205

Cost of sales(4 5,8 8 0)(4 3, 2 07 )

Gross Profit

34,19125,998

Other income

52,2352,659

Selling and distribution expenses

6(a)(28,533)(25,964)

General and administrative expenses

6(a)(8,308)(5,851)

Research and development expenses

6(a)(8,230)(11,227)

Equity accounted loss of joint venture entity

13(b)(1,494) (414)

Operating Loss

(10,139)(14,799)

Finance income125347

Finance costs

6(a)(2,652)(3,878)

Loss before tax

6(12,666)(18,330)

Tax expense

7(58)(58)

Loss after tax attributable to owners of the parent(12,724)(18,388)

Basic and diluted loss per share ($)

25(0.13)(0.19)

Independent Auditor’s Report

To the Shareholders of AFT Pharmaceuticals Limited

OpinionWe have audited the consolidatedfinancial statementsof AFT Pharmaceuticals Limitedand

its subsidiaries (the ‘Group’), which comprise the consolidated balance sheet as at 31

March 2018, and the consolidatedincome statement, statement of comprehensive income,

statement of changes in equity and statement of cash flows for the year then ended, and

notes to theconsolidatedfinancial statements, including a summary of significant

accounting policies.

In our opinion, the accompanying consolidated financial statements, on pages 31to 57,

present fairly, in all material respects, theconsolidatedfinancial position of the Group as

at 31 March 2018, and itsconsolidatedfinancial performance and cash flows for the year

then ended in accordance with New Zealand Equivalents toInternational Financial

Reporting Standards (‘NZ IFRS’) and International Financial Reporting Standards (‘IFRS’).

Basis for opinionWe conducted our audit in accordance with International Standards on Auditing (‘ISAs’)

and International Standards on Auditing (New Zealand) (‘ISAs (NZ)’). Our responsibilities

under those standards are further described in the Auditor’s Responsibilities for the Audit

of the Consolidated Financial Statements section of our report.

We believe that the audit evidence we have obtained is sufficient and appropriate to

provide a basis for our opinion.

We are independent of the Group in accordance with Professional and Ethical Standard 1

(Revised) Code of Ethics for Assurance Practitioners issued by the New Zealand Auditing

and Assurance Standards Boardand the International Ethics Standards Board for

Accountants’ Code of Ethics for Professional Accountants, and we have fulfilled our other

ethical responsibilities in accordance with these requirements.

Other than in our capacity as auditor and the provision of taxation advice, we have no

relationship with or interests in the Company or any of its subsidiaries. These services

have not impaired our independence as auditor of the Company and Group.

Audit materialityWe consider materiality primarily in terms of the magnitude of misstatement in the

financial statements of the Groupthat in our judgement would make it probable that the

economic decisions of a reasonably knowledgeable person would be changed or influenced

(the ‘quantitative’ materiality). In addition, we also assess whether other matters that

come to our attention during the audit would in our judgement change or influence the

decisions of such a person (the ‘qualitative’ materiality). We use materiality both in

planning the scope of our audit work and in evaluating the results of our work.

We determined materiality for the Group financial statements as a whole to be $1 million.

Key audit mattersKey audit matters are those matters that, in our professional judgement, were of most

significance in our audit of the consolidated financial statements of the current period.

These matters were addressed in the context of our audit of the consolidated financial

statements as a whole, and in forming our opinion thereon, and we do not provide a

separate opinion on these matters.

3233AFT PHARMACEUTICALS LIMITED
Annual Report 2018

FINANCIAL STATEMENTS

Consolidated Statement of Comprehensive Income

For the year ended 31 March 2018

$NZ000’s 20182017

Loss after tax(12,724)(18,388)

Other comprehensive income

May be subsequently reclassified to profit and loss:

Foreign currency translation reserve74356

Other comprehensive income/(loss) for the year, net of tax74356

Total comprehensive loss for the year

attributable to owners of the parent(12,650)(18,032)

Consolidated Statement of Changes in Equity

For the year ended 31 March 2018

$NZ000’s Note

Share

capital

Redeemable

preference

shares

reserve

Share

options

reserve

Foreign

currency

translation

reserve

Retained

earnings

Total

equity

Balance 31 March 201653,902 - 65(100)(25,637) 28,230

Loss after tax - - - -(18,388)(18,388)

Other comprehensive income -- -356 -356

Total comprehensive income---356(18,388)(18,032)

Issue of redeemable preference shares

179,124 - - - -9,124

Movement in share options reserve - -230 - -230

Capital raising expenses

17(82) - - - -(82)

Balance 31 March 201762,944 - 295256 (4 4,025)19,470

Loss after tax - - - -(12,724)(12,724)

Other comprehensive income - - -74 -74

Total comprehensive income---74(12,724)(12,650)

Preference dividends accumulated

17-483---483

Issue of share capital1,065----1,065

Capital raising expenses

17(266)----(266)

Movement in share options reserve - -135 - -135

Preference dividends paid or

accumulated

17----(895)(895)

Balance 31 March 201863,743483430330( 57, 6 4 4)7, 3 4 2

3435AFT PHARMACEUTICALS LIMITED
Annual Report 2018

FINANCIAL STATEMENTS

Consolidated Balance Sheet

As at 31 March 2018

$NZ000’s Note 20182017

Assets

Current assets

Inventories

824,41222,198

Trade and other receivables

916,95416,051

Cash and cash equivalents

106,77015,905

Derivative assets

20176-

Total current assets

48,31254,154

Non-current assets

Property, plant and equipment

11330386

Intangible assets

125,1182,548

Deferred income tax assets

7708610

Investment in joint venture entity

13(b)2,135 627

Total non-current assets8,2914,171

Total assets

56,60358,325

Liabilities

Current liabilities

Trade and other payables

141 7, 3 9 114,549

Provisions

151,098564

Current income tax liability118112

Derivative liabilities

20-204

Total current liabilities18,60715,429


Non-current liabilities

Interest bearing liabilities

1630,65423,426

Total liabilities49,26138,855


Equity

Share capital1763,74362,944

Retained earnings( 5 7, 6 4 4 )(44,025)

Share options reserve

19(b)430 295

Redeemable preference shares reserve483-

Foreign currency translation reserve330256

Total equity

7, 3 4 219,470

Total liabilities and equity

56,60358,325

Net tangible assets per ordinary share $0.02 $0.17

For and on behalf of the Board who authorised these financial statements for issue on 23 May 2018.

Consolidated Statement of Cash Flows

For the year ended 31 March 2018

$NZ000’s Note 20182017

Cash flows from Operating Activities

Receipts from customers79,27866,491

Interest received125347

Payments to suppliers and employees(88,296)(83,043)

Tax (paid) / received(149)16

Interest and finance cost paid(1,862)(2,873)

Net cash used in operating activities

18(10,904)(19,062)

Cash flows from Investing Activities

Purchases of property, plant and equipment(70)(122)

Purchases of intangible assets(2,783)(620)

Investment in joint venture(3,002)(856)

Net cash used in investing activities

(5,855)(1,598)

Cash flows from Financing Activities

Proceeds from issue of share capital1,0659,124

Share issue costs(188)(82)

Dividends paid(41 2)-

New borrowings

167, 1 3 5-

Net cash generated from financing activities

7, 6 0 09,042

Net decrease in cash(9,159)(11,618)

Impact of foreign exchange on cash and cash equivalents24(4 57 )

Opening cash and cash equivalents15,9052 7, 9 8 0

Closing cash and cash equivalents6,77015,905

Hartley Atkinson

Managing Director and

Chief Executive Officer

David Flacks

Chairman

3637AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

Notes to the Financial Statements

For the year ended 31 March 2018

(c) Critical accounting estimates and judgements

In preparing these financial statements the Group made estimates and assumptions concerning the future. These estimates

and assumptions may differ from the subsequent actual results. Estimates and judgements are continually evaluated and are

based on historical experience and other factors, including expectations or future events that are believed to be reasonable

under the circumstances. The recognition of deferred tax (detailed within note 7) and treatment of research and development

costs (detailed within note 12) are considered critical estimates and judgements. It is not expected that these estimates and

judgements will have a significant risk of causing a material adjustment to the carrying amounts of assets and liabilities within

the next financial year.

(d) Foreign currency translation

(i) Functional and presentation currency

Items included in the financial statements of the subsidiaries’ operations are measured using the currency of the primary

economic environment in which they operate (the ‘functional currency’). The consolidated financial statements are presented

in New Zealand dollars (NZ$), which is the Company’s functional currency and the Group’s presentation currency.

(ii) Transactions and balances

Foreign currency transactions are translated into the functional currency using the exchange rates prevailing at the dates

of the transactions. Foreign exchange gains and losses resulting from the settlement of such transactions and from the

translation at year end exchange rates of monetary assets and liabilities denominated in foreign currencies, are recognised

in the income statement.

(iii) Foreign operations

The results and balance sheets of all foreign operations (none of which has the currency of a hyperinflationary economy)

that have a functional currency different from New Zealand dollars are translated into the presentation currency as follows:

• assets and liabilities for each balance sheet presented are translated at the closing rate at the date of that balance sheet

• income and expenses for each income statement and statement of comprehensive income are translated at average

exchange rates, unless this is not a reasonable approximation of the cumulative effect of the rates prevailing on the

transaction dates, in which case income and expenses are translated at the dates of the transactions.

• exchange differences arising are recognised in other comprehensive income and accumulated in equity.

(e) Revenue recognition

Revenue comprises the fair value for the sale of goods, excluding Goods and Services Tax (GST), rebates and discounts.

• The sales of goods are recognised when the product is delivered to the customer.

• Royalties are recognised when licencees have made sales of product which attract royalties to the Company.

(f) Other income recognition

Other income comprises research and development grant and licensing income:

• Research and development grant

Research and development grant income is recognised when eligible research and development expenses are incurred and

conditions relating to the grant are satisfied.

• Licencing income

Licencing income comprises milestone payments due under licencing agreements. Milestone payments represent a minor

portion of the economic benefits of the licencing agreements (the primary benefits being the sale of product and royalties

earned on licensee sales). The milestones are recognised as income according to the terms of each licencing agreement.

(g) Finance income recognition

Finance income comprises interest income that is recognised on a time-proportion basis using the effective interest method.

1. General information

AFT Pharmaceuticals Limited (the “Company”) is a company that is incorporated and domiciled in New Zealand. It is

registered under the Companies Act 1993. These financial statements comprise AFT Pharmaceuticals Limited and its

subsidiaries (together referred to as the “Group”). The Group is a pharmaceutical distributor and developer of

pharmaceutical intellectual property.

The financial statements of the Group have been prepared in accordance with the requirements of the Companies Act 1993,

Financial Reporting Act 2013 and the Financial Markets Conduct Act 2013. As Group financial statements are prepared and

presented for AFT Pharmaceuticals Limited and its subsidiaries, separate financial statements for AFT Pharmaceuticals

Limited are not required to be prepared under the Companies Act 1993.

These financial statements are authorised for issue on 23 May 2018 by the directors.

2. Statement of accounting policies

The financial statements have been prepared under the historical cost convention with the exception of derivative

instruments revalued to fair value.

(a) Basis of preparation

The consolidated financial statements of the Group have been prepared in accordance with Generally Accepted Accounting

Practice in New Zealand (NZ GAAP). The Group is a for-profit entity for the purposes of complying with NZ GAAP.

The consolidated financial statements comply with New Zealand equivalents to International Financial Reporting Standards

(NZ IFRS), other New Zealand accounting standards and authoritative notices that are applicable to entities that apply

NZ IFRS. The consolidated financial statements also comply with International Financial Reporting Standards (IFRS), and

interpretations issued by the IFRS Interpretations Committee (IFRS IC) applicable to companies reporting under IFRS.

The accounting policies presented below have been applied consistently to all periods presented in these consolidated

financial statements.

The reporting currency used in the preparation of these consolidated financial statements is New Zealand dollars,

rounded where necessary to the nearest thousand dollars.

(b) Principles of consolidation

Subsidiaries

The consolidated financial statements incorporate the assets and liabilities and the results of the parent and its subsidiaries

controlled at year end.

Subsidiaries are all entities over which the Group has control. The Group controls an entity when the Group is exposed to,

or has rights to, variable returns from its involvement with the entity and has the ability to affect those returns through its

power over the entity. Subsidiaries are fully consolidated from the date on which control is transferred to the Group.

They are deconsolidated from the date that control ceases.

The acquisition method of accounting is used to account for the subsidiaries of the Group. The cost of an acquisition is

measured as the fair value of the assets given, equity instruments issued and liabilities incurred or assumed at the date

of exchange. Identifiable assets acquired and liabilities and contingent liabilities assumed in a business combination are

measured initially at their fair values at the acquisition date. The excess of the cost of acquisition over the fair value of

the Group’s share of the identifiable net assets acquired is recorded as goodwill. If the cost of acquisition is less than the

Group’s share of the fair value of the identifiable net assets of the subsidiary acquired, the difference is recognised

in profit or loss.

Inter-company transactions, balances and unrealised gains on transactions between subsidiary companies are eliminated.

Unrealised losses are also eliminated unless the transaction provides evidence of the impairment of the asset transferred.

Joint venture

Where the Company has joint control in a joint venture, the principles of equity accounting are adopted. In these cases, the

Company’s investment is recognised in the balance sheet and its share of after tax profits less losses of the joint venture are

recognised in the profit and loss, with the value of the Company’s investment carrying value adjusted accordingly.

3839AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

2. Statement of accounting policies (continued)

(h) Property, plant and equipment

All plant and equipment is stated at historical cost less depreciation and any impairment losses. Historical cost includes

expenditure that is directly attributable to the acquisition of the items. Subsequent costs are included in the asset’s carrying

amount or recognised as a separate asset, as appropriate, only when it is probable that future economic benefits associated

with the item will flow to the Company and Group and the cost of the item can be measured reliably. All other repairs and

maintenance are charged to the income statement during the financial period in which they are incurred.

Depreciation of property, plant and equipment is calculated using the diminishing value method which apportions the cost of

the assets over their useful lives. The Group has the following classes of property, plant and equipment and depreciation rates:

Category Depreciation rate (%)

Plant and machinery 21% to 80%

Furniture and fixtures 9% to 60%

Vehicles 26% to 36%

An asset’s carrying amount is written down immediately to its recoverable amount if the asset’s carrying amount is

greater than its estimated recoverable amount.

Gains and losses on disposal are determined by comparing proceeds to carrying amounts and are included in the

income statement.

(i) Intangible assets

Finite useful life

Acquired patents, capitalised development costs and software have a finite life and are carried at cost less accumulated

amortisation. Patents are amortised over a useful economic life of 20 years, capitalised development costs over the life of

the relevant patent or period of expected benefit, and software over 3 – 4 years.

Indefinite useful life

Acquired trademarks are considered to have indefinite useful lives whilst they continue to protect revenue streams.

Trademarks are carried at cost less accumulated impairment. Indefinite useful life assets are tested for impairment annually

or when impairment indicators exist. The asset’s carrying amount is written down immediately to its recoverable amount if

its carrying amount is greater than its estimated recoverable amount.

(j) Goods and services tax (GST)

The income statement and the statement of comprehensive income have been prepared so that all components are stated

exclusive of New Zealand, Australian and Malaysian GST. All items in the balance sheet are stated net of GST, with the

exception of accounts receivable and payable, which include GST invoiced. All components of the statement of cash flows

are stated exclusive of GST.

(k) Income tax

The income tax expense recognised for the period is based on the accounting profit or loss, adjusted for non-taxable and

non-deductible differences.

Current tax is calculated by reference to the amount of income tax payable, calculated using tax laws that are enacted or

substantively enacted at balance date.

Deferred income tax is recognised on temporary differences arising between the tax bases of assets and liabilities and their

carrying amounts in the financial statements. Deferred income tax is determined using tax rates (and laws) that have been

enacted or substantively enacted by the balance sheet date and are expected to apply when the related deferred income tax

asset or liability is settled. Deferred income tax assets are recognised to the extent that it is probable that future taxable profit

will be available against which the temporary differences can be utilised.

(l) Inventories

Inventories are stated at the lower of cost and net realisable value. Cost is determined on a weighted average cost basis.

Net realisable value is the estimated selling price in the ordinary course of business less the estimated costs of completion

and the estimated costs necessary to make the sale.

(m) Leased assets

Operating leases are those in which all the risks and rewards are substantially retained by the lessor. Lease payments are

charged in the income statement on a straight line basis over the term of the lease.


(n) Trade receivables

Trade receivables are recognised initially at fair value and subsequently measured at amortised cost, less provision for

doubtful debts and provision for customer rebates. Bad debts are written off in the year in which they are identified.

Collectibility of trade receivables is reviewed on an ongoing basis. Debts which are known to be uncollectible are written off.

A provision for doubtful receivables is established when there is objective evidence that the Group will not be able to collect

all amounts due according to the original terms of receivables. The amount of the provision is the difference between the

asset’s carrying amount and the present value of estimated future cash flows, discounted at the effective interest rate.

The amount of the provision is recognised in the income statement.

(o) Trade payables

These amounts represent liabilities for goods and services provided to the Group prior to the end of the financial period

which are unpaid. These amounts are incurred and are usually paid within 30 days of recognition.

(p) Borrowings

Borrowings are initially recognised at fair value plus transaction costs incurred. Borrowings are subsequently measured at

amortised cost. Any difference between the proceeds (plus transaction costs) and the redemption amount is recognised

in the income statement over the period of the borrowings using the effective interest method.

Borrowings are classified as current liabilities unless the Group has an unconditional right to defer settlement of the liability

for at least 12 months after the balance sheet date. Borrowing costs are expensed as incurred.

(q) Share capital

Ordinary shares, and the now-converted preferred shares, are classified as equity. Both carried equal voting rights.

Preferred shares attracted a dividend yield. Redeemable preference shares also form part of share capital.

(r) Cash and cash equivalents

Cash and cash equivalents includes cash on hand, deposits held at call with financial institutions, other short term investments

with original maturities of three months or less that are readily convertible to known amounts of cash and which are subject to

an insignificant risk of change in value, and bank overdrafts. Bank overdrafts are shown within borrowings in current liabilities

on the balance sheet.

(s) Employee entitlements

Liabilities for wages and salaries, including non monetary benefits, annual leave, and accumulating sick leave expected to be

settled within 12 months of the reporting date are recognised in trade payables or provisions in respect of employees’ services

up to the reporting date and are measured at the amounts expected to be paid when the liabilities are settled. Liabilities for

non-accumulating sick leave are recognised when the leave is taken and measured at the rates paid or payable. The liability

for employee entitlements that are not expected to be settled within 12 months is carried at the present value of estimated

future cash flows. Staff share options are valued at fair value as calculated independently using the Black Scholes model.

(t) Impairment of non-financial assets

Assets are reviewed for impairment whenever events or changes in circumstances indicate that the carrying amount may

not be recoverable. An impairment loss is recognised for the amount by which the asset’s carrying amount exceeds its

recoverable amount. The recoverable amount is the higher of an asset’s fair value less costs to sell and value in use. For the

purposes of assessing impairment, assets are grouped at the lowest levels for which there are separately identifiable cash

flows (cash generating units). Indefinite useful life assets are tested for impairment annually and whenever there are indicators

of impairment while finite useful life assets are tested only when there are indicators of impairment.

(u) Derivative financial instruments

The Group benefits from the use of derivative financial instruments to manage foreign currency exposures. The fair value

of forward exchange contracts is calculated using discounted cashflows by reference to contractual exchange rates for

contracts in place and the forward exchange rate at year-end, considered level 2 of the fair value hierarchy.

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

4041AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

2. Statement of accounting policies (continued)

(v) Research and development

Research is the original and planned investigation undertaken with the prospect of gaining new knowledge and understanding.

This includes: direct and overhead expenses for research, pre-clinical trials and costs associated with clinical trial activities.

All research costs are expensed when incurred.

Development is the application of research findings to a plan or design for the production of new or substantially improved

processes or products prior to the commencement of commercial production. When a project reaches the stage where it is

reasonably certain that future expenditure can be recovered through the process or products produced, expenditure that is

directly attributable or reasonably allocated to that project is recognised as a development asset. The asset will be amortised

from the date of commencement of commercial production of the product to which it relates on a straight line basis over

the life of the relevant patent or period of expected benefit. Development assets are reviewed annually for any impairment

in their carrying value.

(w) Earnings per share

Basic earnings per share is computed by dividing net earnings by the weighted average number of ordinary shares

outstanding during each period. Preferred shares are considered to be anti-dilutive for the earnings per share calculation.

(x) Change in classification

During 2018, the Group modified the classification of provisions for customer rebates from “Provisions” to “Trade and

Other Receivables” to reflect more appropriately the receipts expected from customers.

Comparative amounts in the Balance Sheet were restated for consistency. As a result, for FY2017, $3,386k was reclassified

from “Provisions” to “Trade and Other Receivables”. Additionally, $75k which is held on term deposit for an NZX bond has

been reclassified from “Cash” to “Prepayments”.

(y) Correction of error

During 2018, the Group determined that goods in transit should be accounted for according to Incoterms, other than for

specific ownership terms in the contracts. Previously, the Group recognised inventory once it had inspected and accepted

the goods as per its rights under the contracts. As a result of this change, as at 31 March 2017 there was $3,480k of goods

in transit which had not been recorded. As a consequence, inventories and trade and other payables were understated.

The change has been recorded in these financial statements by restating each of the affected financial statement line items

for prior periods.

The following table summarises the impact on the Group’s consolidated financial statements, of items (x) and (y).

Consolidated Balance Sheet

For the year ended 31 March 2017

Impact of correction of error

$NZ000’sAs previously reportedAdjustmentsAs restated

Inventories18,7183,48022,198

Trade and other receivables19,362(3,311)16,051

Cash15,980(75)15,905

Total current assets54,0609454,154

Total assets58,2319458,325

Trade and other payables11,0693,48014,549

Provisions3,950(3,386)564

Total current liabilities15,3359415,429

Total liabilities38,7619438,855

There is no impact on the Group’s total equity, basic or diluted earnings per share, net tangible assets per ordinary share,

total comprehensive loss or cash flows for the year ended 31 March 2017.

3. Standards or interpretations not yet effective

No new standards that have been issued and are effective for the periods beginning 1 April 2017 are considered to materially

impact the recognition, measurement or disclosure of these financial statements. Below are new standards and amendments

that have been issued that are not yet effective:

NZ IFRS 9, ‘Financial instruments’, addresses the classification, measurement and recognition of financial assets and financial

liabilities. The complete version of NZ IFRS 9 was issued in September 2014. It replaces the guidance in NZ IAS 39 that relates

to the classification and measurement of financial instruments. NZ IFRS 9 retains but simplifies the mixed measurement

model and establishes three primary measurement categories for financial assets: amortised cost, fair value through other

comprehensive income and fair value through profit or loss. The basis of classification depends on the entity’s business

model and the contractual cash flow characteristics of the financial asset. Investments in equity instruments are required to

be measured at fair value through profit or loss with the irrevocable option at inception to classify equity instruments that

are not held for trading at fair value through comprehensive income. There is now a new expected credit losses model that

replaces the incurred loss impairment model used in NZ IAS 39.

For financial liabilities there were no changes to classification and measurement except for the recognition of changes in own

credit risk in other comprehensive income, for liabilities designated at fair value through profit or loss. NZ IFRS 9 relaxes the

requirements for hedge effectiveness by replacing the bright line hedge effectiveness tests. It requires an economic relationship

between the hedged item and hedging instrument and for the ‘hedged ratio’ to be the same as the one management actually

uses for risk management purposes. Contemporaneous documentation is still required but is different to that currently

prepared under NZ IAS 39. The standard is effective for accounting periods beginning on or after 1 January 2018. Early

adoption is permitted. The Group intends to adopt NZ IFRS 9 in the period beginning 1 April 2018, however, no material

impact is expected as no derivatives used by the Company currently qualify for hedge accounting.

NZ IFRS 15 ‘Revenues from Contracts with Customer’

The Group will implement the new standard effective 1 April 2018. The new standard will replace NZ IAS 18 ‘Revenue’ and NZ

IAS 11 ‘Construction Contracts’. NZ IFRS 15 establishes a comprehensive framework for determining whether, how much and

when revenue is recognised and also contains new requirements related to presentation. The core principle in that framework

is that revenue should be recognised dependent on the transfer of promised goods or services to the customer for an

amount that reflects the consideration which should be received in exchange for those goods or services. The objective of

the standard is to provide a five-step approach to revenue recognition that includes identifying contracts with customers,

identifying performance obligations, determining transaction prices, allocating transaction prices to performance obligations,

and recognising revenue when or as performance obligations are satisfied. Judgement will need to be applied, including

making estimates and assumptions for multiple-element contracts in identifying performance obligations, in constraining

estimates of variable consideration and in allocating the transaction price to each performance obligation and to lease

components (if any). The new standard will result in an increased volume of disclosure information in the Consolidated

Financial Statements.

Changes introduced by the standard relevant to AFT

The new standard provides new requirements and additional guidance that are relevant to the AFT Group, notably in the

following areas:

• the Group’s “Sale of goods” are derived from the sale of pharmaceuticals where control transfers to our customer and

our performance obligations are satisfied at the time of shipment to or receipt of the products by the customer. We do

not expect NZ IFRS 15 to significantly change the timing or amount of revenue recognised under these agreements.

• the Group’s “Royalty income” consists of royalty income from the out-licensing of intellectual property (IP), which is

recognised as earned. We do not expect NZ IFRS 15 to significantly change the timing or amount of revenue recognised

on these royalty arrangements as the standard’s royalty exception will apply to these revenues.

• out-licensing contracts may be entered into with no further obligations or may include commitments to late-stage

development, regulatory approval or manufacturing. These may be settled by a combination of up-front payments,

milestone payments, and reimbursement for services provided. Whether to consider these commitments as a single

performance obligation or separate ones, or even being in scope of NZ IFRS 15, is not straight forward and requires some

judgement. Depending on the conclusion, this may result in all revenue from the contract being estimated at inception

and either recognised at a point in time or spread over the time. The outcome under the new standard may differ to the

Group’s current treatment. The new standard provides an exemption for sales-based royalties for licences of intellectual

property which will continue to be recognised as revenue as underlying sales are incurred. Based on the Group’s current

out-licencing contracts, the impact of the new standard is however not considered to be material.

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

4243AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

3. Standards or interpretations not yet effective (continued)

Transition approach and use of practical expedients

The Group will apply the full retrospective method for the transition. Certain practical expedients permitted by the standard

during the transition will also be used, notably the relief to not restate contracts that began and were completed in FY2018 or

were completed before 1 April 2017 and to not provide in FY2019 the disclosure requirement as per NZ IFRS 15 paragraph 120

for the comparative FY2018 period (‘amount of the transaction price allocated to the remaining performance obligations’).

Since the new standard, including the use of practical expedients, is not expected to materially modify the timing or amounts

of revenue recognised for FY2018, no restatement is expected to be necessary.

Presentational changes

As a result of implementing NZ IFRS 15, the Group will make a presentational change to the consolidated income statement

in FY2019 and will create new notes for Revenue and Other Income to include the increased volume of required disclosure

information.

NZ IFRS 16 Leases

Under adoption of the new NZ IFRS 16, a portion of the annual operating lease costs, which are currently fully recognised as a

functional expense, will be recorded as interest expense. The capitalised value of the leases will be amortised as depreciation,

while the lease liability will be amortised as ongoing lease payments are made.

In addition, a portion of the annual lease payments recognised in the cash flow statement as a reduction of the lease liability,

will be recognised as an outflow from financing activities. These are currently fully recognised as an outflow from operating

activities.

The Group does not expect the changes to significantly affect overall cashflow nor expenses and net profit, however the

costs will be recognised in different classifications (interest, depreciation and liability reduction).

There are no other NZ IFRS or NZ IFRIC interpretations that are not yet effective that would be expected to have a material

impact on the Group.

4. Revenue from operations

$NZ000’s 20182017

Sale of goods79,88269,047

Royalty income189158

Total revenue80,07169,205

5. Other income

$NZ000’s 20182017

Research and development grant409512

Licensing income1,8261,597

Other income -550

Total other income2,2352,659

In FY2017, the Company purchased emergency supplies of Metoprolol at a cost of $823,000, which was damaged in transit

and written off as part of Cost of Sales during the year. An insurance recovery of $550,000 was made against this cost,

which was reported as other income.

6(a). Net operating profit

$NZ000’s Note 20182017

Loss before tax (12,666)(18,330)

After charging the following specific expenses:

Finished goods material component of cost of goods sold45,40441,671

Inventory write off4761,536

Audit fees and review of financial statements

6(b)193149

Rental expense – premises528502

Operating leases – motor vehicles and equipment450422

Share options expense135 230

Short-term employee emoluments:

Selling and distribution expenses6,6836,233

General and administrative expenses1,8991,594

Research and development expenses1,2821,362

9,8649,189

Research and development expenses:

Product development6,5219,222

New market development1,7092,005

8,23011,227

Depreciation:

Plant and machinery8899

Furniture and fixtures2729

Vehicles1115

126143

Amortisation (included in General and Administration expenses):

Patents11599

Software9984

214183

Finance costs:

Interest3,4963,186

Foreign exchange losses/(gains)(818)710

Other financing costs(26)(18)

2,6523,878

Research is the original and planned investigation undertaken with the prospect of gaining new knowledge and understanding.

This includes: direct and overhead expenses for research, pre-clinical trials and costs associated with clinical trial activities.

All research costs are expensed when incurred.

Development is the application of research findings to a plan or design for the production of new or substantially improved

processes or products prior to the commencement of commercial production. When a project reaches the stage where it is

reasonably certain that future expenditure can be recovered through the process or products produced, expenditure that is

directly attributable or reasonably allocated to that project is recognised as a development asset. The asset will be amortised

from the date of commencement of commercial production of the product to which it relates on a straight-line basis over the

period of expected benefit. Development assets are reviewed annually for any impairment in their carrying value.

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

4445AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

6(b). Fees paid to auditors

$NZ000’s 20182017

Audit of financial statements

Audit of annual financial statements – Deloitte (2017: PwC)129126

Review of half year financial statements - PwC6423

Total fees for audit and review services193149

Other services

Tax due diligence services – Deloitte19-

Total fees paid to auditors212149

Deloitte 148-

PwC64149

7. Income tax

The income tax expense recognised for the period is based on the accounting profit or loss, adjusted for non-taxable and

non-deductible differences.

Current tax is calculated by reference to the amount of income tax payable, calculated using tax laws that are enacted or

substantively enacted at balance date.

Deferred income tax is recognised on temporary differences arising between the tax bases of assets and liabilities and their

carrying amounts in the financial statements. Deferred income tax is determined using tax rates (and laws) that have been

enacted or substantively enacted by the balance sheet date and are expected to apply when the related deferred income tax

asset or liability is settled. Deferred income tax assets are recognised to the extent that it is probable that future taxable profit

will be available against which the temporary differences can be utilised.

$NZ000’s 20182017

(a) Tax expense

Loss before tax(12,666)(18,330)

Tax calculated at domestic tax rates applicable*(1,862)(5,049)

Expenses not deductible4384

Current year losses not recognised2,3235,094

Previous year losses now utilised(603)(197)

Non resident withholding tax160121

Prior year adjustment(3)5

Tax expense/(benefit)5858

Comprising:

Current tax(4 0)117

Deferred tax

98(59)

5858


* Calculated using the pre tax profit / loss and tax rate in New Zealand (28%) and Australia (30%)

$NZ000’s 20182017

(b) Deferred tax balance

Provisions708610

708610

Deferred tax assets relating to unused tax loss carry-forwards and to deductible temporary differences are recognised if it is

probable that they can be offset against future taxable profits or existing temporary differences. As at 31 March 2018, the

Group recognised deferred tax assets on temporary differences totalling $708,000 (2017: $610,000) since it was foreseeable

that temporary differences could be offset against future taxable profits. On the basis of the approved business plans of

subsidiaries, AFT Pharmaceuticals Limited considers it probable that temporary differences can be offset against future

taxable profits. There is no expected change in capital structure in the near future which is expected to affect the

recoverability of the recognised deferred tax assets.

The amount of tax losses carried forward that is available for future utilisation is $45,964,000 (FY2017: $39,815,000).

No deferred tax asset has been recognised in relation to these losses.

$NZ000’s 20182017

(c) Imputation and franking credits available for use

NZD252600

AUD319319

8. Inventories

Inventories are stated at the lower of cost and net realisable value. Cost is determined on a weighted average cost basis.

Net realisable value is the estimated selling price in the ordinary course of business less the estimated costs of completion

and the estimated costs necessary to make the sale.

$NZ000’s 2018

Restated

2017

Finished goods25,66422,526

Provision for obsolescence(1,252)(328)


24,41222,198


Inventory on hand comprises pharmaceutical goods ready for resale.

The value of inventory is transferred to cost of sales in the income statement when sold.

9. Trade and other receivables

Trade receivables are recognised initially at fair value and subsequently measured at amortised cost, less provision for

doubtful debts and provision for customer rebates. Bad debts are written off in the year in which they are identified.

Collectibility of trade receivables is reviewed on an on-going basis. Debts which are known to be uncollectible are written

off. A provision for doubtful receivables is established when there is objective evidence that the Group will not be able to

collect all amounts due according to the original terms of receivables. The amount of the provision is the difference between

the asset’s carrying amount and the present value of estimated future cash flows, discounted at the effective interest rate.

The amount of the provision is recognised in the income statement. Customer rebates are based on the customer’s ability to

achieve certain sales targets and are computed using the expected rebate percentage for sales made during the period.

$NZ000’s 2018

Restated

2017

Trade receivables 19,8231 7, 4 0 3

Less provision for customer rebates(5,044)(3,386)

Prepayments2,1752,034


16,95416,051

Ageing of overdue trade debtors but not considered impaired

$NZ000’s 1-30 Days31-60 Days61-90 Days90+ DaysTotal

31 March 20182,79743324143,268

31 March 2017323 1673- 493

All balances are expected to be settled within the next 12 months.

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

4647AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

10. Cash and cash equivalents

Cash and cash equivalents includes cash on hand, deposits held at call with financial institutions, other short-term

investments with original maturities of three months or less that are readily convertible to known amounts of cash and

which are subject to an insignificant risk of changes in value, and bank overdrafts. Bank overdrafts are shown within

borrowings in current liabilities on the balance sheet.

$NZ000’s 2018

Restated

2017

Cash at bank6,74515,876

Cash on hand2529

Total cash6,77015,905

Cash at bank earns, on average, less than 1% of interest.

11. Property, plant and equipment

All plant and equipment is stated at historical cost less depreciation and any impairment losses. Historical cost includes

expenditure that is directly attributable to the acquisition of the items. Subsequent costs are included in the asset’s carrying

amount or recognised as a separate asset, as appropriate, only when it is probable that future economic benefits associated

with the item will flow to the Company and Group and the cost of the item can be measured reliably. All other repairs and

maintenance are charged to the income statement during the financial period in which they are incurred.

Depreciation of property, plant and equipment is calculated using the diminishing value method that apportions the cost of

the assets over their useful lives. The Group has the following classes of property, plant and equipment and depreciation rates:

Category Depreciation Rate (%)

Plant and machinery 21% to 60%

Furniture and fixtures 9% to 60%

Vehicles 26% to 36%

An asset’s carrying amount is written down immediately to its recoverable amount if the asset’s carrying amount is greater

than its estimated recoverable amount. Gains and losses on disposal are determined by comparing proceeds to carrying

amounts and are included in the income statement.

$NZ000’s

Plant and

machinery

Furniture

and fixturesVehiclesTotal

(a) Cost

Balance 31 March 2016694 396 218 1,308

Additions104 18 - 122

Disposals ----

Balance 31 March 2017798 414 218 1,430

Additions43121570

Disposals--(32)(32)

Balance 31 March 20188414262011,468

(b) Depreciation

Balance 31 March 2016(537)(192)(172)(901)

Depreciation(99)(29)(15)(143)

Disposals -- - -

Balance 31 March 2017(636)(221)(187)(1,044)

Depreciation(88)(27)(11)(126)

Disposals--3232

Balance 31 March 2018(724)(248)(166)(1,138)

(c) Carrying amounts

Balance 31 March 2017162 193 31 386

Balance 31 March 201811717835330

12. Intangible assets

Capitalised development costs

Development projects are regularly reviewed throughout the year by a staff committee comprising the CEO, CFO, GM

Development and Financial Controller. The status of each project is measured against the requirements of NZ IAS 38

and where projects are probable to generate economic benefits, the relevant costs incurred during the financial year are

capitalised. The Group considers technical feasibility, resources required and intention of completing the project in making

this assessment.

Finite useful life

Acquired patents, capitalised development costs and software have a finite life and are carried at cost less accumulated

amortisation. Patents are amortised over a useful economic life of 20 years, capitalised development costs over the life of

the relevant patent or period of expected benefit, and software over 3 – 4 years.

Indefinite useful life

Acquired trademarks are considered to have indefinite useful lives while they continue to protect revenue streams.

Trademarks are carried at cost less accumulated impairment. Indefinite useful life assets are tested for impairment annually

or when impairment indicators exist. The asset’s carrying amount is written down immediately to its recoverable amount if

the asset’s carrying amount is greater than its estimated recoverable amount.

$NZ000’s Trademarks

Capitalised

development

costsPatentsSoftwareTotal

(a) Cost

Balance 31 March 2016439 -1,978 260 2,677

Additions171 -204 254 629

Disposals -- (9) - (9)

Balance 31 March 2017610 -2,173 514 3,297

Additions842,46523412,784

Disposals-----

Balance 31 March 20186942,4652,4075156,081

(b) Amortisation

Balance 31 March 2016 --(338)(228)(566)

Amortisation--(99)(84)(183)

Disposals -- - - -

Balance 31 March 2017 --(437)(312)(749)

Amortisation --(115)(99)(214)

Disposals -----

Balance 31 March 2018 --(552)(411)(963)

(c) Carrying amounts

Balance 31 March 2017610 -1,736 202 2,548

Balance 31 March 20186942,4651,8551045,118

Trademarks are acquired to protect the current and future revenue streams of the Group.

They are considered to have an indefinite useful life while they continue to protect revenue streams.

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

4849AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

13(a). Investment in subsidiaries

Interest held


2018

%

2017

%

Country of

incorporationPrincipal activities

AFT Pharmaceuticals (AU) Pty Ltd100%100%AustraliaDistribution of pharmaceuticals

in Australia

AFT Pharmaceuticals Singapore Pte Ltd100%100%SingaporeRegistration of pharmaceuticals

in Singapore

AFT Pharmaceuticals (S.E. Asia) Sdn Bhd100%100%MalaysiaDistribution of pharmaceuticals

in Malaysia

AFT Orphan Pharmaceuticals Limited65%65%New ZealandNo activity

AFT Limited Partner Limited100%100%New ZealandPartner in Dermatology

Specialties LP

AFT Dermatology Limited100%100%New ZealandDistribution of pharmaceuticals

All subsidiaries have a balance date of 31 March.

13(b). Investment in joint partnership

$NZ000’s 20182017

Interest in joint venture company at cost4,345 1,343

Equity accounted earnings of joint venture partnership(2,210) (716)

Net equity investment in joint venture partnership2,135 627

The joint venture partnership of the Group and its activities are as follows:


2018

% Interest

held

2017

% Interest

held

Dermatology Specialties LP (incorporated in New Zealand)50% 50%

Principal activities: Development and distribution of pharmaceuticals

$NZ000’s 20182017

Balance at start of year 627 185

Investment during the year3,002 856

Share of current year loss(1,494) (414)

Dividend received- -

Balance at end of year2,135 627

13(b). Investment in joint partnership (continued)

The following table summarises the financial information relating to the Group’s joint venture partnership and represents

100% of the joint venture partnership net assets, revenues and net profits.

$NZ000’s 20182017

Extracts from joint venture partnership balance sheet (unaudited)

Current assets- -

Non-current assets2,189 2,175

Current liabilities(96) (95)

Non-current liabilities- -

Net assets2,093 2,080

Extracts from joint venture partnership income statement (unaudited)

Revenue- -

Net profit after taxation(2,989) (828)

The joint venture did not have any contingent liabilities or capital commitments at balance date (2017: nil).

14. Trade and other payables

These amounts represent liabilities for goods and services provided to the Group prior to the end of the financial period

which are unpaid. These amounts are incurred and are usually paid within 30 days of recognition.

$NZ000’s 2018

Restated

2017

Trade payables7, 3 3 510,828

GST payable1,1891,161

Employee entitlements932615

Other payables7, 9 3 51,945

1 7, 3 9114,549

15. Provisions

$NZ000’s 2018

Additional

provisionsUtilised2017

Additional

provisionsUtilised2016

Supplier rebates1,0981,098(564)564 564 (661)661

1,0981,098(564)564564 (661)661

Supplier rebates are based on profit sharing arrangements with suppliers which are estimated on achieving expected set

margin targets and are expected to be utilised within the next 12 months.

16. Interest bearing liabilities

Borrowings are initially recognised at fair value plus transaction costs incurred. Borrowings are subsequently measured at

amortised cost. Any difference between the proceeds (plus transaction costs) and the redemption amount is recognised in

the income statement over the period of the borrowings, using the effective interest method.

Borrowings are classified as current liabilities unless the Group has an unconditional right to defer settlement of the liability

for at least 12 months after the balance sheet date. Borrowing costs are expensed as incurred.

$NZ000’s 20182017

CRG (Capital Royalty Partners) loans30,65423,426

30,65423,426

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

5051AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

16. Interest bearing liabilities (continued)

$NZ000’s

Opening balance of CRG loan 1 April 201723,426

Capitalised interest1,139

Additional loans drawn down7, 1 3 5

Gain on FX translation(1,046)

Closing balance 31 March 201830,654

The term loan agreement with CRG commenced in May 2014 and had a facility draw down of up to USD$30 million by

October 2016. USD$15 million was drawn down. Initially this facility was for a six year term with the first four years being

interest only, and the principal to be repaid in equal quarterly instalments in years five and six.

In September 2017, a new loan facility of USD$10 million was entered into, which includes a minimum mandatory drawdown

of USD$5 million on or before 31 March 2018. This was drawn down in December 2017. A second drawdown for the balance is

available at the Company’s option on or before 30 September 2018.

The repayment terms for all facilities were amended in September 2017 to interest only until maturity, and the principal to be

repaid in full on 31 March 2020.

The loans have a general security over the assets of the Group together with a group guarantee. Interest is fixed at 13.5%

p.a. The loans are denominated in United States dollars (USD) and during the period NZD$1,046,000 (FY2017 $260k) was

recognised as unrealised foreign exchange gains. The carrying amount of the CRG loans are substantially in line with the fair

market value as at balance sheet date.

All covenants relating to the loan and BNZ facility have been complied with during the year (refer note 24).

17. Share capital

Ordinary shares are classified as equity. Preferred shares are classified as equity, they attract a dividend yield and do not

have ordinary share voting rights.

SharesShares

2018

Number

2017

Number

2018

$’000

2017

$’000

Ordinary share capital97,308,01996,834,838 5 7, 0 5 855,994

Less capital-raising costs--(2,439)(2,174)

Redeemable preference shares3,330,0003,330,0009,1249,124

100,638,019100,164,838 63,74362,944

$NZ000’s 20182017

Share capital at beginning of the year62,94453,902

Issue of Redeemable preference shares-9,124

Issue of Ordinary shares1,065-

Less capital raising costs(266)(82)

63,74362,944

FY2017

On 24 March 2017, the Company issued 3,330,000 redeemable preference shares at $2.74 each. These shares attract a

dividend of 9.4% accruing quarterly, which may be satisfied in cash either in full or in part or deferred indefinitely at the

Company’s absolute discretion.

They do not carry any right to vote except at meetings of an ‘interest group’ of holders of redeemable shares.

They may be redeemed at the option of the Company at any time two years or more after issue. On redemption, the Company

would pay the issue price plus unpaid dividends accrued to the date of redemption. The redemption can only be settled in cash.

After three years from issue, they may be converted to ordinary shares at the option of the holder in multiples of 100,000.

The holder would receive one ordinary share for every redeemable share held and a number of ordinary shares calculated by

dividing the amount of any accumulated dividends by the issue price. Conversion of the redeemable preference shares may

only be settled through the issuance of shares. Once the holder has elected to convert, neither the issuer not the holder can

be obligated to settle in any other manner.

Optional conversion events arise if one of a number of conditions occur. These conditions were notified to NZX and ASX at

the time of issue of the redeemable preferences shares and are available on the Company website (www.aftpharm.com).

FY2018

In May 2017, a share purchase plan was issued to existing shareholders, who could elect to purchase shares @NZ$2.25 per

share (AUD$2.11) which was a 3% discount to the volume weighted average price of an AFT share on the NZX main board for

the 5 day period ending on 23 May 2017. Shareholders could subscribe for a minimum of $1,000 and maximum of $15,000

worth of shares at that price. Shareholders subscribed for 473,181 ordinary shares, raising $1,064,657.

18. Reconciliation of loss after tax with net cash flow from operating activities

$NZ000’s 2018

Restated

2017

Loss after tax(12,724)(18,388)

Non-cash items:

Depreciation126143

Amortisation214183

Impact of foreign exchange on cash and cash equivalents24456

Share options expense135230

Interest expense capitalized to loan principle1,139525

Unrealised gain on USD denominated loan(1046)(260)

Share in loss of JV entity1,494414

Movement in working capital:

(Increase)/decrease in inventories(2,214)1,261

(Increase)/decrease in trade and other receivables(1,080)(5,273)

Increase/(decrease) in trade and other payables3,1711,509

Increase/(decrease) in income tax(143)138

Net cash used in operating activities(10,904)(19,062)

19(a). Related parties

The Group had related party relationships with the following entities:

Related party Nature of relationship

CRG (Capital Royalty Partners) Shareholder of both ordinary shares and redeemable preference

The following transactions were carried out with these related parties:

(i) Loans

$NZ000’s 20182017

Capital Royalty Partners (refer note 16)30,65423,426

Total loan balances30,65423,426

(ii) Key management compensation

$NZ000’s 20182017

Directors fees286289

Executive salaries1,0841,092

Short term benefits127238

Options expense2981

Key management compensation1,5261,700

Key management includes external directors, the Chief Executive Officer, the Chief of Staff, the Chief Financial Officer and

the Director of International Business Development. These positions are mainly responsible for the planning, controlling and

directing the activities of the business. The Chief of Staff is the spouse of the Chief Executive Officer.

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

5253AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

19(b). Staff share options

Staff share options are valued at fair value as calculated independently using the Black Scholes model. The options vest over

up to four years from date of issue.

Movements in the number of share options outstanding and their related weighted average exercise prices are as follows:

2018 2017


Average

exercise price

$ per share

Options

‘000’s

Average

exercise price

$ per share

Options

‘000’s

Balance at beginning of year2.80850 2.80861

Issued-- - -

Forfeited-(157) - (11)

Exercised-- - -

Lapsed- - - -

Balance at end of year2.80693 2.80 850

Weighted average share price for options exercised during the period $nil (2017: $nil).

Of the 693,000 outstanding options, 135,969 are currently exercisable (2017: nil).

Share options outstanding at the end of the year have the following expiry dates, exercise dates and exercise prices:

Expiry month

Exercise

month

Exercise

price20182017

April 2020December 20172.80135,969 151,629

April 2020December 20182.805 5 7, 0 3 1 698,371

Total share options outstanding693,000850,000

The weighted average remaining contractual life of options outstanding at the end of the period was 2 years (2017: 3 years).

Share options reserve

$NZ000’s20182017

Balance at beginning of year(295)(65)

Current year amortisation(135) (230)

Balance at end of year(430) (295)

20. Financial risk management

(a) Managing financial risk

The Group’s activities expose it to various financial risks as detailed below.

• Market risk

Management is of the opinion that the Group’s exposure to market risk at balance date is defined as:

Risk factor Description Sensitivity

(i) Currency risk Exposure to changes in foreign exchange rates on

assets and liabilities of the subsidiary, and USD

denominated borrowings As below

(ii) Interest rate risk Exposure to changes in interest rates on borrowings As below

(iii) Other price risk No commodity securities are bought, sold or traded Nil

• Foreign exchange risk

The Group benefits from the use of derivative financial instruments to manage foreign currency exposures.

The fair value of forward exchange contracts is calculated by reference to current forward exchange rates at year end and

the contract exchange rates, considered level 2 of the fair value hierarchy.

The Group purchases goods and services from overseas suppliers in a number of currencies, primarily AUD, USD, EUR and

GBP and has borrowings that are denominated in US dollar amounts. This exposes the Group to foreign currency risk. The

Group manages foreign currency risk through use of derivative arrangements, in particular forward exchange contracts.

The exposure is monitored on a regular basis based on Group foreign exchange policies. Future revenues from markets

outside Australasia will be denominated primarily in USD and EUR which will provide a natural hedge against these costs.

In the current year (FY2018) Foreign Exchange gains totalled $817,992 (2017: $710,000 gain) of which $1,046,000

(2017: $260,000 gain) were unrealised gains on the USD denominated CRG loan. Future revenues from markets outside

Australasia will be derived in USD which will be used towards repaying this debt as it falls due. The balance of the losses are

derived from the restatement of the cash balances at the spot rate on the year end balance date of 31 March 2018 and the

change in spot rates during the time between when expenses are recorded in the general ledger and when they are paid.

In total, the Group had assets and liabilities denominated in the following currencies:

Assets

NZ$000’s

CurrencyLiabilities

NZ$000’s

12,960AUD4,366

134USD33,596

202MYR62

251SGD24

30EUR2,897

-GBP64

A 1% increase or decrease in foreign exchange rates on assets and liabilities will reduce/increase equity by $111,000

(2017: $53,000) and reduce/increase the profit or loss by $354,000 (2017: $341,000).

The following forward foreign exchange contracts were held at the end of the 2018 financial year:

Forward Foreign Exchange Contracts

Buy currency

Buy currency

amount (‘000)

Sell amount

$NZ000’s

Buy amount

31-Mar-18

$NZ000’s

Fair value

$NZ000’s

EUR2,5504,2904,394104

GBP19736538722

USD6,0008,2688,31850

Total benefit as at 31 March 2018176

All contracts mature within one year from 31 March 2018.

The following forward foreign exchange contracts were held at the end of the 2017 financial year:

Forward Foreign Exchange Contracts

Buy currency

Buy (sell) currency

amount (‘000)

Sell (buy) amount

$NZ000’s

Buy (sell) amount

31-Mar-17

$NZ000’s

Fair value

$NZ000’s

EUR3,0124,8064,656(150)

GBP5441,027979(4 8)

USD2,7303,9023,9097

AUD(750)(807)(820)(13)

Total exposure as at 31 March 2017(204)

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

5455AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

20. Financial risk management (continued)

• Interest rate risk

Borrowings are at a fixed interest rate, which exposes the Group to fair value interest rate risk. There are no specific

derivative arrangements to manage this risk.

• Credit risk

Financial instruments, which potentially subject the Group to credit risk, principally consist of accounts receivable.

Regular monitoring is undertaken to ensure that the credit exposure remains within the Group’s normal terms of trade.

The Group has one significant concentration of credit risk at 31 March 2018 with the largest debtor being $3,510,000 (2017:

$7,640,667). There has been no past experience of default and no indications of default in relation to this debtor. There are

no impaired receivables at 31 March 2018 (2017: nil).

The Group’s cash and short-term deposits are placed with high credit quality financial institutions. Accordingly, the Group

has no significant concentration of credit risk other than bank deposits, with 8.3% of total assets at the Bank of New

Zealand (2017: 23.9%), 3.8% at NAB Bank (2017: 3.3%) and 0% with ANZ (2017: 0%). The carrying value of financial assets

represents the maximum exposure to credit risk.

• Liquidity risk

Liquidity risk is the risk that the Group may encounter difficulty in raising funds at short notice to meet its commitments

and arises from the need to borrow funds for working capital. The directors monitor the risk on a regular basis and actively

manage the cash available to ensure the net exposure to liquidity risk is minimised. Since May 2014, there has been a $1m

BNZ overdraft immediately available.

The liquidity/maturity profile of the liabilities is as follows:

Liquidity Profile

$NZ000’s

31 March 2018 < 1 Year1-2 Years2-5 Years> 5 YearsTotal

Trade and other payables(16,122)---(16,122)

Borrowings(2,806)(36,458)--(39,264)

Derivative liabilities (outbound)(1 2,747)---(1 2,747)

Derivative liabilities (inbound)12,923---12,923

Totals(18,752)(36,458)--(55,210)

31 March 2017

Trade and other payables(14,549) - - -(14,549)

Borrowings (2,144) (14,454) (13,283)-(29,881)

Derivative liabilities (outbound)(9,132) - - -(9,132)

Derivative liabilities (inbound)8,928 - - -8,928

Totals(16,897) (14,454) (13,283)-(4 4,634)

(b) Fair values

The carrying value of financial assets and liabilities (trade receivables and trade payables) approximates their fair value.

Trade receivables are valued net of provision and trade payables are valued at their original amounts by contract.

21. Segment reporting

Operating Segments

$NZ000’s

31 March 2018 AustraliaNew ZealandSoutheast AsiaRest of worldTotal

Revenue49,1932 7,0 9 61,2862,49680,071

Other income-721-1,5142,235

Depreciation and amortisation253087-340

Equity accounted loss of joint venture entity---(1,494)(1,494)

Gain / (Loss) before tax538(4,598)(698)(7,907)(12,666)

Finance income / (loss)4121-125

Finance costs(719)(2,027)94-(2,652)

Total assets25,70628,6221402,13556,603

Property, plant and equipment3927417-330

Intangible assets---5,1185,118

Investment in joint venture entity---2,1342,134

Total liabilities5,25442,65186-47, 9 91

Capital expenditure11509-70

31 March 2017

Revenue3 7,0 6 4 29,168 1,005 1,968 69,205

Other income - 550 -2,109 2,659

Depreciation and amortisation25 294 7 -326

Equity accounted loss of joint venture entity---(414)(414)

Loss before tax(3,633)(5,782)(689)(8,226)(18,330)

Finance income -347 - -347

Finance costs(26)(3,728)(124) -(3,878)

Total assets (restated)19,451 37,254 993 62758,325

Property, plant and equipment54 317 15 -386

Intangible assets -- -2,5482,548

Capital expenditure19 722 10 -751

Operating segments are reported in a manner consistent with the internal reporting provided to the chief operating

decision-maker (CODM). For the purposes of NZ IFRS 8 the CODM is a group comprising the Board of Directors, together

with the Chief Executive Officer, the Chief of Staff, the Chief Financial Officer and the Director of International Business

Development. This has been determined on the basis that it is this group that determines the allocation of the resources

to segments and assesses their performance.

The Group has four operating segments based on geographical location reportable under NZ IFRS 8, as described below,

which are the Group’s strategic groupings of business units. The following summary describes the operations in each of the

Group’s reporting segments:

New Zealand – Includes the Head Office function for the Group, supplier relationships and procurement of all stock for the

Group, all regulatory activity, all marketing activity and all finance activity. The sales and distribution activity principally

relates to the New Zealand market.

Australia – Includes the sales and distribution activity relating to the Australian market.

Southeast Asia – Includes the sales and distribution activity relating to the Southeast Asian market (Brunei, Hong Kong,

Malaysia, Philippines, Singapore and Vietnam).

Rest of World – Includes the out-licensing of IP developments to markets in which AFT does not have a presence and

the export of products to export markets (Balkans, Iraq, Pacific Islands, Saudi Arabia, United Arab Emirates). The costs

of research and development and new market development activity not specific to the other segments are expensed

to this segment.

Major Customers – Revenues from one customer of the Australian segment (being a licensed wholesaler) represents

approximately NZ$38.5m (2017: NZ$15.5m) and from one customer of the New Zealand segment (also being a licensed

wholesaler) represents approximately $14.6m (2017: $13.9m) of the Group’s total revenues.

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

5657AFT PHARMACEUTICALS LIMITED
Annual Report 2018

NOTES TO THE FINANCIAL STATEMENTS

22. Contingent liabilities

In May 2015, AFT Pharmaceuticals Limited signed as guarantor of AFT Pharmaceuticals (AU) Pty Limited for its five-year

lease contract with Investec Limited for the premises occupied in Sydney, Australia. A deposit of AUD$75,000 has been

placed with NAB as security for this lease. The Company has also placed NZD$75,000 on term deposit with the BNZ as

security for a guarantee issued by the BNZ in favour of the NZX, should the Company ever default on any of its payment

obligations to NZX.

23. Commitments

(a) Capital commitments

The Group has no capital commitments at 31 March 2018 (2017: nil).

(b) Lease commitments

Operating leases are those in which all the risks and rewards are substantially retained by the lessor. Lease payments are

charged in the income statement on a straight-line basis over the term of the lease.

$NZ000’s 20182017

Due within one year843890

Due later than one year but within five years1,9532,261

Due later than 5 years1,065 1,750

3,8614,901

The above includes leases for property (with lease terms of 2 to 8 years) and vehicles and equipment (with lease terms

of up to 4 years.

(c) Other commitments

The Company has entered into contracts to complete clinical trials overseas. These contracts call for stage or milestone

payments to be made progressively when those stages or milestones are achieved. Certain conditions allow for the termination

of the trials, with future obligations extinguished. The aggregate expected amounts to be paid under these contracts is

$4.0m (2017: $4.0m).

24. Management of capital

The Group’s objectives when managing capital are to:

• Safeguard the Group’s ability to continue as a going concern so that it can continue to provide returns to its

shareholders, and

• Maintain a strong capital base to support the development of its business.

The Group meets these objectives through a mix of equity capital and borrowings. The level and mix of capital is

determined by the Group’s internal Corporate Governance Policies.

The long-term debt in the form of the CRG Loan was used to replace the trade facility from the BNZ in May 2014.

Under the CRG Loan Agreement, there is a covenant requiring a minimum bank balance of NZ$4m at each month end.

Under the BNZ facility, there is a covenant requirement that the facility, comprising an overdraft and letter of credit facility,

must not exceed the total of 70% of acceptable debtors plus 40% of acceptable stock.

The Group has complied with both the CRG and BNZ covenants during the 2018 and 2017 financial years.

In March 2017 the Group issued 3,330,000 Redeemable Preference Shares raising $9.1m, and in May 2017 an issue of

ordinary shares was offered to existing shareholders, resulting in the issue of 473,181 ordinary shares and raising an

additional $1,064,657. Details are covered in note 17.

Notes to the Financial Statements (continued)

For the year ended 31 March 2018

Going concern assumption

At 31 March 2018, the outstanding balance on interest bearing loans with CRG amounted to $30.5m (2017: $23.4m). At the

same time, the Group held a cash balance of $6.8m (2017: $16.0m). The Group incurred a net loss in the period of $12.7m

(2017: net loss of $18.4m) and had a net operating cash outflow for the period of $11.0m (2017: $19.1m).

During the period ended 31 March 2018, a new loan facility of US$10m was entered into with CRG of which US$5m has been

drawn and US$5m is available for drawdown (refer note 16). A further $1m of additional share capital was also raised from

existing shareholders (refer note 17).

The CRG loan is due for repayment in full on 31 March 2020 (refer to note 16).

The Directors have approved internal forecasts through to 31 March 2020, considered achievability of the assumptions under

these forecasts, reviewed the existing working capital against Group requirements and considered forecast compliance with

applicable debt covenants. The key revenue assumptions, which like all assumptions, are subject to a degree of uncertainty are:

• the ability to execute further licensing agreements for the key innovative products, Maxigesic, Pascomer and NasoSurf;

• the ability to generate future international revenues from the existing and potential licensing agreements for the key

innovative products, Maxigesic, Pascomer and NasoSurf; and

• the continued Australian sales growth for Maxigesic as the market adjusts for the re-scheduled codeine-based painkillers

from over-the-counter to prescription only, which took effect on 1 February 2018 (Maxigesic is codeine-free and is therefore

exempt and remains available over-the-counter).

The directors actively monitor and manage these key revenue growth plans, together with their associated uncertainties, and

have also taken into account the ability of the Group to significantly reduce and or defer forecast development and marketing

spend should this be required, in order to preserve funds.

After considering the uncertainties and mitigations described above, the Directors have a reasonable expectation that the

Group will be in a position to repay this loan on or before 31 March 2020 from a combination of positive cash flows, issuance

of new equity or by establishing a replacement facility if required.

25. Earnings per share

Basic earnings per share is computed by dividing net earnings by the weighted average number of ordinary shares

outstanding during each period.

The calculation of diluted earnings per share assumes the conversion of all dilutive potential ordinary shares in determining

the denominator.

$NZ000’s 20182017

Earnings used in the calculation of basic and diluted earnings per share

Loss after tax(12,724)(18,388)

Weighted average ordinary shares for the purposes of basic and diluted earnings per share 97,248,87196,837,838

Basic and diluted loss per share ($)(0.13)(0.19)

26. Dividends per share

No dividends have been declared to the ordinary shareholders of the parent company during the current year, nor in FY2017.

Gross dividends of $894,506 were declared on the Redeemable Preference Shares, with $411,701 paid in cash and withholding

taxes, and $482,805 accumulated in a reserve for future settlement per the terms described at note 17.

27. Subsequent events

On 30 April 2018, the Group announced that it had concluded its divestment of non-core hospital products by divesting

to Baxter Healthcare a range of non-core hospital products currently sold in Australia. The expected completion date is

1 June 2018. For FY2018 sales of these products in Australia were NZ$5.2m and stock on hand was NZ$1.0m.

5859AFT PHARMACEUTICALS LIMITED
Annual Report 2018

STATUTORY DISCLOSURES

Statutory Disclosures

Executive Director Remuneration

The executive directors, Hartley Atkinson and Marree Atkinson, receive remuneration and other benefits in their respective

executive roles as Chief Executive Officer and Chief of Staff and, accordingly, do not receive director fees.

The table below sets out the total remuneration and value of other benefits earned by or paid to each executive director of

AFT during, and in respect of, the financial period ended 31 March 2018:

Base SalaryTaxable

Benefits

1

Subtotal

Pay for PerformanceTotal

Remuneration

STILT I

4

Subtotal

Hartley Atkinson

$428,978

$9,035$438,013$76,225

2

-$76,225$514,238

Marree Atkinson

$114,053-$114,053$11,425

3

-$11,425$125,478

1

Taxable benefits include a car allowance.

2

The short-term incentive stated was earned in FY2017 and paid in FY2018. Hartley earned a short-term incentive for FY2018 of $119,842 from a full

potential of $248,472. This will be paid in FY2019.

3

The short-term incentive stated was earned in FY2017 and paid in FY2018. Marree earned a short-term incentive for FY2018 of $11,388. This will be

paid in FY2019.

4

Neither executive director was issued any form of long-term incentive during the financial period.

Employee Remuneration

The table below sets out the number of employees or former employees of AFT and its subsidiaries, not being directors of

AFT, who, in their capacity as employees received remuneration and other benefits during the period ended 31 March 2018

totalling at least $100,000 per annum. The remuneration of those employees paid outside of New Zealand has been

converted into New Zealand dollars.

Remuneration Range (NZD)

Total Number

of Employees

$100,000-$110,0004

$110,001-$120,0009

$120,001-$130,0004

$130,001-$140,0007

$140,001-$150,0001

$150,001-$160,000-

$160,001-$170,000-

$170,001-$180,0004

$180,001-$190,000-

$190,001-$200,0001

$200,001-$210,0001

$210,001-$220,0001

$220,001-$230,0001

$270,001-$280,0001

$280,001-$290,0001

Total number of employees and former employees35

The table includes base salaries and short-term incentives paid during FY2018 and long-term incentives vested or exercised

during FY2018. The table does not include long-term incentives that have been granted and have not yet vested. Where

the individual is a KiwiSaver member, contributions of 3% of gross earnings towards that individual’s KiwiSaver scheme

are included in the above table. Where the individual works in Australia contributions of 9.5% of gross earnings towards

Australian Superannuation are included in the table above.

Non-Executive Director Remuneration

AFT’s shareholders have approved a total cap of $575,000 per annum for non-executive directors’ fees, for the purposes

of the NZX Listing Rules. This annual fee pool has not been increased since it was approved by shareholders in 2015. AFT

currently pays directors’ fees which, in aggregate, amount to approximately $300,000 per annum (subject to exchange

rate fluctuations). More information about the remuneration payable to directors is set out in AFT’s Corporate Governance

Statement which is located on the investor centre of the Company’s website.

The Board has agreed that the following fixed annual fees will apply to all non-executive directors during FY2019

(these remain unchanged from FY2018):

Position

Fees Per Annum

(Paid in NZD except

where stated)

Board of DirectorsChair$95,000

Non-Executive Director$40,000

Audit and Risk CommitteeCommittee Chair $ 7, 5 0 0

Committee Member$5,000

Remuneration and Nominations CommitteeCommittee Chair $ 7, 5 0 0

Committee Member$5,000

Regulatory and Product Development Oversight CommitteeCommittee Chair $ 7, 5 0 0

Committee Member$5,000

1

Fee payable to non-United States (US) based directors. US based directors receive USD$50,000.

2

Fee payable to non-US based directors. US based directors receive USD$5,000.

Non-executive directors received the following directors’ fees, remuneration and other benefits from the Company in the year

ended 31 March 2018:

Remuneration and Value of Other Benefits Received in FY2018

Director

Non-Executive

Directors’

Board Fees

Audit and Risk

Committee Fees

Remuneration

and Nominations

Committee Fees

Regulatory

and Product

Development

Oversight

Committee Fees

Shares and

Other Payments

or Benefits

1

Total

Remuneration

Jim Burns

2

$69,968 $6,997$6,997--$83,962

David Flacks$95,000

(Chairman)

$5,000---$100,000

Nate Hukill

3

- -----

Jon Lamb

$40,000 $ 7, 5 0 0

(Chairman)

$ 7, 5 0 0

(Chairman)

--$55,000

Doug Wilson

$40,000--$ 7, 5 0 0

(Chairman)

-$ 47, 5 0 0

Total$244,968$19,497$14,497$7, 5 0 0-$286,462

1

In addition to director fees, AFT meets costs incurred by non-executive directors that are incidental to the performance of their duties. This includes

paying the costs of directors’ travel. As these costs are incurred by AFT to enable directors to perform their duties, no value is attributable to them as

benefits to directors for the purposes of this table.

2

Fees disclosed in New Zealand Dollars. Jim Burns receives fees paid in USD. These fees have been converted into NZD in the above table, calculated

at an exchange rate of 1: 0.715

3

Nate Hukill agreed not to receive any directors’ fees during the financial year ended 31 March 2018.

1

2

2

60AFT PHARMACEUTICALS LIMITED
Annual Report 2018

61

Diversity

The respective numbers and proportions of men and women at various levels within the AFT workforce as at 31 March 2017

and 31 March 2018 are set out in the table below:

FemaleMale

2018201720182017

No.%No.%No.%No.%

Directors

114%1

14%686%686%

Officers

1

440%327%660%873%

Senior Employees

2

229%233%571%466%

Overall Workforce

5461%4956%3439%3944%

1

Officers are considered to be the CEO and his direct reports (Management Team). Note that CEO, Hartley Atkinson, and Chief of Staff, Marree

Atkinson are included in both the number of Directors and Officers reported.

2

Senior Employees are considered to be direct reports to Officers.

The Board’s assessment of AFT’s performance against its Diversity Policy is set out in AFT’s Corporate Governance

Statement, which can be found on the investor centre of the Company’s website.

Board and Committee Attendance

The table below shows the number of Board and Committee meetings each director was eligible to attend and attended

during the year ended 31 March 2018:

DirectorBoard

Audit and Risk

Committee

Remuneration

and Nominations

Committee

1

Regulatory and New

Product Development

Committee

Hartley Atkinson

9/9-2/2

2/2

Marree Atkinson

8/9--2/2

Jim Burns

9/94/42/2-

David Flacks

9/94/4--

Nate Hukill

7/ 9---

Jon Lamb

7/ 94/41/2-

Doug Wilson

9/9--2/2

1

The Remuneration and Nominations Committee carried out certain functions during the year via circular resolution.

Director Independence

As at 31 March 2018 (and the date of this Annual Report), the Board comprised seven directors:

• David Flacks – Independent, Non-executive Director and Chairman

• Jon Lamb – Independent, Non-executive Director

• Doug Wilson – Independent, Non-executive Director

• Jim Burns – Independent, Non-executive Director

• Nate Hukill – Non-independent, Non-executive Director

• Hartley Atkinson – Executive Director and Chief Executive Officer

• Marree Atkinson – Executive Director and Chief of Staff

A biography of each director is set out on pages 20 and 21 of this Annual Report.

The Board has determined, based on information provided by directors regarding their interests, that as at 31 March 2018

(and the date of this Annual Report) David Flacks, Jon Lamb, Doug Wilson and Jim Burns are independent directors.

The Board has also determined that Hartley Atkinson and Marree Atkinson are not independent directors due to also

being executives and having major shareholding interests in AFT. The Board has also determined that Nate Hukill is not

independent due to his relationship with CRG, a major shareholder in AFT.

Statutory Disclosures (continued)

Director Interest Disclosures

Directors have given general notices disclosing interests pursuant to section 140(2) of the Companies Act 1993. All of

those interests (and any changes to interests) notified and recorded in AFT’s Interests Register during the financial year

ended 31 March 2018 are set out below:

DirectorEntityRelationship

Hartley AtkinsonAFT Orphan Pharmaceuticals LimitedDirector

AFT Pharmaceuticals Pty LimitedDirector

AFT Pharmaceuticals Singapore PTE LimitedDirector

AFT Pharmaceuticals (SE Asia) SDN BHDDirector

Atkinson Family TrustTrustee/Discretionary Beneficiary

AFT Limited Partner LimitedDirector

DSGP LimitedDirector

Dermatology Specialties, L.P.Director of AFT Limited Partner

Limited (LP of Dermatology

Specialties)

AFT Dermatology LimitedDirector

Marree AtkinsonAtkinson Family TrustDiscretionary Beneficiary

James BurnsPrecera Bioscience (formerly SanoAppointed Director

Informed Phenomics Health IncAppointed Director

Assurex Health, IncCeased to be Chairman/Director

Symmetry Surgical, IncCeased to be Director

Vermillion, IncDirector

David FlacksHarmoney Corp LimitedAppointed Chairman

NZX Regulatory Governance CommitteeAppointed Chairman

NZX Markets Disciplinary TribunalCeased to be Director

Vero Liability Insurance New Zealand LimitedDirector

Vero Insurance New Zealand LimitedDirector

Flacks & Wong LimitedDirector

Asteron Life LimitedDirector

NZ Venture Investment FundDirector

Upside Biotechnologies LimitedChairman

Nate HukillCapital Royalty Group entitiesPresident/Shareholder

CRG Investment CommitteeChairman

Valeritas IncDirector

Jon LambZoono LimiteAppointed Executive Chairman

Redwood Medical LimitedCeased to be Director

Rivers One LimitedTruste e

Redvers LimitedDirector

Project X Trustee LimitedDirector

Coronation Equities LimitedDirector

Three Dots LimitedDirector

Doug WilsonAdherium LimitedCeased to be Chairman

Mainz Consulting LimitedDirector

There were no entries in the Interests Register for the purposes of section 140(1) of the Companies Act 1993.

STATUTORY DISCLOSURES

62AFT PHARMACEUTICALS LIMITED
Annual Report 2018

63

In accordance with Section 148(2) of the Companies Act 1993, directors disclosed the following acquisitions or disposals of

relevant interests in AFT ordinary shares during the financial year ended 31 March 2018:

Name

Date of

Acquisition

/Disposal

Number of

Shares

Acquired

/(Disposed)

Nature of

Relevant Interest

Details of

Acquisition/Disposal

Consideration

Paid/Received

(NZD)

James Burns16 -J un -176,667 ordinary

shares

Registered holder and beneficial

owner of ordinary shares.

Acquisition of shares

under Share Purchase

Plan.

$15,000

4 -J ul -1714,000 ordinary

shares

Registered holder and beneficial

owner of ordinary shares.

On market acquisition

during permitted

trading period.

$32,200

10 -J ul -1720,000 ordinary

shares

Registered holder and beneficial

owner of ordinary shares.

On market acquisition

during permitted

trading period.

$46,000

David Flacks1 5 -J un -1725,000 ordinary

shares

Joint registered holder and

beneficial owner of ordinary

shares as trustee of Waitemata

Family Trust.

On market acquisition

during permitted

trading period.

$ 5 7, 5 0 0

16 -J un -176,667 ordinary

shares

Joint registered holder and

beneficial owner of ordinary

shares as trustee of Waitemata

Family Trust.

Acquisition of shares

under Share Purchase

Plan.

$15,000

Jon Lamb16 -J un -176,667 ordinary

shares

Power to control the exercise of

the right to vote as trustee of the

Rivers One Trust which holds the

shares in Rivers One Limited.

Acquisition of shares

under Share Purchase

Plan.

$15,000

Doug Wilson25 - M ay-1750,022/

(50,022)

ordinary shares

Beneficial interest as beneficiary

of trust.

Power to control the exercise of

the right to vote as director and

shareholder of Gillespie Nominee

Limited.

Off-market transfer of

shares to new trustee

entity. The underlying

beneficial holders

remain unchanged.

n/a

16 -J un -176,667 ordinary

shares

Beneficial interest as beneficiary

of trust.

Power to control the exercise of

the right to vote as director and

shareholder of Gillespie Nominee

Limited.

Acquisition of shares

under Share Purchase

Plan.

$15,000

Statutory Disclosures (continued)

In accordance with the NZX Listing Rules, as at 31 March 2018, directors had a relevant interest in AFT ordinary shares

as follows:

NameRelevant InterestPercentage

Hartley Atkinson

1

72,964,94274.98 3%

James Burns100,4170.103%

David Flacks115,4310.119%

Jon Lamb2 0 7, 9 7 20.214%

Doug Wilson56,6890.058%

1

Hartley Atkinson also has a relevant interest in 730,000 redeemable preference shares (21.9% of the total redeemable preference shares on issue),

which may in the future convert into ordinary shares.

For the purposes of section 161 of the Companies Act 1993, the following entries were made in the Interests Register in

relation to the payment of remuneration and other benefits to directors:

DateDirectorParticulars of Board Authorisation

16 June 2017Hartley Atkinson

Maree Atkinson

The payment of remuneration and the provision of other benefits

by the Company to each of Hartley Atkinson and Marree Atkinson

on the terms set out in a letter of amendment to the relevant

employment agreement.

For the purposes of section 162 of the Companies Act 1993, an entry was made in the Interests Register in relation to

insurance effected for directors of AFT, in relation to any act or omission in their capacity as directors.

Shareholdings

As at 30 April 2018, there were 97,308,019 AFT ordinary shares on issue, each conferring on the registered holder the right to

vote on any resolution at a meeting of shareholders, held as follows:

Size of ShareholdingNumber of Ordinary HoldersNumber of Ordinary Shares

1 to 1,000

3483 7. 2 %171,301

0.2%

1,001 to 5,000

37339.8%1,021,1801.1%

5,001 to 10,000

10611.3%804,4440.8%

10,001 to 50,000

849.0%1,674,1501.7%

50,001 to 100,000

91.0%590,9370.6%

100,001 and over

161.7%93,046,00795.6%

Total

936100.0%97, 3 0 8 ,01 9100.0%

As at 30 April 2018, there were 50 individuals holding a total of 694,000 options to acquire shares issued by AFT under its

employee long-term incentive scheme. The options are unlisted and carry no voting rights.

As at 30 April 2018, there were 5 shareholders holding a total of 3,330,000 redeemable preference shares issued by AFT.

The redeemable preference shares may convert into ordinary shares in certain circumstances. The redeemable preference

shares are unlisted and do not carry any right to vote except at meetings of an “interest group” of holders of Redeemable

Shares.

There is currently no on-market buy-back of the Company’s ordinary shares.

STATUTORY DISCLOSURES

6465AFT PHARMACEUTICALS LIMITED
Annual Report 2018

Set out below are details of the 20 largest holders of AFT ordinary shares as at 30 April 2018:

Shareholder

1

Number of

Ordinary Shares Held%

1.Hartley Atkinson + Colin McKay72,964,94274.98 %

2.Capital Royalty Partners II – Parallel Fund B (Cayman) L.P.6,499,5086.68%

3.National Nominees New Zealand Limited – Nzcsd <NNLZ90>3,468,8103.56%

4.Capital Royalty Partners II – Parallel Fund A L.P.3,285,5893.38%

5.Capital Royalty Partners II L.P.2,444,4152.51%

6.HSBC Nominees A/C NZ Superannuation Fund Nominees Limited – NZCSD <SUPR40>1,006,6671.03%

7.JPMorgan Chase Bank NA NZ Branch-Segregated Clients Acct – NZCSD <CHAM24>875,0230.90%

8.Capital Royalty Partners II (Cayman) L.P.769,5030.79%

9.FNZ Custodians Limited446,0660.46%

10.HSBC Nominees (New Zealand) Limited – NZCSD <HKBN90>41 7, 9 9 30.43%

11.Rivers One Limited2 0 7, 9 7 20.21%

12.Hamish Stewart Atkinson + Karen Winifred Atkinson + Andrew John Marriott190,0000.20%

13.Joseph Wallace Carson125,0000.13%

14.Joeri Yvonne Jozef Sels123,1000.13%

15.Citibank Nominees (New Zealand) Limited – NZCSD <CNOM90>121,0020.12%

16.James Burns100,4170.10%

1 7.David Mark Flacks + Adina Rita Betty Halpern90,4310.01%

18.BNP Paribas Nominees Pty Ltd <IB Au Noms Retailclient DRP>75,7500.08%

19.Barbara Tubby + Colin Tubby + Malcolm Tubby75,2180.08%

20.Custodial Services Limited <A/C 3>63,4120.07%

1

The shareholding of New Zealand Central Securities Depository Limited (custodian for members trading through NZClear) has been re-allocated to

the applicable members.

According to notices given to AFT under the Financial Markets Conduct Act 2013, the following persons were substantial

product holders in AFT as at 31 March 2018 in respect of the number of quoted voting products noted below. As at the

balance date (31 March 2018) there were 97,308,019 ordinary shares on issue:

Substantial Product Holder

Number of Ordinary Shares

in which Relevant Interest is Held% of Class Held at Date of Last Notice

Capital Royalty Partners Funds

1

12,999,01513.36%

Hartley Campbell Atkinson and Colin McKay as

Trustees of the Atkinson Family Trust72,964,94274.98 %

1

Funds detailed in the substantial product holder notice.

Statutory Disclosures (continued)

Subsidiary Company Directors

The following fees were paid to directors of subsidiary companies during the year ended 31 March 2018. No other directors

of subsidiary companies received director fees:

• Raymond McGregor received A$12,000 during the financial year ended 31 March 2018 in his capacity as a director of

AFT Pharmaceuticals (AU) Pty Limited.

• Hawksford Singapore Pte Ltd received SG$3,600 during the year ended 31 March 2018 in relation to Leong Wai Kuan acting

as a director of AFT Pharmaceuticals Singapore Pte Limited.

• Ilium Corporate Management SDN BHD received MYR3,600 during the year ended 31 March 2018 in relation to Khafnena

Binti Khanafiah and Irdawati Binti Mohamad acting as directors of AFT Pharmaceuticals (SE Asia) SDN BHD.

The following people held office as directors of subsidiary companies as at 31 March 2018:

SubsidiaryDirectors

AFT Pharmaceuticals (AU) Pty Limited (Australia)

Hartley Atkinson, Raymond MacGregor

AFT Pharmaceuticals (SE Asia) SDN BHD (Malaysia)Hartley Atkinson, Khafnena Binti Khanafiah,

Irdawati Binti Mohamad

AFT Pharmaceuticals Singapore Pte Limited (Singapore)

1

Hartley Atkinson, Leong Wai Kuan

AFT Orphan Pharmaceuticals LimitedHartley Atkinson, Andrew Moore, Giles Moss,

Malcolm Tubby

AFT Dermatology Limited

Hartley Atkinson

AFT Limited Partner Limited

Hartley Atkinson

DSGP Limited

Hartley Atkinson, Michael Derby

1

Chia Lai Kuan ceased to be, and Leong Wai Kuan was appointed, a director of AFT Pharmaceuticals Singapore Pte Limited during the financial year

ended 31 March 2018.

There were no entries made in the subsidiary company Interest Registers during the financial reporting period.

STATUTORY DISCLOSURES

66AFT PHARMACEUTICALS LIMITED
Annual Report 2018

67

NZX Waivers

On 21 December 2015, NZX granted the Company a waiver (Original Waiver) from NZX Main Board Listing Rule 5.2.3 in

respect of its quoted shares (Shares) for a period of 12 months to the extent the Rule required the Company to have at least

25% of Shares held by Members of the Public holding at least a Minimum Holding (as that term is defined in the NZX Main

Board Listing Rules). The Original Waiver has expired. On 21 December 2016, a further waiver from NZX Main Board Listing

Rule 5.2.3 was granted to AFT for an additional 12 month period. This waiver was renewed by NZX Regulation for a further

12 month period on 20 December 2017.

The waiver was granted on the following conditions:

• NZX receives an undertaking from the Atkinson Family Trust (AF Trust) that it will not increase its holding in AFT during the

term of the waiver, otherwise than as a result of an allotment pursuant to an offer or issue of shares that is made pro-rata to

all AFT shareholders;

• At least 10% of shares are held by more than 500 Members of the Public, with each Member of the Public holding at least

a Minimum Holding;

• AFT clearly and prominently discloses this waiver, its conditions, and its implications in AFT’s half year and annual reports,

and in any Offer Documents relating to any offer of shares undertaken by AFT, during the period of the waiver;

• AFT consistently monitors the total number of Members of the Public holding shares and the percentage of shares held by

Members of the Public holding at least a Minimum Holding;

• AFT notifies NZX as soon as practicable if there is any material reduction to the total number of Members of the Public

holding at least a Minimum Holding of shares, and/or the percentage of shares held by Members of the Public holding at

least a Minimum Holding; and

• AFT provides NZX with a written quarterly update of the total number of Members of the Public holding shares holding at

least a Minimum Holding and the percentage of shares held by Members of the Public holding at least a Minimum Holding.

The quarterly updates are from the date the waiver is granted, for the period of the waiver. The updates are to be provided

to NZX within ten business days of the end of each quarter.

• AFT provides NZX, with the second quarterly update, an update on the proposed initiatives AFT intends to undertake to

materially increase the percentage of shares held by Members of the Public before the expiry of the waiver.

The implication of the waiver is that the Shares may not be widely held and that there may be reduced liquidity in the Shares

following quotation. A copy of each waiver can be viewed at www.aftpharm.com.

Donations

No donations were made to charities or political parties during the financial reporting period. We donated medicine that was

used in education, prison and government institutions in Fiji.

Credit Rating

AFT does not currently have an external credit rating status.

Statutory Disclosures (continued)

AFT is a company incorporated with limited liability under the New Zealand Companies Act 1993

(Companies Office registration number 873005).

Registered OfficeLevel 1, 129 Hurstmere Road, Takapuna, Auckland 0622, New Zealand

+64 9 488 0232

www.aftpharm.com


Mertons, Level 7, 330 Collins Street, Melbourne, Victoria 3000, Australia

+61 3 8689 9997

Principal

Administration

Office

Level 1, 129 Hurstmere Road, Takapuna, Auckland 0622, New Zealand

+64 9 488 0232

www.aftpharm.com

113 Wicks Road, North Ryde NSW 2113, Australia

+61 2 9420 0420

ARBN: 609 017 969

Directors

(as at date of this

annual report)

Dr Hartley Atkinson

Marree Atkinson

Dr James (Jim) Burns

David Flacks

Nathan (Nate) Hukill

Jon Lamb

Dr Douglas (Doug) Wilson

Share RegistrarComputershare Investor Services Limited

Level 2, 159 Hurstmere Road, Takapuna, Auckland 0622, New Zealand

+64 9 488 8777

enquiry@computershare.co.nz


Computershare Investor Services Pty Limited

Yarra Falls, 452 Johnston Street, Abbotsford VIC 3001, Australia

+61 3 9415 4083

enquiry@computershare.co.nz

AuditorDeloitte

Deloitte Centre, 80 Queen Street, Auckland 1140, New Zealand

+64 9 303 0700

Annual Meeting3 August 2018

Half-Year End30 September 2018

Interim Results

Announcement

November 2018

Financial Year End31 March 2019

Financial calendar

Directory

DIRECTORY

68AFT PHARMACEUTICALS LIMITED
Annual Report 2018

Notes

AFT PHARMACEUTICALS LIMITED
Annual Report 2017

70

Data sourced from publicly available filings. Our datasets may not be complete. Automated analysis can produce errors. If you believe any data on this page is incorrect, please contact us at hello@nzxplorer.co.nz. For informational purposes only. Not investment advice.