Annual Report to shareholders
Released
Released
Announcement PDF
2017
ANNUALREPORT
ABN 73 124 849 065
2017
HIGHLIGHTS
• Dose safety indicated in multiple animal models
• Efficacy in animal models for superbug strains
of E. coli and S. Aureus
• Multiple tests of mutagenicity (cancer) are clear
• Confirmation of production at volumes for
clinical program
• Efficacy established in seven of the top 12 superbug
threats identified by WHO
• Secured up to A$6.05 million investment from
US investor
• Additional global patent advances
b
recce.com.au / Recce Annual Report 2017
CONTENTS
WHO WE ARE
3
MESSAGE FROM THE CHAIRMAN
4
COMPANY PROFILE
6
BOARD OF DIRECTORS &
KEY MANAGEMENT PERSONNEL
10
FINANCIAL REPORT
11
CORPORATE DIRECTORY
IBC
recce.com.au / Recce Annual Report 2017
1
“
“Drug-resistant bacteria kill
about 700,000 people each year,
and that number could rise to 10
million by 2050 without a new
arsenal of drugs”
The Review on Antimicrobial Resistance
Chaired by Jim O’Neill
WHO WE ARE
Recce is a drug discovery and development business
commercialising a new class of synthetic antibiotics to address
the global health challenge of antibiotic resistant superbugs.
Overuse of antibiotics in medicine and
farming has led to the rise of antibioticresistant bacteria worldwide.
The rise of so-called superbugs has
become a global health issue and
one of the greatest threats to human
health according to the World Health
Organisation (WHO).
Recce is developing a portfolio of new
therapies that have the potential to
help address the worldwide threat to
human health posed by drug resistant
bacteria. Recce’s current lead candidate
is a synthetic antibiotic that is being
developed to treat bacterial sepsis,
gastritis and diarrhoea.
Recce is currently completing an
Investigational New Drug application
(IND) application for submission to the
US Food & Drug Administration (FDA)
to gain approval to test its therapy in
humans.
With a low cost out-sourced business
model and a strong patent portfolio,
the business is well positioned, with
management committed to delivering
long-term value to shareholders.
recce.com.au / Recce Annual Report 2017
3
“With your support we
are focused on creating a
commercially successful
enterprise to help address the
global rise of antibiotic
resistant superbugs.”
Executive Chairman, Dr Graham Melrose
MESSAGE FROM THE CHAIRMAN
Building the foundations for long term growth
During the 2017 financial year, Recce Limited continued building the solid foundations for growth and moving towards becoming a
significant international antibiotics business.
Our pre-clinical program continued to make excellent progress as we invested considerable resources in the advance of our
Investigative New Drug (IND) application for submission to the US Food & Drug Administration (FDA).
Operational update
Key operational achievements included the establishment of our first automated manufacturing facility in Sydney to supply our early
clinical trials as well as recruiting a number of key staff to manage and support our production.
The upscaling of our manufacturing capabilities was a key milestone for the period as it broadened our production capacity whilst bringing
our overall Quality Management System (QMS) to a higher standard according to the US Food and Drug Administration’s (FDA) good
laboratory practice (glp) guidelines.
During the reporting period we welcomed a number of highly qualified new employees who together have been crucial to the timely
establishment of our new manufacturing facility in Sydney.
As we grow we expect to make a number of senior management appointments at the appropriate time as our technology advances
through the approval process and we expand our operations in to key geographic markets.
With your support, we are focused on creating a commercially successful business and realising the full potential of our unique Australian
technology.
The danger and effective management of the challenges posed by antibiotic resistance are very real and growing daily. The annual cost to
the Australian and global economy is growing and impacts all of us in some way.
Recce believes we have a unique opportunity to help medical professionals worldwide and to materially grow our business in the process.
4
recce.com.au / Recce Annual Report 2017
Financial management
At the same time our focus is on tightly managing our cash outflows while directing our precious resources towards the rapid
development of our lead candidate.
Recce is committed to delivering an effective low cost treatment demanded by our markets.
The team in Sydney has made excellent progress towards developing our new manufacturing facility and preparing the business
for the next critical stage of development - the start of human clinical trials.
A new approach to antibiotics
For the past decade, many big pharmaceutical companies have ignored investment in new antibiotics. Most of this is due to the
propensity of natural antibiotics to soon develop resistant superbugs soon after their market introduction.
Alternatively, Recce believes it can be part of the solution. Being synthetic means our lead candidate is not prone to resistance
and potentially less expensive to make. Our long term vision is to deliver to the market cost-effective, long-term solutions for the
current threat posed by multiple drug resistant superbugs.
The year ahead
2018 will be a pivotal year for our business as we aim to start a series of first human clinical trials of our lead compound in patients,
beginning with Phase 1 (safety) before progressing to Phase 2 (efficacy) for the treatment of sepsis derived from resistant and/or
non-resistant bacteria in the blood.
At the same time we expect to make
submissions to begin human studies for our
lead candidate to treat antibiotic resistant
strains of H.Pylori and E. coli.
“Thank you to our shareholders who have
supported Recce and continue to show their
strong belief in the future of the Company.”
Your Board of Directors remains focused on
managing this critical phase and conserving
our cash resources and have accordingly not replaced a number of board members who resigned during the reporting period. Our
focus is managing and minimising the risks and costs.
We are proud of the way our small team have responded to the challenges during the reporting period and I believe we have the
right people in place to drive the Company forward and rise to the many challenges we will encounter as we grow.
On behalf of the Board, I would like to sincerely thank our shareholders who continue to support the Company and our vision.
The solid foundations for long term growth are being built and we look forward to providing you with more positive updates as
we progress towards realising the promise our unique Australian technology holds and the potential to help improve the lives of
millions of people and reduce the cost burden of antibiotic resistant superbugs.
Yours sincerely,
Dr Graham Melrose
Executive Chairman / Recce Ltd
recce.com.au / Recce Annual Report 2017
5
COMPANY PROFILE
Our lead compound RECCE® 327 in action
These images show the mode of action of our lead compound. They were taken at the University of Western Australia using a
high-definition electron microscope. Our thanks to Dr Peta Clode and Lyn Kirilak of the Centre for Microscopy, Characterisation and
Analysis at UWA for their time and efforts.
A broad spectrum antibiotic candidate
Recce’s lead drug candidate, RECCE® 327 has shown promising results to date.
Data from pre-clinical studies indicate the compound is effective in treating a wide range of disease-causing bacteria, and the
superbugs of these bacteria.
6
00:00 minutes
00:20 minutes
180 minutes
The first image shows the drug
resistant E. coli bacteria before the
application of RECCE® 327, the
E. coli bacteria cells are healthy,
smooth and intact.
After application of RECCE® 327,
the E. coli bacteria cell membrane
begins to weaken and is disrupted.
E. coli bacteria cells (10e6 cfu/ml)
having their outer membrane
weakened – and finally collapsing
from treatment with
RECCE® 327 (1000 ppm).
Efficacy
Safety
•
Performs as a broad spectrum antibiotic
•
Multiple studies of toxicity in small and large animals
•
Acts against bacteria in both normal and mutated
superbug forms
•
Multiple tests of mutagenicity (cancer) are clear
•
Over 30 studies to date indicate the safety of RECCE® 327.
•
Multiple tests demonstrate efficacy against Gr+ve
S. aureus (Staph) including superbug forms
•
Is suited to administration against sepsis by intra-venous
drip
•
Multiple tests demonstrate efficacy against Gr-ve
E. coli including superbug forms
•
Indicates a wide and safe therapeutic dosing window
•
Rate and MIC/MKC data demonstrate high potency and
broad spectrum activity against range of bacteria
•
Contains a patented polymeric structure, intentionally
designed to overcome the traditional challenges of
bacterial mutation/resistance (superbugs)
•
In-vivo (mice) study against Influenza virus
recce.com.au / Recce Annual Report 2017
COMPANY PROFILE cont.
Strong patent portfolio provides a solid foundation for growth
Recce’s patent portfolio has continued to strengthen with the submission of patent family’s 2 and 3 in all Patent Cooperation
Treaty (PCT) countries.
Recce’s first family of patents protects its unique method of manufacture, antibacterial application and some modes of delivery as
a synthetic polymeric technology for human use. This monopoly is exclusive to Recce until at least 2028.
Provisional patents were lodged and advanced to patent pending statuses covering new modes of delivery and uses of the
synthetic technology including potential antiviral applications, extend to at least 2036.
Our aim is to become a global leader in the supply of new antibiotics that can help address the worldwide crisis of drug
resistant antibiotics.
Patent Family 1 – Granted
protecting Recce’s unique and highly economical manufacturing process
Status
Expiry
Australia
Filed
Granted
2028
USA
Granted
2029
Europe
Granted
2028
Germany
Granted
2028
Spain
Granted
2028
France
Granted
2029
United Kingdom
Granted
2028
Italy
Granted
2028
Sweden
Granted
2028
Japan
Granted
2028
China
Granted
2028
Status
Expiry
Pending
2034
Patent Family 2 – Provisional
protecting Recce’s drug delivery opportunities
Filed
All PCT Countries
Patent Family 3 – Provisional
protecting Recce’s anti-viral and anti-cancer applications
Filed
All PCT Countries
Status
Expiry
Pending
2034
Trade Marks – Approved and Registered
protecting RECCE® for use on antibiotic and pharmaceutical products and services
Filed
Status
Expiry
Australia
Registered
2026
USA
Registered
2026
Europe
Registered
2026
Japan
Registered
2026
China
Registered
2026
recce.com.au / Recce Annual Report 2017
7
COMPANY PROFILE cont.
Growth also supported by legislative and financial initiatives
Supportive US legislation
In the US, the Generating Antibiotic Incentives Now (GAIN) Act was passed to incentivize the development of new antibiotics in
response to the growing threat of antibiotic resistance and a lack of antibiotic products in drug manufacturers’ pipelines. The
legislation gives an extra five years patent exclusivity to new antibiotics that treat serious or life-threatening illnesses without
generic drug competition. A further five years market exclusivity is also available for molecules that the FDA defines as a ‘New
Chemical Entity’ (NCE). Additionally, the FDA provides a framework to award ‘Expedited Review Status’. Recce believes it will be
eligible to benefit from these additional advantages.
Non-dilutive funding grants
Two key programs, the US Biomedical Advanced Research & Development Agency (BARDA) Broad Spectrum Antimicrobials
program, and the European Innovative Medicines Initiative (IMI) New Drugs For Bad Bugs (ND4BB) program, provide direct financial
support to nearly 20 percent of all antibiotics currently under development globally.
In 2016 a new initiative called CARB-X, was launched as one of the world’s largest public-private partnerships focused on preclinical
discovery and development of new antimicrobial products. CARB-X will give US$44 million in its first year and up to $350 million
in the next five years in grants to small companies developing new antibiotics and diagnostics. CARB-X funds come from the US
government and a public-private initiative in the UK. The goal is to get at least two new drugs into human trials in the next five
years.
The World Health Organisation (WHO) is working to urgently raise awareness and action on antibiotic
resistant bacteria
To help governments, researchers and industry focus their resources on antibiotic resistance, the WHO has published a priority list
of 12 antibiotic-resistant bacteria.
Priority 1: CRITICAL
• Pseudomonas aeuginosa, carbapenem-resistant
• Enterobacteriacae, carbapenem-resistant, ESBL-producing
• Acinetobacter baumannii, carbapenem-resistant
RECCE® 327
1
2
Not tested
Priority 2: HIGH
• Enterococcus faecium, vancomycin-resistant
3
• Staphylococcus aureus, methicillin-resistant, vancomycin-intermediate
and resistant
4
• Helicobacter pylori, clarithromycin-resistant
5
• Neisseria gonorrhoeae, cephalosporin-resistant, fluoroquinolone-resistant
6
• Campylobacter spp., fluoroquinolone-resistant
Not tested
• Salmonellae, fluoroquinolone-resistant
Not tested
Priority 3: MEDIUM
• Streptococcus pneumoniae, penicillin-non-susceptible
1
2
3
4
5
6
7
8
7
• Haemophilus influenzae, ampicillin-resistant
Not tested
• Shigella spp., fluoroquinolone-resistant
Not tested
Active in vitro against Recce’s own superbug of this bacterium
Active in vivo against a member of this family CRE E. coli
Active in vitro against a very closely related species, Enterococcus faecalis, Vancomycin resistant
Active both in vitro and in vivo against MRSA, Methicillin-resistant Staphyloccocus aureus.
Active both in-vitro and in vivo against three strains (2 of which were superbugs)
Active in vitro (superbug not available)
Active in-vitro against related superbug Klebsiella pneumoniae
recce.com.au / Recce Annual Report 2017
“
“Antimicrobial resistance is a
global health emergency that will
seriously jeopardise progress in
modern medicine”
Dr Tedros Adhanom Ghebreyesus
Director-general of the WHO
BOARD OF DIRECTORS &
KEY MANAGEMENT PERSONNEL
Dr Graham Melrose
Executive Chairman
BSc (Hons), PhD (UWA), MBA (Macq), FRACI, C Chem, FAICD
Founder and inventor. Former Chief Research Executive of Johnson & Johnson
(Aust) Pty Ltd in Sydney, with global responsibilities, particularly in Asia-Pacific.
Michele Dilizia
Executive Director
BSc (Med Sci), Grad Dip Bus (Mkting), BA (Journ), GAICD, MASM
Co-inventor and qualified medical scientist; specialisation in medical
microbiology & regulatory affairs.
James Graham
Executive Director
BCom (Entrepreneurship), GAICD
Extensive experience in marketing, business development and
commercialisation of early stage technologies with global potential.
Peter Williams
CFO and Company Secretary
BBus, FCPA, MAICD
Accomplished senior ASX finance professional with significant local and
international experience. Former VP Finance with BHP World Minerals
reporting to the CEO.
Arthur Kollaras
Principal Engineer
BSc Beng (Chem), PhilEng (Enviro)
Highly qualified in chemical engineering and microbiology, has significant
experience taking a new technology concept to pilot plant and full scale FDA
standards and production internationally.
Dr Justin Ward
Senior Quality Chemist
BSc (Chem), Ph.D (Chem), MRACI, CChem
A quality control expert who has worked with leading pharmaceutical
companies. He will bring Recce’s research and development laboratory in Perth
up to US FDA standard.
10
recce.com.au / Recce Annual Report 2017
FINANCIALREPORT
For the year ending 30 June 2017
Recce Limited Consolidated Entity ABN: 73 124 849 065
CONTENTS
DIRECTORS’ REPORT
12
AUDITOR’S INDEPENDENCE DECLARATION
30
CORPORATE GOVERNANCE STATEMENT
31
CONSOLIDATED STATEMENT OF PROFIT OR LOSS
AND OTHER COMPREHENSIVE INCOME
44
CONSOLIDATED STATEMENT OF FINANCIAL POSITION
45
CONSOLIDATED STATEMENT OF CASH FLOWS
46
CONSOLIDATED STATEMENT OF CHANGES IN EQUITY
47
NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS
48
DIRECTORS’ DECLARATION
74
INDEPENDENT AUDIT REPORT
75
ADDITIONAL STOCK EXCHANGE INFORMATION
79
CORPORATE DIRECTORY
IBC
DIRECTORS’ REPORT
Your Directors present their report on the Group for the year ended 30 June 2017.
Directors
The names of Directors in office at any time during or since the end of the year are:
•
•
•
•
•
r Graham Melrose
D
Ms Michele Dilizia
Mr James Graham
Dr Dominic Barnes
Ms Bernadette Murdoch
Appointed 14 May 2016 – Resigned 20 January 2017
Appointed 26 May 2016 – Resigned 21 November 2016
Directors have been in office since the start of the financial year to the date of this report unless otherwise stated.
Company Secretary
The following person held the position of Company Secretary at the end of the financial year:
•
Mr Peter John Williams — Bachelor of Business, FCPA, MAICD.
Mr Williams has worked for Recce Ltd since 19 May 2015 as Chief Financial Officer and Company Secretary. Mr Williams was appointed Company Secretary on 3 June 2015.
1. Principal Activities
The principal activities of the Group during the financial year were related to the research and development of antibiotic drugs.
2. Operating Results
The loss of the Group amounted to $3,025,504 (2016: $4,840,358 loss)
3. Dividends Paid or Recommended
No dividends have been paid or declared for payment.
4. Review of Operations
Research & Development Activities
During the year the Company undertook a wide range of Efficacy, Safety & Chemistry related tests for the purposes of gathering
data to support its Investigational New Drug (IND) application to the Food and Drug Administration in the USA.
A range of announcements related to these tests and supporting activities were released as follows:
12
•
On 13 July 2016 it was announced that an anti-viral test, conducted by a Contract Research Organisation (CRO) in the US,
showed efficacy in-vitro against Influenza virus
•
On 20 July 2016 the Company announced that three separate laboratory screening tests for genetic toxicity indicated that
RECCE® 327 is not carcinogenic (does not cause cancer)
•
On 28 July 2016 the Company announced that it had scaled up manual manufacturing capabilities in its Perth facilities, producing 9 litres of RECCE® 327 over one week and expansion to Sydney
•
On 15 August 2016 the Company announced that it had again in-vivo (mice) increased the “normal” dose of RECCE® 327 by
at least a factor of 4, with no toxicity observed
•
On 31 October 2016 the Company announced that it had employed chemistry and manufacturing experts to support its
quality assurance and scale-up process as well as the advancing of its patent family 2 application
•
On November 2016 the Company announced that dose escalation in a cancer mouse model showed tolerance without animal
deaths. Inhibition of colon carcinoma growth was not significant
recce.com.au / Recce Annual Report 2017
DIRECTORS’ REPORT cont.
•
On 20 December 2016 the Company announced that an anti-viral test, conducted by a CRO in the US, showed efficacy in-vivo
(mice) against Influenza virus
•
On 18 January 2017 the Company announced that an anti-bacterial test, conducted by a CRO in the US, showed Recce’s lead
compound reduces illness in mice infected by resistant E. coli bacteria. It further showed not only a better ‘Health score’ than
those treated using last line of defence antibiotic Tigecycline but a better weight loss score
•
On 23 February 2017 the Company announced that it had suspended its anti-cancer program to focus on commercialising its
synthetic lead compound against resistant bacteria and viruses. It further announced that its patent family 3 application had
progressed from a provisional to patent pending status across all jurisdictions party to the International Patent Cooperation
Treaty (PCT)
•
On 24 February 2017 the Company announced that it had captured RECCE® 327 in action against E. coli bacteria using
University of Western Australia’s sophisticated electron microscope. This was important as the images reinforced Recce’s
unique and patented mechanism of action at a cellular level
•
On 27 March 2017 the Company announced that in a further in-vivo (dogs) safety test, conducted by a CRO in the US, the
intravenous infusion of RECCE® 327 at 70 mg/Kg over four hours was well tolerated
•
On 10 April 2017 the Company released an operational update informing shareholders that its IND application was on
schedule, it had moved into larger animal species and began work on its automated manufacture facility. The Company further
confirmed it had demonstrated efficacy against 7 of the top 12 bacterial threats identified and priority-categorised by the
World Health Organisation and opportunities for additional market exclusivity
•
On 19 May 2017 the Company announced that it had successfully completed a chemical analysis and structural study at a
CRO in the US. The study had shown RECCE® 327 could be tracked in the blood of study animals - enabling researchers to
trace its path. The tests also confirmed the compound’s structure, chemical stability and mode of action as outlined in its
patents and manufacturing process
•
On 16 June 2017 the Company announced that it had successfully secured up to A$6.05 million investment agreement with
US institutional investor The Lind Partners over 2 years to support its IND application and Phase 1 clinical trials
•
On 22 June 2017 the Company announced it had completed construction of a wholly owned production facility in Macquarie
Park, Sydney with expected outputs capable of supporting RECCE® 327 through both Phase 1 and Phase 2 human trials.
So where does that leave us? With now over 30 pre-clinical studies completed, results favourably indicate that RECCE® 327:
•
Does not cause healthy cells to mutate (cancer)
•
Destroys Gram positive and Gram negative bacteria - broad spectrum
•
Acts against bacteria in both normal and mutated superbug forms – with the same ease
•
Contains a patented polymeric structure, intentionally designed to overcome the traditional challenges of bacterial mutation/
resistance (superbugs)
•
Is suited to administration against sepsis by intra-venous drip
•
Has a wide and safe therapeutic dosing window
5. Financial Position
The Directors believe that the Group is in a position to meet all its commitments as and when they fall due.
recce.com.au / Recce Annual Report 2017
13
DIRECTORS’ REPORT cont.
6. Significant Changes in State of Affairs
On 15 July 2016 3,543,000 Class A Performance Shares were converted to ordinary shares and on 16 January 2017 a further
1,059,000 Class A Performance Shares were converted to ordinary shares. Although these conversions related to the Company
achieving the milestone applicable to these Performance Shares on 16 February 2016, the Performance Shares allocated to
G Melrose were restricted from conversion as a result of the application of section 606(1) of the Corporations Act 2001. The
restrictions related to these Performance Shares was lifted on these dates.
On 16 June 2017 the Company announced it had signed a Share Purchase and Convertible Security Agreement, whereby the
Company could receive over a 24 month period, up to A$6.05 million from a US institutional investor, the Australian Special
Opportunity Fund LP (ASOF). ASOF made an initial upfront investment of $300,000 by way of a $250,000 24 month interest free
unsecured convertible security (with a face value of $300,000) and a $50,000 equity investment that was satisfied by the issue of
ordinary shares. Subsequent investments, subject to certain conditions, be made in monthly equity tranches of $50,000 that can
be increased up to $250,000 by mutual consent between Recce and ASOF.
7. Future Developments, Prospects and Business Strategies
The Group continues its strategy of having its antibiotic drug tested for safety, efficacy and chemistry to enable the Group to lodge
its application for Investigational New Drug (IND) status with the Food and Drug Administration (FDA) in the USA.
8. Environmental Issues
The Group is not aware of any environmental issue.
9. Subsequent Events
On 20 July 2017 the Company announced that its manufacturing facility in Sydney was producing at name-plate standard its
antibiotic compounds at volumes in preparation for human clinical trials.
On 31 July 2017 the Company announced the following:
•
It had positive data from additional pre-clinical studies that confirmed that RECCE® 327 was equally effective in killing Gram
Positive and Gram Negative bacteria and their superbug form;
•
That the preferred mode of delivery of RECCE® 327 was via an IV drip; and
•
That independent experts had reviewed Recce’s draft IND and recommended that Recce should proceed to a pre-IND meeting
with the US FDA.
On 7 July 2017 the Group issued a purchase order in relation to the purchase of an Acquity UPLC – H Class at a cost of $138,301.
This piece of equipment will be used to analyse Recce’s lead compound RECCE® 327.
No other matter or circumstance has arisen since 30 June 2017, which has significantly affected, or may significantly affect the
state of affairs of the Group in subsequent financial years.
14
recce.com.au / Recce Annual Report 2017
DIRECTORS’ REPORT cont.
10. Information on Directors
Dr Graham Melrose
Chairman (Executive)
Qualifications
BSc(Hons), PhD, MBA, FRACI,
CChem, FAICD
Experience
Founder of Recce and inventor of RECCE antibiotics.
Previously, founded Chemeq Ltd and under his leadership and
R&D direction, achieved over a three-year period, the top capital gain of all companies listed on the ASX, and an average
market capitalisation of approximately $500 million.
Interest in Shares
30,375,003 Ordinary Shares*
6,075,000 Class B Performance Shares*
6,075,000 Class C Performance Shares*
6,075,000 Class D Performance Shares*
*held jointly with wife Olga Mary Melrose
Special Responsibilities
Chairman of the Board of Directors
Directorships held in other listed entities
during the last three years
Nil
Earlier, a senior academic in the University of NSW’s Department of Applied Organic Chemistry; visiting research scientist
at Oxford and Munich universities.
Executive Director and Chief Research Executive of Johnson &
Johnson (Aust) Pty Ltd in Sydney, with global responsibilities,
particularly in the Asia-Pacific.
Established and operated for some ten years, an industry-leading marketing consultancy.
Mr James Graham
Director (Executive)
Qualifications
BCom (Entrepreneurship), GAICD
Interest in Shares
Direct
1,868,601 Ordinary Shares
389,712 Class B Performance Shares
389,712 Class C Performance Shares
389,712 Class D Performance Shares
Experience
Appointed a Director on 23 June 2015.
Indirect
345,000 Ordinary Shares
Committee-member of WA Angel Investors; entrepreneurship
and marketing.
1,436,250 Ordinary Shares
Previously, General Manager of start-up marine company with
sales in Australia, Asia and Europe.
356,250 Class C Performance Shares
Investor (Non-professional) in ASX-listed technology companies.
Special Responsibilities
Member of the Audit and Risk Management Committee.
Closely involved in the early growth and direction of Recce –
initiated and facilitated funding.
356,250 Class B Performance Shares
356,250 Class D Performance Shares
Directorships held in other listed entities
during the last three years
Nil
recce.com.au / Recce Annual Report 2017
15
DIRECTORS’ REPORT cont.
Ms Michele Dilizia
Director (Executive)
Qualifications
BSC (Med Sci), Grad Dip Bus (Mkting),
BA (Journ), GAICD, MASM
Experience
Appointed a Director on 23 June 2015.
Qualified Medical Scientist; specialisation is medical microbiology.
Interest in Shares
2,886,061 Ordinary Shares
577,212 Class B Performance Shares
577,212 Class C Performance Shares
577,212 Class D Performance Shares
Special Responsibilities
Member of the Nomination and Remuneration Committee.
Directorships held in other listed entities
during the last three years
Nil
Earlier a successful executive career in public relations and
marketing for a leading retail chain.
Began with journalism and then post-graduate qualifications
in business.
Market research consultant, which included marketing development of health-care and pharmaceutical products.
Dr Dominic Barnes
Director (Non-Executive)
Interest in Shares
Nil
Qualifications
FAICD, MMedSc, MBA, MBBS
Special Responsibilities
Dominic was Chairman of the Nomination and Remuneration
Committee and was a member of the Audit and Risk Management Committee.
Experience
Appointed a director on 14 May 2016 –
Resigned 20 January 2017
Has had directorships or senior regulatory appointments with
the Australian subsidiary companies of leading global pharmaceutical companies: Shire, AstraZeneca and Johnson & Johnson; he is also a leading member of medical, government and
academic institutions in Australia.
16
recce.com.au / Recce Annual Report 2017
Directorships held in other listed entities
during the last three years
Nil
DIRECTORS’ REPORT cont.
Ms Bernadette Murdoch
Director (Non-Executive)
Interest in Shares
Qualifications
Bachelor Public Relations. Completed a
Bachelor of Arts in Public Relations at
RMIT University including an exchange
program with Leeds Metropolitan University, UK.
Special Responsibilities
Bernadette was Chairperson of the Audit and Risk Management Committee and was a member of the Nomination and
Remuneration Committee.
Experience
Appointed a director on 26 May 2016 –
Resigned 21 November 2016
20,000 Ordinary Shares at the time of resignation.
Directorships held in other listed entities
during the last three years
Nil
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