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Benitec Biopharma Inc.

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FY2014 Annual Report · Benitec Biopharma Inc.
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Contents

CHAIRMAN AND THE CEO’S LETTER 

DIRECTORS’ REPORT 

AUDITOR’S INDEPENDENCE DECLARATION 

CORPORATE GOVERNANCE STATEMENT 

FINANCIAL STATEMENTS 

DIRECTORS’ DECLARATION 

INDEPENDENT AUDIT REPORT 

SHAREHOLDER INFORMATION 

CORPORATE DIRECTORY 

1

2

15

16

19

42

43

46

INSIDE BACK COVER

Cover Image (left to right):  
Dr Michael Graham, Benitec’s Chief Scientist and discoverer of ddRNAi and  
Dr David Suhy, Benitec’s Senior Vice President of Research & Development and creator of TT-034.

Chairman’s and CEO’s letter

Dear Shareholder,
We are pleased to present Benitec Biopharma’s Annual Report for 2014. 
Once in a generation a technology is developed that has the potential to radically change the current approach to disease treatment. Before penicillin 
there was fresh air and mercury baths. Think of what medicine was like before X-rays, MRI, organ transplants, IVF, or monoclonal antibodies. Now 
we are on the verge of turning the knowledge from the human genome project into targeted gene therapy drugs for a number of currently untreatable 
or incurable diseases. Benitec Biopharma’s gene silencing technology represents such a transformational technology for medicine. 
During the last year Benitec has made very significant progress toward delivering on this potential. This can be seen by comparing Benitec today 
with the company’s key performance indicators 12 months ago. In September 2013 the company had a market capitalisation of AUD$24.8 million, a 
share price of AUD$0.29, AUD$1.58 million in the bank, few institutional investors and no programs in the clinic. 
The Board and management team are very proud to report that one year later Benitec has a market capitalisation of around AUD$110 million, over 
AUD$30 million in the bank, 10 institutional healthcare investors and our lead compound, TT034 a “single shot cure” for Hepatitis C is in the clinic. 
These achievements have been made against the backdrop of a significant rise in the acceptance of RNAi as a treatment modality. siRNA-based 
companies such as Alnylam, Dicerna and Arrowhead also saw large increases in their valuation over the past 12 months. Your Board believes that 
Benitec is well positioned to continue to leverage the success of RNAi through the commercialisation of ddRNAi. 
Benitec became a clinical stage biotechnology company when, in January 2014, the US Food and Drug Administration (FDA) provided the company 
with clearance to began a phase I/II(a) clinical trial for TT-034. The fact that this clearance to proceed was provided within 30 days of the 
Investigational New Drug (IND) Application being submitted was a major validation of the work that our team put into this program. Even more 
important when considering that this was the first time the FDA had provided clearance for the commencement of a clinical trial for a systemically 
delivered ddRNAi therapeutic.  The progress and challenges of the trial and our measures in response have been reported on in Company 
announcements and we remain confident and committed to this program.
In February 2014 with the assistance of Lodge Partners (Melbourne) and Maxim Investment Bank (New York) Benitec was able to raise over AUD$30 
million in a private placement, predominantly from US-based healthcare institutional investors. This raising was important for a number of reasons; 
first it validated ddRNAi’s position in the RNAi therapeutic space, specialist healthcare institutions who had invested in US-based RNAi companies 
such as Alnylam, Dicerna and Arrowhead were acknowledging the opportunity that Benitec represented. Secondly these funds will enable Benitec 
to advance TT-034 to the conclusion of a Phase II(b) trial at which point we believe the drug, if successful, should deliver optimal partnering value. 
Thirdly, as a result of securing these funds, Benitec was able to open the Company’s own laboratory in Northern California providing the Company 
with the capability of advancing the other programs in our pipeline such as Hepatitis B, AMD, Lung Cancer and OPMD. Being able to advance these 
programs through the pre-clinical pathway highlights the depth and strength of Benitec’s approach to commercialising ddRNAi. 
During May 2014 Benitec’s Senior Vice President of Research and Development, Dr David Suhy was present at Duke Medical Research Unit when 
the first patient in our groundbreaking trial was given a sub-therapeutic dose of TT-034. It was particularly gratifying for Dr Suhy to be present 
at this significant event; Dr Suhy first drew his proposed structure for TT-034 on a white board in California eight years earlier. In June 2014, the 
independent Data Safety Monitoring Board (DSMB) for the TT-034 trial gave the all clear to dose the second patient, indicating that they saw no 
treatment-related adverse events with the first patient. Importantly laboratory results from the first patient demonstrated that TT-034 had been able 
to transduce liver cells and produce small but detectable amounts of shRNA, a very encouraging result considering this dose was sub-therapeutic. 
In a further significant development for Benitec’s ddRNAi technology, our licensee Calimmune, was given approval by the FDA to begin treating their 
second cohort of patients in the company’s groundbreaking Phase I/II trial of Cal-1, a stem cell based therapeutic candidate for HIV/AIDS therapeutic.  
This approval was further evidence of the safety of ddRNAi technology. 
Benitec has continued an aggressive strategy to raise the company’s profile and increase awareness of our achievements, and during 2013 – 2014 
we have presented at or attended the following events:

•  Ausbiotech 2013 – Brisbane
•  Over 30 investor and partnering meetings around the 2014 JP 

Morgan Healthcare Conference – San Francisco

•  ASX Spotlight - New York & London

•  BioPharma Europe - Barcelona
•  Bio 2014 - San Diego
•  Three Tickers – Brisbane and Melbourne
•  Broker Meets Biotech – Perth & Brisbane

It is becoming clear from these meetings that both investors and pharmaceutical industry representatives are now much more aware and interested 
in the potential that Benitec and ddRNAi offers as a value proposition than they were twelve months ago. 
The last 12 months has in many ways been transformational for your Company. Whilst many challenges remain in bringing a first-in-man therapy 
through to clinical validation, Benitec now has the resources to achieve its goals. We thank you for your ongoing support and look forward to an 
exciting next twelve months.

Peter Francis 
Chairman 

Peter French 
CEO and Managing Director

Benitec Biopharma Ltd Annual Report 2014  Page 1

 
 
Directors’ Report

Back (from left to right): Dr David Suhy, Mr Carl Stubbings, Mr Iain Ross, Dr John Chiplin, Dr Michael Graham. Front (from left to right): Dr Peter French, Mr Peter Francis, Mr Greg West

The Directors of Benitec Biopharma Limited (‘the Company’ or 
‘Benitec’) and its controlled entities (‘the Group’) present their report 
for the financial year ended 30 June 2014.

Mr Kevin Buchi BA, MBA, CPA
Non-Executive Director  
Appointed 14 April 2013

NON-EXECUTIVE DIRECTORS
The following persons were Directors of Benitec Biopharma Limited 
during or since the end of the financial year. 

Names, qualifications experience and special 
responsibilities

Mr Peter Francis LLB, GRAD DIP (INTELLECTUAL PROPERTY) 
Non-Executive Chairman 
Appointed 23 February 2006 

Mr Peter Francis is a partner at Francis Abourizk Lightowlers (FAL), a 
firm of commercial and technology lawyers with offices in Melbourne, 
Australia. He is a legal specialist in the areas of intellectual property 
and licensing and provides legal advice to a large number of 
corporations and research bodies. 

Other Current Directorships of Listed Companies: None

Former Directorships of Listed Companies in last three years 
Xceed Capital Limited.

Page 2  Benitec Biopharma Ltd Annual Report 2014

Mr. Buchi served as Chief Executive Officer of Cephalon, Inc. through 
its $6.8 billion acquisition by Teva Pharmaceutical Industries in 
October 2011. After the acquisition Mr. Buchi served as Corporate 
Vice President, Global Branded Products of Teva Pharmaceuticals. Mr. 
Buchi joined Cephalon in 1991 and held various positions, including 
Chief Operating Officer, Chief Financial Officer and Head of Business 
Development prior to being appointed CEO. 

Mr. Buchi currently serves as President and CEO and a member of the 
Board of Directors of TetraLogic Pharmaceuticals. Mr Buchi is also on 
the Board of Directors of Stemline Therapeutics, Inc., Forward Pharma 
A/S, Alexza Pharmaceuticals, Inc. and Epirus Biopharmaceuticals.

Mr Buchi originally trained as a synthetic organic chemist for the 
Eastman Kodak Company graduating from Cornell University with 
a Bachelor of Arts degree in chemistry. He holds Master’s degree 
in management from Kellogg Graduate School of Management at 
Northwestern University and is a Certified Public Accountant.

Other Current Directorships of Listed Companies 
Stemline Therapeutics, Inc. and Alexza Pharmaceuticals, Inc.

Former Directorships of Listed Companies in last three years 
Mesoblast Limited (Australia).

Directors’ Report

Dr Mel Bridges BAPPSC, FAICD 
Non-Executive Director 
Appointed 12 October 2007 
Resigned 18 June 2014

Dr Mel Bridges has more than 30 years’ experience as a CEO and 
public company director in the global biotechnology and healthcare 
industry. During this period, he founded and managed successful 
diagnostics, biotechnology and medical device businesses. He has 
successfully raised in excess of $300 million investment capital in the 
healthcare/biotech sector and been directly involved in over $1 billion 
in M&A and related transactions.

The businesses that Dr Bridges has founded have won numerous 
awards including the Queensland Export Award, Australian Small 
Business of the Year, Queensland Top 400, BRW’s Top 100 Fastest 
Growing Companies for seven consecutive years and The Australian 
Quality Award.

Dr Bridges has an Honorary Doctorate from Queensland University of 
Technology

Other Current Directorships of Listed Companies

ALS Ltd, Tissue Therapies Ltd.

Former Directorships of Listed Companies in last three years

Alchemia Limited (October 2003 to July 2013), Genetic Technologies 
Limited (December 2011 to November 2012), Leaf Energy Limited 
(August 2010 to September 2012), and Genera Biosystems Limited 
(December 2008 to November 2010).

Dr Bridges retired from the Board in June 2014.

Dr John Chiplin PH.D. 
Non-Executive Director  
Appointed 1 February 2010 

Dr. Chiplin is CEO of Polynoma LLC, an immuno-oncology company 
currently running one of the world’s largest (Phase III) melanoma trials. 
Prior to Polynoma, he was the founding CEO of Arana Therapeutics, 
a world leading antibody developer, and a director of Domantis, Inc., 
prior to their acquisition by Cephalon & GSK respectively.

Dr Chiplin’s investment vehicle, Newstar Ventures Ltd., has funded 
more than a dozen early stage companies in the past ten years. Dr. 
Chiplin’s Pharmacy and Doctoral degrees are from the University of 
Nottingham. In addition to Benitec Biopharma, he currently serves on 
the board of ScienceMedia, Inc. and Adalta Pty.Ltd

Other Current Directorships of Listed Companies: None

Former Directorships of Listed Companies in the last three years 
Arana Therapeutics Ltd., Calzada Ltd., Healthlinx, Ltd., Progen 
Pharmaceuticals Ltd., and Medistem, Inc.

Mr Iain Ross BSc, CH.D. 
Non-Executive Director  
Appointed 1 June 2010 

Mr Ross brings over 30 years’ experience in the international life 
sciences sector to the Board of Benitec. Following a career with 
Sandoz, Fisons, Hoffman La Roche and Celltech, he has undertaken 
and had input to a number of company turnarounds and start-ups as 
a board member on behalf of banks and private equity groups. He has 
led and participated in 4 IPOs, has direct experience of life science 

mergers and acquisitions both in the UK and USA and has raised more 
than £250m in the biotech sector.

He is a Qualified Chartered Director and currently he is Chairman of 
Ark Therapeutics Group plc (LSE); Biomer Technology Limited and 
Pharminox Limited; and a non-executive director of Tissue Therapies 
Limited (ASX), Novogen Limited (ASX) and Anatata Lifesciences 
Limited. He is also Vice Chairman of the Council of Royal Holloway, 
University of London. 

Other Current Directorships of Listed Companies 
Ark Therapeutics Group plc, Tissue Therapies Limited,  
Novogen Limited 

Former Directorships of Listed Companies in last three years: Coms plc

CHIEF EXECUTIVE OFFICER & MANAGING DIRECTOR

Dr Peter French MBA, PH.D.
Chief Executive Officer and Managing Director  
Appointed 26 August 2013

Peter French is a cell and molecular biologist who has been 
extensively involved in both basic and clinical medical research 
and commercialisation of biological intellectual property. He has 
an MBA in Technology Management and a PhD in cell biology. Dr 
French is a Past President of the Australia and New Zealand Society 
for Cell and Developmental Biology, and represented Australia’s 
biological scientists on the Board of FASTS, Australia’s peak 
government lobbying organization for science and technology. Dr 
French has conducted cell and molecular research in a broad range 
of areas relevant to Benitec’s DNA-directed RNAi based therapeutic 
technology, including cancer, HIV/AIDS, neurobiology, immunology and 
inflammatory disease.

He obtained his PhD in 1987 for work performed at CSIRO on the 
characterisation of the keratin composition of the developing wool 
fibre. He carried out postdoctoral research at the Children’s Medical 
Research Foundation, Sydney, on the role of glycoprotein expression in 
neuronal development. In 1989 he became Principal Scientific Officer 
and Manager of the Centre for Immunology, St Vincent’s Hospital, 
Sydney. Over the past 15 years Dr French has been extensively 
involved in Australia’s biotechnology industry, initially founding the 
stem cell company Cryosite (ASX:CTE), and then taking up leadership 
roles at other biotechnology companies prior to joining Benitec in 2009 
as its Chief Scientific Officer. Peter was appointed Chief Executive 
Officer of Benitec in June 2010 and Managing Director in August 2013.

Other Current Directorships of Listed Companies: None

Former Directorships of Listed Companies in last three years: None

COMPANY SECRETARY

Mr Greg West CA 
Appointed 26 May 2011 

Mr West is a Chartered Accountant with experience in the Biotech 
sector. He is a Director and Audit Committee Chairman of UOWE 
Limited (a business arm of Wollongong University), and a Director and 
Audit Committee Chairman of IDP Education Pty Ltd and Education 
Australia Limited. He worked at PWC and has held senior finance 
executive roles in financial services and investment banking with 
Bankers Trust, Deutsche Bank, NZI, and with other financial institutions.

Benitec Biopharma Ltd Annual Report 2014  Page 3

Directors’ Report

Interests in the shares and options of the company and 
related bodies corporate

Employees

The Group had 13 employees as at 30 June 2014 (2013: 7 employees). 

At the date of this report, the interest of the Directors in the shares 
and options of Benitec Biopharma Limited were:

Dividends

Director 

Number of  
Ordinary Shares  
(*after the July 2014 
securities consolidation) 

Number of Options over 
Ordinary Shares 
(*after the July 2014  
securities consolidation)

Mr Peter Francis 

327,250 

Dr Peter French 

342,554 

Mr Kevin Buchi 

615,385 

Dr John Chiplin 

263,020 

Mr Iain Ross 

66,364 

1,716,924

2,849,231

646,154

410,563

407,500

* A resolution to consolidate the Company’s securities (shares, 
options and warrants) was approved at the General Meeting on 17 
July 2013. The securities consolidation was on a 25:1 basis meaning 
that shareholders have 1 consolidated security for every 25 securities 
held before Friday 19 July 2013. Capital raisings and securities 
consolidation are referred to on page 12. 

Unless otherwise stated, all numbers of securities in this document 
are after the 19 July 2013 consolidation. 

CORPORATE INFORMATION

Corporate Structure

Benitec Biopharma Limited (‘the Company’ or ‘Benitec’) is a company 
limited by shares and is incorporated and domiciled in Australia. The 
Company has prepared a consolidated financial report incorporating 
the entities that it controlled during the financial year (‘the Group’), 
which are described in note 11 of the financial statements.

– 

Principal Activities

Benitec Biopharma Limited is an ASX-listed biotechnology company 
(ASX: BLT, OTC: BTEBY) based in Sydney, Australia. The company 
has a pipeline of in-house and partnered therapeutic programs 
based on its patented gene-silencing technology, ddRNAi. Benitec 
is developing treatments for chronic and life-threatening human 
conditions such as Hepatitis C, Hepatitis B, wet age-related macular 
degeneration, cancer-associated pain, drug resistant lung cancer 
and oculopharyngeal muscular dystrophy based on this technology. 
In addition, Benitec has licensed ddRNAi technology to other 
biopharmaceutical companies who are progressing their programs 
towards the clinic for applications including HIV/AIDS, retinitis 
pigmentosa and Huntington’s disease. Benitec generates revenue from 
licensing its technology and research and development grants. 

The principal activities of the Group during the year were progressing 
programs through the clinic, the commercialisation of Benitec’s unique 
Intellectual Property, development of the Company’s therapeutic 
pipeline and pre-clinical programs, funding, and protection and 
building the IP estate. 

Page 4  Benitec Biopharma Ltd Annual Report 2014

No dividends in respect of the current or previous financial year have 
been paid, declared or recommended for payment.

OPERATING AND FINANCIAL REVIEW

Operating review

Benitec’s ddRNAi approach is significantly different to other gene 
silencing methodologies: it induces the target cell to continuously 
manufacture specific silencing molecules resulting in long term 
silencing of the disease-associated gene after just a single treatment. 
While there are other technologies for inhibiting gene activity, in 
most cases these treatments must be regularly re-administered. It is 
believed that only ddRNAi is able to achieve long-term gene silencing 
from a single treatment administration.

The key elements of Benitec’s strategy to generate a competitive and 
appropriate return for stakeholders are to:

•  Validate that ddRNAi will be safe and effective in a clinical 

setting. The Company has made substantial progress towards this 
goal, namely:
– 

In late May 2014, the Duke Medical Research Unit, 
commenced dosing in the Company’s “first-in-man” clinical 
trial of its hepatitis C virus (HCV) treatment, TT-034. 
Demonstrating its safety and efficacy should be a significant 
value inflection point in addition to “validating” ddRNAi as a 
transformational platform for targeting multiple diseases. This 
would be expected to enhance interest from pharmaceutical 
companies in collaborating with Benitec on developing 
ddRNAi therapies in areas of mutual interest. 
In December Benitec’s collaborator, University of NSW 
Children’s Cancer Institute, was able to confirm increased 
survival in a preclinical in-vivo lung cancer model. The 
Company filed a pre-pre IND submission with the US Food and 
Drug Administration (FDA) to discuss options for preclinical 
toxicology testing. 

•  Optimise the Company’s share register by consolidating the 

number of shares issued and expanding the number of institutional 
investors. 
– 

In July 2013 Benitec announced a 25:1 consolidation of the 
Company’s stock. The post consolidation share price of $0.27.5 
has been significantly improved on the company trading above 
$1.00 for the majority of 2014. 
In February 2014 Benitec announced that the company had 
completed a $31.5M private placement which included US 
and international institutional investors including: RA Capital 
Management, Perceptive Advisors, Special Situation Funds 
and Sabby Management. 
In June 2014 Benitec advised it had established a sponsored 
Level 1 American Depositary Receipt (ADR) program facility 
trading in the Over-The-Counter (OTC) market in the United 
States. The Benitec ticker for the ADR is: BTEBY. The primary 
benefit of the ADR program is to widen the secondary capital 
market for the Company allowing Benitec shares to be traded 
more easily for U.S. investors. 

– 

– 

 
 
 
Directors’ Report

•  Secure funding to accelerate the clinical development of Benitec’s 
programs. The $31.5 million capital raise finalised in April is 
enabling the Company to:
–  Fund TT-034 into Phase I/II(b) and to advance other programs 
in the Company’s pipeline with particular emphasis on lung 
cancer, AMD and HBV. 

–  Expand the Company’s in-house capability with the opening of 

its own laboratory in northern California.

–  Appoint key personnel: Benitec has recruited a number 
of experienced and highly qualified scientific, program 
management and Intellectual Property resources to support the 
accelerated clinical development of the Company’s programs. 

Successful execution of these elements is enhancing Benitec’s 
opportunities to engage with the pharmaceutical industry and achieve 
successful commercial outcomes for the Company’s programs. 

Strategic Advantage

Benitec’s ddRNAi technology is a form of RNA interference (RNAi) that 
can ‘silence’ or shut down disease-causing genes. Recently there has 
been an increasing awareness of the value of gene silencing and RNAi 
as a therapeutic modality; Companies operating in this segment – such 
as Alnylam, Arrowhead, Dicerna, Tekmira, Bluebird Bio and Isis – have 
seen significant increases in their valuation. In particular, Alnylam has 
grown its company’s market capitalisation from around $1 Billion to 
over $4 Billion over the last two years. Benitec’s ddRNAi technology 
has a number of differential advantages over RNAi: the most important 
is its ability to silence a disease-causing gene for long periods with a 
single administration, whereas conventional RNAi requires continuous 
administration. 

Big pharma is demonstrating a renewed interest in RNAi and gene 
therapy. Benitec’s ddRNAi technology offers an optimised combination of 
these approaches, and the TT-034 clinical trial, if successful, will provide 
validation of the technology for treating a wide range of diseases. 

In-house Programs

Focus

Indication Partners/Collaborators Discovery

Pre-clinical

Clinical

Hepatitis C

Infectious 
Disease

Hepatitis B

Biomics  
Biotechnology (JV)

Non Small  
Cell* Lung 
Cancer

Cancer  
Associated 
Pain

University of New 
South Wales (RC)

Stanford University 
(RC)

Cancer

Ocular 
Disease

AMD**

Stanford University 
(RC)

Genetic 
Disease

OPMD***

Royal Holloway  
London University (RC)

RC = research collaboration
JV = joint venture

*and other chemotherapy-resistant cancers    
**Age-Related Macular Degeneration   
***Oculopharyngeal Muscular Dystrophy, and orphan disease

Benitec has six in-house development programs underway. Following 
the acquisition of Tacere in November 2012, the Company decided to 
put most of these programs on hold whilst focusing on advancing the 
hepatitis C therapeutic, TT-034, towards the clinic. With the securing of 
the major fund raising in April 2014, the Company is re-activating the 
other pipeline programs. Highlights over the previous 12 months include:

•  Hepatitis C – “TT-034”. In 2014 TT-034 became Benitec’s first 
clinical stage treatment achieving the following key milestones:

–  Allowance by the FDA to proceed with a clinical trial for TT-

034 was received in mid-January. Of particular note, the New 
Drug Application (NDA) was accepted by the Agency within 30 
days of receipt with no significant changes. 

–  Commencement of screening and patient recruitment at Duke 

Medical Research Unit.

–  The first patient was dosed in late May.
–  The first patient experienced no treatment-related adverse 
events and, importantly, there was evidence of liver 
transduction and production of short hairpin RNAs (shRNA).

–  Approval by the Data Safety Monitoring Board (DSMB) to 

proceed with the clinical trial with no modification following 
review of the safety parameters of the first patient after 6 
weeks following the single administration. 

–  A paper describing TT-034 was accepted for publication in 
the prestigious scientific journal Nature Molecular Therapy 
Nucleic Acids.

–  University of California San Diego (UCSD) has joined the 

Duke Clinical Research Unit to concurrently screen and enrol 
patients, boosting patient recruitment. 

•  Chemotherapy-resistant lung cancer – “Tribetarna™”. 

Benitec’s lung cancer program targeting the gene responsible for 
chemotherapy resistance, beta III tubulin, has made encouraging 
progress toward the clinic. Significant milestones in the last 12 
months include:

–  Significantly increased survival observed in a preclinical in vivo 
model of lung cancer following intravenous administration of 
the ddRNAi-based therapeutic, Tribetarna™ in combination 
with cisplatin, confirming previously reported results.

–  Dr Craig Lewis appointed Chief Medical Adviser. Dr Lewis is 

a medical oncologist at Sydney’s Prince of Wales Hospital; he 
has a major interest in clinical trial research in lung cancer, 
breast cancer and sarcoma. 

–  Professor Maria Kavallaris (Benitec’s collaborator on 

Tribetarna™) was acknowledged by the prestigious National 
Health and Medical Research Council (NHMRC)’s List of High 
Achievers in Health and Medical Research Award. 
–  Pre-pre IND submission filed with the US FDA and a 

teleconference held to discuss guidance on appropriate 
toxicology studies to be conducted for this first-in-man 
therapeutic approach.

•  Wet age-related macular degeneration (AMD). A focus of 
Benitec’s US laboratory has been the testing and optimisation 
of suitable vectors to deliver ddRNAi constructs to the retina. In 
parallel the Company has identified suitable animal models to 
complete the validation of this therapy. The single-administration 
approach permits the possibility of use as a prophylactic, 
preventing any development of retinal damage before AMD 
develops thus offering both a treatment and a preventative 
solution to this important healthcare problem.

Benitec Biopharma Ltd Annual Report 2014  Page 5

Directors’ Report

•  Hepatitis B – ‘Hepbarna™’ Hepatitis B virus (HBV) infection is 
currently incurable and represents a significantly larger public 
health problem than HCV. Hepbarna™ is similar in design to TT-
034, utilizing the same delivery vector, enabling it to leverage 
much of the toxicity and biodistribution data obtained in the 
Company’s HCV clinical development program. In conjunction with 
the Company’s collaborator, Biomics Biotechnologies, Benitec is 
optimising the design of DNA constructs, and the Company’s US 
laboratory is preparing to undertake a range of in vitro validation 
experiments.  

•  Neuropathic pain. The research collaboration with Professor 
David Yeomans at Stanford University will focus in the first 
instance on re-validating the previously developed constructs  
in vivo.

•  Genetic disease – ‘Pabparna™’. Benitec’s treatment for 

oculopharyngeal muscular dystrophy (OPMD) – which is being 
developed in collaboration with the Royal Holloway, University of 
London – continues to progress. 

•  Huntington’s disease – Benitec’s non-exclusive license allows 
uniQure to develop a treatment for Huntington’s disease using 
the company’s ddRNAi gene silencing technology. uniQure listed 
on the NASDAQ in early 2014, raising around $90M so is wel 
resourced to be able to advance this program towards the clinic.
•  Retinitis pigmentosa – Benitec’s licensee Genable Technologies 
Ltd is developing GT308 for retinitis pigmentosa using ddRNAi 
to silence the disease-causing mutant gene. Genable was been 
granted orphan drug designation from the FDA; this status means 
Genable will gain seven years of market exclusivity in the US once 
the product is approved. 

•  Breast cancer – Benitec has granted a license to Regen 

Biopharma for the development of a ddRNAi-based therapy called 
dCellVax. Regen recently announced the successful silencing of 
the IDO gene in dendritic cells, an approach that in animal models 
has demonstrated the ability to induce regression of breast cancer. 

Licensed Programs

Intellectual Property

In addition to the Company’s in-house development programs, Benitec 
has licensed its ddRNAi technology to four biotech companies. As 
each of these companies advances their clinical development their 
success further validates ddRNAi. Each program is outlined below:

Focus

Indication Partners/Collaborators Discovery

Pre-clinical

Clinical

Infectious 
Disease

HIV/AIDS

Licensed to  
Calimmune

Cancer

Cancer Vac-
cines

Licensed to  
Regen BioPharma

Ocular 
Disease

Retina 
Pigmentosa

Licensed to  
Genable

Genetic 
Disease

Huntington’s 
Disease

Licensed to  
uniCure

•  HIV/AIDS – Benitec’s US-based licensee Calimmune Inc. has 
recently received approval to commence dosing patients in the 
second cohort of their Phase I/II stem cell-based clinical trial in 
people living with HIV/AIDS. Approval to move into the second 
group of patients confirms that there were no safety issues or 
treatment-related adverse events observed during the dosing of 
the first cohort. The Cal-1 therapy utilises ddRNAi-based gene 
silencing technology along with additional proprietary technology 
to reduce the ability of HIV to enter immune cells. The trial is 
entitled “Safety Study of a Dual Anti-HIV Gene Transfer Construct 
to Treat HIV-1 Infection”.  

Page 6      Benitec Biopharma Ltd Annual Report 2014

Benitec’s patent estate includes a combination of technology patents 
and program-specific patents. Technology patents are based on 
research in the 1990’s conducted by Dr Michael Graham (now Chief 
Scientist at Benitec) and colleagues at CSIRO. These patents form 
the basis for a dominant position in DNA-directed gene silencing 
for therapeutic use in humans. The program patents are aimed at 
establishing strategic patent protection for Benitec’s programs in 
development in key jurisdictions including the US, Europe, Australia, 
China, Japan and Canada

Key developments:
• 

International patent application filed for the AMD program. This 
patent filing is aimed at the use of ddRNAi in the treatment of 
wet age-related macular degeneration including identifying target 
sequences for RNAi activity.

•  European opposition hearing was conducted for the Graham 

European patent EP1555317 in the presence of patent opponents, 
BASF SE and Galapagos NV. Despite a favourable preliminary 
ruling, the formal hearing reversed its initial findings and upheld 
the opposition, revoking this Graham patent. Benitec, along with 
CSIRO, has the opportunity to appeal this decision. The Graham 
patent family also includes two pending applications in Europe, 
EP070008204 and EP10183258.

•  Benitec has licensed third party IP to strengthen its position in 
Europe. The company has executed a license agreement with 
Galapagos NV in Europe, which grants Benitec the rights to use 
RNAi in human therapeutics and diagnostics under the Galapagos 
patent EP1444346. The rights include the right to sub-license.

•  The European Waterhouse patent EP1068311 has been scheduled 
for an opposition hearing at The Hague in January 2015. The 
opponents to this patent are BASF SE, Strawman Limited, 
Carnegie Institution of Washington/University of Washington and 
Syngenta International AG. The preliminary review from the EPO is 
favourable.  

Directors’ Report

Technology patents 

Title

Patent number

Filing date

Status

Genetic constructs for delaying or 
repressing the expression of a target 
gene (Graham patent family)1

Control of gene expression (Graham 
family patent)

Methods and means for obtaining 
modified phenotypes (Waterhouse 
patent family)2

US 6,573,099

19 June 1998

Graham patent family member; granted 3 June 2003; Re-
examination Certificate (US90/008096) issued 8 March 2011

WO199904929

19 March 1999

Granted
US (8067383, 8168774, 7754697, 8048670, 8053419), Australia, 
Canada, Europe (under opposition), UK, Hong Kong, India, Japan, 
Korea, Mexico, New Zealand, Singapore, South Africa

Pending
US, Brazil, China, Europe, Japan, Mexico

WO1999053050

7 April 1999

Granted
US, Australia, China, Europe (under opposition), New Zealand

Genetic Silencing

WO2001070949

16 March 2001

Pending
US, Canada, Europe, Japan

Granted
Singapore, South Africa, UK

Pending
Brazil

Double-stranded nucleic acid

WO2004106517

3 June 2004

Granted
Australia, New Zealand, Singapore, South Africa

1 Benitec has an exclusive, irrevocable worldwide license from CSIRO for human therapeutics 
2 Benitec has an exclusive, irrevocable worldwide license from CSIRO for human therapeutics

Program specific patents 

Title

Patent number

Filing date

Status

Multiple promoter expression 
cassettes for simultaneous delivery 
of RNAi agents (Hepatitis C)

WO2005087926

4 March 2005

Granted
US (7727970, 8283461, 8691967), Australia, Canada, China, 
Europe, Israel, Japan, Korea

Pending
China, Europe

RNAi expression constructs 
(Hepatitis C)

WO2006084209

3 February 2006

Granted
US (7803611, 8076471), Australia, China, New Zealand

RNAi expression constructs with 
liver-specific enhancer/promoter 
(Hepatitis virus)

Minigene expression cassette 
(Hepatitis)

US 8,008,468

16 February 2006

Granted on 30 August 2011

Pending
US, Europe, Canada, Hong Kong, 

US 8,129,510

30 March 2007

Granted on 6 March 2012

HBV treatment (Hepatitis B)

WO2012055362

27 October 2011

Pending
Australia, Brazil, Canada, China, Hong Kong, Europe, India, 
Korea, Russia, US

Pain treatment

WO2013126963

28 February 2013

PCT filed

Age related macular degeneration 
treatment (AMD)

WO2014107763

8 January 2014

PCT filed

Benitec Biopharma Ltd Annual Report 2014      Page 7

Directors’ Report

Commercialisation 

Cash Flows

Business development has remained a major focus for Benitec in 
2013 – 2014. Executing an appropriate partnering agreement with a 
suitable commercial pharmaceutical company is a key goal for the 
Company. The review and subsequent allowance to proceed with 
the TT-034 clinical trial by the FDA combined with agreement by the 
DSMB to dose the second patient in this “first-in-man” clinical trial 
has created a significant increase in interest from the pharmaceutical 
industry. These successes provide early stage validation of ddRNAi in 
the Company’s other programs, any one of which could be a “company 
maker” in their own right. 

The $31.5 million injection of capital will enable Benitec to negotiate 
with potential partners from a strong financial position.

Raising Benitec’s profile

Benitec’s commercial profile continues to grow. Two more firms 
initiated coverage of Benitec during 2013 – 2014: Shaw Stockbrokers 
recommended a “buy” rating with target price of $3.00 and New York-
based Maxim Group also recommended a “buy” rating with a target 
price of $4.00. Lodge Partners, who had initiated coverage in 2012 
– 2103, updated their target price to $3.20 maintaining their “buy” 
recommendation. 

Benitec continued to raise its profile as an innovator and leader in 
gene silencing with Dr Peter French appearing on ABC TV’s “The 
Business” and “The 7:30 Report”. Dr Peter French also recorded an 
in-depth interview on Brisbane Radio 4BC. 

The Company cash flows consist of income from licensing the 
Company’s technology, proceeds from issue of shares, interest income, 
Research and Development grant receipts, payments to employees and 
suppliers to exploit the Company’s intellectual property portfolio and 
the maintenance of the required regulatory corporate structures.

Capital raisings - June & July 2013

Benitec announced a capital management update on 6 June 2013, 
including details of a Private Placement and share purchase plan (SPP). 
The private placement raised $7,900,000 and was subscribed to by 
several new institutional investors, along with Benitec management 
and directors and existing sophisticated investors at $0.275 per share 
(after consolidation). The June & July 2013 placement was made in 
two stages:

•  $412,000 was raised under the Company’s 15% placement 

capacity, in accordance with ASX Listing Rule 7.1, and settled on 
14 June 2013; and

•  $7,488,000 was raised following shareholder approval, settled on 

24 July 2013. 

A General Meeting was held on 17 July 2013 where shareholders 
approved the second stage of the private placement, together with 
a 25-for-1 consolidation of the Company’s issued securities. The 
securities consolidation means that shareholders have 1 consolidated 
security for every 25 securities held before Friday 19 July 2013. All 
numbers of securities in this report are after the consolidation on 19 
July 2013.

Benitec has entered into agreements to raise AUD 31,496,514 from international 
institutional investors comprising leading US healthcare and biotechnology funds.

In the print media, Benitec featured in The Australian Way, QANTAS’ 
in-flight magazine, Business Review Weekly, and Hospital & Aged 
Care, as well as being featured in stories in The Australian, Brisbane 
Times and The Geelong Independent. 

Benitec completed production of a video summarising ddRNAi’s mode 
of action highlighting its advantages compared with conventional 
RNAi; the video can be viewed on the Company’s website 
http://www.benitec.com/videos.php

Financial Overview

Benitec’s net loss for the year to 30 June 2014 was $7,039,109 
compared to a net loss of $3,847,960 for the previous corresponding 
period. Operating revenue of $1,373,773 (2013: $1,464,182) included 
Research and Development Grants received totalling $775,833 (2013: 
$824,333). Expenses totalled $8,867,247 (June 2013: $4,952,142)

Benitec’s current assets at 30 June 2014 were $34,447,525 (June 
2013: $1,722,590), with current liabilities of $954,680 (June 2013: 
$1,110,370). 

The SPP raised $2,820,000 and closed on 29 July 2013. The SPP was 
conducted on the same terms as the private placement, with shares 
allotted to participants in the SPP on 6 August 2013. 

Capital raisings – February and April 2014

On 24 February 2014 Benitec announced it has entered into agreements 
for a Private Placement to raise AUD $31,496,514 from international 
institutional investors who include US based RA Capital Management, 
Perceptive Advisors, Special Situations Funds and Sabby Management, 
as well as existing Australian investors. The international institutional 
investors comprised leading US healthcare and biotechnology 
funds and their participation represents significant support for and 
recognition of Benitec’s ddRNAi development programs.

The Placement involved the purchase of 29,435,994 ordinary shares at a 
price of AUD $1.07 per ordinary share. In addition, the investors received 
free attaching options expiring in five-years to purchase 13,246,204 
ordinary shares at an exercise price of AUD $1.26 per ordinary share. 
The February and April 2014 Placement was made in two stages: 

Page 8      Benitec Biopharma Ltd Annual Report 2014

Directors’ Report

•  $15,748,255 representing 14,717,995 ordinary shares, with 

There were no ESOP options which lapsed during the financial year.

6,623,099 options. The placement was made without shareholder 
approval on 28 February 2014; and was ratified by shareholders’ at 
a general meeting on 10 April 2014; and

•  $15,748,259 representing 14,717,999 ordinary shares, with 
6,623,105 options. The placement was made after receiving 
shareholder approval at a general meeting on 10 April 2014.

Ordinary Shares

67,867,428 ordinary shares were issued during the year through 
private placements at prices ranging from $0.275 to $1.07 per share. 
In addition, 955,002 ordinary shares were released from escrow to the 
Tacere vendors during the year at $0.375 per share.

Options

At the date of this Directors’ Report, the Company has a total of 
23,320,173 options to acquire ordinary shares in the Company. 
Unless otherwise noted, all options are unlisted, restricted and are 
categorised as follows:

Non-Executive Director Options on issue were:

Grant Date 

Expiry Date 

Exercise Price  Number

13 July 2010 

19 August 2014 

$0.5700 

26 September 2011  26 September 2016  $1.2500 

120,000

1,600,000

26 September 2011  26 September 2016  $1.2500 

      1,200,000 

10 November 2013  18 May 2018 

$0.6250 

       400,000 

Total 

3,320,000

Summary of Shares, Options and Warrants on Issue –  
30 June 2014
The Company had 114,898,992 listed ordinary shares and no listed 
options on issue at reporting date. There are 14,467,095 unlisted 
options and 245,078 warrants on issue, details of which are included 
in note 16 (b) to the financial statements.

Employee Share Option Plan 

Directors’ Options 

Warrants 

Unlisted Options 

Total 

5,288,000

3,320,000

245,078

14,467,095

23,320,173

Unissued Shares
As at the date of this report, there were 23,320,173 options over 
unissued ordinary shares, details of which are included in note 16 (b) 
to the financial statements. Option holders do not have the right, by 
virtue of the option, to participate in any share issue of the Company 
or any related body corporate or in the interest issue of any other 
registered scheme related to the Company.

Further details of the unissued shares under option are provided in 
Note 16(b)

Employees Share Option Plan (ESOP)
Options issued to employees are made through the Employee Share 
Option Plan (ESOP). The expiry dates for options granted under the 
ESOP are set out below. The expiry date for options held by any 
employee who has resigned will be determined by the Board or will 
expire within twelve months of resignation. The Board has the power 
to adjust, amend and cancel the ESOP. Non-Executive Directors are 
excluded from the ESOP.

Options on issue under the Employees Share Option Plan are:

Grant Date 

Expiry Date 

Exercise Price  Number

13 July 2010 

19 August 2014 

$0.510 

       260,000 

17 November 2011  17 November 2016  $1.250 

      1,800,000 

7 February 2012 

7 February 2017 

$1.250 

       168,000 

Shares issued as a result of the exercise of Options
During the year 547,088 shares were issued on the exercise of options 
issued by the Company (2013: nil). 

Significant changes in the state of affairs

During the year the Company commenced a US based Phase I/IIa clinical 
trial in Hepatitis C and arranged net equity funding of $39.6 million. 
These and other important events in the year are considered in the 
‘Operation of Operations’ section of this Directors Report. Other than 
this, there were no significant changes in the Company’s state of affairs.

Significant events after the reporting date 

No other matters or circumstances have arisen since 30 June 2014 
which have significantly affected or may significantly affect the 
operations of the Group, the results of those operations or the state of 
affairs of the Group, in subsequent financial years. 

18 July 2012 

18 July 2017 

$1.250 

       400,000 

Likely developments and expected results

16 November 2012  16 November 2017  $1.250 

       400,000 

22 August 2013 

22 August 2018 

15 May 14 

15 May 19 

$1.250 

$1.500 

Total 

      2,080,000 

       180,000 

5,288,000 

Benitec will continue to progress programs through the clinic, seek 
commercialisation opportunities with big Pharma and others for 
the Company’s unique Intellectual Property; develop its therapeutic 
pipeline and pre-clinical programs, protect and build the Company’s IP 
estate and secure adequate funding. 

Benitec Biopharma Limited is listed on the Australian Securities 
Exchange (ASX) and is subject to the continuous disclosure 
requirements of the ASX Listing Rules which require timely disclosure 
of information which may affect security values or influence 
investment decisions, and information in which security holders, 
investors and ASX have a legitimate interest.

Benitec Biopharma Ltd Annual Report 2014      Page 9

 
 
 
 
The performance of executives is measured against criteria agreed 
annually with each executive and is based predominantly on the overall 
success of the Company in achieving its broader corporate goals. 
Bonuses and incentives are linked to predetermined performance 
criteria. The Board may, however, exercise its discretion in relation 
to approving incentives, bonuses, and options, and can recommend 
changes to the CEO’s recommendations. The policy is designed 
to attract the highest calibre of executives and reward them for 
performance that results in long-term growth in shareholder wealth.

Executives may be invited to participate in the Employee Share  
Option Plan. 

Australian executives or directors receive a superannuation guarantee 
contribution required by the government and do not receive any other 
retirement benefits.

All remuneration paid to directors and executives is valued at the cost 
to the Company and expensed. Options are valued using the Black-
Scholes methodology. 

The Board policy is to remunerate non-executive directors at 
market rates for comparable companies for time, commitment, and 
responsibilities. The Board as a whole determines payments to the 
non-executive directors and reviews their remuneration annually, 
based on market practice, duties, and accountability. The maximum 
aggregate amount of fees that can be paid to non-executive directors 
is subject to approval by shareholders at the Annual General Meeting. 
Fees for non-executive directors are not linked to the performance 
of the consolidated entity. However, to align directors’ interests with 
shareholder interests, the directors are encouraged to hold shares in 
the Company.

Performance Based Remuneration
Each executive’s remuneration package has a performance-based 
component. The intention of this approach is to facilitate goal 
congruence between executives with the business and shareholders. 
Generally, the executive’s performance based remuneration is tied 
to the Company’s successful achievement of certain key milestones 
relating to its operating activities, as well as the Company’s overall 
financial position.

Company Performance, Shareholder Wealth, and Directors’ and 
Executives’ Remuneration
The remuneration policy has been tailored to increase goal congruence 
between shareholders, directors, and executives. Two methods are 
applied in achieving this aim, the first being a performance based bonus 
based on achievement of key corporate milestones, and the second 
being the issue of options to the majority of directors and executives to 
encourage the alignment of personal and shareholder interests.

Directors’ Report

Environmental regulation

The Group’s operations are not subject to any significant environmental 
regulations under either Commonwealth or State legislation.

Meetings of Directors

The number of meetings of the Directors held during the year and the 
number of meetings attended by each director was as follows:

Board of Directors  Risk & Audit Committee
Attended 

Attended 

Held 

Held

Peter Francis 

Peter French 

John Chiplin 

Kevin Buchi 

Iain Ross 

Mel Bridges 

13 

11 

13 

11 

11 

11 

13 

11 

13 

13 

13 

13 

2 

- 

2 

- 

- 

2 

2

-

2

-

-

2

Committee membership
Due to the small number of Directors, it was determined that the 
Board would undertake all of the duties of a properly constituted 
Remuneration and Nomination Committee, with Dr John Chiplin acting 
as Chairman.

The Audit and Risk Committee was chaired by Dr Bridges and met 
twice during the financial year. Mr Iain Ross now chairs the Audit and 
Risk Committee.

Remuneration report (audited)

This report details the nature and amount of remuneration for each 
director of the Company, and for all key management personnel.

The information provided in the Remuneration Report has been audited 
as required by s308 (3c) of the Corporations Act 2001.

Remuneration Philosophy
The remuneration policy of the Company is to align director and 
executive objectives with shareholder and business objectives by 
providing a fixed remuneration component and offering long-term 
incentives based on key performance areas. The Board believes the 
remuneration policy to be appropriate and effective in its ability to 
attract and retain the best executives and directors to run and manage 
the consolidated entity, as well as create goal congruence between 
directors, executives, and shareholders.

The Board is responsible for determining the appropriate remuneration 
package for the CEO, and the CEO is in turn responsible for determining 
the appropriate remuneration packages for senior management.

Executives typically receive a base salary (which is based on factors 
such as experience and comparable industry information), options, and 
performance incentives. The Board reviews the CEO’s remuneration 
package, and the CEO reviews the other senior executives’ 
remuneration packages, annually by reference to the consolidated 
entity’s performance, executive performance, and comparable 
information within the industry.

Page 10  Benitec Biopharma Ltd Annual Report 2014

 
 
Directors’ Report

Details of Remuneration for Year Ended 30 June 2014
Table 1.  Non-Executive Director Remuneration for the year ended 30 June 2014

Short Term

Post Employment

Equity

Total

Salary & Fees

Cash 
Bonus

Non 
Monetary 
Benefits

Super-
annuation

Termination 
Benefits

Options

% of 
remuneration 

consisting of 
options

Peter Francis

John Chiplin

Iain Ross

Kevin Buchi

Mel Bridges

2014
2013
2014
2013
2014
2013
2014
2013
2014
2013

$

113,328 
 113,328 

53,000    

    50,000 
58,000  
   50,000 
53,000
10,972
58,000   
   55,000 

$

  -  
  -  
  -  
  -  
  -  
  -  
  -  
  -  
  -  
  -  

$

  -  
  -  
  -  
  -  
  -  
  -  
  -  
  -  
  -  
  -  

$

  -  
  -  
  -  
  -  
  -  
  -  
  -  
  -  
  -  
  -  

$

-
-
-
-
-
-
-
-
-
-

$

$

27,556
137,728
6,890
34,444
6,890
34,444
103,098
-
6,890
34,444

140,884
  251,056 
59,890
    84,444 
64,890
    84,444 
156,098
    10,972 
64,890
    89,444 

19.6%
54.9%
11.5%
40.8%
10.6%
40.8%
66.0%
0.0%
10.6%
38.5%

There was no performance related remuneration payable to non-executive directors during the year. 

Table 2.  Remuneration of key management personnel for the year ended 30 June 2014

Short Term

Post Employment

Equity

Total

% of re 

 muneration

Salary & 
Fees

Cash 
Bonus

$

$

Non 
Monetary 
Benefits
$

300,000
 249,800 
252,000
240,000
195,000
185,000
217,902
135,662
217,391
162,333

150,000
 - 
50,000
 - 
30,000
 - 
87,160
 - 
50,000
 - 

-
-
-
-
-
 - 
-
 - 
-
 - 

Peter French

Carl Stubbings

2014
2013
2014
2013
Michael Graham 2014
2013
2014
2013
2014
2013

David Suhy

Greg West

Peter French 

Carl Stubbings 

Michael Graham 

David Suhy 

Greg West 

Fixed 
remuneration 

At risk -  
STI 

53.5% 

79.6% 

84.0% 

65.9% 

78.2% 

25.3% 

14.7% 

11.9% 

26.4% 

16.7% 

Super-
annuation

Termination 
Benefits

Options

 consisting 
of options 

Perfor-
mance 
based

$

17,775
15,775 
17,775
15,775
17,775
15,775
-
  -  
17,775
14,610

At risk - 
Options

21.2%

5.7%

4.1%

7.7%

5.1%

$

-
  -  
-
  -  
-
  -
-
  -  
-
  -

$

$

126,061
104,167 
19,391
54,166  
10,417
52,083 
25,360
38,710
15,461
2,790 

539,836
369,742
339,166
309,941
253,192
252,858
330,422
174,372
300,627
179,733

21.2%
28.2%
5.7%
17.5%
4.1%
20.6%
7.7%
22.2%
5.1%
1.6%

46.5%
28.2%
20.4%
17.5%
16.0%
20.6%
34.1%
22.2%
21.8%
1.6%

Benitec Biopharma Ltd Annual Report 2014      Page 11

 
 
 
Directors’ Report

Options Issued as part of remuneration for the year ended 30 June 2014 
Options can be issued to executives as part of their remuneration. Options are issued to executives to increase goal congruence with Company 
objectives. During the year ended 30 June 2014, 2,080,000 options (2013: 800,000) were granted to executives and the 2013 Annual General 
Meeting approved the grant of 400,000 options to Director Kevin Buchi. There were no other options issued to directors as part of their 
remuneration.

Balance 
1 July 13 

Granted as 
Remuneration 

Options 
Acquired 

Options 
Exercised 

Balance at 
30 June 14 

Total Vested  Exercisable 
at 30 June 14  at 30 June 14

Total 

Directors 

Peter Francis 

Mel Bridges 

John Chiplin 

Iain Ross 

Kevin Buchi 

1,660,000 

460,000 

410,563 

407,500 

246,154 

3,184,217 

- 

- 

- 

- 

400,000 

400,000 

36,924 

61,539 

61,539 

- 

- 

- 

- 

61,539 

- 

- 

1,696,924 

1,696,924 

1,696,924

521,539 

410,563 

407,500 

646,154 

521,539 

410,563 

407,500 

512,820 

521,539

410,563

407,500

512,820

160,002 

61,539 

3,682,680 

3,549,346 

3,549,346 

Specified Executives 

Peter French 

Carl Stubbings 

Mick Graham 

David Suhy 

Greg West 

1,449,231  

1,400,000  

412,308  

600,000  

400,000  

120,000  

200,000  

- 

200,000  

280,000  

2,981,539  

2,080,000  

- 

- 

- 

- 

- 

- 

- 

- 

- 

- 

- 

- 

2,849,231  

1,449,231  

1,449,231 

612,308  

600,000  

600,000  

400,000  

 145,641  

600,000  

133,333  

80,000  

145,641 

600,000 

133,333 

80,000 

5,061,539  

2,408,205  

2,408,205 

* Refers to securities purchased during the financial year not as part of remuneration.

Options Issued to Directors and Specified Executives in the year ended 30 June 2014

Percentage 
remuneration 
that are 
options

Number 
granted in 
the year 
to 30 June 
2014

Grant  
date

Value per 
option at 
grant date 
($)

Number 
vested

Number 
lapsed

Exercise 
price ($) 

Vesting and 
first exercise 
date

Last 
exercise 
date

Non-Executive Directors
Kevin Buchi

Specified Executives
Peter French
Carl Stubbings
David Suhy
Greg West

66.0%

400,000

10-Nov-13

$ 0.42

266,666

21.2% 1,400,000
200,000
5.7%
200,000
7.7%
280,000
5.1%

22-Aug-13
22-Aug-13
22-Aug-13
22-Aug-13

$ 0.18
$ 0.18
$ 0.18
$ 0.18

-
-
-
-

-

-
-
-
-

$ 0.63

10-Nov-13

18-May-18

$ 1.25
$ 1.25
$ 1.25
$ 1.25

22-Aug-14
22-Aug-14
22-Aug-14
22-Aug-14

22-Aug-18
22-Aug-18
22-Aug-18
22-Aug-18

The options were provided at no cost to the recipients. All options expire on the earlier of their expiry date or termination of the individual’s 
employment or an expiry date which may be determined by the Board. The Board has the power to adjust, amend and cancel the ESOP. Non-
Executive Directors are excluded from the ESOP.

There were no options issued to staff or directors in the period since the end of the financial year and the issuing of this report.

Page 12  Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
  
  
  
  
  
 
 
 
 
 
 
 
 
 
Directors’ Report

Number of Shares held by Key Management Personnel
No shares were granted as remuneration to staff or directors

Balance 
1 July 2013 

Received as  
Remuneration 

Upon Options  
Exercised  

Securities 
Purchased 

Balance
30 June 14

Non-Executive Directors 

Peter Francis 

Mel Bridges 

John Chiplin 

Iain Ross 

Kevin Buchi 

Specified Executives 

Peter French 

Carl Stubbings 

Michael Graham 

David Suhy 

Greg West 

89,487 

165,200 

47,634 

30,000 

615,385 

947,706 

332,615 

37,009 

47,448 

- 

-  

417,072 

-  

-  

- 

- 

- 

- 

- 

- 

-  

- 

-  

- 

-  

-  

61,539 

- 

- 

61,539 

-  

- 

-  

- 

-  

- 

237,763 

226,544 

153,847 

36,364 

- 

654,518 

9,939 

87,470 

-  

- 

-  

327,250

391,744

263,020

66,364

615,385

1,663,763

342,554

124,479

47,448

-

-

97,409 

514,481

Consequences of performance on shareholder wealth
In considering the Group’s performance and benefits for shareholder wealth, the Board have regard to the following indices in respect of the 
current financial year and the previous five financial years:

Loss per share (cents per share) 

Dividends (cents per share) 

Net loss ($ 000’s) 

Share price ($’s) 

2014 

(7.62) 

- 

(6,889) 

1.15 

2013 

(8.25) 

- 

(3,488) 

0.38 

2012 

(10.75) 

- 

(4,113) 

0.43 

2011 

(17.00) 

- 

(3,535) 

0.70 

2010 

(5.25) 

- 

(4,641) 

0.65 

2009

(20.00)

-

-2,471

0.58

Payments to Related Parties of Directors
Legal services at normal commercial rates totalling $119,804 (2013: $103,492) were provided by Francis Abourizk Lightowlers, a law firm in which 
Mr Peter Francis is a partner and has a beneficial interest.

Consultancy fees were paid for executive duties totalling $40,000 (2013: $40,000) provided by NewStar Ventures Ltd, a corporation in which Dr 
John Chiplin is a director and has a beneficial interest.

Employment Contracts
The employment conditions of Dr Peter French, the Chief Executive Officer and Managing Director, are formalised in a contract of employment 
prepared on his appointment as Chief Executive Officer and dated 4 June 2010. Dr French’s appointment with the Company may be terminated 
with the Company giving six months’ notice or by Dr French giving six months’ notice. The Company may elect to pay Dr French an equal amount to 
that proportion of his salary equivalent to six months’ pay in lieu of notice, together with any outstanding entitlements due to him. The Company 
may, at any time, by notice in writing terminate Dr French’s contract immediately in the event of serious misconduct. 

The employment conditions of Carl Stubbings, the Chief Business Officer, are formalised in a contract of employment dated 28 May 2012. Mr 
Stubbing’s appointment with the Company may be terminated with the Company giving three months’ notice or by Mr Stubbings giving three 
months’ notice. The Company may elect to pay Mr Stubbings an equal amount to that proportion of his salary equivalent to three month’s pay in 
lieu of notice, together with any outstanding entitlements due to him. The Company may, at any time, by notice in writing terminate the contract 
immediately in the event of serious misconduct.

Benitec Biopharma Ltd Annual Report 2014      Page 13

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
AUDITOR INDEPENDENCE
The Directors received the declaration included on page 15 of this 
annual report from the auditor of Benitec Biopharma Limited.

The directors are satisfied that the provision of non-audit services 
during the year is compatible with the general standard of 
independence for auditors imposed by the Corporations Act. The 
Directors and management assess the provision of non-audit services 
before engagement to be satisfied that the auditor did not compromise 
the auditor independence requirements of the Corporations Act. 

PROCEEDINGS ON BEHALF OF COMPANY
No person has applied for leave of Court to bring proceedings on 
behalf of the Company or intervene in any proceedings to which the 
Company is a party for the purpose of taking responsibility on behalf of 
the Company for all or any part of those proceedings.

NON-AUDIT SERVICES
Non-audit services provided by Grant Thornton, the Company’s 
auditors, during the year ended 30 June 2014 relate to taxation advice 
and corporate advisory services for which fees of $24,000 (2013: 
$43,230) were paid.

This report has been made in accordance with a resolution of the 
Directors.

Peter Francis 
Chairman 

Sydney 
22 August 2014

Directors’ Report

 The employment conditions of Dr Michael Graham, the Chief 
Scientific Officer, are formalised in a contract of employment dated 
1 January 2012. Dr Graham’s appointment with the Company may be 
terminated with the Company giving three months’ notice or by Dr 
Graham giving three months’ notice. The Company may elect to pay 
Dr Graham an equal amount to that proportion of his salary equivalent 
to three month’s pay in lieu of notice, together with any outstanding 
entitlements due to him. The Company may, at any time, by notice 
in writing terminate the contract immediately in the event of serious 
misconduct.

The employment conditions of Dr David Suhy, Senior Vice President, 
Research and Development, are formalised in a contract of 
employment dated 28 August 2012. Dr Suhy’s appointment with the 
Company may be terminated with the Company effectively giving 
three months’ notice. The Company may elect to pay Dr Suhy an equal 
amount to that proportion of his salary equivalent to three month’s pay 
in lieu of notice, together with any outstanding entitlements due to 
him. The Company may, at any time, by notice in writing terminate the 
contract immediately in the event of serious misconduct.

The employment conditions of Mr Greg West, the Company Secretary, 
are formalised in a contract of employment dated 23 August 2011.  
Mr West’s appointment with the Company may be terminated with the 
Company giving two months’ notice or by Mr West giving two months’ 
notice. The Company may elect to pay Mr West an equal amount to 
that proportion of his salary equivalent to two month’s pay in lieu of 
notice, together with any outstanding entitlements due to him. The 
Company may, at any time, by notice in writing terminate the contract 
immediately in the event of serious misconduct.

This concludes the Remuneration Report which has been audited.

Indemnification and insurance of Directors and Officers
The Company has entered into Deeds of Indemnity with the Directors, 
the Chief Executive Officer and the Company Secretary, indemnifying 
them against certain liabilities and costs to the extent permitted by law. 

The Company has also agreed to pay a premium in respect of a contract 
insuring the Directors and Officers of the Company. Full details of the 
cover and premium are not disclosed as the insurance policy prohibits 
the disclosure.

CORPORATE GOVERNANCE
In recognising the need for the highest standards of corporate 
behaviour and accountability, the Directors of Benitec Biopharma 
Limited observe the ASX principles of corporate governance. The 
Company’s corporate governance statement is included on page 16 of 
this annual report.

Page 14      Benitec Biopharma Ltd Annual Report 2014

 
 
Auditor’s Independence Declaration

Benitec Biopharma Ltd Annual Report 2014      Page 15

Corporate Governance Statement

The Board of Directors is responsible for establishing the corporate 
governance framework of the Group. The Board guides and monitors 
the business and affairs of Benitec on behalf of its shareholders by 
whom they are elected and to whom they are accountable.

The Company’s corporate governance reflects the ASX Corporate 
Governance Council’s principles and recommendations. The following 
commentary summarises the Company’s compliance with the ASX 
Corporate Governance Council’s recommendations.

•  Dr Bridges, Dr Chiplin, Mr Ross and Mr Buchi do not have any 

previous association with the Company or any other relationships 
that are relevant to their independence.

The Board continually assesses its membership and makes 
appointments to complement and enhance the existing skill base 
of the Board. The Board has established a Remuneration and 
Nominations Committee comprising of all non-executive directors. 
Formal letters of appointment are used for all new NEDs.

PRINCIPLE 1 
Lay solid foundations for management and oversight

The Board has adopted a formal charter that sets out their 
responsibilities. This charter is posted on the Company’s website 
www.benitec.com. The Board sets objectives, goals and strategic 
direction along with a policy framework which management then 
works within to manage day-to-day business. The Board monitors 
this on a regular basis. There is clear segregation between the Board 
and management. Any functions not reserved for the Board and not 
expressly reserved for members by the Corporations Act and ASX 
Listing Rules are reserved for senior executives.

Senior executives are subject to a formal performance review process 
on an annual basis. The focus of the performance review is to set 
specific objectives, and monitor performance against them for each 
executive, that are aligned with the Company’s business objectives. 
An annual review of the performance of each senior executive was 
conducted in accordance with this process during the year.

PRINCIPLE 2 
Structure the Board to add value

Details on the Board members and their qualifications are included in 
the Directors’ Report. The Board has a policy of maintaining a majority 
of independent directors. The current Board composition is four 
independent Non-Executive Directors (NEDs). The Board has resolved 
that a majority of the members of each Board committee should be 
NEDs. The Board has approved that, where necessary, NEDs should 
meet during the year in absence of management at such times as they 
determine necessary.

Directors are considered to be independent when they are 
independent of management and free from any business or other 
relationship that could materially interfere with the exercise of their 
independent judgement. The Board assesses director independence 
on an annual basis, or more often if it feels it is warranted, depending 
on disclosures made by individual Directors. In the context of director 
independence, to be considered independent a NED may not have a 
direct or indirect material relationship with the Company. The Board 
has determined that a material relationship is one which has, or has 
the potential to, impair or inhibit a Director’s exercise of judgement on 
behalf of the Company and its shareholders.

The Board has concluded that all NEDs are independent. In reaching 
this conclusion, the Board considered that:

•  Mr Francis, the Non-Executive Chairman, is a principal of Francis 
Abourizk Lightowlers, a material professional adviser to the 
Company. Notwithstanding this association, the Board is satisfied 
that it will not interfere with the independent exercise of his 
judgment.

Page 16  Benitec Biopharma Ltd Annual Report 2014

The Company’s Constitution provides that:

• 

the maximum number of Directors shall be ten unless amended by 
a resolution at a General Meeting of Shareholders;

•  one third of the Directors (excluding the Managing Director and 
rounded down) must retire from office at the Annual General 
Meeting (AGM) each year; such retiring Directors are eligible for 
re-election;

•  Directors appointed to fill casual vacancies must submit to 

• 

election at the next general meeting; and
the number of Directors necessary to constitute a quorum is not 
less than two Directors currently in office.

The duties of a nomination committee have been assumed by the 
Board due to the size and scale of the Company. 

The Board carries out a Board performance assessment on an annual 
basis. In the last review, the Board undertook a detailed review of its 
performance and that of its committees and individual Directors. This 
involved a self-assessment process which required the completion 
and evaluation of questionnaires on Board and management matters. 
The results of this review were collated and analysed by the Board. 
Following recent changes to the Board, the next review is expected to 
take place during the year ended 30 June 2015.

PRINCIPLE 3 
Promote ethical and responsible decision-making

The Board and management ensure that the business processes of 
Benitec are conducted according to sound ethical principles. The Board 
has established a formal Code of Conduct in this regard. This code is 
posted on the Company’s website.

All Directors and employees of the Company are expected to act with 
the utmost integrity and objectivity, striving at all times to enhance the 
reputation and performance of the Company. 

All Directors and employees of the Company are made aware of their 
obligations under the Corporations Act 2001 with regard to trading in 
the securities of the Company. In addition, the Company has adopted a 
Share Trading Policy, which is reviewed and updated on a regular basis 
as required. This policy is posted on the Company’s website.

Board members who have or may have a conflict of interest in any 
activity of the Company or with regard to any decision before the 
Board, notify the Board of such and a decision is made as to whether 
the Board member concerned is to be excluded from making decisions 
that relates to the particular matter. The Company’s constitution allows 
a Director to enter into any contract with the Company other than that 
of auditor for the Company, subject to the law.

The Board has determined that Directors are able to seek independent 
professional advice for Company related matters at the Company’s 
expense, subject to the instruction and estimated cost being approved 
by the Chairman in advance as being necessary and reasonable.

 
 
 
Corporate Governance Statement

Diversity Policy

Diversity includes, but is not limited to, gender, age, ethnicity and 
cultural background. The company is committed to diversity and 
recognises the benefits arising from employee and board diversity and 
the importance of benefiting from all available talent. A copy of the 
company’s diversity policy is available on the Benitec website. 

The diversity policy outlines the requirements for the Board to develop 
measurable objectives for achieving diversity, and annually assess 
both the objectives and the progress in achieving those objectives. 
Accordingly, the Board has developed the following objectives 
regarding gender diversity and aims to achieve these objectives over 
the next few years as director and senior executive positions become 
vacant and appropriately qualified candidates become available:  

2014 

2015 

2016

Women on the Board 

Women in senior management roles 

Women employees in the company 

- 

3 

5 

- 

4 

6 

-

5

6

PRINCIPLE 4 
Safeguard integrity in financial reporting

The Board has established an Audit and Risk Committee which meets 
at least twice through the year.  Mr Iain Ross has been appointed to 
chair the Committee and Mr Peter Francis is the other independent 
director on the Committee. Dr Mel Bridges chaired the Audit and Risk 
Committee until his retirement on 18 June 2014.

The members of the Committee have significant financial, business 
and legal backgrounds, expertise and qualifications, full particulars of 
which are contained in this annual report, as are details of meetings of 
this Committee.

The Committee is responsible for the appointment of the Company’s 
auditors and has a formal charter, which is posted on the Company’s 
website. The charter is reviewed annually to ensure that it is in line 
with emerging market practices which are in the best interests of 
shareholders.

The main objective of the Committee is to assist the Board in 
reviewing any matters of significance affecting financial reporting and 
compliance of the consolidated entity including:

•  exercising oversight of the accuracy and completeness of the 

financial statements;

•  making informed decisions regarding accounting and compliance 

• 

policies, practices, and disclosures;
reviewing the scope and results of operational risk reviews, 
compliance reviews, and external audits; and

•  assessing the adequacy of the consolidated entity’s internal 
control framework including accounting, compliance, and 
operational risk management controls based on information 
provided or obtained.

“Compliance” refers to compliance with laws and regulations, internal 
compliance guidelines, policies and procedures, and other prescribed 
internal standards of behaviour.

All other directors, the auditors and the Chief Financial Officer are 
invited to attend Committee meetings. The Committee meets with the 
auditors without management in attendance so that there can be open 
and frank communication between the Committee and the auditor.

The Committee has the power to conduct or authorise investigations 
into, or consult independent experts on, any matters within the 
Committee’s scope of responsibility. 

The Committee also considers the independence of the auditor. The 
Company requires that the audit partner be rotated every five years 
and, on an annual basis, the auditor provides a certificate to the 
Committee confirming their independence. 

The Chief Executive Officer and Chief Financial Officer have certified 
to the committee that the Group’s financial reports present a true and 
fair view, in all material respects, of the Group’s financial condition 
and operational results and are in accordance with relevant accounting 
standards.

PRINCIPLE 5 
Make timely and balanced disclosure

The Board is committed to inform its shareholders and the market 
of any major events that influence the Company in a timely and 
conscientious manner. The Board is responsible for ensuring that 
the Company complies with the continuous disclosure requirements 
as set out in ASX Listing Rule 3.1 and the Corporations Act 2001. 
The Company’s Communication Protocols have been posted on the 
Company’s website.

Any market sensitive information is discussed by the Board before it 
is approved to be released to the market. The Company’s procedure 
is to lodge the information with the ASX and make it available on the 
Company’s website shortly thereafter. All executives of the Company 
have been made aware of the Company’s obligations with regard to 
the continuous disclosure regime.

PRINCIPLE 6 
Respect the rights of shareholders

The Board ensures that its shareholders are fully informed of matters 
likely to be of interest to them. The Company provides all obligatory 
information such as annual reports, half yearly reports and other ASX 
required reports in accordance with the law and regulations.

Notices of shareholders meetings, annual and extraordinary, are 
distributed in a timely manner and are accompanied by all information 
that the Company has obtained.

The Company is always available to be contacted by shareholders 
for any query that the shareholders may have. The queries can be 
submitted by telephone, email or fax to the Company’s office. 

The chairman encourages questions and comments at the AGM 
ensuring that shareholders have a chance to obtain direct response 
from the CEO and other appropriate Board members. The Company 
requests that the auditors attend the AGM and are available to answer 
any questions with regard to the conduct of the audit and their report.

Benitec Biopharma Ltd Annual Report 2014  Page 17

 
 
 
 
 
 
Corporate Governance Statement

PRINCIPLE 7 
Recognise and manage risk

The Directors continually monitor areas of significant business 
risk, recognising that there are inherent risks associated with the 
management, funding and commercialisation of biotechnology projects.

The Board has delegated the responsibility for the establishment and 
maintenance of a framework for risk oversight and the management of 
risk for the Group to the Risk and Audit Committee.

The Committee’s role is to provide a direct link between the Board and 
the external function of the Company. This includes:

•  Monitoring corporate risk assessment and the internal controls 

instituted;

•  Monitoring the establishment of an appropriate internal control 
framework, including information systems, and considering 
enhancements;

•  Reviewing reports on any defalcations, frauds and thefts from the 

Company and action taken by managements;

•  Reviewing policies to avoided conflicts of interest between the 

Company and members of management; and

•  Considering the security of computer systems and applications, 
and the contingency plans for processing financial information in 
the event of a systems breakdown.

The Chief Executive Officer and Chief Financial Officer have made 
representations to the Committee on the system of risk management 
and internal compliance and control which implements the policies 
adopted by the Board. The Chief Executive Officer and Chief Financial 
Officer have also represented that, to the best of their knowledge, 
the Company’s risk management and internal compliance and control 
system is operating efficiently and effectively in all material respects. 

PRINCIPLE 8 
Remunerate fairly and responsibly

After considering the size and nature of the Company business the 
Board have accepted the responsibilities of the Remuneration and 
Nomination Committee rather than establishing separate committee. 
The Board, acting as the Remuneration and Nomination Committee, 
ensures that the Company’s remuneration levels are appropriate in the 
markets in which it operates and are applied, and seen to be applied, 
fairly. 

The Company’s remuneration policy is described in the Remuneration 
Report contained within the Directors’ Report.

The business of the Committee has been dealt with as part of the 
regular Board meetings as needed. The Board has access to senior 
management of the Company and may consult independent experts 
where the Board considers it appropriate to carry out the duties of the 
Committee.

Currently the Company pays directors’ fees to the NEDs. As stated 
in the Directors’ Report, businesses associated with directors may 
receive fees for professional services provided to the Company in 
addition to their duties as a NED.

Page 18  Benitec Biopharma Ltd Annual Report 2014

 
 
Financial Statement and Notes to the Financial Statements

CONSOLIDATED STATEMENT OF PROFIT OR LOSS AND OTHER COMPREHENSIVE INCOME

For the Year Ended 30 June 2014

Continuing Operations 

Revenue 

Other income 

Royalties & licence fees 

Research and development 

Employment related 

Share based expense 

Impairment costs 

Travel related costs 

Consultants costs 

Occupancy costs 

Corporate expenses 

Foreign exchange translation 

Loss before income tax  

Income tax benefit 

Note 

2 

2 

4 

2014 
$ 

597,940 

775,833 

1,373,773 

(192,753) 

(3,757,869) 

(2,444,015) 

(355,116) 

- 

(585,359) 

(652,839) 

(121,582) 

(646,315) 

(111,399) 

(8,867,247) 

(7,493,474) 

454,365 

2013
$

639,849

824,333

1,464,182 

(30,000)

(1,280,012)

(1,832,065)

(518,749)

(1,503,296)

(345,826)

(336,570)

(100,153)

(531,686)

1,526,215

(4,952,142) 

(3,487,960) 

-   

Loss for the year attributable to members of the parent entity 

(7,039,109) 

(3,487,960)

Other Comprehensive Income 

Items that may be reclassified subsequently to profit and loss 

Other Comprehensive Income for the year, Foreign exchange translation, net of tax  

Total Comprehensive Income for the year 

Total Comprehensive Income attributable to members of the parent entity   

7,747 

(7,031,362) 

(7,031,362) 

(1,313,792)

(4,801,752)

(4,801,752)

Earnings per share (cents per share) 

Basic and diluted for loss for the year attributable  
to ordinary equity holders of the parent entity 

Cents per share, with the comparative adjusted  
for the share consolidation at 25:1 in July 2013 

6 

(7.81) 

(8.25)

This statement should be read in conjunction with the notes to the financial statements.

Benitec Biopharma Ltd Annual Report 2014  Page 19

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Financial Statement and Notes to the Financial Statements

CONSOLIDATED STATEMENT OF FINANCIAL POSITION

As at 30 June 2014

CURRENT ASSETS 
Cash and cash equivalents 
Trade and other receivables 
Other current assets 

TOTAL CURRENT ASSETS 

NON-CURRENT ASSETS 
Property, plant and equipment 

TOTAL NON-CURRENT ASSETS 

TOTAL ASSETS 

CURRENT LIABILITIES 
Trade and other payables 
Provisions 

TOTAL CURRENT LIABILITIES 

TOTAL LIABILITIES 

NET ASSETS 

EQUITY 
Contributed equity 
Reserves 
Accumulated losses 

TOTAL EQUITY 

Note 

8 
9 
10 

12 

13 
15 

16 
17 

2014 
$ 

31,359,199 
121,587 
2,966,739 

2013
$

1,587,299
105,073
30,218

34,447,525 

1,722,590

47,677 

47,677 

28,120

28,120

34,495,202 

1,750,710

788,169 
166,511 

954,680 

954,680 

1,011,733
98,637

1,110,370

1,110,370

33,540,522 

640,340

129,185,676 
640,773 
(96,285,927) 

89,609,248
277,910
(89,246,818)

33,540,522 

640,340

This statement should be read in conjunction with the notes to the financial statements.

Page 20      Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  
 
 
 
 
 
 
 
 
 
 
  
 
 
Financial Statement and Notes to the Financial Statements

Note 

8 

26 

CONSOLIDATED STATEMENT OF CASH FLOWS

For the Year Ended 30 June 2014

CASH FLOWS FROM OPERATING ACTIVITIES 
Receipts from customers 
Research and development grants 
Interest received 
Income tax benefit 
Payments to suppliers and employees   

Net cash used in operating activities 

CASH FLOWS FROM INVESTING ACTIVITIES 
Business acquisition 
Purchase of property, plant and equipment 

Net cash provided by investing activities 

CASH FLOWS FROM FINANCING ACTIVITIES 
Net proceeds from issue of shares 

Net cash provided by financing activities 

Net decrease in cash held 
Exchange differences on cash and cash equivalents 
Cash and cash equivalents, beginning of year  

Cash and cash equivalents, end of year 

8 

This statement should be read in conjunction with the notes to the financial statements.

2014 
$ 

260,310 
775,833 
321,116 
454,365 
(11,081,963) 

(9,270,339) 

- 
(32,365) 

(32,365) 

39,075,618 

39,075,618 

29,772,914 
(1,014) 
1,587,299 

31,359,199 

2013
$

566,754
824,333
133,011

(4,256,694)

(2,732,596)

143,603
(9,889)

133,714

1,086,844

1,086,844

(1,512,038)
23,457
3,075,880

1,587,299

Benitec Biopharma Ltd Annual Report 2014      Page 21

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Financial Statement and Notes to the Financial Statements

CONSOLIDATED STATEMENT OF CHANGES IN EQUITY

For the Year Ended 30 June 2014

Contributed 
Equity 
$ 

Share-based  
Payments 
Reserve 
$ 

Foreign 
exchange  
translation  Accumulated 

Reserve 
$ 

Losses 
$ 

Total
$

Balance at 1 July 2012 

87,348,819 

1,394,142 

- 

(86,080,047) 

2,662,914   

Loss for the year 
Other comprehensive income for year 
Total comprehensive income for year 

Share issue to Tacere on business acquisition 
Transfer to Accumulated Losses the Share Based 
Payments Reserve no longer required 
Share Based Payments 
Share issues, net of transaction costs 
Transactions with owners 

- 
- 
- 

1,173,585 

- 
-  
1,086,844 
2,260,429 

-  
- 
- 

- 

(321,189) 
518,749 
- 
197,560 

- 
(1,313,792) 
(1,313,792) 

(3,487,960) 
- 
(3,487,960) 

(3,487,960)
(1,313,792)
(4,801,752)

- 

- 
- 
- 
- 

- 

1,173,585

(321,189) 
-  
-  
321,189 

-
518,749
1,086,844
2,779,178

Balance 30 June 2013 

89,609,248 

1,591,702 

(1,313,792) 

(89,246,818) 

640,340

Loss for the year 
Other comprehensive income for year 
Total comprehensive income for year 
Share Based Payments 
Share issues, net of transaction costs 
Transactions with owners 

- 
- 
-  
- 
39,576,428 
39,576,428 

-  
- 
-  
355,116 
- 
355,116 

- 
7,747 
7,747 
- 
- 
- 

(7,039,109) 
- 
(7,039,109) 
-  
-  
- 

(7,039,109)
7,747
(7,031,362)
355,116
39,576,428
39,781,544

Balance 30 June 2014 

129,185,676 

1,946,818 

(1,306,045) 

(96,285,927) 

33,540,522

This statement should be read in conjunction with the notes to the financial statements.

Page 22      Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 1: SUMMARY OF SIGNIFICANT  
ACCOUNTING POLICIES

(a) Basis of Preparation

The financial report covers Benitec Biopharma Limited and its controlled 
entities as a consolidated entity (“Group”). Benitec Biopharma Limited is 
a listed public company, incorporated and domiciled in Australia.

The consolidated general purpose financial statements of the Group 
have been prepared in accordance with the requirements of the 
Corporations Act 2001, Australian Accounting Standards and other 
authoritative pronouncements of the Australian Accounting Standards 
Board. Compliance with Australian Accounting Standards results in full 
compliance with the International Financial Reporting Standards (IFRS) as 
issued by the International Accounting Standards Board (IASB). Benitec 
Biopharma Limited is a for-profit entity for the purpose of preparing 
financial statements. The consolidated financial statements for the 
year ended 30 June 2014 (including comparatives) were approved and 
authorised for issue by the board of directors on 22 August 2014.

The consolidated financial statements have been prepared using the 
measurement bases specified by Australian Accounting Standards for 
each type of asset, liability, income and expense. The measurement 
bases are more fully described in the accounting policies below.

(b) Principles of Consolidation
A controlled entity is any entity controlled by Benitec Biopharma Limited 
whereby Benitec Biopharma Limited has the power to control the 
financial and operating policies of an entity so as to obtain benefits from 
its activities.

All inter-company balances and transactions between entities in the 
consolidated entity, including any unrealised profits or losses, have been 
eliminated on consolidation. Accounting policies of controlled entities 
have been changed where necessary to ensure consistencies with those 
policies applied by the parent entity.

Where controlled entities have entered or left the consolidated entity 
during the year, their operating results have been included/excluded from 
the date control was obtained or until the date control ceased.

A list of controlled entities is contained in note 11 to the financial 
statements. All controlled entities have a June financial year-end except 
for Benitec Ltd (UK) which has a December year-end.

(c) Accounting Standards
New and revised standards that are effective for these financial 
statements
A number of new and revised standards are effective for annual periods 
beginning on or after 1 July 2013. Information on these new standards is 
presented below.

AASB 10 Consolidated Financial Statements
AASB 10 supersedes AASB 127 Consolidated and Separate Financial 
Statements (AASB 127) and AASB Interpretation 112 Consolidation 
- Special Purpose Entities. AASB 10 revises the definition of control 
and provides extensive new guidance on its application. These new 
requirements have the potential to affect which of the Group’s investees 
are considered to be subsidiaries and therefore to change the scope of 
consolidation. The requirements on consolidation procedures, accounting 
for changes in non-controlling interests and accounting for loss of control 
of a subsidiary are unchanged.

Management has reviewed its control assessments in accordance with 
AASB 10 and has concluded that there is no effect on the classification 
(as subsidiaries or otherwise) of any of the Group’s investees held during 
the period or comparative periods covered by these financial statements.

AASB 11 Joint Arrangements
AASB 11 supersedes AASB 131 Interests in Joint Ventures (AAS 131) 
and AASB Interpretation 113 Jointly Controlled Entities- Non-Monetary-
Contributions by Venturers. AASB 11 revises the categories of joint 
arrangement, and the criteria for classification into the categories, with 
the objective of more closely aligning the accounting with the investor’s 
rights and obligations relating to the arrangement. In addition, AASB 
131’s option of using proportionate consolidation for arrangements 
classified as jointly controlled entities under that Standard has been 
eliminated. AASB 11 now requires the use of the equity method 
for arrangements classified as joint ventures (as for investments in 
associates).

AASB 13 Fair Value Measurement
AASB 13 clarifies the definition of fair value and provides related 
guidance and enhanced disclosures about fair value measurements. It 
does not affect which items are required to be fair-valued. The scope 
of AASB 13 is broad and it applies for both financial and non-financial 
items for which other Australian Accounting Standards require or permit 
fair value measurements or disclosures about fair value measurements, 
except in certain circumstances.

AASB 13 applies prospectively for annual periods beginning on or after 
1 January 2013. Its disclosure requirements need not be applied to 
comparative information in the first year of application. The Group has 
however included as comparative information the AASB 13 disclosures 
that were required previously by AASB 7 Financial Instruments: 
Disclosures.

Amendments to AASB 119 Employee Benefits
The 2011 amendments to AASB 119 made a number of changes to the 
accounting for employee benefits. The amendments which impact the 
Group related to the following:

-  Under the amendments, employee benefits ‘expected to be settled 
wholly’ (as opposed to ‘due to be settled’ under the superseded 
version of AASB 119) within 12 months after the end of the reporting 
period are short-term benefits, and are therefore not discounted 
when calculating leave liabilities. As the Group does not expect all 
annual leave for all employees to be used wholly within 12 months 
of the end of reporting period, annual leave is included in ‘other long-
term benefit’ and discounted when calculating the leave liability. 
This change has had no impact on the presentation of annual leave 
as a current liability in accordance with AASB 101 Presentation of 
Financial Statements. 

Management have assessed the impact of this change and noted that it 
is not material to the Group for the year ended 30 June 2013 and  
30 June 2014.

Accounting Standards issued but not yet effective and not been 
adopted early by the Group
At the date of authorisation of these financial statements, certain new 
standards, amendments and interpretations to existing standards have 
been published but are not yet effective, and have not been adopted 
early by the Group. Management anticipates that all of the relevant 
pronouncements will be adopted in the Group’s accounting policies for 
the first period beginning after the effective date of the pronouncement. 

Benitec Biopharma Ltd Annual Report 2014      Page 23

Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

Information on new standards, amendments and interpretations that are 
expected to be relevant to the Group’s financial statements is provided 
below. Certain other new standards and interpretations have been issued 
but are not expected to have a material impact on the Group’s financial 
statements.

AASB 2014-1 Amendments to Australian Accounting Standards 
Part A of AASB 2014-1 makes amendments to various Australian 
Accounting Standards arising from the issuance by the International 
Accounting Standards Board (IASB) of International Financial 
Reporting Standards Annual Improvements to IFRSs 2010-2012 Cycle 
and Annual Improvements to IFRSs 2011-2013 Cycle. Among other 
improvements, the amendments arising from Annual Improvements to 
IFRSs 2010-2012 Cycle: 

(a) clarify that the definition of a ‘related party’ includes a management 
entity that provides key management personnel services to the reporting 
entity (either directly or through a group entity); and 

(b) amend AASB 8 Operating Segments to explicitly require the disclosure 
of judgements made by management in applying the aggregation criteria. 

Part E of AASB 2014-1 makes amendments to Australian Accounting 
Standards to reflect the AASB’s decision to defer the mandatory 
application date of AASB 9 Financial Instruments to annual reporting 
periods beginning on or after 1 January 2018. Part E also makes 
amendments to numerous Australian Accounting Standards as a 
consequence of the introduction of Chapter 6 Hedge Accounting into 
AASB 9 and to amend reduced disclosure requirements for AASB 
7 Financial Instruments: Disclosures and AASB 101 Presentation of 
Financial Statements. 

Accounting for Acquisitions of Interests in Joint Operations 
The amendments to IFRS 11 state that an acquirer of an interest in a 
joint operation in which the activity of the joint operation constitutes a 
‘business’, as defined in IFRS 3 Business Combinations, should: 

- 

- 

apply all of the principles on business combinations accounting 
in IFRS 3 and other IFRSs except principles that conflict with the 
guidance of IFRS 11. This requirement also applies to the acquisition 
of additional interests in an existing joint operation that results in the 
acquirer retaining joint control of the joint operation (note that this 
requirement applies to the additional interest only, i.e. the existing 
interest is not remeasured) and to the formation of a joint operation 
when an existing business is contributed to the joint operation by 
one of the parties that participate in the joint operation; and 
provide disclosures for business combinations as required by IFRS 3 
and other IFRSs. 

The Australian Accounting Standards Board (AASB) is expected to issue 
the equivalent Australian amendment shortly. 

AASB 9 Financial Instruments 
AASB 9 introduces new requirements for the classification and 
measurement of financial assets and liabilities. These requirements 
improve and simplify the approach for classification and measurement of 
financial assets compared with the requirements of AASB 139. The main 
changes are: 

(a) Financial assets that are debt instruments will be classified based on 
(1) the objective of the entity’s business model for managing the financial 
assets; and (2) the characteristics of the contractual cash flows. 

(b) Allows an irrevocable election on initial recognition to present gains 
and losses on investments in equity instruments that are not held for 

Page 24  Benitec Biopharma Ltd Annual Report 2014

trading in other comprehensive income (instead of in profit or loss). 
Dividends in respect of these investments that are a return on investment 
can be recognised in profit or loss and there is no impairment or recycling 
on disposal of the instrument. 

(c) Financial assets can be designated and measured at fair value through 
profit or loss at initial recognition if doing so eliminates or significantly 
reduces a measurement or recognition inconsistency that would arise 
from measuring assets or liabilities, or recognising the gains and losses 
on them, on different bases. 

(d) Where the fair value option is used for financial liabilities the change 
in fair value is to be accounted for as follows: 

- 

- 

The change attributable to changes in credit risk are presented in 
other comprehensive income (OCI); and 
The remaining change is presented in profit or loss. 

If this approach creates or enlarges an accounting mismatch in the profit 
or loss, the effect of the changes in credit risk are also presented in profit 
or loss. 

(d) Revenue

Revenue from the granting of licenses is recognised in accordance 
with the terms of the relevant agreements and is usually recognised 
on an accruals basis, unless the substance of the agreement provides 
evidence that it is more appropriate to recognise revenue on some 
other systematic rational basis. Interest revenue is recognised on a 
proportional basis taking into account the interest rates applicable to the 
financial assets. Revenue from the rendering of a service is recognised 
upon the delivery of the service to the customers. All revenue is stated 
net of the amount of goods and services tax (GST). 

Government grants are recognised at fair value where there is 
reasonable assurance that the grant will be received and all grant 
conditions will be met. Grants relating to expense items are recognised 
as income over the periods necessary to match the grant costs they are 
compensating. Grants relating to assets are credited to deferred income 
at fair value and are credited to income over the expected useful life of 
the asset on a straight line basis.

Research and Development Grant revenue is recognised as income when 
it is received.

(e) Income Tax

The charge for current income tax expense is based on the loss for the 
year adjusted for any non-assessable or disallowed items. It is calculated 
using tax rates that have been enacted or are substantially enacted by 
reporting date. 

Deferred tax is accounted for using the liability method in respect of 
temporary differences arising between the tax bases of assets and 
liabilities and their carrying amounts in the financial statements. No 
deferred income tax will be recognised from the initial recognition of an 
asset or liability, excluding a business combination, where there is no 
effect on accounting or taxable profit or loss. 

Deferred tax is calculated at the tax rates that are expected to apply to 
the period when the asset is realised or liability is settled. Deferred tax 
is credited in the statement of comprehensive income except where it 
relates to items that may be credited directly to equity, in which case 
the deferred tax is adjusted directly against equity. Deferred income tax 
assets are recognised to the extent that it is probable that future tax 

Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

profits will be available against which deductible temporary differences 
can be utilised.

The amount of benefits brought to account or which may be realised in 
the future is based on the assumption that no adverse change will occur 
in income taxation legislation and the anticipation that the consolidated 
entity will derive sufficient future assessable income to enable the 
benefit to be realised and comply with the conditions of deductibility 
imposed by the law.

Benitec Biopharma Limited and its wholly-owned Australian 
subsidiary has formed an income tax consolidated group under the Tax 
Consolidation Regime. Benitec Biopharma Limited is responsible for 
recognising the current and deferred tax assets and liabilities for the 
tax consolidated group. The Group notified the ATO on 12 February 2004 
that it had formed an income tax consolidated group to apply from 1 July 
2002. No tax sharing agreement has been entered between entities in 
the tax consolidated group. 

(f) Critical Accounting Estimates and Judgments
The Directors evaluate estimates and judgments incorporated into the 
financial report based on historical knowledge and best available current 
information. Estimates assume a reasonable expectation of future events 
and are based on current trends and economic data, obtained both 
externally and within the Group. 

Key estimates – share-based payments transactions
The Group measures the cost of equity-settled transactions with 
employees by reference to the fair value of the equity instruments at 
the date at which they are granted. The fair value is determined using a 
Black-Scholes model, using the assumptions detailed in note 21.

Key judgements – tax losses
Given the company’s and each individual entities’ history of recent 
losses, the Group has not recognised a deferred tax asset with regard 
to unused tax losses and other temporary differences, as it has not 
been determined whether the company or its subsidiaries will generate 
sufficient taxable income against which the unused tax losses and other 
temporary differences can be utilised.

Key judgements – compound financial instruments
The Group measures the fair value of the liability component using the 
prevailing market interest rate for similar convertible instruments.

(g) Impairment of Non-Financial Assets
The Group assesses at each reporting date whether there is an indication 
that an asset may be impaired. If any such indication exists, or when 
annual impairment testing for an asset is required (i.e. Goodwill, 
intangible assets with indefinite useful lives and intangible assets 
not yet available for use), the Group makes an estimate of the asset’s 
recoverable amount. An asset’s recoverable amount is the higher of its 
fair value less costs to sell and its value in use and is determined for an 
individual asset, unless the asset does not generate cash inflows that 
are largely independent of those from other assets or groups of assets 
and the asset’s value in use cannot be estimated to be close to its fair 
value. In such cases the asset is tested for impairment as part of the cash 
generating unit to which it belongs. When the carrying amount of an 
asset or cash-generating unit exceeds its recoverable amount, the asset 
or cash-generating unit is considered impaired and is written down to its 
recoverable amount. 

In assessing value in use, the estimated future cash flows are discounted 
to their present value using a pre-tax discount rate that reflects current 
market assessments of the time value of money and the risks specific 
to the asset. Impairment losses relating to continuing operations are 
recognised in those expense categories consistent with the function of 
the impaired asset unless the asset is carried at revalued amount (in 
which case the impairment loss is treated as a revaluation decrease). 

(h) Cash and Cash Equivalents
Cash and cash equivalents includes cash on hand, deposits held at call 
with banks, other short-term highly liquid investments with original 
maturities of three months or less, and bank overdrafts. Bank overdrafts 
are shown within short term borrowings in current liabilities on the 
statement of financial position.

(i) Trade and Other Receivables
Trade receivables, which generally have 30 day terms, are recognised 
and carried at original invoice amount less an allowance for any 
uncollectible amounts. An estimate for doubtful debts is made when 
collection of the full amount is no longer probable. Bad debts are written 
off when identified.

(j) Property, Plant and Equipment
Each class of property, plant and equipment is carried at cost or fair value 
less, where applicable, any accumulated depreciation and impairment 
losses.

Plant and equipment
Plant and equipment are measured on the cost basis less depreciation 
and impairment losses. The carrying amount of plant and equipment 
is reviewed annually by directors to ensure it is not in excess of the 
recoverable amount from these assets. The recoverable amount is 
assessed on the basis of the expected net cash flows that will be 
received from the assets employment and subsequent disposal. The 
expected net cash flows have been discounted to their present values in 
determining recoverable amounts.

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 
group and the cost of the item can be measured reliably. All other repairs 
and maintenance are charged to the statement of comprehensive income 
during the financial period in which they are incurred.

Depreciation
The depreciable amount of all fixed assets including capitalised lease 
assets is depreciated on a diminishing value basis over their useful lives 
to the consolidated entity commencing from the time the asset is held 
ready for use. Leasehold improvements are depreciated over the shorter 
of either the unexpired period of the lease or the estimated useful lives 
of the improvements.

The depreciation rates used for plant and equipment were 20-33 %. The 
assets’ residual values and useful lives are reviewed, and adjusted if 
appropriate, at each reporting date. 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 disposals are determined by comparing proceeds 
with the carrying amount. These gains and losses are included in the 
statement of comprehensive income. When assets which have been 

Benitec Biopharma Ltd Annual Report 2014  Page 25

Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

revalued are sold, amounts included in the revaluation reserve relating to 
that asset are transferred to retained earnings.

(k) Leases

Leases of fixed assets are classified as finance leases where the Group 
has substantially all the risks and benefits incidental to the ownership of 
the asset, but not the legal ownership.

Finance leases are capitalised by recording an asset and a liability at the 
lower of the amounts equal to the fair value of the leased property or the 
present value of the minimum lease payments, including any guaranteed 
residual values. Lease payments are allocated between the reduction of 
the lease liability and the lease interest expense for the period. Leased 
assets are depreciated on a straight-line basis over their estimated useful 
lives where it is likely that the consolidated entity will obtain ownership 
of the asset or over the term of the lease. Lease payments for operating 
leases, where substantially all the risks and benefits remain with the 
lessor, are charged as expenses in the periods in which they are incurred.

Lease incentives under operating leases are recognised as a liability and 
amortised on a straight-line basis over the life of the lease term.

(l) Financial Instruments

Recognition
Financial instruments are initially measured at cost on trade date, 
which includes transaction costs, when the related contractual rights or 
obligations exist. Subsequent to initial recognition these instruments are 
measured as set out below.

Loans and receivables
Loans and receivables are non-derivative financial assets with fixed or 
determinable payments that are not quoted in an active market and are 
stated at amortised cost using the effective interest rate method.

Financial liabilities
Non-derivative financial liabilities are recognised at amortised cost, 
comprising original debt less principal payments and amortisation.

Compound instruments
The component parts of compound instruments (convertible notes) 
issued by the Group are classified separately as financial liabilities and 
equity in accordance with the substance of the contractual arrangement. 
The liability component is recorded on an amortised cost basis using 
the effective interest method until extinguished upon conversion or at 
the instrument’s maturity date. The equity component is determined by 
deducting the amount of the liability component from the fair value of 
the compound instrument as a whole. This is recognised and included in 
equity, net of income tax effects, and is not subsequently remeasured.

Fair value
Fair value is determined based on current bid prices for all quoted 
investments. Valuation techniques are applied to determine the fair value 
for all unlisted securities, including recent arm’s length transactions, 
reference to similar instruments and option pricing models.

Impairment
At each reporting date, the group assess whether there is objective 
evidence that a financial instrument has been impaired. In the case 
of available-for-sale financial instruments, a prolonged or significant 
decline in the value of the instrument is considered to determine 
whether impairment has arisen. Impairment losses are recognised in the 
statement of comprehensive income.

Page 26  Benitec Biopharma Ltd Annual Report 2014

(m) Intangibles

Research and development
Expenditure during the research phase of a project is recognised as an 
expense when incurred. Development costs are capitalised only when 
technical feasibility studies identify that the project will deliver future 
economic benefits and these benefits can be measured reliably.

Development costs have a finite life and are amortised on a systematic 
basis matched to the future economic benefits over the useful life of the 
project.

Goodwill
Goodwill, representing the excess of the cost of acquisition over the 
fair value of the identifiable assets, liabilities and contingent liabilities 
acquired, is recognised as an asset and not amortised, but tested at least 
annually for impairment and whenever there is an indication that the 
goodwill may be impaired. Any impairment is recognised immediately in 
profit or loss and is not subsequently reversed

Refer to Note 1 (g) for a description of impairment testing procedures.

(n) Trade and Other Payables

Trade payables and other payables are carried at amortised costs and 
represent liabilities for goods and services provided to the group prior to 
the end of the financial year that are unpaid and arise when the group 
becomes obliged to make future payments in respect of the purchase of 
these goods and services.

(o) Employee Benefits

Provision is made for the Group’s liability for employee benefits arising 
from services rendered by employees to reporting date. Employee 
benefits that are expected to be settled within one year have been 
measured at the amounts expected to be paid when the liability is 
settled, plus related on-costs. Employee benefits payable later than one 
year have been measured at the present value of the estimated future 
cash outflows to be made for those benefits. 

(p) Provisions

Provisions are recognised when the Group has a legal or constructive 
obligation, as a result of past events, for which it is probable that an 
outflow of economic benefits will results and that outflow can be reliably 
measured. 

(q) Contributed Equity

Ordinary shares are classified as equity. Incremental costs directly 
attributable to the issue of new shares or options are shown in equity as 
a deduction, net of tax, from the proceeds. 

(r) Share-based Payment Transactions

Benefits are provided to employees of the Group in the form of share-
based payment transactions, whereby employees render services in 
exchange for shares or rights over shares (‘equity-settled transactions’). 
The plan currently in place to provide these benefits is the Employee 
Share Option Plan (ESOP), which provides benefits to senior executives.

The cost of these equity-settled transactions with employees is 
measured by reference to the fair value at the date at which they are 
granted. The fair value is determined using a Black-Scholes model. 

Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

In valuing equity-settled transactions, no account is taken of any 
performance conditions, other than conditions linked to the price of the 
shares of Benitec Biopharma Limited (‘market conditions’).

The cost of equity-settled transactions is recognised, together with 
a corresponding increase in equity, over the period in which the 
performance conditions are fulfilled, ending on the date on which the 
relevant employees become fully entitled to the award (‘vesting date’).

The cumulative expense recognised for equity-settled transactions at 
each reporting date until vesting date reflects (i) the extent to which 
the vesting period has expired and (ii) the number of awards that, in 
the opinion of the directors of the group, will ultimately vest. This 
opinion is formed based on the best available information at reporting 
date. No adjustment is made for the likelihood of market performance 
conditions being met as the effect of these conditions is included in the 
determination of fair value at grant date.

No expense is recognised for awards that do not ultimately vest, except 
for awards where vesting is conditional upon a market condition.

Where the terms of an equity-settled award are modified, as a minimum 
an expense is recognised as if the terms had not been modified. In 
addition, an expense is recognised for any increase in the value of the 
transaction as a result of the modification, as measured at the date of 
modification. Where an equity-settled award is cancelled, it is treated 
as if it had vested on the date of cancellation, and any expense not 
yet recognised for the award is recognised immediately. However, if a 
new award is substituted for the cancelled award, and designated as a 
replacement award on the date that it is granted, the cancelled and new 
award are treated as if they were a modification of the original award, as 
described in the previous paragraph.

The dilutive effect, if any, of outstanding options is reflected as additional 
share dilution in the computation of earnings per share.

(s) Earnings per Share

Basic earnings per share is calculated as net profit attributable to 
members of the parent, adjusted to exclude any costs of servicing equity 
(other than dividends) and preference share dividends, divided by the 
weighted average number of ordinary shares, adjusted for any bonus 
element.

Diluted earnings per share is calculated as net profit attributable to 
members of the parent, adjusted for:

•  costs of servicing equity (other than dividends) and preference  

• 

share dividends;
the after tax effect of dividends and interest associated with dilutive 
potential ordinary shares that have been recognised as expenses; 
and

•  other non-discretionary changes in revenues or expenses  

during the period that would result from the dilution of potential 
ordinary shares;

divided by the weighted average number of ordinary shares and dilutive 
potential ordinary shares, adjusted for any bonus element.

(t) Foreign Currency Transactions and Balances

Functional and presentation currency
The functional currency of each of the Group’s entities is measured 
using the currency of the primary economic environment in which that 
entity operates. The consolidated financial statements are presented in 

Australian dollars which is the parent entity’s functional and presentation 
currency.

Transaction and balances
Foreign currency transactions are translated into functional currency 
using the exchange rates prevailing at the date of the transaction. 
Foreign currency monetary items are translated at the year-end exchange 
rate. Non-monetary items measured at historical cost continue to be 
carried at the exchange rate at the date of the transaction. Non-monetary 
items measured at fair value are reported at the exchange rate at the 
date when fair values were determined.

Exchange differences arising on the translation of monetary items are 
recognised in the statement of comprehensive income, except where 
deferred in equity as a qualifying cash flow or net investment hedge. 
Exchange differences arising on the translation of non-monetary items 
are recognised directly in equity to the extent that the gain or loss is 
directly recognised in equity, otherwise the exchange difference is 
recognised in the statement of comprehensive income.

Group companies
The financial results and position of foreign operations whose functional 
currency is different from the Group’s presentation currency are 
translated as follows:

•  Assets and liabilities are translated at year-end exchange rates 

• 

prevailing at that reporting date.
Income and expenses are translated at average exchange rates for 
the period. 

•  Retained profits are translated at the exchange rates prevailing at 

the date of the transaction.

(u) Goods and Services Tax (GST)

Revenues, expenses and assets are recognised net of the amount of 
GST, except where the amount of GST incurred is not recoverable from 
the Australian Tax Office. In these circumstances the GST is recognised 
as part of the cost of acquisition of the asset or as part of an item of the 
expense. Receivables and payables in the statement of financial position 
are shown inclusive of GST. 

Cash flows are presented in the statement of cash flows on a gross 
basis, except for the GST component of investing and financing activities, 
which are disclosed as operating cash flows.

(v) Comparative Figures

When required by Accounting Standards, comparative figures have 
been adjusted to conform to changes in presentation for the current 
financial year. 

(w) Going Concern

The directors have prepared the financial statements on a going 
concern basis after taking into consideration the net loss for the year of 
$7,039,109 and the cash and cash equivalents balance of $31,359,199, 
The directors have recognised the capital raisings in 2013 and 2014, 
performed a review of the cash flow forecasts, considered the cash 
flow needs of the Group, and believe that the strategies in place are 
appropriate to generate funding which will be sufficient to maintain the 
going concern status of the Group. If these strategies are unsuccessful 
then the Group may need to realise its assets and extinguish liabilities 
other than in the ordinary course of business and at amounts different to 
those disclosed in the financial report.

Benitec Biopharma Ltd Annual Report 2014  Page 27

Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 2: REVENUE FROM CONTINUING OPERATIONS 
Revenue 
Licensing revenue and royalties 
Finance income - interest received 

Other income 
Federal Government Research and Development Grants 

Total revenue and other income 

NOTE 3: LOSS FOR THE YEAR 
(a) Expenses incurred by continuing operations 
Items included in Statement of Comprehensive Income 
Depreciation 
Included in Occupancy expenses 
Depreciation of plant and equipment 
Employee benefits expense 
Included in Employment related expenses 
Wages and salaries 
Superannuation costs 
(b) Expenses
Research and development costs consist of:
Project expenses 
Other IP related expenses 

2014 
$ 

2013
$

276,824 
321,116 

597,940 

775,833 

1,373,773 

  521,140
118,709

639,849

824,333

1,464,182

12,808 

29,794

2,109,860  
89,090 

3,310,014  
447,855 

3,757,869 

1,759,745
72,320

1,075,844
204,168

1,280,012

NOTE 4:  INCOME TAX EXPENSE
(a)   The prima facie tax on loss from ordinary activities before income tax is reconciled to the income tax as follows:

Prima facie tax payable on loss from ordinary activities before income tax at 30% (2013: 30%) 
Add Tax effect of: 
Non-deductible share-based payment expense 
Non-assessable foreign currency translation provision 
Non-deductible legal fees 
Capital items deductible 
Other non-deductible items 
Deductible items not included in operating result 
Deferred tax asset not brought to account 

Income tax benefit  

Income tax benefit reported in the income statement 

 (2,248,042) 

(1,046,388)

106,535 
 (2,324) 
15,906 
 (231,942) 
19,500 
4,800 
2,335,567 

- 

454,365 

155,625
457,865
9,326
(58,863)
46,843
(48,354)
483,947

-

-

The income tax benefit was a cash refund of income tax in the US in Tacere Therapeutics Inc. (a wholly owned subsidiary).

Page 28  Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

(b)  The parent entity, acting as the Head Entity, notified the Australian Taxation Office on 12 February 2004 that it had formed a Tax Consolidated 

Group applicable as from 1 July 2002.  No tax sharing agreement has been entered between entities in the tax consolidated group.

(c)  As at 30 June 2014, the Tax Consolidated Group has estimated carry-forward tax losses of $13,103,412 (2013: $11,751,713) calculated at 30% 
of the accumulated annual Australian tax losses. The tax losses have not been recognised in the financial statements and the capacity of the 
Tax Consolidated Group to use the tax losses will be subject to conforming with regulatory tests. The deferred tax asset relating to temporary 
differences (calculated at 30%) was $49,953 (2013: $29,591). 

The Tax Consolidated Group also has Australian capital tax losses for which no deferred tax asset is recognised in the financial statements 
of $381,588 (2013: $381,588). The capacity of the Tax Consolidated Group to use the capital tax losses will be subject to conforming with 
regulatory tests.

The recoupment of available tax losses as at 30 June 2014 is contingent upon the following:
(i) 

the Consolidated Group deriving future assessable income of a nature and of an amount sufficient to enable the benefit from the losses to 
be realised;

(ii)  the conditions for deductibility imposed by tax legislation continuing to be complied with; and
(iii)  there being no changes in tax legislation which would adversely affect the Tax Consolidated Group from realising the benefit from the losses.

NOTE 5: AUDITOR’S REMUNERATION   
Audit Services 
Remuneration of Grant Thornton Audit Pty Ltd for: 
- auditing or reviewing the financial report 
Other Services 
Remuneration of Grant Thornton Australia Limited for:  
- taxation compliance and corporate advisory services 

2014 
$ 

2013
$

73,238 

54,000

24,000 

43,230

NOTE 6: EARNINGS PER SHARE 
Basic earnings per share is calculated by dividing the net loss for the year attributable to ordinary shareholders by the weighted average number 
of ordinary shares on issue during the year.
Diluted earnings per share amounts are calculated by dividing the net loss attributable to ordinary shareholders by the weighted average number 
of ordinary shares on issue during the year (adjusted for the effects of dilutive options) and the weighted average number of ordinary shares that 
would be issued on conversion of all dilutive potential ordinary shares.

2014 
$ 

2013
$

Loss after income tax used in the calculation of basic EPS and dilutive EPS 

(7,039,109) 

(3,487,960)

Weighted average number of ordinary shares for basic and diluted earnings per share 
Weighted average number of converted, lapsed or cancelled potential ordinary shares  
included in diluted earnings per share 
Outstanding options to acquire ordinary shares are not considered dilutive for the years ended 30 June 2014 and 30 June 2013.
Classification of securities   
No securities or convertible debt instruments could be classified as potential ordinary shares under AASB 133 and therefore have not been 
included in determination of dilutive EPS.

-  

Number 
90,432,177  

Number
41,688,975 

- 

Benitec Biopharma Ltd Annual Report 2014  Page 29

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 7:  KEY MANAGEMENT PERSONNEL 

(a) Details of Key Management Personnel 

(i) Non-Executive Directors  
Mr Peter Francis 
Dr John Chiplin 
Mr Iain Ross 
Mr Kevin Buchi 
Dr Mel Bridges 

Chairman - Non-Executive 
Director - Non-Executive 
Director - Non-Executive 
Director - Non-Executive 
Director - Non-Executive 

(ii) Specified Executives 
Dr Peter French 

Chief Executive Officer  
and Managing Director  

Appointed on 23 February 2006
Appointed on 1 February 2010
Appointed on 1 June 2010
Appointed on 11 April 2014
Appointed on 12 October 2007
Resigned 18 June 2014 

Dr Michael Graham 
Mr Greg West 
Mr Carl Stubbings 
Dr David Suhy 

Chief Scientific Officer 
Company Secretary 
Chief Business Officer 
Senior VP Research and Development  Appointed on 1 October 2012

Appointed as Managing Director on 26 August 2014
Appointed Chief Executive Officer on 4 June 2010
Appointed Chief Scientific Officer on 4 August 2009
Appointed on 1 January 2012
Appointed on 26 May 2011
Appointed on 2 July 2012

(b) Key management personnel remuneration includes the following expenses:

Short term employee benefits 
    Salaries including bonuses 
Post-employment benefits 
    Superannuation 
Share-based payments 

Total Remuneration 

2014 
$ 

1,859,719 

71,100 
348,013 

2,278,832 

2013
$

1,252,095

61,935
492,976

1,807,006

During the year no key management personnel exercised options which were granted either under ESOP or by a General Meeting of Members to 
Non-Executive Directors

NOTE 8: CASH AND CASH EQUIVALENTS 
Cash at bank 
Deposits at call 

Reconciliation of Cash Flow from Operations with Loss after Income Tax
Loss after Income Tax 
Non-cash flows included in operating loss: 
Impairment 
Foreign exchange on intercompany balances 
Depreciation 
Share-based payments 
Foreign currency translation unrealised 
Changes in assets and liabilities: 
(Increase)/decrease in other assets 
Decrease in receivables 
Decrease/(increase) in payables 
Increase/(decrease) in employee provisions 

Net cash flows from operations 

Page 30  Benitec Biopharma Ltd Annual Report 2014

288,945 
31,070,254 

31,359,199 

614,746
972,553

1,587,299

(7,039,109) 

(3,487,960)

- 
- 
12,808 
355,116 
8,761 

(2,936,521) 
(16,514) 
277,246 
67,874 

(9,270,339) 

1,503,296
(1,526,215)
29,794
518,749
(23,457)

(13,163)
22,393
200,452
43,515

(2,732,596)

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 9: TRADE AND OTHER RECEIVABLES 
CURRENT 
Sundry Debtors 

NOTE 10: OTHER ASSETS 
CURRENT 
Prepayments 
Prepaid clinical trials * 
Other current assets 

2014 
$ 

2013
$

121,587 

105,073

26,679 
2,700,000 
240,060 

2,966,739 

14,190
-
16,028

30,218

* Prepaid clinical trials - The Company announced on 3 June 2013 that it had committed to moving its non-small cell lung cancer therapeutic, into 
clinical development. The Company is using European-based clinical research organisation Clinical Trials Group (CTGCRO) to manage both the 
initial clinical development and trials. The Company made prepayments in the September quarter 2013 in order to secure favourable commercial 
terms with CTGCRO for the conduct of the trials.

NOTE 11: CONTROLLED ENTITIES 

(a) Controlled entities: 

Parent Entity: 
Benitec Biopharma Limited 

Controlled entities of Benitec Biopharma Limited: 
Benitec Australia Limited 
Benitec Biopharma Limited 
Benitec, Inc. 
Benitec LLC 
RNAi Therapeutics, Inc. 
Tacere Therapeutics, Inc. 

(b) Controlled entities acquired or disposed: 

Country of Incorporation 

Percentage Owned

2014 

2013

Australia 

Australia 
United Kingdom 
USA 
USA 
USA 
USA 

100% 
100% 
100% 
100% 
100% 
100% 

100%
100%
100%
100%
100%
100%

No controlled entities were acquired or disposed during the financial year.

Benitec Biopharma Ltd Annual Report 2014  Page 31

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 12: PROPERTY, PLANT AND EQUIPMENT  
At cost 
Accumulated depreciation 

Total Property, Plant and Equipment 

2014 
$ 

127,795 
(80,118) 

47,677 

2013
$

95,431
(67,311)

28,120

Movements in Carrying Amounts 
Movement in the carrying amounts for each class of property, plant and equipment between the beginning and the end of the current financial year.

Total 
$

30,803
27,111
-
(29,794)

28,120

32,365
-
(12,808)

47,677

Leasehold 
Improvement 
$ 

Plant and 
Equipment 
$ 

19,043 
27,111 
- 
(28,244) 

17,910 

32,365 
- 
(11,258) 

39,016 

Balance at 30 June 2012 
Additions 
Less Disposals 
Depreciation expense 

Balance at 30 June 2013 

Additions 
Less Disposals 
Depreciation expense 

Balance at 30 June 2014  

NOTE 13: GOODWILL 
The net carrying amount of goodwill can be analysed as follows: 

Gross carrying amount 
Balance at 30 June 2012  
Acquired through business combination  

Balance at 30 June 2013  

Acquired through business combination 

Balance at 30 June 2014 

Accumulated impairment 
Balance at 30 June 2012  
Impairment loss recognised in the year 

Balance at 30 June 2013  

Impairment loss recognised in the year 

Balance at 30 June 2014 

Net book value 
At 30 June 2013 

As at 30 June 2014 

Goodwill Impairment

11,760 
- 
- 
(1,550) 

10,210 

- 
- 
(1,550) 

8,660 

$

-
1,503,296

1,503,296 

- 

1,503,296 

-
(1,503,296)

(1,503,296)

-

(1,503,296) 

-

-

A review of the carrying value of the goodwill which arose on the acquisition of Tacere Therapeutics Inc. was undertaken in the 2013 financial 
year. The recoverable amounts of the cash generating units to which the goodwill was allocated were determined based on value-in-use 
calculations. This review identified that the full value of the goodwill should be impaired and as such a non-cash impairment charge of $1,503,296 
was booked in the 2013 financial year.

Page 32  Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 14: TRADE AND OTHER PAYABLES 

CURRENT 
Unsecured liabilities 
Trade creditors 
Sundry creditors and accrued expenses 
Deferred consideration - Tacere vendors 

NOTE 15: PROVISIONS   
CURRENT 
Provision for employee benefits 

2014 
$ 

572,557 
215,612 
- 

788,169 

2013
$

279,994
374,560
357,179

1,011,733

166,511 

98,637

NOTE 16: CONTRIBUTED EQUITY  
The share capital of the Company consists only of fully paid ordinary shares; the shares do not have a par value. All shares are equally eligible 
to receive dividends and the repayment of capital and represent one vote at the shareholders’ meeting of the Company. The Board monitors 
capital funding requirements in its competitive landscape and continues to actively manage its cash requirements as part of a broader capital 
management program to ensure adequate capital is in place to fund the company’s operations. 
(a) Ordinary Shares, reported in post consolidation share numbers for 2014 and 2013 
114,898,992 (2013: 46,076,562) issued and fully paid ordinary shares 

Contributed Equity at the beginning of the reporting period, (after applying the 25:1 consolidation) 
Placements in March to June 2013 
Placement in July 2013  
Share Purchase Plan August 2013 
Issued to Tacere shareholders on purchase of Tacere 
Tacere escrow shares released October 2013 
Options exercised during the year 
Placements in February and April 2014  
Transaction costs relating to share issues during the year 

Contributed Equity at the close of the reporting period 

At the beginning of reporting period  
Shares issued during the year 

89,609,248 
- 
7,618,326  
2,820,000  
- 
357,190  
185,503  
31,496,504  
(2,901,095) 

129,185,676 

Number 
46,076,562 
68,822,430 

114,898,992 

87,348,819
1,262,000
-
-
1,173,585
-
-
-
 (175,156)

89,609,248

Number
38,825,141
7,251,421

46,076,562

(b) Share options 
At the end of the financial year, there were 23,320,173 unissued ordinary shares (2013: 17,594,313) over which options were outstanding.
Details 

Exercise Price 

Expiry Date 

Number

Strategic Advisor warrants 

ESOP Options 

NED Options 

Unlisted Options - placement 

Unlisted other options 

4 August 2014 

19 August 2014 

19 August 2014 

18 February 2015 

10 April 2015 

22.500 

0.510 

0.570 

0.325 

2.500 

245,078 

260,000 

120,000 

662,767 

480,000 

Benitec Biopharma Ltd Annual Report 2014  Page 33

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 15: CONTRIBUTED EQUITY (continued)
Unlisted other options 

NED Options 

ESOP Options 

NED Options 

ESOP Options 

ESOP Options 

ESOP Options 

NED Options 

ESOP Options 

Unlisted options - placement 

ESOP Options 

23 October 2015 

26 September 2016 

17 November 2016 

26 September 2016 

7 February 2017 

18 July 2017 

16 November 2017 

18 May 2018 

22 August 2018 

28 February 2019 

15 May 2019 

4.250 

1.250 

1.250 

1.250 

1.250 

1.250 

1.250 

0.625 

1.250 

1.260 

1.500 

78,125 

1,600,000 

1,800,000 

1,200,000 

168,000 

   400,000 

 400,000 

400,000 

2,080,000 

13,246,203 

180,000 

23,320,173  

Since 30 June 2013, the following options were issued under the ESOP:

Expiry date 

Exercise price  

Issue date 

Number 

Weighted average
share price 

Volatility 

Risk free rate

22 August 2018 

15 May 2019 

1.250 

1.500 

22 August 2013 

2,080,000 

15 May 2014 

180,000 

$0.29 

$0.30 

112% 

100% 

3.55%

2.60%

2,260,000 

Rights over shares are provided to employees under the Employee Share Option Plan (ESOP). The cost of these equity-settled transactions with 
employees is measured by reference to the fair value at the date at which they are granted. The fair value is determined using a Black-Scholes 
model. In valuing equity-settled transactions, no account is taken of any performance conditions, other than conditions linked to the price of the 
shares of Benitec Biopharma Limited (‘market conditions’).

The following information was factored in to the Black-Scholes model for the options issued under ESOP this year: 
i.  weighted average share price as shown above
ii.  exercise prices were as shown above 
iii.  expected volatility was  as shown above and was determined by reference to Bloomberg for the Benitec share price based on historical 

volatility

iv.  option life is 5 years
v.  The risk-free interest rate used was as shown above

There were no options issued to staff or directors in the period from 30 June 2014 to the date this report was issued. 

Page 34  Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 17: RESERVES 
Share-based payments reserve 
At the beginning of the reporting period 
Share based payments 
Transferred to Accumulated Losses Reserve no longer required 

Foreign currency translation reserve 
At the beginning of the reporting period 
Foreign currency translation  

Total Reserves 

2014 
$ 

2013
$

1,591,702 
355,116 
- 

1,946,818 

(1,313,792) 
7,747  

(1,306,045)  

640,773 

1,394,142
518,749
(321,189)

1,591,702

-
(1,313,792)

(1,313,792)

277,910

Nature and purpose of Reserves 
Share Based Payments Reserve
The Share-based Payments Reserve represents the expense attributed to options based on a Black Scholes valuation method for vested options.
Foreign currency translation reserve
The Foreign currency translation reserve represents the currency translation movements of subsidiary company balances denominated in foreign 
currencies at year end.

NOTE 18: OPERATING SEGMENTS
Business Segments 
The Group had only one business segment during the financial year, being the global commercialisation by licensing and partnering of patents and 
licences in biotechnology, more specifically in functional genomics, with applications in biomedical research and human therapeutics.
Geographical Segments
Business operations are principally conducted in Australia, with laboratory and other activities in the USA.

Geographical location 

Segment Revenues  

Segment Results 

2014 
$ 

2013 
$ 

2014 
$ 

2013 
$ 

Carrying Amount of 
Segment Assets

2014 
$ 

2013
$

Australia 

External customers 
Interest revenue 
Other income 

United States of America 
External customers 
Interest revenue 
Other income 

274,413 
321,116 
775,833 

521,140 
118,709 
823,354 

1,371,362 

1,463,203 

2,411 
- 
- 

2,411 

- 
- 
979 

979 

(7,495,377) 

(3,220,240) 

34,433,803 

1,507,350

1,903 

(267,720) 

61,399 

243,360

1,373,773 

1,464,182 

(7,493,474) 

(3,487,960) 

34,495,202 

1,750,710

Accounting Policies
Segment revenues and expenses are directly attributable to the identified segments and include joint venture revenue and expenses where a 
reasonable allocation basis exists. Segment assets include all assets used by a segment and consist mainly of cash, receivables, inventories, 
intangibles and property, plant and equipment, net of any allowances, accumulated depreciation and amortisation. Where joint assets correspond 
to two or more segments, allocation of the net carrying amount has been made on a reasonable basis to a particular segment. Segment liabilities 
include mainly accounts payable, employee entitlements, accrued expenses, provisions and borrowings. Deferred income tax provisions are not 
included in segment assets and liabilities.

Benitec Biopharma Ltd Annual Report 2014  Page 35

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 19:  FINANCIAL RISK MANAGEMENT OBJECTIVES AND POLICIES
The Group’s principal financial instruments comprise receivables, payables, cash and short-term deposits. The Group manages its exposure to key 
financial risks, including interest rate and currency risk in accordance with the Company financial risk management policy. The objective of the 
policy is to protect the assets and provide a solid return.

The main risks arising from the financial instruments are interest rate risk, liquidity risk, foreign currency risk and credit risk. The Board reviews 
and agrees policies for managing each of these risks and they are summarised below.   

Risk Exposures and Responses

Interest rate risk
The Group generates income from interest on surplus funds. At reporting date, the Group had the following mix of financial assets and liabilities 
exposed to Australian variable interest rate risk that are not designated in cash flow hedges:

Financial Assets 

Cash and cash equivalents 
Financial Liabilities 

Net Exposure 

2014 
$ 

31,359,199 
- 

31,359,199 

2013
$

1,587,299
-

1,587,299

The policy is to analyse the Company’s interest rate exposure across the Groups financial assets and liabilities. Consideration is given to the return 
on funds invested, alternative financing, the mix of fixed and variable interest rates and hedging positions. The Group currently has short term 
deposits at variable interest rates.  The average interest rate applying to cash deposits in the year was 3.67% (2013 4.00%).
The following sensitivity analysis is based on the interest rate risk exposures in existence at the reporting date:
At 30 June 2014, if interest rates had moved, as illustrated in the table below, with all other variables held constant, the judgment of reasonably 
possible movements in post-tax profit and equity would have been as follows:

+1% (100 basis points) 

-0.5% (50 basis points) 

Post Tax Result 
Higher/ (Lower) 

Equity 
Higher/ (Lower)

2014 
$ 

143,625 

(71,812) 

2013 
$ 

12,797 

(6,399) 

2014 
$ 

143,625 

(71,812) 

2013
$

12,797

(6,399)

Liquidity risk
The Group’s objective is to obtain revenue from commercialisation and to continue to access funding markets. The Group has a pipeline of 
programs to take its research and development to the clinic and potentially originate licensing transactions with pharmaceutical companies.  
Trade payables and other financial liabilities originate from the financing of the ongoing research and development programs in addition to the 
operations of the business generally.
The table below reflects all contractually fixed pay-offs and receivables for settlement, repayments and interest resulting from recognised financial 
assets and liabilities as at 30 June 2014.  ash flows for financial assets and liabilities with fixed amount or timing are presented with their 
respective discounted cash flows for the respective upcoming fiscal years.
The remaining contractual maturities of the Group’s financial liabilities are:

6 months or less 
6-12 months 
1-5 years 
Over 5 years 

2014 
$ 

788,169 
- 
- 
- 

788,169 

2013
$

1,011,733
-
-
-

1,011,733

Maturity analysis of financial assets and liabilities based on management’s expectation
The table below reflects management’s expectation of the maturity of financial assets and liabilities. 
These assets are considered in the context of the Group’s overall liquidity risk. The Group has established a risk reporting process overseen by the 
board which monitors existing financial assets and liabilities and provides information to enable effective risk management. The Board regularly 
evaluates managements rolling forecasts of liquidity which includes assessments of cash income and outgoings.  

Page 36      Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

≤6 months 
$ 

6-12 months 
$ 

1-5 years 
$ 

>5 years 
$ 

Financial assets 
Cash and cash equivalents 23,359,199 

Trade and other receivables  121,587 

Financial Liabilities 
Trade and other payables 

Net Maturity 

(788,169) 

22,692,617 

8,000,000 

- 

- 

8,000,000 

- 

- 

- 

- 

- 

- 

- 

- 

Total
$

31,359,199

121,587

(788,169)

30,692,617

Foreign currency risk
The Group has transactional currency exposures.  Such exposure arises from licensing fees and royalties as well as expenditure by the Group in 
currencies other than the unit’s measurement currency. With the exception of unrealised movements on intercompany loans, foreign currency 
income and expenditure accounts for less than 15% of the Groups transactions and therefore management have assessed that movements in 
foreign exchange would not materially impact the financial statements. 

Credit risk
Credit risk arises from the financial assets of the Group, which comprise cash and cash equivalents, and trade and other receivables.  The Group’s 
exposure to credit risk arises from potential counter party payment default, with a maximum exposure equal to the carrying amount.  Exposures at 
each reporting date are assessed and disclosed in the financial statements.

The Group does not hold any credit derivatives to offset its credit exposure.  The Group trades only with recognised, creditworthy third parties and 
as such collateral is not requested. The Group does not securitise its trade and other receivables.  

Customers who wish to trade on credit terms are subject to credit assessment procedures which may include an assessment of their independent 
credit rating, financial position, past experience and industry reputation.  Receivable balances are regularly monitored. There are no significant 
concentrations of credit risk within the Group.

NOTE 20: FINANCIAL INSTRUMENTS

Fair values

Fair values of financial assets and liabilities are equivalent to carrying values due their short term to maturity.

NOTE 21: SHARE BASED PAYMENTS 

Benitec Biopharma Limited Employees Share Option Plan (ESOP): 

Description of plan 
The Group may from time to time issue employees options to acquire shares in the parent at a fixed price.  Each option when exercised entitles the 
option holder to one share in the Company.  Options are exercisable on or before an expiry date, do not carry any voting or dividend rights and are 
not transferable except on death of the option holder. 

Share Options granted during the year 
The following options were issued to executives by Benitec Biopharma Limited under its ESOP and are unlisted.
Executive  

Exercise Price 

Grant Date 

Number 

Peter French 

22 August 2013 

1,400,000 

David Suhy 

Greg West 

22 August 2013 

22 August 2013 

Carl Stubbings 

22 August 2013 

Tin Mao 

Shin-chu Kao 

15 May 2014 

15 May 2014 

200,000 

280,000 

200,000 

90,000 

90,000 

2,260,000 

$1.250 

$1.250 

$1.250 

$1.250 

$1.500 

$1.500 

Expiry Date

22 August 2018

22 August 2018

22 August 2018

22 August 2018

15 May 2019

15 May 2019

Benitec Biopharma Ltd Annual Report 2014      Page 37

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 21: SHARE BASED PAYMENTS (continued)
There were no options issued to directors in the year to 30 June 2014. The closing market price of an ordinary share of Benitec Biopharma Limited 
(ASX Code: BLT) on the Australian Securities Exchange at 30 June 2014 was $1.15 (30 June 2013: $0.375, after adjusting for the securities 
consolidation in July 2013)
The following table shows the number and weighted average exercise price (WAEP) of share options issued under the ESOP:
2014 
Number 

2013 
Number 

2014 
WAEP 

2013
WAEP

Outstanding at the beginning of the year 

Granted during the year 

Exercised during the year 

Lapsed or forfeited during the year 

Outstanding at the end of the year 

Options exercisable at the end of the year 

3,028,000 

2,260,000 

- 

- 

5,288,000 

2,178,667  

Details of ESOP share options outstanding as at end of year: 

Grant Date   

13 July 2010 

  Expiry Date 

  19 August 2014 

17 November 2011 

  17 November 2016 

7 February 2012 

18 July 2012 

  7 February 2017 

  18 July 2017 

16 November 2012 

  16 November 2017 

22 August 2013 

28 May 2014 

  22 August 2018 

  18 May 2019 

1.200 

1.270  

 -  

- 

1.229 

Exercise Price 

$0.510 

$1.250 

$1.250 

$1.250 

$1.250 

$1.250 

$1.500 

2,440,000 

800,000 

- 

-212,000 

3,028,000 

1,456,000 

2014 
Number 

260,000  

1,800,000  

168,000  

400,000  

400,000  

2,080,000  

180,000  

5,288,000  

1.147

1.250 

 - 

0.792

1.200 

2013
Number

260,000 

1,800,000 

168,000 

400,000 

400,000 

-

-

3,028,000 

The weighted average remaining life of the options issued under the ESOP at 30 June 2014 was 3 years and 3 months. 
(2013: 3 years and 4 months)

NOTE 22: EVENTS SUBSEQUENT TO REPORTING DATE 
No matters or circumstances have arisen since 30 June 2014 which have significantly affected or may significantly affect the operations of the 
Group, the results of those operations or the state of affairs of the Group, in subsequent financial years. 

NOTE 23: CONTINGENT LIABILITIES
In January 2010, the Company reached a settlement with the CSIRO to replace the existing Licence Agreement and Commercial Agreement with a 
new exclusive Licence Agreement for the use of intellectual property and the Capital Growth Agreement with the issue of ordinary shares. As part 
of the settlement, a Transition Agreement was put in place in order to facilitate the change from the old agreements to the new agreement and to 
deal with a number of other matters. 

Under the terms of the Transition Agreement, the Company agreed to pay CSIRO an amount of $297,293 for past patent costs only in the event of 
a trigger event, being either a corporate transaction or an insolvency event.

Scientific work on the therapeutic programs  

On 18 December 2012 Benitec announced the appointment of Synteract Inc. as the Company’s Clinical Research Organisation responsible for the 
progression of TT-034 into Phase I/II (a) Clinical Trials in the USA. Benitec has negotiated a contract with favourable commercial terms, in some 
instances requiring prepayment, for Synteract to continue to manage the Clinical Trials throughout 2014 and 2015.  

Benitec announced plans on 3 June 2014 to progress its non-small cell lung cancer (NSCLC) therapeutic Tribetarna™ into Phase II clinical trials 
in late 2014 calendar year. The Company had reached agreement to use European-based clinical research organisation Clinical Trials Group 
(CTGCRO) to manage the trial, and subsequently negotiated favourable commercial terms which included prepayments covering the clinical trial 

Page 38  Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

and consulting services. 

The Company has contracted for scientific work on the therapeutic programs, as described above, and payments due within the next twelve 
months total approximately $2,092,500 (2013: $4,178,261)

NOTE 24: CAPITAL MANAGEMENT POLICIES AND PROCEDURES 
The Group’s capital management objectives are to ensure the Group has the ability to fund its activities, to continue as a going concern; and to 
provide value to shareholders.

The Group’s capital management plan targets appropriate cash levels to service expected future cash flow needs based on the forecasts for 
current and future programs and business running costs.  Management assesses the Group’s capital requirements in order to maintain an efficient 
overall financing structure.  The Group manages the capital structure and makes adjustments to it in the light of changes in access to funding, 
business conditions and the risk characteristics of the business.  In order to maintain appropriate funding the Group may issue new shares. The 
amounts managed as capital by the Group for the reporting periods under review are as shown in the statement of financial position.

NOTE 25: RELATED PARTY TRANSACTIONS 

Transactions with Directors and Director-related Entities: 
Legal services paid / payable to Francis Abourizk Lightowlers,  
a law firm in which Mr Peter Francis is a partner and has a beneficial interest. 
Consultancy fees for executive duties paid/payable to NewStar Ventures Ltd,  
a corporation in which Dr John Chiplin is a director and has a beneficial interest. 

2014 
$ 

108,913 

40,000 

2013
$

103,492

40,000

Transactions between related parties are on normal commercial terms and the conditions no more favourable than  
those available to other non-related parties. There are no outstanding balances as at 30 June 2014 (2013: nil).

NOTE 26: BUSINESS COMBINATION – TACERE THERAPEUTICS INC. ACQUISITION IN OCTOBER 2012
Benitec announced an agreement to acquire the US-based RNA interference (RNAi) therapeutics company Tacere Therapeutics Inc. (‘Tacere’) on 
11 October 2012. The acquisition was completed on 30 October 2012 when Benitec acquired 100% of the issued share capital and voting rights of 
Tacere, a company based in the United States. Tacere was a privately held drug development company with a Phase I/II ready program in hepatitis 
C (HCV) that uses Benitec’s novel gene silencing technology.

Benitec acquired Tacere’s extensive HCV program data and materials, as well as an advanced preclinical program for the eye disease macular 
degeneration, The Tacere acquisition provided Benitec with the opportunity to commence Phase I/II clinical trials in 2014.

The consideration for the acquisition was an issue of shares in Benitec Biopharma Limited for USD $1,530,765 plus a potential cash royalty on 
future licensing revenue.  The shares issued as consideration represented 9.5% of the issued capital at the time of the acquisition. 

Further, the agreements with the Tacere vendors provided for AUD $357,179 Benitec Biopharma Limited shares (included in the acquisition 
consideration) be treated as reserve shares and not issued to the Tacere vendors for a period of 12 months from acquisition. The reserve shares 
are accounted for as a creditor in 2013 (refer to note 6). The reserve shares were established by an agreement with the Tacere vendors for the 
purposes of satisfying indemnities to Benitec, if required. The Tacere Vendors also provided a cash escrow of USD $360,000 to provide Benitec 
with additional security should certain pre-acquisition liabilities emerge.

Impairment costs, relating to the goodwill on the acquisition of Tacere of $1,503,296 were recognised in the 2013 financial year. The Tacere 
acquisition goodwill is the excess of the consideration over the fair value of the identifiable assets acquired less liabilities assumed. The 
immediate write off of the goodwill, following the impairment review, was considered to be the most appropriate accounting treatment as the 
intellectual property is a preclinical trial and hence the future economic benefit is uncertain.

Benitec Biopharma Ltd Annual Report 2014  Page 39

 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 26: BUSINESS COMBINATION – TACERE THERAPEUTICS INC. ACQUISITION IN OCTOBER 2012 (continued)
Financial details of the business combination made in the previous financial year (year ended 30 June 2013) were:

Fair value of consideration transferred 
Consideration for the acquisition in October 2012 was the issue of 102,321,345 (pre-consolidation)  
shares in Benitec Biopharma Limited, plus a potential cash royalty on future licensing revenue  

Recognised amounts of identifiable net assets 
Property, plant and equipment  
Cash and cash equivalents 
Amount owing to Benitec Biopharma Limited 
Other liabilities 

Identifiable net assets 

Goodwill on acquisition impaired in the June 2013 financial statements 

Net cash inflow on acquisition 
Acquisition related costs recognised as an expense in the Group corporate expenses 
Post-acquisition loss of Tacere in the period to 30 June 2013 
Post-acquisition loss of Tacere in the period to 30 June 2014 

$

 1,530,765

 17,567
 138,760
 (126,882)
 (1,976)

27,469

 1,503,296

 143,603
77,104
267,720
1,903

Page 40  Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Notes to the Consolidated Financial Statements  
for the Year Ended 30 June 2014

NOTE 27: BENITEC BIOPHARMA LIMITED PARENT COMPANY INFORMATION

ASSETS   
Current assets 
Non-current assets 

TOTAL ASSETS 

LIABILITIES 
Current liabilities 
Non-current liabilities 

TOTAL LIABILITIES 

NET ASSETS 

EQUITY 
Contributed equity 
Share based payments reserve 
Accumulated losses 

TOTAL EQUITY 

FINANCIAL PERFORMANCE  
Loss for the year 
Other comprehensive income 

2014 
$ 

      34,386,167  
                       181,547 

Parent Entity

2013
$

1,478,422
48,999

           34,567,714  

1,527,421

     1,311,608  
- 

1,165,652
-

      1,311,608   

1,165,652

       33,256,106  

361,769

   129,185,675 
      2,096,818 
  (98,026,387) 

89,609,248
1,591,702
(90,839,181)

33,256,106 

361,769

     (7,037,206) 
- 

(4,885,852)
-

TOTAL COMPREHENSIVE INCOME 

     (7,037,206) 

(4,885,852)

Contingent liabilities
The parent entity had no contingent liabilities as at 30 June 2014 (2013: nil), other than the contingent liabilities described in note 22. 
Capital commitments
The parent entity has no capital commitments as at 30 June 2014 (2013: nil).
Significant accounting policies
The accounting policies of the parent are consistent with those of the consolidated entity (Note 1)

Benitec Biopharma Ltd Annual Report 2014  Page 41

 
 
 
 
 
 
 
 
 
 
 
 
 
 
  
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  
 
 
 
 
 
 
 
 
 
 
  
 
 
 
Directors’ Declaration

1. 

In the opinion of the Directors:

(a)  the attached financial statements and notes thereto are in accordance with the Corporations Act 2001, including:

(i)   giving a true and fair view of the financial position and performance of the Company and consolidated entity; and
(ii)  complying with Australian Accounting Standards, including the Interpretations, and the Corporations Regulations 2001. 

(b)  the financial statements and notes thereto also comply with International Financial Reporting Standards, as disclosed in Note 1; and
(c)  as indicated in note 1(w), there are reasonable grounds to believe that the Company will be able to pay its debts as and when they 

become due and payable.

(d)  The remuneration disclosures contained in the Remuneration Report comply with s300A of the Corporations Act 2001

2.  The Directors have been given the declarations by the Chief Executive Officer and Chief Financial Officer required by section 295A of the 

Corporations Act 2001.

Signed in accordance with a resolution of the directors made pursuant to s.295(5) of the Corporations Act 2001. 

On behalf of the Directors

Peter Francis

Director

Sydney

22 August 2014

Page 42  Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
Independent Audit Report

Benitec Biopharma Ltd Annual Report 2014      Page 43

Independent Audit Report

Page 44      Benitec Biopharma Ltd Annual Report 2014

Independent Audit Report

Benitec Biopharma Ltd Annual Report 2014      Page 45

Shareholder Information

1. SHARE AND OPTION HOLDING INFORMATION

a) Distribution of Equity Security Holders

The number of holders and amount of holdings by a range of holding sizes of the ordinary shares and options as at 23 September 2014  
are detailed below.

Range 

Fully Paid Ordinary Shares (ASX:BLT)

1 - 1,000 

1,001 - 5,000 

5,001 - 10,000 

10,001 - 100,000 

100,001 - 9,999,999,999 

b) Marketable parcels

Number of 
holders 

944 

1,547 

563 

822 

117 

3,993 

Number of 
shares held

537,815

4,378,010

4,471,682

25,281,581

80,549,905

115,218,993

The number of holdings of ordinary shares less than a marketable parcel of $500 as at 23 September 2014 is 409.

c) Substantial Shareholders

The names of substantial shareholders listed in the Company’s register as at 23 September 2014 were:

Holder

RA Capital Management LLC 

Dr Christopher Bremner 

Dalit Pty Ltd 

d) Voting rights

Number Of Ordinary 
Shares Held 

% Of Issued 
Capital

14,018,691 

8,013,201 

5,780,497 

12.2

7.0

5.0

The voting rights attached to each class of equity security are as follows:

Each ordinary share holder is entitled to one vote when a poll is called, otherwise each member present at a meeting or by proxy has one vote on 
a show of hands.

Option holders do not have any voting rights until the option is converted into an ordinary share.

Page 46      Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Shareholder Information

e) 20 Largest Ordinary Shareholders as at 23 September 2014

Holder

Citicorp Nominees Pty Limited 

National Nominees Limited 

Dalit Pty Ltd 

MJGD Nominees Pty Ltd 

J P Morgan Nominees Australia Limited 

Irwin Biotech Nominees P/L  

National Nominees Limited  

CSIRO 

HSBC Custody Nominees (Australia) Limited - A/C 2 

Dr Russell Kay Hancock 

Tigcorp Nominees Pty Ltd 

Mr Paul Leonard Grimshaw + Mr Dayne Paul Grimshaw  

Hokkaido Venture Capital Co Ltd 

HSBC Custody Nominees (Australia) Limited 

Montclair Pty Ltd 

Promega Corporation 

Merrill Lynch (Australia) Nominees Pty Limited 

Wilson Engineering Wa Pty Ltd  

Sara Renison 

Mr Jason Scott Ellenport + Mrs Vicky Ellenport  

Totals: Top 20 holders of fully paid ordinary shares  

Total remaining holders balance 

Number Of Ordinary 
Shares Held 

% Of Issued 
Capital

18,439,997 

12,461,673 

5,339,848 

4,323,463 

4,073,729 

3,510,088 

2,407,418 

1,924,658 

1,855,773 

1,050,000 

872,892 

751,594 

653,416 

611,644 

593,134 

519,854 

487,504 

450,000 

447,098 

440,681 

61,214,464 

54,004,529 

16.00

10.82

4.63

3.75

3.54

3.05

2.09

1.67

1.61

0.91

0.76

0.65

0.57

0.53

0.51

0.45

0.42

0.39

0.39

0.38

53.13

46.87

Benitec Biopharma Ltd Annual Report 2014      Page 47

 
 
 
 
 
 
 
 
 
 
 
Shareholder Information

f) Restricted securities

There are no securities on issue subject to restriction agreements.

i) Unquoted securities

As at the date of this report, the Company has unquoted securities as follows:

Details 

Strategic Advisor warrants 

ESOP Options 

NED Options 

Unlisted Options - placement 

Unlisted other options 

Unlisted other options 

NED Options 

ESOP Options 

NED Options 

ESOP Options 

ESOP Options 

ESOP Options 

NED Options 

ESOP Options 

Unlisted options - placement 

ESOP Options 

2. On-Market Buy Back

There is currently no on-market buy back.

3. Listing on Exchanges

Expiry Date 

Exercise Price 

4 August 2014 

19 August 2014 

19 August 2014 

18 February 2015 

10 April 2015 

23 October 2015 

26 September 2016 

17 November 2016 

26 September 2016 

7 February 2017 

18 July 2017 

16 November 2017 

18 May 2018 

22 August 2018 

28 February 2019 

15 May 2019 

22.500 

0.510 

0.570 

0.325 

2.500 

4.250 

1.250 

1.250 

1.250 

1.250 

1.250 

1.250 

0.625 

1.250 

1.260 

1.500 

Number

245,078 

260,000 

120,000 

662,767 

480,000 

78,125 

1,600,000 

1,800,000 

1,200,000 

168,000 

   400,000 

 400,000 

400,000 

2,080,000 

13,246,203 

180,000 

23,320,173 

Trading of the Company’s securities is available on the Australian Securities Exchange Limited (ASX : BLT) and through a  
Level 1 American Depositary Receipt (ADR) program in the Over-The-Counter (OTC : BTEBY) market in the United States.

Page 48      Benitec Biopharma Ltd Annual Report 2014

 
 
 
 
 
 
 
Corporate Directory

BENITEC BIOPHARMA LIMITED

ABN 64 068 943 662

Directors

Mr Peter Francis   Non-Executive Chairman
Dr Peter French 
Dr John Chiplin 
Mr Iain Ross 
Mr Kevin Buchi 

Chief Executive Officer and Managing Director
Non-Executive Director
Non-Executive Director
Non-Executive Director

Chief Executive Officer and Managing Director
Dr Peter French       

Company Secretary
Mr Greg West

Registered Office
Level 16
356 Collins Street
Melbourne Vic 3000
Australia

Principal Place of Business
F6A/1-15 Barr Street
Balmain NSW 2041
Australia

Auditors
Grant Thornton Audit Pty Ltd 
Level 17, 383 Kent Street 
Sydney NSW 2000

Bankers
Westpac Banking Corporation 
274 Darling Street 
Balmain NSW 2041

Share Registry
Computershare Investor Services Pty Limited
Yarra Falls
452 Johnston Street
Melbourne VIC 3067

Stock Exchange Listing
The Company is listed on the Australian Securities Exchange Limited 
ASX Code: BLT

Benitec Biopharma Ltd  
ABN 64 068 943 662 

F6A / 1-15 Barr Street 
Balmain NSW   2041 Australia

Tel:  +61 (0) 2 9555 6986   
Email: info@benitec.com

www.benitec.com