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Pharming Group N.V.Annual Report
2024
Delivering
meaningful
patient outcomes
with advanced
dendrimer
technology
Starpharma is an innovative
biotechnology company with
two decades of experience
in advancing dendrimer
technology from the lab
to the patient.
Our mission is to help patients with significant
illnesses, such as cancer, achieve improved health
outcomes and quality of life through the application
of our unique dendrimer technology.
Contents
01
Highlights
02
Chairman’s Report
06
Key Focus Area 1:
Maximise DEP®
Asset Value
04
Chief Executive
Officer’s Report
09
Key Focus Area 2:
Accelerate Early
Asset Development
11
Key Focus Area 3:
Build Long-Term
Sustainability
14
Directors’ Report
(including
Remuneration Report)
13
Outlook
55
Auditor’s Independence
Declaration
56
Annual Financial
Report
87
Independent
Auditor’s Report
86
Directors’ Declaration
91
Shareholder
Information
93
Intellectual
Property Report
95
Corporate
Directory
Annual Report 2024
Starpharma Holdings Limited
ABN 20 078 532 180
Highlights
Reported the results from all three Phase II clinical trial
programs – DEP® SN38 (DEP® irinotecan), DEP®
cabazitaxel, and DEP® docetaxel. All three programs
provided clinical validation of the DEP® technology; over
350 patients have now been treated using DEP® products.
The trials showed promising anti-cancer activity and
improvements in efficacy, including longer median
progression-free survival (mPFS) and higher overall
survival (OS) rates, than published data on standard-of-
care regimens. The DEP® products also demonstrated
improved tolerability profiles in patients with advanced
cancers, including lower rates of severe adverse events,
compared with standard-of-care treatments. Importantly,
the DEP® treatments extended the lives of many patients
who had failed other therapies and allowed many to live
more fulfilling and enriched lives.
Presented the advantages of Starpharma’s DEP®
dendrimer technology in oncology at multiple
international industry conferences, including the American
Society of Clinical Oncology (ASCO) Annual Meeting in the
US, the ASCO Gastrointestinal Cancers Symposium in the
US, the International Conference on Molecular Targets,
co-hosted by the American Association of Cancer Research
(AACR), National Cancer Institute (NCI), and the European
Organisation for Research and Treatment of Cancer
(EORTC) in the US, and the Society of Nuclear Medicine
and Molecular Imaging (SNMMI) Annual Meeting in Canada.
Partnered with ITROM Pharmaceutical Group to sell
and distribute VivaGel® BV in 13 countries across
the Middle East and North Africa region. Bacterial
vaginosis is highly prevalent in this region, presenting a
market need and commercial opportunity for new and
effective therapeutic approaches. This agreement came
shortly after Starpharma terminated the VivaGel® BV
license to Mundipharma, regained the commercial rights
to Mundipharma’s territories, and received a one-time
A$6.6 million cash payment from Mundipharma.
Generated clinical evidence demonstrating the
effectiveness of VIRALEZE™ in humans. The results from
the post-market clinical study of VIRALEZE™ in COVID-19
patients showed that VIRALEZE™ achieved a statistically
significant reduction in SARS-CoV-2 viral load in the
cohort of patients aged 45 and over. This data will support
the regulatory transition to the new European Medical
Device Regulations, which come into full effect in 2029.
The findings will also support ongoing marketing
and commercial activities.
Achieved Great Place to Work® certification for the
second consecutive year. This external recognition
is a testament to our team’s positive workplace
environment and company culture.
Received a $7.2 million research and development (R&D)
tax incentive refund in October 2023 under the Australian
Federal Government’s R&D Tax Incentive scheme. This tax
refund pertains to eligible domestic and international R&D
activities across Starpharma’s portfolio. The government
scheme is important in supporting local companies like
Starpharma to innovate and grow.
Confirmed plans to progress Starpharma’s DEP® HER2
radiodiagnostic program towards a first-in-human
clinical trial, following promising early-stage imaging
data in HER2-positive (HER2+) cancers. Starpharma’s
DEP® radiopharmaceuticals program continues to
show that DEP® dendrimers are a promising, versatile,
and multifunctional platform for developing precision
radiotheranostics for cancer imaging and therapeutic
applications. This dendrimer technology bridges the
gap between small molecules and large antibodies,
offering the potential to improve performance and
overcome limitations associated with existing
technologies and treatments.
Partnered with Medicxi, a leading life sciences
investment firm, to co-found Petalion Therapeutics,
an asset-centric company focusing on developing
a novel cancer therapy using Starpharma’s dendrimer
technology. Starpharma receives an equity holding
of 22.5% in Petalion in return for licensing certain
intellectual property for the research,development, and
commercialisation of this potential new cancer therapy.
1
Annual Report 2024
Starpharma Holdings Limited
Rob Thomas AO Chairman
Chairman’s Report
Dear shareholders,
On behalf of the Board of Directors,
I am pleased to present Starpharma’s
2024 Annual Report to our fellow
shareholders.
2024 marks a significant year of
transition for Starpharma, highlighted
by Cheryl Maley assuming the role
of CEO after an international search
and Jackie Fairley’s retirement.
Jackie dedicated over 17 years to
our company; we are grateful for her
service and leadership, as well as
her assistance during the transition.
This leadership transition provided us
with a valuable opportunity to reflect on
Starpharma’s journey and learnings and
critically evaluate our current position.
While we believe the current share
price does not reflect the true value of
our dendrimer technology and current
assets, the Board recognises that the
market requires further commercial
validation of our technology. This is our
prime focus.
We are deeply committed to our
mission of helping patients with
significant illnesses, such as cancer,
achieve improved treatment outcomes
and quality of life through the
application of our unique dendrimer
technology.
Under Cheryl’s leadership, we are
confident in our ability to execute
our strategy effectively and improve
shareholder value. Cheryl has already
made a profound impact on
our organisation, and we look forward
to the future with great anticipation.
During FY24, we were pleased to report
positive outcomes from our Phase
II clinical trials of DEP® SN38, DEP®
cabazitaxel, and DEP® docetaxel.
These trials have shown promising
anti-tumour efficacy, including
longer progression-free survival than
published data on standard-of-care
treatment options, and excellent
tolerability profiles in patients with
challenging-to-treat cancers.
These are positive achievements
and demonstrate the abilities of
Starpharma’s DEP® technology
in cementing our core mission of
providing improved treatment options
for patients with significant illnesses.
We went on to showcase our leading
candidates, DEP® SN38 and DEP®
cabazitaxel, at the prestigious ASCO
Annual Meeting in Chicago in June 2024.
This recognition not only underscores
the clinical interest in our Phase II results
but also validates the potential of these
treatments in cancer therapy.
Starpharma’s dendrimer drug delivery
technology has now demonstrated
clinical benefits in over 350 patients,
garnering strong support from clinical
investigators and reinforcing our
leadership in this field. We are at the
forefront of this innovative technology.
While chemotherapy remains
fundamental in cancer treatment,
emerging technologies such as
radiopharmaceuticals and antibody-
drug conjugates (ADCs) necessitate
continuous adaptation and
acceleration of our research
and development efforts. Recent
high-value mergers and acquisitions,
as well as product approvals and
successes, underscore the industry’s
growing interest in these technologies.
Looking forward, our focus on advancing
our DEP® radiopharmaceuticals, including
a radiodiagnostic and radiotherapeutic,
reflects our commitment to research
and development in novel therapeutic
areas.
Collaborations are integral to
Starpharma’s strategy, enabling
broader application of our dendrimer
technology across various therapeutic
areas. We value our partnerships
deeply and continue to evolve our
collaboration models to expedite
progress and maximise value.
We are deeply committed to our mission of
helping patients with significant illnesses, such as
cancer, achieve improved treatment outcomes
and quality of life through the application of our
unique dendrimer technology.
350+patients
have experienced clinical benefits
from Starpharma’s dendrimer drug
delivery technology
2
Annual Report 2024
Starpharma Holdings Limited
The formation of Petalion Therapeutics
in partnership with Medicxi exemplifies
our dedication to exploring new
partnership models and accelerating
early asset development. An important
advantage of the asset-centric
approach is Petalion’s ability to
accelerate development, and this
partnership is progressing well.
Our partnerships with Genentech and
MSD continued to progress, and our
chemistry teams are diligently working
to deliver the desired outcomes for
both partners.
Our commercial products, VivaGel®
BV and VIRALEZE™ Nasal Spray are
important for generating additional
revenue for the company and
supporting our sustainable growth
objectives. We were pleased to
announce that the post-market clinical
study of VIRALEZE™ had shown positive
results, demonstrating its antiviral
efficacy. Additionally, we partnered
with ITROM Pharmaceutical Group to
sell and distribute VivaGel® BV in the
Middle East and North Africa region
after successfully negotiating an exit
from the Mundipharma distribution
agreement. We consider these
developments to be important steps
towards growing revenue from
both products.
Starpharma places great importance
on Environmental, Social, and
Governance (ESG) initiatives, ensuring
responsible business practices. We
aim to minimise our environmental
impact relative to the scale of our
business operations, support our
people, and operate with good
governance. Our people are at the
core of our organisation, and we were
delighted to have achieved Great
Place to Work® certification for the
second consecutive year, recognising
our team’s positive workplace and
company culture. We encourage you
to read our ESG Report 2024, which
provides more details about our
ESG initiatives.
In closing, on behalf of the Board, I wish
to thank Cheryl, our leadership team,
and the entire Starpharma team for
their efforts in recent months. Transition
is not easy, but the Board could not be
more pleased with how it has gone.
The Company’s underperforming share
price places additional pressure on
all of us. I want shareholders to know
that the stock performance has been
explicitly considered in determining
remuneration. For the 2025 financial
year, we have revised the remuneration
framework to increase the proportion of
at-risk performance-based incentives,
both short-term and long-term, for all
employees. This change is designed to
further align employee rewards more
closely with shareholder returns.
The Board of Directors extend sincere
thanks to our shareholders, customers,
and partners for their continued support.
Starpharma is acutely focused on
executing its strategic objectives, which
include maximising DEP® asset value,
accelerating early asset development,
and building a financially sustainable
business that will generate benefits
for patients and shareholders alike.
Rob Thomas AO
Chairman
During FY24, we were pleased to report positive
outcomes from our Phase II clinical trials of
DEP® SN38, DEP® cabazitaxel, and DEP® docetaxel.
These trials have shown promising anti-tumour
efficacy, including longer progression-free survival
than published data on standard-of-care treatment
options, and excellent tolerability profiles in
patients with challenging-to-treat cancers.
3
Annual Report 2024
Starpharma Holdings Limited
Chief Executive Officer’s Report
Cheryl Maley Chief Executive Officer
Dear fellow shareholders,
I am pleased to present Starpharma’s
2024 Annual Report for the first time
as Chief Executive Officer. Since
joining Starpharma, I have observed a
culture of passion and determination
towards realising our mission of helping
patients with significant illnesses,
such as cancer, achieve improved
health outcomes and quality of life
through the application of our unique
dendrimer technology. This mission
and our commitments to advancing
dendrimer technology and boosting
shareholder value are at the forefront
of our priorities.
In acknowledging the current share
price, we are diligently working at
Starpharma to enhance value for our
shareholders. We are not content with
the current position and firmly believe
that it does not reflect the true value of
our company.
As you know, soon after I started with
the company, I, along with the Board
and leadership team, conducted
a comprehensive review of the
business. This rigorous assessment
encompassed every facet of
our operations, from programs,
partnerships, sales, and marketing
to regulatory compliance and
research. The insights gained from
this review, shared with shareholders
in May, underscored our strengths in
innovation, expertise in dendrimer
science, and collaborative ethos.
This evaluation also identified key
opportunities, prompting us to refine
our core value proposition, enhance
execution focus, allocate resources
to strategic priorities, strengthen
commercial capabilities, and improve
shareholder engagement. Guided by
these findings, we established three
pivotal focus areas: maximising DEP®
asset value, accelerating early-stage
development, and building long-
term sustainability.
Since sharing these strategic
imperatives with shareholders
approximately three months ago,
our team has been dedicated to
their realisation.
A key milestone in our plan to maximise
DEP® asset value was the successful
presentation of two oral podium
sessions at the esteemed American
Society of Clinical Oncology (ASCO)
Annual Meeting in June 2024. The
acceptance of Starpharma’s Phase II
clinical data reinforces the promising
potential of DEP® SN38 (DEP®
irinotecan) and DEP® cabazitaxel for
patients with cancer.
Our participation at ASCO was
extremely valuable, as it provided
Starpharma with the opportunity to
establish meaningful connections with
companies with an interest in exploring
dendrimer applications in their product
pipelines. Our presence at the BIO
2024 Conference and the Society
of Nuclear Medicine and Molecular
Imaging (SNMMI) Annual Meeting further
increased our visibility and potential
partner opportunities that could
maximise the value of our assets
and DEP® technology.
Our focus on radiopharmaceuticals is
particularly timely, given the current
momentum in this sector. Starpharma’s
dendrimer technology has great
potential in radiopharmaceuticals,
offering advantages such as enhanced
tumour targeting, rapid blood
clearance, excellent imaging contrast,
and minimal exposure to radiation-
sensitive organs. By advancing our
dendrimer technology in this space,
internally and with partners, we aim
to develop targeted diagnostic and
treatment options that offer significant
advantages over existing regimens and
position us well in a competitive market.
While maximising the value of
Starpharma’s DEP® clinical assets is
our number one priority, accelerating
the advancement of new candidates in
our early asset development program
is crucial to our future success.
Following this year’s comprehensive
review, our scientists are committed to
accelerating this development with a
renewed focus and rigorous research
and development processes.
Our recent strategic partnership
with Medicxi exemplifies this focus
and our approach to innovation.
The formation of Petalion Therapeutics
in collaboration with Medicxi represents
a novel venture for Starpharma, but
it is a partnership model that Medicxi
has demonstrated success with.
The partnership aims to expedite
the development of a promising
oncology asset, leveraging our
collective expertise. This partnership is
progressing well, and we look forward
to sharing relevant updates with you
in the future.
A key milestone in our plan to maximise DEP®
asset value was the successful presentation of two
oral podium sessions at the esteemed American
Society of Clinical Oncology (ASCO) Annual
Meeting in June 2024.
4
Annual Report 2024
Starpharma Holdings Limited
Achieving self-sustainability is a
cornerstone of our long-term strategy,
in tandem with our developmental
efforts. This goal hinges on increasing
revenue from commercialised over-
the-counter products, effective cost
management, optimising our cash
position, and nurturing a culture of
excellence and performance within
our workforce.
Our strategic initiatives are designed
to leverage our strengths, define
our commercial priorities, address
identified opportunities, and position
us for long-term success. We are
resolutely committed to and confident
in our ability to deliver on these
objectives. To ensure transparency and
accountability, we have implemented
robust project management protocols
to monitor and track our progress
internally, progress that will also be
shared with shareholders along the way.
Clinically validated
DEP® dendrimer technology
• More than 350 patients have been
treated with the DEP® dendrimer
technology.
• DEP® dendrimers are easily
scalable, precisely manufactured,
and Good Manufacturing Practice
(GMP) certified.
Flexibility with drug and linker
• Flexibility with the number of payload
molecules and types, such as cytotoxic or
radioisotope, to precisely match the clinical
need and therapy characteristics.
• Linkers tether the payload to the dendrimer
scaffold and can be designed to release the
payload under certain conditions (e.g., low pH,
in the presence of certain enzymes). A variety
of different linkers can be used depending
upon where the drug needs to be delivered.
• Option to use targeting moieties to develop
targeted therapy approaches.
PEG provides stealth,
control clearance, and solubility
• Easier manufacturing and handling
of drugs, minimising unwanted drug
clearance from the body.
Option to use targeting moieties to
develop targeted therapy approaches
• Flexible choice of targeting moiety
(e.g., antibody, antibody mimetics, peptide,
small molecule) provides options for
targeting and can be customised to
specific therapeutic needs.
• Polyvalency, the ability to have multiple
targeting molecules, which can maximise
both the affinity and avidity of the targeting
molecule with the receptor target.
Starpharma’s Validated DEP® Platform
Advantageous flexible, scalable technology for precision targeted medicine
Dendrimers are highly branched, tree-like
macromolecules with a well-defined, 3D
structure. DEP® dendrimers are constructed
in concentric layers of lysine monomers
(generations).
This report is structured to align with
our three strategic pillars and offers
an overview of our progress from
FY24 within each focus area.
Thank you for your continued support
and trust in our vision. We look forward
to sharing our continued progress
with you and achieving new
milestones together.
Cheryl Maley
Chief Executive Officer
Ability to modify
Linker/Chelator and
pharmacokinetics
• Payload release rate and
plasma half-life are tuneable,
allowing management of
both the rate and site of
drug/payload release.
• Dendrimer size and charge
can be adjusted to control
clearance, which can
determine the therapeutic
clearance route based on
the treatment approach or
disease, for instance, via
the kidney, liver, or spleen.
5
Annual Report 2024
Starpharma Holdings Limited
Key Focus Area 1: Maximise DEP® Asset Value
Starpharma’s dendrimer-enhanced
product (DEP®) drug delivery platform
enhances the therapeutic utility of
pharmaceutical drugs by improving
solubility, efficacy, and control over
how the drug is delivered in the body.
This can help reduce specific drug-
related toxicities. The DEP® platform
has shown benefits for a wide range of
drug classes, including small molecule
drugs, peptides, and proteins. It can
also be used in the development of
DEP® radiopharmaceuticals and
DEP® ADCs. The dendrimer technology
offers strategic advantages for
companies seeking to extend patents
on key drugs or enhance the
effectiveness and safety profiles
of developmental therapies.
In FY24, Starpharma achieved
significant milestones by completing
three Phase II clinical studies utilising
the DEP® platform. These studies
demonstrated promising efficacy
against tumours and excellent tolerability.
Treatment with these products also
extended many patients’ lives across
the clinical trials. These clinical results
were presented at prestigious
international oncology conferences
like ASCO. Starpharma’s current focus
centres on optimising the value of its
DEP® clinical assets through strategic
licensing deals, particularly for the
priority products DEP® SN38 and
DEP® cabazitaxel.
Clinically Validated
Technology
DEP® SN38 (DEP® irinotecan)
Phase II Clinical Program Results
DEP® SN38 is a patented nanoparticle
formulation of SN38, which is the active
metabolite of the anticancer drug
irinotecan. SN38 is approximately 1000
times more active than its pro-drug,
irinotecan, but cannot be delivered
directly due to toxicity and insolubility.
Instead, irinotecan must be converted
to SN38 in the liver, leading to
significant patient to patient variability
in efficacy, and the generation of toxic
metabolites that cause significant gut
issues, including severe diarrhoea,
nausea and vomiting.
DEP® SN38 achieves solubilisation
and allows for direct delivery of SN38,
avoiding the need for metabolic
conversion of irinotecan to SN38
in the liver. As a result, DEP® SN38
achieves greater tumour targeting of
SN38 while significantly reducing
severe gastrointestinal side effects.
DEP® SN38 represents a promising new
drug candidate for companies looking
to develop a treatment for platinum-
resistant ovarian cancer and/or
advanced colorectal cancer, which
are both areas of unmet clinical need.
In FY24, Starpharma reported the results
from the Phase II trial of DEP® SN38,
with promising data generated in
advanced colorectal cancer and
platinum-resistant ovarian cancer
indications. DEP® SN38 showed
clinically meaningful improvements in
efficacy, as measured by progression-
free survival and objective responses
when compared to published data on
standard-of-care treatment options.
DEP® SN38 was confirmed to be very
well tolerated and demonstrated a
consistently improved tolerability
profile in patients with advanced
disease. There was a notable lack of
severe gastrointestinal adverse events
and no instances of cholinergic
syndrome, which are both commonly
associated with standard irinotecan.
The lack of severe gastrointestinal
toxicity, which is a common issue with
irinotecan treatment, is a notable
feature of Starpharma’s product,
according to clinical trial investigators.
They have been very encouraged
by the product’s ability to provide
long-term treatment without the
taxing side effects.
Starpharma continues
to lead dendrimer drug
delivery innovation
with its DEP® platform,
driving advancements
in oncology treatments
through enhanced
efficacy, safety, and
targeted delivery
mechanisms.
Product
Target
indication
Research
Preclinical
Phase I
Phase II
Strategy
DEP® SN38
License/co-develop –
ovarian, colorectal
Ovarian and
colorectal
Phase II results reported
DEP® cabazitaxel
License – prostate,
ovarian
Prostate and
ovarian
Phase II results reported
DEP® HER2 radiodiagnostic
Optimise and accelerate
to preclinical
Diagnostic
DEP® HER2 radiotherapeutic
Advance to clinical
Solid cancers
DEP® HER2 ADC
Advance to preclinical
Solid cancers
DEP® docetaxel
Lower priority
Pancreatic and
other cancers
Phase II results reported
DEP® Pipeline and Next Steps
6
Annual Report 2024
Starpharma Holdings Limited
Furthermore, several patients who have
had prolonged responses to therapy
and are experiencing ongoing clinical
benefit continue to receive access to
DEP® SN38 treatment and will be
monitored for safety and any change
to their disease.
These positive efficacy and tolerability
results support the promising clinical
utility and potential commercial
opportunities for DEP® SN38 in the
treatment of advanced colorectal
cancer and platinum-resistant ovarian
cancer. Starpharma is prioritising the
licensing of DEP® SN38 because of
its potential to address significant
unmet needs in advanced colorectal
and platinum-resistant ovarian
cancers, as current treatments
have reported limited efficacy
and high toxicity profiles.
DEP® cabazitaxel Phase II
Clinical Program Results
DEP® cabazitaxel is a dendrimer-
enhanced version of the drug cabazitaxel
(Jevtana®), widely used for treating
metastatic castrate-resistant prostate
cancer (mCRPC). Unlike standard
cabazitaxel, DEP® cabazitaxel is highly
water soluble and does not contain
toxic excipients, such as the detergent
polysorbate 80, eliminating the need
for patients to be treated with steroids
before chemotherapy.
Starpharma’s aqueous DEP® cabazitaxel
formulation offers advantages over
generic cabazitaxel formulations
containing polysorbate 80. Aqueous
formulations are generally better
tolerated by patients with a reduced
risk of allergic reactions. Poorly soluble
drugs can cause hypersensitivity
reactions in some patients, ranging from
mild skin irritation to severe anaphylactic
responses. The improved tolerability
can lead to a smoother treatment
experience for patients, better
adherence to therapy and, from a
physician’s perspective, the drugs can
be administered more easily and reduce
preparation time. These benefits align
with Starpharma’s mission of improving
patient outcomes and quality of life
during treatment.
In FY24, Starpharma announced the
final results from the Phase II trial of
DEP® cabazitaxel. The trial showed
positive anti-tumour efficacy in mCRPC
and other challenging cancers, including
platinum-resistant ovarian and gastro
-esophageal cancers. The efficacy
results, measured by progression-free
survival and disease control, were
clinically meaningful as all patients had
late-stage, hard-to-treat cancers and
had failed multiple therapies prior to
entering Starpharma’s trial.
Continues next page
“The full DEP® irinotecan/DEP® SN38 trial results are very exciting. DEP® SN38 in
heavily pre-treated, advanced cancer patients demonstrated highly encouraging
efficacy results in a range of tumour types. These responses include significant
and sustained tumour shrinkage and disease control in patients with irinotecan-
pre-treated colorectal cancer and platinum-resistant ovarian cancer.
Furthermore, DEP® SN38 exhibits excellent tolerability, with a distinct lack of severe
gastrointestinal toxicity that is a common and problematic feature of standard
irinotecan treatment. Such treatment tolerability, combined with sustained disease
control, has meant that many of our patients, including those who are quite young
with advanced colorectal cancer, have been able to receive long-term treatment
and continue to work and engage socially with their peers, which is very important
for their quality of life.”
Dr Jia (Jenny) Liu MD PhD FRACP, Medical Oncologist and Principal Investigator
at the Kinghorn Cancer Centre, St Vincent’s Hospital in Sydney.
Promising DEP® SN38 and
DEP® cabazitaxel Clinical
Results Showcased at the
2024 ASCO Annual Meeting
The final clinical data from the DEP®
SN38 and DEP® cabazitaxel Phase I/II
clinical trials were showcased at the
2024 ASCO Annual Meeting through
oral podium presentations delivered
by clinical investigators. This milestone
marks a significant achievement for
Starpharma, underscoring the clinical
relevance of the data and the promising
potential of DEP® SN38 and DEP®
cabazitaxel in patient care. Furthermore,
the acceptance of two oral abstracts
at ASCO reflects the clinical interest
in Starpharma’s DEP® technology
platform.
ASCO is a premier global conference
for oncology professionals, offering
a vital platform for presenting new
cancer treatments and the latest
advancements in cancer care and
technologies. These oral presentations
provided Starpharma with a notable
opportunity to showcase its
innovations on an international
stage, emphasising the value
of the DEP® technology.
Each year, ASCO receives tens of
thousands of abstract submissions,
with only a tiny fraction accepted for
presentation as posters or oral talks.
This year, approximately 4% of
accepted abstracts received the
distinction of an oral presentation.
7
Annual Report 2024
Starpharma Holdings Limited
DEP® docetaxel Phase II Clinical
Program Results
DEP® docetaxel is a dendrimer
nanoparticle formulation of the
chemotherapy drug docetaxel
(Taxotere®). Conventional docetaxel is
used to treat breast, lung, and prostate
cancers despite severe side effects such
as neutropenia and hypersensitivity
reactions. In contrast, DEP® docetaxel is
an aqueous detergent-free formulation,
minimising these adverse events and
removing the need for pre-medication
with steroids.
In FY24, Starpharma reported Phase II
results for DEP® docetaxel. The trial
met its objectives, demonstrating
anti-tumour activity across multiple
advanced metastatic cancers,
including pancreatic, lung, and gastro-
oesophageal. The DEP® docetaxel clinical
program also confirmed the product’s
improved tolerability versus conventional
docetaxel in terms of key and sometimes
dose-limiting adverse events.
The company remains open to
proposals from parties interested
in further developing this candidate.
DEP® docetaxel represents an
important part of Starpharma’s
mission to improve cancer therapy
delivery using its advanced dendrimer
technology.
Importantly, DEP® cabazitaxel was also
well tolerated, with almost 90% of the
treatment-related adverse events (AEs)
being mild or moderate, and very few
severe AEs. Patients did not require
routine pretreatment with steroids, and
no severe hypersensitivity reactions or
anaphylaxis were observed following
treatment with DEP® cabazitaxel.
The trial underscored DEP® cabazitaxel’s
favourable safety and tolerability,
positioning it as a promising candidate
for further clinical development
and licensing.
“In our cancer early phase trials unit at Guy’s Hospital, we conduct many studies of novel oncology therapeutics. The results
with DEP® cabazitaxel clearly demonstrate promising and durable anti-cancer activity in very hard-to-treat cancer patients,
not only in prostate cancer patients but also in platinum-resistant ovarian cancer and advanced gastro-oesophageal cancers.
These advanced patients have few treatment options and we have had many patients who benefited from DEP® cabazitaxel
therapy. It was also pleasing to see the limited impact on bone marrow function of this agent given these advanced patients
are often at risk of complications of chemotherapy-induced bone marrow toxicity, especially low neutrophil counts.”
Professor James Spicer, FRCP, MBBS, PhD, Professor of Experimental Cancer Medicine at King’s College London
and Consultant in Medical Oncology and the Principal Investigator for the trial at Guy’s Hospital in London.
Key Focus Area 1: Maximise DEP® Asset Value continued
8
Annual Report 2024
Starpharma Holdings Limited
8
Starpharma Holdings Limited
Key Focus Area 2: Accelerate Early Asset Development
Starpharma’s core value proposition
lies in its ability to effectively utilise
dendrimer technology in a wide range
of applications, particularly in cancer
treatment and diagnosis. The company
is dedicated to expanding its portfolio
of early-stage assets and improving
the efficiency of its developmental
programs. Our future success hinges
on the swift advancement of early-
stage assets through in-house
efforts and partnerships.
In May 2024, Starpharma committed
to intensifying its efforts to develop
saleable assets and secure collaborations
and licensing deals. Since then,
Starpharma has introduced a number of
initiatives to improve internal processes
and efficiencies and accelerate our
research programs. We have also
expanded our business development
team to support the generation of
new collaboration opportunities.
Partnerships are integral to Starpharma’s
business strategy, enabling the
widespread application of its dendrimer
technology across diverse therapeutic
areas and targets. Starpharma is seeking
partnerships that encompass R&D
collaborations, co-development
opportunities, licence agreements,
and technology access.
To advance these goals, Starpharma
places particular emphasis on
progressing existing partnerships
and seeking new partnerships.
In parallel, Starpharma continues to
advance its in-house preclinical program
for DEP® ADCs, focusing on optimising
candidates and conducting further
preclinical studies to demonstrate the
DEP® platform’s advantages in this
high-value therapeutic area.
Advancing DEP®
Radiopharmaceuticals Program
Starpharma is advancing its DEP®
radiopharmaceutical candidates, a
DEP® HER2-radiodiagnostic and a
DEP® HER2-radiotherapeutic. In May
2024, Starpharma announced plans to
initiate a first-in-human clinical study for
its DEP® HER2-radiodiagnostic within
the next 12 months, following promising
preclinical results. These initiatives
underscore Starpharma’s commitment
to innovation and advancing
therapeutic options in oncology.
HER2 is a validated and important
marker in many cancers, such as breast
and gastric cancers. Our aim is to create
a HER2-targeted radiodiagnostic that
enables the real-time and whole-body
evaluation of HER2 status of patients’
cancer. The radiodiagnostic could help
improve the diagnosis, staging and
management of disease, enabling
clinicians to monitor responses to
therapy, guide treatment options, and
assess metastatic spread of disease.
We also aim to develop a HER2 targeted
radiotherapeutic that improves the
treatment of HER2 positive cancers.
Starpharma’s strategic
partnerships and
collaborations provide
value in advancing
its innovative pipeline
and expanding
the therapeutic
reach of its DEP®
technology platform.
Trastuzumab-89Zr
15
0
Trastuzumab-89Zr
DEP® HER2
radiodiagnostic
DEP® HER2
radiodiagnostic
Maximum intensity projection (MIP) PET-CT images of BT474 HER2+ tumour-bearing
mice dosed with either DEP® HER2-89Zr or Trastuzumab-89Zr
→ DEP® HER2 radiodiagnostic achieved
excellent imaging contrast between
tumour and normal tissue, similar to
Trastuzumab.
→ Higher levels of activity are observed
in heart for Trastuzumab at Day 2 and
Day 4, consistent with ex vivo blood
activity data.
→ DEP® HER2 radiodiagnostic
shows uptake in liver, consistent
with macrophage-related clearance
described for nanoparticles in
size range.
Radio-conjugates administered at t=0
Representative mice shown at Day 2 (left side) or Day 4 (right side) after injection
Scale bar (% ID/g) is shown to the right
Heart
Heart
Liver
Liver
Heart
Heart
Tumour
Tumour
Day 2
Day 4
%ID/g
DEP® HER2 radiodiagnostic vs Trastuzumab:
PET/CT Imaging Performance
Radioisotope
DEP® dendrimer
PEG
HER-2 targeted Nanobody
Tumour
Tumour
9
Annual Report 2024
Starpharma Holdings Limited
Key Focus Area 2: Accelerate Early Asset Development continued
Partnership with Medicxi:
Petalion Therapeutics
In April 2024, Starpharma announced
a strategic partnership with Medicxi,
a prominent healthcare and life
sciences investment firm, to
establish Petalion Therapeutics.
This partnership is dedicated to
advancing a novel cancer therapy
leveraging Starpharma’s DEP®
dendrimer platform technology.
Medicxi has committed an initial
investment of up to USD $25 million
to fund Petalion’s development
efforts. Starpharma will license
specific background intellectual
property (IP) essential for research,
development, manufacturing, and
commercialisation to Petalion,
securing a 22.5% stake in the venture.
Dr Mehdi Shahidi, a seasoned
pharmaceutical executive and
clinical oncologist with extensive
experience in drug development,
has been appointed as CEO of
Petalion. Dr Shahidi’s leadership will
guide Petalion’s strategic direction,
leveraging his background as
Corporate Senior Vice President,
Chief Medical Officer, and Global
Head of Medicine at Boehringer
Ingelheim. Additionally, David
McIntyre, Starpharma’s non-
executive director, assumes a
directorship role at Petalion,
ensuring Starpharma’s interests
are represented.
Medicxi’s deep expertise in asset-
centric investments, coupled with
their highly experienced team,
positions them as an ideal partner
for Starpharma. Since signing the
agreement, the teams from
Starpharma and Medicxi have
collaborated closely to advance
various project aspects. One
significant benefit of this partnership
for Starpharma is its capacity for
expedited, agile and flexible
operations while accelerating
learning and demonstrating
R&D progress.
In June 2024, Starpharma was
delighted to host Dr Mehdi Shahidi
and Shyam Masrani, Principal at
Medicxi and Board Chair of Petalion,
at its office in Melbourne (pictured
above). It was fantastic to connect
and introduce them to the wider
Starpharma team, and to discuss
the Petalion project.
Ongoing Collaborations
and Initiatives
Throughout the year, Starpharma
has continued its collaborations with
Genentech and MSD. The details of the
research remain confidential due to
the sensitive nature of their projects.
In these partnerships, Starpharma
provides dendrimer chemistry expertise
and develops functionalised dendrimers
for its partners to test.
In July 2023, AstraZeneca discontinued
the development of AZD0466.
While Starpharma had hoped for a
different outcome, it is important to
recognise that the AZD0466 program
brought several important benefits
to Starpharma’s DEP® platform
technology. These benefits include
demonstrating the ability of DEP® to
expand the therapeutic index of a highly
toxic drug, presenting multiple posters,
presentations, and publications at
major global conferences, generating
intellectual property with applications
outside of the program, and receiving
approximately A$11 million in milestone
payments. These achievements
enhanced the profile of Starpharma’s
DEP® platform and facilitated the
development of new partnerships
with other companies.
In July 2023, Starpharma partnered
with the University of Queensland’s
Hub for Advanced Manufacture of
Targeted Radiopharmaceuticals
(AMTAR Hub) to bolster research and
development efforts for targeted
DEP® radiopharmaceuticals.
In July 2024, Starpharma announced
that it will collaborate with The
University of Technology Sydney
(UTS) and CSIRO on the research and
development of an mRNA vaccine
for antimicrobial-resistant (AMR)
urinary tract infections (UTIs). As
part of the program, Starpharma’s
DEP® dendrimer technology will be
investigated for its ability to improve
the formulation and performance of
the nanoparticle-based mRNA vaccine
candidates being developed by UTS
and CSIRO.
During the year, the DEP® platform’s
adaptability in delivering targeted
radiopharmaceuticals was showcased
at prestigious conferences, including
the Society of Nuclear Medicine and
Molecular Imaging (SNMMI) Annual
Meeting in June 2024, the Targeted
Radiopharmaceuticals Summit in Berlin
in December 2023, and the AACR-NCI-
EORTC Conference in October 2023,
emphasising its potential to advance
cancer imaging and treatment.
Pictured (left to right): Dr Jeremy Paull, VP of Development & Regulatory Affairs, Justin Cahill,
CFO and Company Secretary, Cheryl Maley, CEO, Shyam Masrani, Principal at Medicxi and Chair
of Petalion, Dr Mehdi Shahidi, CEO of Petalion, and Dr Tony Eglezos, VP of Business Development.
10
Annual Report 2024
Starpharma Holdings Limited
Starpharma Holdings Limited
Key Focus Area 3: Build Long-Term Sustainability
Starpharma is dedicated to achieving
long-term self-sustainability by
bolstering revenues, continually
strengthening our intellectual property
position, always striving for a high-
performance culture, and effectively
managing costs. Our current focus
includes increasing revenue, enhancing
efficiency, and reducing costs, all of
which align with our long-term goal
of sustainability.
During FY24, Starpharma initiated
measures expected to reduce fixed
costs by approximately $2 million by
the end of FY25, alongside identifying
further potential savings. The company
anticipates further strides in financial
sustainability, having strengthened
our business development and digital
marketing capabilities.
VivaGel® BV
VivaGel® BV is a novel, non-antibiotic
gel developed by Starpharma for the
treatment of bacterial vaginosis (BV)
and the prevention of recurrent BV
and its symptoms. BV is a common
condition affecting an estimated one
in three women globally. VivaGel® BV
is registered in over 40 countries and
is currently distributed by Aspen in
Australia and New Zealand.
VIRALEZE™ Nasal Spray
VIRALEZE™ is a broad-spectrum
topical antiviral nasal spray developed
by Starpharma to provide added
protection against colds and
respiratory viruses in the nasal cavity.
Viral infections commonly affect
the upper respiratory tract and
can potentially lead to more serious
infections or diseases. VIRALEZE™
is registered in over 35 countries
and is primarily sold online, with
local distribution in a number of
countries in Asia.
Starpharma conducted a post-market
clinical study of VIRALEZE™ in COVID-
19-positive patients. In January 2024,
Starpharma reported results from this
study, demonstrating the effectiveness
of VIRALEZE™ in reducing SARS-CoV-2
viral load, accelerating virus clearance
from the nasal passage, and improving
key COVID-19 symptoms, with statistical
significance in the 45+ age group.
These findings will support compliance
with the new European Medical Device
Regulations (MDR) that will take effect in
2029, as well as Starpharma’s ongoing
marketing efforts.
Sales through Starpharma’s online
channels in the UK and EU increased in
FY24. As part of Starpharma’s strategic
review in May 2024, the company
identified increasing revenue from
the online sales of VIRALEZE™
as a key objective for FY25.
Starpharma has recently implemented
several initiatives to support this goal,
including undertaking a comprehensive
analysis of target users, launching
targeted digital marketing campaigns,
and enhancing the brand’s online
presence. These initiatives are ongoing
and aim to optimise the customer
experience and drive revenue growth.
Throughout the year, Starpharma
continued progressing the application
for marketing authorisation in Australia,
submitting clinical data from the
post-market study to support the
submission. VIRALEZE™ is not approved
for use or supply in Australia, and
Starpharma awaits a decision by the
Therapeutic Goods Administration (TGA).
After ending the agreement with
Mundipharma in August 2023 for a
one-time payment of A$6.6 million and
regaining territorial rights, Starpharma
has actively sought a new partner for
these regions to expand the global
distribution of VivaGel® BV. We
are currently engaged in business
development activities to achieve this
goal in line with our broader strategic
objectives.
In January 2024, Starpharma formed a
partnership with ITROM Pharmaceutical
Group to market VivaGel® BV across 13
countries in the Middle East and North
Africa. ITROM’s extensive network
in both public and private health
sectors positions us well for a planned
FY25 launch following the transfer of
marketing rights from Mundipharma.
In February 2024, Starpharma
concluded a formal dispute resolution
with the FDA regarding VivaGel®
BV’s regulatory pathway in the US.
While the FDA upheld its requirement
for additional clinical efficacy data,
Starpharma has opted not to proceed
with further independent studies at this
time. Instead, we remain committed
to maximising commercial potential
in over 40 approved markets.
Consequently, we mutually agreed
with EDW Pharma, formerly ITF Pharma,
to exit the US license agreement
signed in 2018.
Starpharma is actively
pursuing a path to
financial sustainability
while advancing patient
care and fostering a
responsible, impactful
presence in our industry.
Commercialised Over the Counter (OTC) Products
11
Annual Report 2024
Starpharma Holdings Limited
Starpharma concluded FY24 with a
cash balance of $23.4 million as at
30 June 2024. The Company’s revenue
was $9.8 million, which included
$6.6 million from the commercial
settlement and exit of the VivaGel®
BV license and supply agreement
with Mundipharma, as well as product
sales, royalties, and research revenue
from commercial partners.
The FY24 loss after tax was
$8.2 million, and the company is
pleased to note a consistent downward
trend. Expenditure included investment
in research and development (R&D)
for the DEP® clinical assets, DEP®
radiopharmaceuticals, and DEP®
ADCs, and the post-market clinical
study of VIRALEZE™.
The net operating cash outflows for
the year were $7.0 million, which was
lower than the previous year, with the
$6.6 million Mundipharma settlement
received in August 2023. Investing and
financing cash outflows included the
repayment of the $4.0 million Invest
Victoria R&D cash flow, following the
$7.2 million FY23 R&D Tax Incentive
refund received in October 2023.
Starpharma anticipates an additional
approximately $5.0 million R&D Tax
Incentive refund for FY24 in the first half
of FY25.
Strong Intellectual
Property Position
Starpharma has a strong intellectual
property position with 19 active patent
families, over 150 granted patents,
and more than 40 patent applications
pending. The company is committed
to protecting its existing background
IP for DEP® and generating new IP
in novel areas.
ESG Commitments
Starpharma remains steadfast in its
commitment to ethical conduct,
sustainability, and innovation within
the biopharmaceutical sector.
Our annual ESG report underscores
our dedication to environmental
impact, workplace values, product
safety, and governance principles.
Achieving Great Place to Work®
certification for the second
consecutive year underscores
our positive workplace culture
and commitment to diversity and
inclusivity. Read the full 2024 ESG
Report on our website.
3-Year Financial Summary
FY24
$M
FY23
$M
FY22
$M
Total revenue and other income
9.8
4.3
5.2
Expenditure, including the cost of goods sold
(17.9)
(19.9)
(21.4)
Loss for the period
(8.2)
(15.6)
(16.2)
Net operating cash outflows
(7.0)
(14.3)
(13.2)
Net investing and financing cash inflows (outflows)
(4.8)
(0.5)
2.4
Cash and cash equivalents at end-of-year
23.4
35.2
49.9
12
Annual Report 2024
Starpharma Holdings Limited
Outlook
As Starpharma continues to prioritise its
three strategic imperatives, which are
aimed at driving shareholder value, the
company has defined clear milestones
it aims to achieve in the short and
medium term. These milestones are
weighted within the context of each
strategic imperative, and our resources
are aligned with these weightings to
ensure effective execution and delivery.
As outlined in this Annual Report,
Starpharma’s top priority is to license
a DEP® asset, with DEP® SN38 (DEP®
irinotecan) and DEP® cabazitaxel as our
priority candidates for licensing. Early
asset development is crucial to our
future success, and we are prioritising the
development of new targets in-house.
We see research collaborations as
important to our company’s growth and
are focusing on business development
in novel diagnostic and therapeutic
areas concurrently. Increasing revenue
from the sale of VIRALEZE™ and
VivaGel® BV is also a key focus for
the company, and we have already
implemented a series of measures
designed to achieve this during FY25.
At its core, Starpharma is striving to
enhance shareholder value through
a renewed focus and emphasis on
delivering tangible outcomes for
shareholders. We are confident that
reaching these goals has the potential
to generate significant impacts
for patients and substantial returns
for shareholders, and we are fully
committed to achieving them.
Strategic Priorities
01
02
03
Maximise DEP®
asset value
Accelerate early
asset development
Build long-term
sustainability
Prioritising DEP® SN38
and DEP® cabazitaxel
Advancing DEP®
radiopharmaceuticals
and partnerships
Increasing revenue,
strengthening IP position
and fostering a high-
performance culture
Annual Report 2024
13
Starpharma Holdings Limited
Directors’ Report
The directors are pleased to present this report on the consolidated entity (referred to hereafter as the “group”, “company”,
or “Starpharma”) consisting of Starpharma Holdings Limited (the “Parent Entity”) and the entities it controlled at the end of, or during,
the year ended 30 June 2024.
Directors
The following persons were directors of Starpharma Holdings Limited at the date of this report and during the whole of the
financial year:
R B Thomas, AO (Chairman)
L Cheng
D J McIntyre
J R Davies
R Basser
J K Fairley (retired as Chief Executive Officer and Managing Director on 8 January 2024)
C Maley (appointed as Chief Executive Officer and Managing Director on 8 January 2024)
Information on Directors
Robert B Thomas AO
BEc, MSAA, SF Fin, FAICD, FRSN
Independent non-executive director (appointed 4 December 2013) and Chairman from 13 June 2014
Experience:
Mr Thomas has a strong background in financial services and capital markets and is a non-executive
director of several Australian listed companies. He was previously a Partner of Potter Partners
(now UBS), where he was also Head of Research.
Mr Thomas is the former Chief Executive Officer (CEO) of County NatWest Securities and then
became CEO and then Chairman of Citibank Corporate and Investment Bank in Australia. Mr Thomas
has also held the position of Chairman at Australian Wealth Management Ltd (ultimately IOOF Ltd),
TAL (Australia’s largest life insurance company) and HeartWare® International Inc, the second
largest global manufacturer of left ventricular assist heart pumps. Mr Thomas is currently a
non-executive director of ASX-listed Biotron Limited and Clarity Pharmaceuticals Limited.
Mr Thomas is also Chair of AusBio Ltd, Grahger Investments, Chair of the State Library of NSW
Foundation and a director of O’Connell Street Associates.
For many years Mr Thomas was regarded as one of Australia’s leading financial analysts and
regularly lectured with Financial Services Institute of Australia (FINSIA). He has considerable
expertise in Mergers & Acquisition (M&A) and capital markets including advising on the floats of
Commonwealth Bank of Australia and Qantas, and vast experience in Audit and Risk Management.
Mr Thomas is also approved under the NSW prequalification scheme for Audit and Risk Committee
Independent Chairs and Members for government/public sector agencies and has previously
served as the Chairman of the Audit and Risk Committee of Virgin Australia Limited (for 11 years),
HeartWare® International Inc, REVA Medical Limited and the State Library of NSW.
Mr Thomas holds a Bachelor of Economics from Monash University, a Diploma of Business
(Accounting) from Swinburne and is a fellow of FINSIA. Mr Thomas is also a Master Stockbroker,
a Fellow of the Australian Institute of Company Directors and a Fellow of the Royal Society of
New South Wales.
Committee membership:
Member of Remuneration and Nomination Committee.
Member of Audit and Risk Committee.
Other current directorships
of ASX listed entities:
Biotron Limited and Clarity Pharmaceuticals Limited.
14
Annual Report 2024
Starpharma Holdings Limited
Directorships of other
ASX listed entities within
last three years:
None.
Specific skills and
experience areas
In addition to Mr Thomas’ significant finance and M&A/capital markets experience, Mr Thomas’
non-executive roles with various ASX listed companies have deepened his skills and experience in
relation to accounting/corporate finance; audit and risk; governance; licensing and commercialisation
of innovation; strategy and risk management; occupational health & safety (“OH&S”); and
remuneration. He has also had significant experience with US-based companies as they progress
from research to commercialisation.
Interests in Starpharma
Holdings Limited:
1,900,000 ordinary shares.
Cheryl Maley
BSc, DipEd, MBA, GAICD
Chief Executive Officer and Managing Director (appointed 8 January 2024)
Experience:
Cheryl has over 25 years of experience in the pharmaceutical industry, including 20 years in
leadership roles at well-known and leading organisations, including Novartis and AbbVie.
Her previous roles include nine years at Novartis in senior commercial and executive roles
and various sales and marketing positions with AbbVie/Abbott, Servier Laboratories,
and Wyeth Pharmaceuticals.
Cheryl has extensive experience leading pharmaceutical innovation, marketing strategies,
and business growth across Australia, Asia, and international markets. She has a strong
commercial background and a proven record of successful product launches and patient
access and reimbursement to innovative medicines.
During her nine-year career at Novartis, Cheryl held senior leadership positions, responsible for
new products, commercialisation, strategy, and reimbursement matters. She also held General
Management roles in both the Philippines and Australia.
Cheryl most recently served as the Acting CEO and Strategic Advisor at Biointelect, a firm
specialising in strategic planning and commercialisation for the biopharmaceutical and medical
device sector.
Committees:
Attends Board Committee meetings by invitation.
Other current directorships
of ASX listed entities:
None.
Directorships of other
ASX listed entities within
the last three years:
Clarity Pharmaceuticals Limited.
Medlab Clinical Limited.
Specific skills and
experience areas:
With more than 25 years of experience in senior leadership and executive positions for
pharmaceutical and biotechnology companies, Cheryl has significant knowledge and leadership
skills in pharmaceutical innovation and development, product commercialisation, business
development, sales and marketing, strategy and risk management.
Interests in Starpharma
Holdings Limited:
125,000 ordinary shares.
2,278,428 employee performance rights.
15
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
Jacinth (Jackie) K Fairley
BSc, BVSc (Hons), MBA, GAICD, FTSE
Chief Executive Officer and Managing Director (appointed 1 July 2006 and retired on 8 January 2024)
Experience:
Dr Jackie Fairley has more than 30 years of operational experience in the pharmaceutical and
biotechnology industries working in senior management roles with companies including CSL
Limited (CSL) and Faulding (now Pfizer). In those roles Dr Fairley had responsibilities which included
clinical, regulatory, business development, product development and general management.
At Faulding Dr Fairley was responsible for global product development, regulatory affairs and
business development for Faulding’s hospital business which operated in more than 60 countries.
Dr Fairley holds first class honours degrees in Science (pharmacology and pathology) and Veterinary
Science from Melbourne University and was a practicing veterinary surgeon prior to joining CSL.
Whilst at CSL Dr Fairley obtained a Master of Business Administration from the Melbourne Business
School, where she was the recipient of the prestigious Clemenger Medal. Dr Fairley is also a graduate
of the Australian Institute of Company Directors.
Dr Fairley is a non-executive director of the listed investment company Mirrabooka Investments
Limited and a member of the Invest Victoria Advisory Board (IVAB) and Carnegie Venture Capital’s
investment Committee. Dr Fairley has previously served on the Melbourne Business School Board,
the Australian Federal Government’s Commonwealth Science Council and Pharmaceutical Industry
Working Group, and the Australian Federal Ministerial Biotechnology Advisory Council.
Committees:
Attended Board Committee meetings by invitation.
Other current directorships
of ASX listed entities:
Mirrabooka Investments Limited.
Directorships of other
ASX listed entities within
the last three years:
None.
Specific skills and
experience areas:
With more than 30 years’ experience in executive roles up to and including as CEO and executive
director of ASX listed and unlisted pharmaceutical and biotechnology companies, Dr Fairley’s
experience covers all key areas described in the Board skills matrix. In particular, Dr Fairley has
significant leadership skills in healthcare and scientific research; pharmaceutical development;
international experience; licensing and commercialisation of innovation; business development;
strategy and risk management; and M&A/capital markets.
Interests in Starpharma
Holdings Limited:
4,055,434 ordinary shares.
6,432,648 employee performance rights.
Directors’ Report continued
Information on Directors continued
16
Annual Report 2024
Starpharma Holdings Limited
David McIntyre
CPA, LL.B., MBA and B. Econs (Acc)
Independent non-executive director (appointed 1 March 2020)
Experience:
Mr McIntyre has more than 20 years of executive experience including 18 years in the life sciences
sector, having held various C-suite level roles at Tessa Therapeutics, Inc., AVITA Therapeutics, Inc.,
HeartWare® International, Inc., and Braeburn, Inc.
Mr McIntyre’s experience also includes seven years as a Partner at Apple Tree Partners, a multi-
billion-dollar life science venture capital and growth equity fund, giving him a deep knowledge of,
and extensive contacts in, the US pharma, medical device and biotech markets. During this time,
Mr McIntyre served as a non-executive director of several US life science companies.
Prior to entering life sciences, Mr McIntyre practiced as a senior attorney at Baker & McKenzie and
KPMG specialising in M&A, initial public offerings, and corporate law and also held various senior
finance roles in both multinational companies and small growth companies.
Mr McIntyre is based in the US and brings to the table an international lens on life science licensing
and commercialisation, marketing and business and development, and M&A/capital markets.
Mr McIntyre has significant experience in the areas of accounting/corporate finance, audit and
risk, strategy and risk management.
Mr McIntyre holds a Bachelor of Economics (Accounting) from the University of Sydney, Australia,
a Bachelor of Laws from the University of Technology, Sydney, and a Master of Business Administration
from Duke University Fuqua School of Business (Fuqua Scholar) from Durham, North Carolina, in the
US. Mr McIntyre is a Certified Practising Accountant and is also admitted as a legal practitioner of
the Supreme Court of New South Wales and of the High Court of Australia.
Mr McIntyre is Starpharma’s nominated director on the Board of Petalion Therapeutics Limited
(Petalion), which is an associate of the Group (see Note 24 of the Financial Statements).
Starpharma holds a 22.5% equity stake in Petalion, with the remaining equity owned by Medicxi,
a UK based venture capital fund. Mr McIntyre does not draw a separate fee from Starpharma or
Petalion for this Directorship.
Committee membership:
Chair of Audit and Risk Committee.
Other current directorships
of ASX listed entities:
None.
Directorships of other
ASX listed entities within
the last three years:
None.
Specific skills and
experience areas:
With more than 20 years of executive experience including 18 years in the life science sector,
Mr McIntyre’s experience covers all key areas described in the Board skills matrix. In particular,
Mr McIntyre has substantial expertise in accounting/corporate finance, audit and risk; M&A/
capital markets; governance; licensing and commercialisation of innovation; strategy and risk
management, having held executive roles including Chief Financial Officer and Chief Operating
Officer. He has also had significant experience with US based companies in the medical device,
biotechnology and pharmaceutical sector.
Interests in Starpharma
Holdings Limited:
16,240 ordinary shares.
17
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
Lynda Cheng
B.Com, LLB (Hons), GAICD
Independent non-executive director (appointed 1 August 2021)
Experience:
Ms Cheng has a strong background in finance with more than 25 years of experience as a finance
executive including more than 15 years at Visy Industries/Pratt Holdings and 10 years in investment
banking. She has significant commercial and international corporate expertise including
experience in financial services, manufacturing, export finance, infrastructure, education as well as
market entry, growth and technology.
Ms Cheng is currently Director of Corporate Development and Mergers & Acquisitions at Visy
Industries/Pratt Holdings and has held various other roles in the group including CFO. Ms Cheng’s
earlier roles include as a lawyer at Blake Dawson, before moving into investment banking with J.P.
Morgan in its Melbourne, Sydney, San Francisco and New York offices.
Ms Cheng is currently an independent, non-executive member of the board of directors at JRJJ
Capital, the parent company of Merricks Capital, in an observer/advisory capacity. Ms Cheng
previously served as a non-executive director of Export Finance Australia, a member of the
Australian Government’s International Development Policy Expert Panel and Deputy Chair and
Chair of the Finance, Audit and Risk committee of South East Water.
Ms Cheng holds a Bachelor of Law (Honours) and Commerce degree, majoring in actuarial studies
and economics, from the University of Melbourne, and is a graduate member of the Australian
Institute of Company Directors.
Committee membership:
Member of Audit and Risk Committee.
Chair of Remuneration and Nomination Committee.
Other current directorships
of ASX listed entities:
None.
Directorships of other
ASX listed entities within
the last three years:
None.
Specific skills and
experience areas:
With over 25 years’ experience as a finance executive, including substantial international
experience and several non-executive directorships, Ms Cheng’s experience covers the majority
of key areas described in Starpharma’s Board skills matrix. In particular, she has substantial
expertise in accounting/corporate finance, audit and risk; M&A/capital markets; strategy and risk
management; governance; as well as business development. Ms Cheng has had involvement in
the commercialisation of new innovations during her tenure at South East Water and also while
working with disruptive technology companies in Silicon Valley.
Interests in Starpharma
Holdings Limited:
170,555 ordinary shares.
Directors’ Report continued
Information on Directors continued
18
Annual Report 2024
Starpharma Holdings Limited
Jeff R Davies
PhD, BSc (Hons)
Independent non-executive director (appointed 1 April 2022)
Experience:
Dr Davies is a former CSL executive with over 35 years of biopharmaceutical experience, holding
senior executive roles at CSL, including Executive Vice President & General Manager at CSL
for the Asia-Pacific region, and Global Head of Plasma Product Research and Development
at CSL-Behring, Switzerland.
As Executive Vice President & General Manager at CSL for the Asia-Pacific region, Dr Davies
had overall P&L responsibility for the commercial and operational aspects of the business and
oversaw the pharmaceutical, plasma, vaccine, and diagnostic businesses in Australia, New Zealand,
China, and the broader Asia-Pacific region.
As the Global Head of CSL-Behring’s Plasma Product Research and Development portfolios,
Dr Davies oversaw and played an important role in the development of leading products,
including the multi-billion-dollar Privigen® immunoglobulin product. Dr Davies was part of CSL’s
due diligence teams, which led to the acquisitions of the Plasma Fractionation businesses of
Swiss Red Cross (2000) and Aventis Behring (2003), thus transforming CSL into a global company.
Dr Davies is a partner and founding director of Centre for Biopharmaceutical Excellence,
a pharmaceutical consulting firm. Dr Davies has held a number of senior industry board and
advisory roles, including representation on the Pharmaceutical Industry Council, the Australian
Red Cross Advisory Board and Medicines Australia.
Dr Davies holds a PhD in Biochemistry from Monash University and is a graduate of the London
Business School’s Senior Executive Program.
Committee membership:
Member of Remuneration and Nomination Committee.
Other current directorships
of ASX listed entities:
None.
Directorships of other
ASX listed entities within
the last three years:
None.
Specific skills and
experience areas:
With over 35 years of experience within the biopharmaceutical industry, Dr Davies is an
accomplished executive skilled in R&D, product development and commercialisation strategy;
business development, manufacturing and clinical and regulatory affairs. Dr Davies has significant
leadership skills and experience in commercialising scientific research for healthcare products.
Interests in Starpharma
Holdings Limited:
929,687 ordinary shares.
19
Annual Report 2024
Starpharma Holdings Limited
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Russell Basser
MB.BS FRACP MD
Independent non-executive director (appointed 20 February 2023)
Experience:
Dr Basser is a medical oncologist and former corporate executive with over 30 years of international
medical and biopharmaceutical experience, including 21 years at CSL.
Dr Basser has substantial expertise in international drug and vaccine development, having held
multiple senior executive roles at CSL, including Senior Vice President (SVP) of Research and
Development at CSL Seqirus; Chief Medical Officer at CSL Limited/CSL Behring; and SVP of
Global Clinical Research and Development at CSL Behring/CSL Limited. During his time at CSL,
Dr Basser was responsible for globalising CSL’s Clinical Research and Development group and
for conception and execution of CSL’s clinical trial strategies across a broad range of therapeutic
areas from Phase 1 to commercialisation. Dr Basser was a founding member of CSL Seqirus’ executive
leadership team in 2015 as SVP of Research and Development until his retirement in April 2022.
Prior to joining CSL, Dr Basser was a practicing medical oncologist at the Royal Melbourne and
Western Hospitals and had an appointment at the Ludwig institute for Cancer Research.
Committee membership:
Member of Remuneration and Nomination Committee.
Other current directorships
of ASX listed entities:
Medical Developments International.
Directorships of other
ASX listed entities within
the last three years:
None.
Specific skills and
experience areas:
With over 20 years of executive experience in the biotechnology industry and 10 years as
a practicing clinical oncologist, Dr Basser has significant leadership skills and experience in
healthcare/scientific research; pharmaceutical product development; international executive
experience and skills in regulation/public policy; commercialisation of innovation; business
development; governance; strategy; and risk management.
Interests in Starpharma
Holdings Limited:
71,428 ordinary shares.
Company Secretary
Mr Justin Cahill commenced as Chief Financial Officer and Company Secretary on 3 April 2023. Mr Cahill has extensive
corporate finance and leadership experience in the biopharmaceutical, food and agricultural sectors for both ASX-listed
and private companies.
Principal Activities
The principal activities of the group consist of research, development and commercialisation of dendrimer products for
pharmaceutical and healthcare applications. Activities within the group are directed towards the development of precisely
defined nano-scale materials, including the development of SPL7013 (astodrimer sodium) as a vaginal gel, VivaGel® BV, for the
management of bacterial vaginosis, VIRALEZE™ antiviral nasal spray; and as an antiviral condom coating. Starpharma is also
applying its proprietary dendrimers to drug delivery to create improved pharmaceuticals and has developed the valuable DEP®
(Dendrimer Enhanced Product) delivery platform.
Result
The financial report for the group for the financial year ended 30 June 2024, and the results herein, have been prepared in
accordance with Australian Accounting Standards.
The consolidated loss after income tax attributable to ordinary shareholders for the financial year ended 30 June 2024 was
$8,165,000 (2023: $15,638,000), with revenue of $9,756,000 (2023: $4,208,000). The net operating cash outflows for the
year were $6,977,000 (2023: $14,311,000). The cash balance at 30 June 2024 was $23,360,000 (June 2023: $35,180,000).
Directors’ Report continued
Information on Directors continued
20
Annual Report 2024
Starpharma Holdings Limited
Dividends and Distributions
No dividends were paid or declared in respect to the financial year ended 30 June 2024 (2023: Nil).
Review of Operations
Key Focus Area 1: Maximise DEP® Asset Value
Starpharma’s DEP® drug delivery platform is being used to enhance the therapeutic utility of drugs through improved solubility,
efficacy and pharmacokinetic control, and reductions in specific drug-related toxicities. Starpharma’s innovative and proprietary
DEP® platform has shown advantages across a wide range of drug classes. It has the potential to provide benefits to small
molecule drugs, peptides, and proteins, as well as to the development of radiotheranostics and antibody-drug conjugates
(ADCs). The dendrimer technology could benefit companies looking to enhance the outcome of a drug currently in development
to improve efficacy and/or reduce toxicity or extend patents of key drugs in their portfolio.
During FY24, Starpharma completed its three DEP® Phase II clinical studies and reported results. With the full clinical dataset
now in hand and beginning to share results at oncology conferences such as ASCO, Starpharma’s top priority is to maximise
the value of the DEP® clinical assets. The key objective is to successfully convert priority assets DEP® SN38 (DEP® irinotecan)
and DEP® cabazitaxel into license deals.
Key activities until the date of this report include:
Starpharma reported the results from the Phase II clinical trial programs of DEP® SN38, DEP® cabazitaxel, and DEP® docetaxel.
The three programs have clinically validated the DEP® platform technology and have generated valuable data supporting
further development of the DEP® clinical candidates. This will provide value in areas of unmet clinical need and knowledge
and experience to advance future high-value DEP® candidates towards clinical trials and commercialisation.
The DEP® SN38 Phase II clinical program met its objectives, with endpoints demonstrating positive anti-tumour efficacy in
heavily pre-treated patients with a range of difficult-to-treat, advanced, metastatic cancers, including colorectal cancer and
platinum-resistant ovarian cancer. The trial also confirmed the product’s favourable safety and tolerability profile. Several
patients who have had prolonged responses to DEP® SN38 therapy and are experiencing ongoing clinical benefit continue
to receive access to DEP® SN38 treatment and will be monitored for safety and any change to their disease.
The promising results from the DEP® SN38 trial were presented as an oral presentation at the ASCO Annual Meeting in June 2024.
The presentation generated significant interest from clinicians and the oncology community attending the conference,
highlighting the challenges that treating physicians see each day and the benefit the DEP® technology can bring to patients
undergoing treatment.
Earlier in the year, interim data on DEP® SN38 were presented at the International Conference on Molecular Targets and
Cancer Therapeutics, co-hosted by the American Association of Cancer Research (AACR), National Cancer Institute (NCI),
and the European Organisation for Research and Treatment of Cancer (EORTC) in the US (AACR-NCI-EORTC) in October 2023.
Additional nonclinical data on DEP® SN38 in combination with immune-oncology agents were also presented at this conference.
The DEP® cabazitaxel Phase II clinical trial met its objectives, with endpoints demonstrating positive anti-tumour efficacy in
advanced, metastatic castrate-resistant prostate cancer, platinum-resistant ovarian cancer, and gastro-oesophageal cancers.
The trial also confirmed the safety and tolerability of DEP® cabazitaxel.
The full results from the Phase II trial of DEP® cabazitaxel were presented as an oral presentation at the American Society of
Clinical Oncology (ASCO) Annual Meeting in June 2024, and data on the efficacy of the product in gastroesophageal cancers
were presented at the ASCO Gastrointestinal Cancers Symposium in January 2024.
Acceptance of two oral presentations at the 2024 ASCO Annual Meeting was a significant achievement for Starpharma,
demonstrating the significance and value of the data generated in the Phase II clinical programs of DEP® SN38 and
DEP® cabazitaxel.
The DEP® docetaxel Phase II clinical program met its objectives, with endpoints demonstrating encouraging anti-tumour activity
in multiple advanced, metastatic cancers, including pancreatic cancer, gastro-oesophageal cancer, non-small cell lung cancer,
and cholangiocarcinoma. The safety and tolerability of DEP® docetaxel were also confirmed. These results were demonstrated
in the monotherapy and combination arms, where DEP® docetaxel was administered either as a monotherapy or combination
therapy with other anti-cancer agents, nintedanib or gemcitabine.
21
Annual Report 2024
Starpharma Holdings Limited
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Review of Operations continued
Starpharma continues to undertake business development partnering activities for its DEP® assets. As part of its business
review and to clearly prioritise the most significant commercial opportunities for the DEP® assets, Starpharma conducted a
comprehensive commercial evaluation of each DEP® clinical asset to determine the best path forward for identifying the ideal
partner to maximise the assets’ value. This evaluation considered each asset’s commercial potential in terms of indication,
region, country, and time to market. Following the outcomes of the commercial evaluation, Starpharma’s partnering priorities
have shifted to focusing on DEP® SN38 and DEP® cabazitaxel, with active business development outreach paused for DEP®
docetaxel. Whilst DEP® docetaxel still represents a commercial opportunity, the priority of our internal resourcing is to focus
on progressing commercial discussions for DEP® SN38 and DEP® cabazitaxel.
In parallel with business development activities for DEP® SN38 and DEP® cabazitaxel, Starpharma is developing two DEP®
radiopharmaceutical candidates, a DEP® HER2-radiodiagnostic and a DEP® HER2-radiotherapeutic. In May 2024, Starpharma
announced it is prioritising the development of the DEP® HER2-radiodiagnostic towards a first-in-human clinical study to initiate
within the next 12 months and, in parallel, continue the development of a DEP® HER2-radiotherapeutic.
Earlier in the year, Starpharma’s DEP® HER2-radiodiagnostic demonstrated a favourable biodistribution profile with excellent
imaging contrast between tumour and normal tissues, as well as rapid uptake and high levels of tumour accumulation in a
HER2-positive (HER2+) breast cancer model. The application, versatility, and benefits of the DEP® platform for targeted delivery
of radiopharmaceuticals were presented at the Society of Nuclear Medicine and Molecular Imaging (SNMMI) Annual Meeting
in June 2024, the Targeted Radiopharmaceuticals Summit in Berlin in December 2023, and the AACR-NCI-EORTC Conference
in October 2023.
Presentations at international industry conferences are important for demonstrating the advantageous application of dendrimers
in drug delivery and raising the profile of Starpharma’s DEP® platform within the oncology community. They also present significant
opportunities for business development. While in the US for ASCO and in Canada for the SNMMI conference, Starpharma also
attended BIO 2024. Attending all three of these conferences proved highly valuable from a partnering perspective, as a high
number of meetings with companies from Europe and the US interested in applying dendrimers to their pipeline products,
including radiopharmaceuticals, were generated.
Key Focus Area 2: Accelerate Early Asset Development
Starpharma is intensifying its efforts to develop saleable assets and secure collaborations and licensing deals. The company’s key
objective is to increase the number of assets in early development and enhance the efficiency of our early development activities.
Key activities until the date of this report include:
In April 2024, Starpharma announced a strategic partnership with Medicxi, a leading life sciences investment firm dedicated
to financing companies developing innovative medicines, to co-found an asset-centric company called Petalion Therapeutics.
Petalion is focusing on developing a novel targeted asset using Starpharma’s DEP® dendrimer platform technology.
During the year, Starpharma continued its research collaborations with Genentech and MSD. In these partnerships,
Starpharma provides dendrimer chemistry expertise and develops functionalised dendrimers for its partners to test.
Starpharma’s in-house preclinical DEP® antibody-drug conjugates (ADCs) program continues with candidate optimisation
and further preclinical studies to demonstrate the DEP® platform’s benefits in this high-value area.
Starpharma partnered with the University of Queensland’s Hub for Advanced Manufacture of Targeted Radiopharmaceuticals
(AMTAR Hub) in July 2023 to advance the research and development of Starpharma’s targeted DEP® radiopharmaceuticals.
On 31 July 2023, following communication from AstraZeneca on 28 July 2023 and the subsequent release of their H1 and Q2 2023
results announcement that day, Starpharma reported that AstraZeneca had made the decision to discontinue the development
of AZD0466 after an internal review prompted by a small number of asymptomatic adverse events that were unrelated to
Starpharma’s dendrimer drug delivery technology.
Key Focus Area 3: Build Long-Term Sustainability
Starpharma aims to become a self-sustaining organisation by increasing revenues and the value of its intellectual property and
managing costs effectively. The company’s key focus areas in the short term include growing revenue, improving efficiency,
and reducing costs to support our long-term self-sustaining goal. Starpharma has multiple revenue streams with short to
medium-term opportunities, including from DEP® asset partnerships and the marketed products VivaGel® BV and VIRALEZE™.
Directors’ Report continued
22
Annual Report 2024
Starpharma Holdings Limited
Key activities until the date of this report include:
VivaGel® BV is a non-antibiotic topical gel for the treatment of bacterial vaginosis (BV) and the prevention of recurrent BV.
It is registered in over 40 countries, including the UK, Europe, Southeast Asia, South Africa, Australia, and New Zealand.
In June 2024, Starpharma successfully achieved regulatory certification of VivaGel® BV under the new EU Medical Device
Regulations (MDR), which recently introduced a range of more stringent requirements to demonstrate medical device safety
and performance, including an increased need for clinical evidence. Certification under the EU MDR gives renewed certainty
about the status of VivaGel® BV in Europe. It is an important factor for potential commercial partners in this region, as the new
regulations introduce significant hurdles that other products that make claims for treatment of BV may not be able to overcome.
In February 2024, Starpharma completed the formal dispute resolution process with the US Food and Drug Administration (FDA) in
relation to VivaGel® BV. The FDA maintained that they require additional clinical efficacy data to be generated for the regulatory
approval of VivaGel® BV for BV in the US. Starpharma is not planning to pursue further clinical studies for VivaGel® BV on its own
at this time. Starpharma remains committed to leveraging the VivaGel® BV development program and is working to maximise the
commercial potential for VivaGel® BV in the more than 40 markets where it has already been approved. The decision by the FDA
does not alter the approval status in the countries where VivaGel® BV is already registered. Following this outcome, Starpharma
and EDW Pharma, formerly ITF Pharma, mutually agreed to exit the license agreement for VivaGel® BV in the US, signed in 2018.
In January 2024, Starpharma partnered with ITROM Pharmaceutical Group for the sales and distribution of VivaGel® BV across
13 countries in the Middle East and North Africa region. ITROM has a strong presence in the region’s public and private health
sectors, maintaining strong relationships with key opinion leaders, specialist physicians, hospital chains and retail outlets.
Since entering this agreement, Starpharma and ITROM have been working closely to transfer relevant VivaGel® BV marketing
authorisations from Mundipharma and prepare for launch in the Middle East market. ITROM has achieved registration for VivaGel®
BV in Saudi Arabia.
This new partnership with ITROM followed the reversion of VivaGel® BV rights to Starpharma under a settlement agreement
with Mundipharma in August 2023. Under the settlement, Starpharma received a one-time A$6.6 million cash payment from
Mundipharma in August 2023, and the VivaGel® BV commercial rights reverted to Starpharma.
Starpharma’s partner, Aspen, continues to market VivaGel® BV in Australia and New Zealand under the brand name Fleurstat® BVgel.
VIRALEZE™ is a topical antiviral barrier nasal spray for colds and respiratory viruses, including coronaviruses. It is registered in
over 35 countries, including Europe, the UK, and Asia. VIRALEZE™ is not approved for use or supply in Australia, where the review
by the Therapeutic Goods Administration (TGA) for the SPL7013 nasal spray as a medical device is ongoing. Starpharma has
provided the TGA with clinical data from the post-market study that was completed during FY24, and Starpharma is awaiting an
outcome from the TGA.
In parallel with seeking marketing authorisation in Australia, Starpharma applied to amend the TGA Poisons Standard to ensure
accurate labelling of the nasal spray, should approval be achieved. The TGA announced its final decision in May 2024 in support
of Starpharma’s application to amend the Standard. This outcome means that if a nasal spray containing astodrimer sodium were
approved for sale in Australia, the product could be labelled appropriately for nasal spray applications and sold in pharmacies.
This outcome is separate from, and does not influence, the application for marketing authorisation.
Starpharma reported the results of the post-market clinical study of VIRALEZE™ in participants with COVID-19 in January 2024.
The results showed that VIRALEZE™ reduced SARS-CoV-2 viral load and increased the rate of virus clearance from the nose, and in
parallel, improved key symptoms of COVID-19, including loss of smell. This benefit was statistically significant in all age cohorts
45+ years but was not significant when patients below 40 years of age were included. As seen in a previously announced trial
in healthy volunteers, VIRALEZE™ was well-tolerated.
The results from the VIRALEZE™ clinical study provide clinical evidence of the performance of VIRALEZE™ in humans that will
support regulatory processes for the transition to the new European Medical Device Regulations (MDR), which will come into full
effect in 2029. The data will also support ongoing marketing and commercial activities for the product. Starpharma submitted
its application for EU MDR certification in April 2024, which is under review by the Regulator.
Starpharma continues to market VIRALEZE™ online through dedicated product webstores and Amazon UK. Starpharma also has
commercial partners in several international markets, where the product is distributed online and in retail outlets, including pharmacies.
Starpharma continues to pursue additional commercial opportunities for its VIRALEZE™ and VivaGel® BV products in line with its
strategic priorities.
Starpharma and Okamoto signed a contract extension for the VivaGel® Condom product. This agreement covers Japan and
several other Asian markets. Okamoto continues marketing in Japan and regulatory activities in several other Asian markets.
23
Annual Report 2024
Starpharma Holdings Limited
Directors’
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Consolidated Financial
Statements
Notes to the Consolidated
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Corporate
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Review of Operations continued
Key Personnel Changes
Cheryl Maley commenced as Starpharma’s Chief Executive Officer and Managing Director on 8 January 2024. Upon Cheryl’s
commencement, Dr Jackie Fairley retired from the position. Dr Fairley was available to provide advisory support to the CEO and
Board as needed until June 2024.
Matters Subsequent to the End of the Financial Year
No matters or circumstances have arisen since 30 June 2024 through the date of this report that have significantly affected,
or may significantly affect:
(a) the consolidated entity’s operations in future financial years, or
(b) the results of those operations in future financial years, or
(c) the consolidated entity’s state of affairs in future financial years.
Strategy, Future Developments and Prospects
The company aims to generate value through the development and commercialisation of its patented dendrimer technology for
pharmaceutical and healthcare applications. The company’s focus is on maximising the value of its DEP® drug delivery platform,
accelerating early asset development, and building long-term sustainability. Starpharma intends to achieve this through a
combination of internally funded and partnered projects. The company commercialises its development pipeline with corporate
partners via licensing and sales and distribution agreements at various stages in a product’s development lifecycle; depending
on the product, patent opportunity, a partner’s commercial strategy and relative strength of product and market expertise,
comparison of current and future potential returns.
Starpharma has extensive expertise in developing dendrimers, with clinically validated technology, a strong intellectual property
(IP) position, and a portfolio of clinical-stage assets, early-stage research, partnerships, and commercial products. Starpharma’s
strategy is to extract the highest value from its patented technology, including licensing priority DEP® product candidates,
advancing its DEP® radiopharmaceuticals program and partnerships, increasing revenue, further strengthening its IP position,
and fostering a high-performance culture.
Proceedings on Behalf of the Company
No proceedings have been brought or intervened in on behalf of the company with leave of the Court under section 237
of the Corporations Act 2001.
Review of Financials
Income statement
30 June 2024
$’000
30 June 2023
$’000
Revenue
9,756
4,208
Cost of goods sold
(632)
(1,120)
Other income
–
135
Research and product development expense (net of R&D tax incentive)
(10,053)
(11,239)
Commercial and regulatory operating expense
(3,664)
(3,854)
Corporate, administration and finance expense
(3,572)
(3,768)
Loss for the period
(8,165)
(15,638)
Directors’ Report continued
24
Annual Report 2024
Starpharma Holdings Limited
Income statement
The reported loss for the year was $8,165,000 (2023: $15,638,000). The loss included nonrecurring revenue of $6,553,000 relating
to the commercial settlement and termination of the VivaGel® BV license and supply agreement with Mundipharma in August 2023.
The consolidated loss adjusted for the Mundipharma settlement was $14,718,000, a 6% decrease on the prior year loss.
Revenue for the year was $9,756,000 (2023: $4,208,000), comprising $8,289,000 (2023: $2,939,000) for product sales,
royalty and license, and research revenue from commercial partners, and interest income on cash invested of $1,467,000
(2023: $1,269,000). Revenue included a nonrecurring $6,553,000 from the Mundipharma commercial settlement. Excluding the
Mundipharma settlement, adjusted revenue was $3,203,000, a 24% decrease on prior year revenues, with lower product sales
in the current period.
Research and product development expense was $10,053,000 (2023: $11,239,000) and includes the costs of the internal
DEP® drug delivery programs, including DEP® SN38, DEP® cabazitaxel, DEP® docetaxel, DEP® ADCs and DEP® radiotheranostics,
as well as the post-market clinical study of VIRALEZE™. A contra research and development expense of $5,527,000 (2023:
$7,631,000) has been recognised for eligible research and development activities under the Australian Government’s R&D Tax
Incentive program.
Commercial and regulatory operating expense includes expenditure related to commercialisation of both VivaGel®, VIRALEZE™
and DEP® portfolios, including business development, marketing, regulatory, supply chain and quality assurance activities.
The decrease in expense from the prior year reflects cost reduction initiatives implemented, including for employment costs,
IT support costs, and ongoing product stability studies.
Corporate, administration and finance expense include corporate costs, gains/losses on foreign currency held, and interest
expense on borrowings. The decrease in expense from the prior year reflects cost reduction initiatives implemented, including
for insurances.
Balance sheet
At 30 June 2024, the group’s cash position was $23,360,000 (June 2023: $35,180,000). Trade and other receivables of $7,151,000
(June 2023: $9,169,000) includes $5,527,000 (June 2023: $7,244,000) receivable from the Australian Government under the
R&D tax incentive program. Trade and other payables of $4,013,000 (June 2023: $7,667,000) have decreased primarily due
to lower accruals associated with expenditure on research programs.
Statement of cash flows
The net operating cash outflows for the year were $6,977,000 (2023: $14,311,000). The net cash outflows from financing activities
were $4,747,000 (2023: $83,000 inflow) and included the repayment of the $4,000,000 Invest Victoria R&D loan.
Earnings Per Share
2024
2023
Basic/diluted loss per share
($0.02)
($0.04)
25
Annual Report 2024
Starpharma Holdings Limited
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Risk Management
The group is subject to business risks typical of companies operating
in the biotechnology and pharmaceutical sectors at the development
and early commercialisation phase. Any investment in these sectors is
considered high-risk. Company management has implemented a risk
management and internal control system in order to manage the
group’s material business risks.
The company’s risk management system comprises four steps:
1) risk identification, 2) analysis, 3) implementation of mitigation controls
and actions, and 4) monitoring and reporting of identified risks.
The Audit and Risk Committee, on behalf of the Board, monitors the risk
management system to ensure it is operating effectively and receives
reports on material risks. The material and specific risks of the industry
sector and the group identified through the company’s risk management
system include, but are not limited to:
• Scientific, technical and clinical – product development requires a
high level of scientific rigour, the outcomes of which cannot be known
beforehand. Activities are experimental in nature, so the risk of failure,
unexpected outcomes or delay is material. The company is introducing
steps to further strengthen the new candidate selection criteria to help
further mitigate this inherent risk
• Key development activities, including clinical trials, are undertaken by specialist contract research organisations, and there are
risks in designing and completing those activities, including managing the quality and timelines of these activities.
• Regulatory – company products and their testing may not be approved, or may be delayed, amended or withdrawn, by regulatory
bodies (e.g. US Food and Drug Administration) whose approvals are necessary before products can be sold in market. Changes
in the regulatory environment may also impact product development and commercialisation. Breach of regulations, local or
international law, or industry codes of conduct may subject the company to financial penalties and reputational damage.
• Financial – the group currently, and since inception, does not receive sufficient recurrent income to cover operating expenses.
Although current cash reserves are sound, there is no certainty that additional capital funding may not be required in the future,
and no assurance can be given that such funding will be available if required.
• Intellectual property (IP) – commercial success requires the ability to develop, obtain and maintain commercially valuable patents,
trade secrets and confidential information. Securing, defending and maintaining IP across multiple countries and preventing
the infringement of the group’s exclusive rights involves managing complex legal, scientific and factual issues. The company
must also operate without infringing upon the IP of others.
• Product manufacturing and supply – the company is required to manufacture and supply product under certain licensing
and distribution agreements, and under highly stringent quality and regulatory requirements. The manufacture of product
is undertaken by specialist, regulatory approved, third party contract manufacturing organisations experienced in the
sector. There is a risk of quality/failure of manufacture and a risk that supply chain disruptions lead to manufacturing and
supply delays/interruptions, which could impact profitability and/or damage relationships with partners. Further, changes in
economic circumstances may increase the cost and availability of product, negatively impacting the business.
• Commercialisation – the company predominately relies upon commercial partners to market, distribute and in some cases
finalise development and registration of its products on its behalf. There are risks in establishing and maintaining these
relationships, and with the manner in which partners execute and deliver on these agreements.
• Product acceptance and competitiveness – a developed product may not be considered by key opinion leaders (e.g. doctors),
reimbursement authorities (e.g. Pharmaceutical Benefits Scheme listing) or the end customer to be an effective alternative to
products already on market, or other products may be preferred.
2
Analyse
3
Actions &
Controls
1
Identify
4
Monitor
& Report
Risk
Management
Process
Directors’ Report continued
26
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Starpharma Holdings Limited
• Product liability – a claim or product recall may significantly impact the company. Insurance, at an acceptable cost, may not
be available or adequate to cover liability claims or any product recall costs (if any) if a product is found to be unsafe.
• Key personnel – the company’s success and achievements against timelines depend on key members of its highly qualified,
specialised and experienced management and scientific teams. The ability to retain and attract such personnel is important.
• Grant and R&D incentives – the company may undertake R&D activities part-funded by incentive programs (e.g. R&D tax incentive)
and other competitive grants. There is no certainty that grants or incentive programs will continue to be available to the
company, and changes in government policy may reduce their applicability.
• Cyber security and data protection – the company recognises the increasing risk associated with cyber security and the
potential impact on business operations and has taken steps in recent years to improve controls relating to protection of
Company data. Management continues to review processes and controls to ensure the company remains current with the
evolving cyber security climate.
In accordance with good business practice in the pharmaceutical industry, the group’s management actively and routinely employs
a variety of risk management strategies. These are broadly described in the Corporate Governance Statement available at
http://www.starpharma.com/corporate_governance.
Health and Safety
The Board, Chief Executive Officer and senior management team of the company are committed to providing and maintaining
a safe and healthy working environment for the company’s employees and anyone entering its premises or with connections
to the company’s business operations. Employees are encouraged to actively participate in the management of occupational
health and safety (OH&S) issues. The company has adopted an OH&S Policy and has an established OH&S Committee as part
of its overall approach to workplace safety. The OH&S Committee provides a forum for management and employees to consult
on health and safety matters. The primary role of the OH&S Committee is to coordinate the development and implementation
of the OH&S Policy and procedures, to consider any work-related safety matters or incidents, and to ensure compliance with
relevant legislation and guidelines. The OH&S Committee includes representatives of management and employees from each
operational area generally in proportion to the number of people working in the area and the perceived safety risks associated
with working in that area.
The OH&S Committee meets monthly, and updates on OH&S matters are provided at Board meetings.
Environment and Regulation
The group is subject to environmental regulations and other licences in respect of its research and development facilities and
there are adequate systems in place to ensure compliance with relevant federal, state and local environmental regulations.
The Board is not aware of any breach of applicable environmental regulations by the group. There were no significant changes
in laws or regulations during the 2024 financial year or since the end of the year affecting the business activities of the group,
and the Board is not aware of any such changes in the near future.
27
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Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
Meetings of Directors
The number of meetings of the company’s Board of Directors and of each committee held during the year ended 30 June 2024,
and the number of meetings attended by each director are listed in the table below.
Directors
Board
Audit and Risk
Committee
Remuneration
and Nomination
Committee
R B Thomas
Chairman
8 of 8
3 of 3
3 of 3
C Maley
CEO & Managing Director1
4 of 4
N/A
N/A
J K Fairley
CEO & Managing Director2
4 of 4
N/A
N/A
D J McIntyre3
6 of 8
3 of 3
N/A
L Cheng
8 of 8
3 of 3
3 of 3
J R Davies
8 of 8
N/A
3 of 3
R Basser
7 of 8
N/A
2 of 3
“N/A” denotes that the director is not a member of the relevant committee.
1. C Maley was appointed as Chief Executive Officer and Managing Director on 8 January 2024.
2. J K Fairley retired as Chief Executive Officer and Managing Director on 8 January 2024.
3. The two Board meetings that D J McIntyre was unable to attend were due to unforeseen and unavoidable travel delays that prevented him joining
the scheduled meetings.
Directors’ Report continued
28
Annual Report 2024
Starpharma Holdings Limited
Remuneration Report
The remuneration report for the year ended 30 June 2024 sets out remuneration information for non-executive directors,
and KMP executives of the group. The remuneration report is presented under the following sections:
1.
Introduction
2. Remuneration governance
3. Non-executive director remuneration policy
4. Executive remuneration policy
5. Executive remuneration outcomes, including link to performance
6. Details of remuneration
7.
Executive employment agreements
8. KMP equity holdings
9. Details of equity incentives affecting current and future remuneration
1. Introduction
Remuneration strategy
Starpharma aims to ensure that its remuneration strategy aligns the interests of its executives and employees with those of its
shareholders. In framing its remuneration strategy, the Board is conscious that Starpharma only has a small number of employees
(~40) so endeavours to keep its remuneration relatively straightforward. Starpharma’s staff are required to have specialist
knowledge and experience allowing them to develop products over the medium to long term. The fact that Starpharma operates
in a global pharmaceutical industry environment also influences its remuneration strategy.
The remuneration structure comprises fixed remuneration, short-term incentives (“STI”) in both cash and equity and equity-based
long-term incentives (“LTI”). Starpharma’s remuneration structure is transparent and based on Key Performance Indicators (“KPIs”),
which are designed to align with the interests of shareholders and to reward performance across multi-year timeframes related
to product development value-adding milestones. In some cases, the Board may exercise discretion to take account of events
and circumstances not envisaged.
The Remuneration and Nominations Committee and Board explicitly considered the FY24 share price underperformance in
determining the STI cash bonus and STI deferred equity incentives awarded for FY24, and in setting appropriate remuneration
for directors and executives for the forward year.
As a result of a strategic review of the company following the commencement of Ms Cheryl Maley as CEO in January 2024,
there are some revisions to the company remuneration strategy, which will come into effect in FY25. The main changes to the
remuneration strategy impact performance pay outcomes for all employees of Starpharma. The organisation has reviewed its
incentive framework, and this will be enhanced in FY25 to more closely align with shareholder interests. In terms of STI and LTI
outcomes, there will be adjustments made to the weighting of KPIs that increase the proportion of at-risk incentives for all staff.
Another change to be implemented in FY25 is the methodology used for offering performance rights to staff. Performance
rights are an important incentive and retention tool and have been an important element of the company’s remuneration
framework. For many years, the company has sought to maintain or, at times, increase the face value of the annual offer of
performance rights to our staff. To make the offer of performance rights more sustainable for the company, from FY25,
the company will take a more measured approach in determining the face value of rights offered to staff, which will lead
to a reduction in the face value of rights offered for the LTI program, across all positions in the company.
CEO Transition
Following the announcement of Dr Fairley’s intention to retire (ASX announcement dated 9 June 2023), the Board undertook
an extensive international search and selection process to recruit a successor to Dr Fairley. Dr Fairley made an outstanding
contribution to Starpharma since assuming the role of CEO in 2006, and the Board was determined to ensure a smooth
handover to a new CEO and a successful transition period. To this end, and recognising the knowledge and experience of
the organisation that would leave with Dr Fairley, the Board implemented some retention measures to help ensure stability
during a newly appointed CEO’s transition. The Board identified a number of positions in the company that would be crucial
to a newly appointed CEO’s success and put in place retention measures for those employees. The first measure was a cash-
based retention payment, which was offered to 7 employees, totalling $390,000. The cash retention payment is payable
in October 2024, 9 months after the start date of the new CEO. The second measure was the offer of performance rights,
totalling 315,000 rights granted to 4 employees. These rights vest in June 2025, 17 months after the new CEO commenced.
These transition retention arrangements are dependent on continued employment with the company; the Board may exercise
discretion to bring forward the payment date and, or, the vesting of rights included in this offer.
29
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
Remuneration Report continued
1. Introduction continued
Key management personnel
The remuneration report details the remuneration arrangements for key management personnel (“KMP”), who are defined as
those persons having authority and responsibility for planning, directing and controlling the major activities of the company,
directly or indirectly, including any director (whether executive or otherwise) of the parent.
Following the appointment of Ms Cheryl Maley as CEO and Managing Director in January 2024 a review of the business was
undertaken, resulting in a refreshed company strategy. This has led to a change in KMP Executive members, compared to FY23.
From January 2024, the Board has assessed the KMP to be the Chair, Non-Executive Directors, CEO & Managing Director, and
Chief Financial Officer. These individuals are responsible for planning, directing and controlling the activities of the Group.
They participate in all meetings of the Board and its committees and have a central role in developing corporate strategy.
Previous KMP positions, VP Business Development and VP Development & Regulatory Affairs, are no longer classified as KMP
from January 2024 as their roles cover discrete areas of the Group’s operations, rather than the Group itself.
The table below outlines the KMP of the group during the financial year ended 30 June 2024. Profiles for each of the directors and
company secretary can be found at the beginning of the Directors’ Report.
Non-executive directors
R B Thomas
Non-executive Chairman
D J McIntyre
Non-executive Director
L Cheng
Non-executive Director
J R Davies
Non-executive Director
R Basser
Non-executive Director
KMP Executives
C Maley
Chief Executive Officer & Managing Director commenced 8 January 2024
J K Fairley
Chief Executive Officer & Managing Director retired 8 January 2024
J W Cahill
Chief Financial Officer & Company Secretary
J R Paull1
VP, Development & Regulatory Affairs
A Eglezos1
VP, Business Development
1. For the reasons explained above, J R Paul and A Eglezos are no longer assessed as KMP from January 2024.
2. Remuneration Governance
The Remuneration and Nomination Committee, consisting of at least three independent non-executive directors, advises the
Board on remuneration policies and practices generally, and makes specific recommendations on remuneration packages
and other terms of employment for non-executive directors, KMP executives and other senior executives. Where required,
external remuneration advice may be sought by the Remuneration and Nomination Committee or the Board.
Specifically, the Board approves the remuneration arrangements of the CEO, including awards made under the STI and LTI
plans, following recommendations from the Remuneration and Nomination Committee. The Board approves, having regard
to recommendations made by the CEO to the Remuneration and Nomination Committee, the level of remuneration, including
STI and LTI awards, for executives. The Board also sets the aggregate fee pool for non-executive directors (which is subject to
shareholder approval) and non-executive director fee levels.
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Starpharma Holdings Limited
The company’s remuneration structure aims to:
• attract and retain exceptional people to lead and manage the group and to support the internal development of executive
talent within the group, recognising that Starpharma is operating in a competitive global pharmaceutical industry environment;
• align KMP and executive remuneration structures to shareholder returns, as executives are set both short-term and long-term
performance targets, which are linked to the core activities necessary to build competitive advantages and shareholder value;
• motivate and reward the executive team whilst aligning performance elements/KPIs to the interests of shareholders; and
• create a respectful culture based on performance and innovation through appropriately structured individual assessments.
Information on the Remuneration and Nomination Committee’s role, responsibilities and membership is outlined in the charter
available at http://www.starpharma.com/corporate_governance.
Benchmarking
Starpharma undertakes extensive salary and remuneration benchmarking each year for executive staff and non-executive
positions. Starpharma benchmarks fixed and total remuneration against employment positions of comparable specialisation,
size, and responsibility within the industry. Fixed remuneration is supplemented by providing incentives in the form of cash and
equity (variable remuneration) to reward performance.
Performance reviews
At the beginning of a performance period all staff have KPIs set specific to their role. At the conclusion of the performance period,
a performance review against these KPIs is conducted, and this feeds into the annual salary review process. The performance
reviews consider behavioural and cultural aspects of performance, as well as objective planning and professional and personal
development. The objective of the salary review is to ensure that all employees are appropriately remunerated based on
performance, that remuneration is competitive within the relevant industry sector, and that increases in employees’ skills and
responsibilities are recognised. As part of the process, each employee’s performance is assessed against their pre-agreed
individual KPIs and/or business unit performance and corporate KPIs, and this assessment determines, subject to business
considerations such as cash availability, if an incentive award is payable and, if so, at what level. During the year, a performance
review of all staff took place in accordance with this process.
Use of remuneration consultants
If remuneration consultants are to be engaged to provide remuneration recommendations as defined in section 9B of the
Corporations Act 2001, they are to be engaged by and report directly to the Remuneration and Nomination Committee.
No remuneration consultants were engaged to provide such remuneration services during the financial year.
As part of the group’s commitment to continuous improvement, the Remuneration and Nomination Committee and the Board
consider comments made by shareholders and proxy advisers on remuneration-related issues. Members of the Remuneration
and Nomination Committee routinely engage with proxy advisers to discuss a range of governance and remuneration matters.
Trading in company securities
The trading of shares issued to participants under any of the company’s employee equity plans is governed by the
company’s securities dealing policy. All employees and directors are prohibited from entering into any hedging
arrangements over unvested securities and from margin lending on Starpharma securities. Further information regarding
the company’s dealing in securities policy is set out in the Corporate Governance Statement, and the policy is available at
http://www.starpharma.com/corporate_governance.
Clawback of remuneration
In the reasonable opinion of the Board, if a KMP executive has acted fraudulently or dishonestly, the Board may determine that
any equity right (including an exercisable, vested right) should lapse.
31
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Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
3. Non-executive Director Remuneration Policy
Determination of fees and the maximum aggregate fee pool
The Board seeks to set non-executive directors’ fees at a level which provides the group with the ability to attract and retain
non-executive directors of the highest calibre with relevant professional expertise. The fees also reflect the demands which are
made on, and the responsibilities of, the non-executive directors, whilst incurring a cost which is acceptable to shareholders.
Non-executive directors’ fees and the aggregate fee pool are reviewed annually by the Remuneration and Nomination Committee
against fees paid to non-executive directors in a group of comparable peer companies within the pharma/biotechnology
sector and relevant companies in the broader ASX-listed market. The Chairman’s fees are determined by the Remuneration
and Nomination Committee independently of the fees of non-executive directors based on the same role, again using
benchmarking data from comparable companies in the biotechnology sector. The Board is ultimately responsible for approving
any changes to non-executive director fees upon consideration of recommendations put forward by the Remuneration and
Nomination Committee.
The company’s constitution and the ASX listing rules specify that the non-executive directors’ maximum aggregate fee pool
shall be determined from time to time by a general meeting of shareholders. The latest determination was at the AGM held on
20 November 2014, when shareholders approved an aggregate fee pool of $550,000. The Board will not seek any increase
in the non-executive directors’ maximum fee pool at the 2024 AGM.
Fee policy
Non-executive directors’ fees consist of base fees and committee fees. The payment of committee fees recognises the additional
time, responsibility and commitment required by non-executive directors who serve on board committees. The Chairman of the
Board is a member of all committees but does not receive any committee fees in addition to the base fee.
Non-executive directors did not receive bonuses or forms of equity securities, or any performance-related remuneration
during the financial year. Statutory superannuation contributions are required under the Australian superannuation guarantee
legislation to be paid on any fees paid to Australian directors. There are no retirement allowances paid to non-executive directors.
The non-executive directors’ fees reported below include any statutory superannuation contributions.
Fees paid in FY24
The aggregate amount paid to non-executive directors for the year ended 30 June 2024 was $462,606 (2023: $436,119). The details
of remuneration for each non-executive director for the years ended 30 June 2024 and 30 June 2023 are outlined in the tables in
section 6.
From 1 July 2024, non-executive director fees will be subject to a modest increase of 2.5%, inclusive of a 0.5% increase in the
compulsory superannuation contribution, as set out below.
Annual non-executive directors’ fees
Proposed fees
from 1 July 2024
$
Actual fees to
30 June 2024
$
Board fees
Chair (no additional fees for serving on Board committees)
140,372
136,948
Base fee for other non-executive directors
73,328
71,540
Committee fees
Audit and Risk Committee
Chair
11,500
11,500
Member
5,500
5,500
Remuneration and Nomination Committee
Chair
11,500
11,500
Member
5,500
5,500
Remuneration Report continued
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Starpharma Holdings Limited
4. Executive Remuneration Policy
(a) Approach to setting and reviewing remuneration
The group aims to reward executives with a level and mix of remuneration appropriate to their position, skills, experience, and
responsibilities whilst being market competitive and enabling the company to retain staff and, at the same time, structuring
awards which conserve cash reserves.
The Remuneration and Nomination Committee, together with the Board, actively reviews the group’s remuneration structure
and benchmarks the overall package and proportion of fixed remuneration, short-term incentives and long-term incentives
against relevant industry comparators to ensure the policy objectives are met and are in line with good corporate practice for
Starpharma’s size, industry and stage of development. Remuneration levels are considered annually through the remuneration
review, which considers industry benchmarks and the performance of the group and the individual.
Starpharma undertakes remuneration benchmarking each year with reference to multiple industry peers, together with, where
appropriate, other benchmarking reports which apply to specific positions. A group of peer companies from within the pharma/
biotechnology sector are included in the benchmarking exercise. In the benchmarking conducted for FY24, the peer companies
included Bionomics, Clarity Pharmaceuticals, Clinuvel, Immutep, Impedimed, Imugene, Incannex Heatlhcare, Mayne Pharma,
Medical Developments International, Mesoblast, Monash IVF, Nanosonics, Neuren, Opthea, Paradigm Biopharmaceuticals,
Polynovo, Race Oncology, Rhythm Biosciences, Syntara, Telix, and 4DMedical. Starpharma typically reviews and develops
this benchmark list of peer companies annually to add and remove companies based on their current operations, size,
market capitalisation, and the complexity of their business. For some executive roles it may be necessary to add or modify
the composition of the peer group to ensure comparable roles are benchmarked.
In reviewing the benchmarking data and determining the level of CEO pay, the Board considers the experience and calibre
of its CEO in comparison to Starpharma’s industry peers, ensuring that remuneration is commensurate with talent, skills and
experience. There are no guaranteed base pay increases or bonuses in any executive contracts.
FY24 included a transition of CEO’s, with Dr Jackie Fairley retiring as CEO & Managing Director on 8 January 2024 and Ms Cheryl
Maley commencing on the same date. As a result of the transition, the outgoing and incoming CEO performance pay will be
assessed on a pro-rata basis. Ms Cheryl Maley has a maximum STI cash opportunity of $70,000 (as per the ASX announcement
dated 10 November 2023) for FY24. Retiring CEO Dr. Fairley had a maximum STI cash opportunity of $275,855 (as disclosed
in the Notice of Meeting for the November 2023 AGM), this opportunity was based on a full 12 months of executive service.
Other executives do not have a pre-specified maximum cash bonus entitlement; however, bonuses are awarded from a target
shared pool for executives as a percentage of total fixed remuneration, based on personal and business unit KPIs and subject
to cash availability. For FY25, as part of updates to the remuneration strategy, executives will have pre-specified maximum
cash bonus. This will be aligned to both company and individual performance objectives. Any bonus award is at risk and subject
to performance. The Remuneration and Nomination Committee considers that this approach provides flexibility in rewarding
superior executive performance and is appropriate for the size of the company at this time, enabling it to manage its cash
reserves as required. For FY24, the STI target cash bonus pool for executives other than the CEO was 24% of fixed remuneration
to align with the strategy to balance the STI ‘at risk’ portions of remuneration for other executives between cash and equity.
33
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Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
4. Executive Remuneration Policy continued
(b) Remuneration principles and strategy
The group’s executive remuneration strategy is designed to attract, motivate and retain high-performing individuals and align
the interests of executives with shareholders, recognising it is operating in the international pharmaceutical industry, and is
summarised below.
Remuneration strategy linkages to group objectives
Align the interests of executives with shareholders:
• The remuneration framework incorporates “at risk”
components, which are determined by performance,
through STI and LTI.
• Performance is assessed against a suite of measures
relevant to the success of the group and generating
growth and returns for shareholders.
Attract, motivate and retain high performing individuals:
• The remuneration offering is competitive for companies
of similar size and complexity within the industry
through benchmarking.
• The mix of short and longer-term remuneration
encourages retention and performance across multiple
years as appropriate for the lifecycle of the group.
Component
Vehicle
Purpose
Link to performance
Fixed remuneration
Base salary, superannuation
contributions and other
benefits (breakdown of
fixed remuneration is at
the executive’s discretion).
To provide competitive
fixed remuneration set
with reference to the role,
market and experience.
Group and individual
performance are
considered during the
annual remuneration review.
Short-term incentives (STI)
(Performance period
of less than 3 years)
Cash and equity
The equity instrument is
currently performance
rights, which is based on a
performance assessment,
with a 1-year performance
period and deferred vesting
of a further one year, subject
to continued employment.
Rewards executives for their
contribution to achievement
of business outcomes.
Deferred equity acts as a
retention tool and aligns with
interests of shareholders.
Allocation of cash bonuses
and vesting of equity linked
to internal KPIs, both business
unit and corporate, over
the medium term, which
are important drivers of
value and typical within the
biotechnology industry.
For example, achievement
of specified development,
clinical, regulatory and
commercial milestones.
Long-term incentives (LTI)
(Performance period
of 3 years or more)
Equity
The equity instrument is
currently performance
rights with a 3-year
performance period.
Rewards executives for their
contribution to the creation
of shareholder value over
the longer term, acts as a
retention tool and aligns with
interests of shareholders.
Vesting of grants are
dependent on internal
measures, both business unit
and corporate over the longer
term; and total shareholder
return (TSR) relative to the
S&P/ASX300 Index.
The target remuneration mix is outlined in the diagrams below.
Target Remuneration Mix
LTI Equity
40%
STI
Cash Bonus
& Equity
25%
Total Fixed
35%
CEO
LTI Equity
30%
STI
Cash Bonus
& Equity
20%
Total Fixed
50%
OTHER
KMP
EXEC
Remuneration Report continued
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Starpharma Holdings Limited
The STI and LTI components of remuneration are variable and are linked to pre-determined performance conditions, such as
KPIs, that are designed to reward executives based on the company’s performance, the performance of the relevant business
unit and demonstrated individual superior performance. The details are outlined in Section 5 of this report.
To achieve the target remuneration mix, the below performance pay structure was applied in FY24 and is consistent with the
prior year.
FIXED
STI – CASH
STI – EQUITY
LTI – EQUITY
Performance
Review
Performance
Review
Apr – June
AGM Date (shareholder approval)
Face Value
of Equity @
3−month
VWAP to
30 June
Year 1
July – June
Year 2
July – June
Year 3
July – June
Performance
Review
Vesting
Date
Deferral
Date
(c) Details of executive equity incentive plans
Short-Term Incentives (STI) – includes cash bonus and short-term equity
The group operates an annual STI program available to executives comprised of cash and equity incentives. The STI is ‘at risk’
remuneration and subject to achieving clearly defined KPIs.
Who participates?
Executives, comprising the CEO, Other KMP executives, and non-KMP executives.
How are STIs delivered?
Cash bonus and performance rights are both based on a 1-year performance period, with the
performance rights conditional upon a deferred vesting date of a further one year, subject to
continued employment.
Providing some rights that vest in the short term allows the company to preserve cash by offering
equity as a short-term incentive in addition to smaller cash bonuses. This is common practice for
companies at a similar stage of their lifecycle.
During FY24, the CEO and executives were awarded STI equity with a 1-year performance
period (1 July 2023 to 30 June 2024), with a deferred vesting date of 30 June 2025 dependent
on continued employment to the vesting date.
What is the STI opportunity? The CEO Cash STI opportunity for FY24 for Ms Maley was an amount of up to $70,000,
representing 25% of her Total Fixed Remuneration, on a full year basis. The award of STI for FY24
has been made on a pro-rata basis based on the achievement of Board approved KPIs.
KMP executives were awarded STI equity for the 1 July 2023 to 30 June 2024 performance period
based on the achievement of their pre-determined KPIs.
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Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
4. Executive Remuneration Policy continued
(c) Details of executive equity incentive plans continued
Starpharma Short-Term Incentives (STI) – includes cash bonus and short-term equity continued
What are the STI
performance conditions
for FY24?
Actual STI payments awarded to each executive depend on the extent to which they meet
specific KPIs set at the beginning of the period. The KPIs are typical of a biotechnology company
at Starpharma’s stage of development and may include corporate KPIs and business unit KPIs
relating to strategic and operational objectives. Details of the corporate KPIs for performance,
which were assessed during FY24, are explained in section 5 of the remuneration report. Given the
company’s stage of development, financial metrics (such as earnings per share) are not entirely
relevant in linking pay to performance.
The proportion of performance measures applicable in determining STI awards for the CEO
and other executives are noted in the table below:
Corporate KPIs
Business units KPIs
STI cash bonus
CEO 100%
Other executives 100%
STI performance rights
CEO 100%
Other executives 30%
Other executives 70%
Details regarding LTI performance conditions are contained on page 44.
How is performance
assessed?
For the CEO, at the end of each performance period (typically annually), after consideration of
actual performance against KPIs, the Remuneration and Nomination Committee recommends
for Board approval of the amount of STI to be paid from the maximum entitlement.
For executives other than the CEO, the Remuneration and Nomination Committee seeks
recommendations from the CEO and then makes recommendations to the Board.
When is performance
assessed and when are
awards paid or vested?
The performance period aligns with the financial year. Performance is assessed following the
end of the financial year to allow for timely disclosure of performance-related awards in the
annual remuneration report. This is usually within two months of the end of the financial year.
The STI cash component is paid approximately three months following the end of the financial year
and once the performance assessment review is complete.
For STI equity, a proportion of rights, based on the performance assessment, will be available
(deferred) to vest on 30 June of the following year, subject to continued employment at that date.
Any rights forfeited based on the performance assessment will be forfeited within the first three
months of the new financial year following the performance assessment.
Once performance rights have vested, executives can elect to convert vested rights into shares
during prescribed exercise windows throughout future periods. The Performance Rights Plan
was updated at the November 2023 AGM, so the maximum period for exercising vested rights is
now 5 years from the grant date.
Is performance against
KPIs disclosed?
Whilst the company’s policy is not to disclose commercially sensitive information, consistent with
best practice disclosure obligations, it will retrospectively disclose the achievement of corporate
KPIs to the extent commercially practicable.
Specific metrics are applied to each KPI to assist in the assessment undertaken for each
performance period. In some cases, the Board may exercise discretion to take account of events
and circumstances not envisaged when a KPI was set.
Contractual entitlement?
Only the CEO has an STI cash bonus entitlement, whereby the maximum amount achievable is set.
There is no predetermined STI equity entitlement. No other executive service agreements contain
any contractual entitlement to STI cash or equity.
Remuneration Report continued
36
Annual Report 2024
Starpharma Holdings Limited
What happens if
an executive leaves?
If an employee ceases employment, all unvested rights lapse. For a ‘good leaver’, the Board, at
its discretion, may pro-rata the vesting of performance rights up to the date the employment
agreement ends.
In certain circumstances, the Board may determine the accelerated vesting of rights if the
employee ceases employment due to death, illness, permanent disability, redundancy, or any other
exceptional circumstance approved by the Board. The Board determination is after considering
the portion of the performance period that has elapsed and the extent to which performance
conditions have been met.
What happens on a
change of control?
Board discretion, after considering the portion of the performance period that has elapsed
and the extent to which performance conditions have been met.
What happens in the case
of fraud/dishonesty?
If, in the opinion of the Board, an employee has acted fraudulently or dishonestly, the Board may
determine that any unvested right granted to that employee, or any vested right, not exercised,
would lapse.
Re-testing
There is no re-testing of KPIs in subsequent years if performance conditions are not met.
How is the conversion
of performance rights
to shares satisfied?
The conversion of performance rights is currently satisfied by the issue of new shares, rather than a
purchase of shares on market, to conserve the company’s cash reserves. This is common practice
for companies at a similar stage of their lifecycle. This is reviewed periodically, and purchases of
shares on market may be undertaken in the future if appropriate.
Are performance rights
eligible for dividends?
Performance rights – whether unvested or vested and not exercised, are not eligible to receive
dividends.
Long-Term Incentives (LTI) – Equity
Participation in these plans is at the Board’s discretion. For key appointments, an initial allocation of long-term equity incentives
may be offered as a component of the initial employment agreement. The LTI is ‘at-risk’ remuneration and subject to achieving
the relevant KPIs.
Who participates?
Executives, comprising the CEO, Other KMP executives, and non-KMP executives.
How are LTIs delivered?
Performance rights with a performance/vesting period of 3 years or more. The LTI performance
rights awarded during FY24 have 3-year performance periods for all executives.
What is the LTI opportunity? The CEO’s LTI opportunity for FY24 was 40% of total remuneration. For Other KMP executives,
the LTI opportunity for FY24 was 30% of total remuneration.
What are the LTI
performance conditions
for the performance
period to 30 June 2024?
Corporate KPIs reflect long-term (3-year) strategic, operational and financial management
objectives. These relate to key value creating events and significant milestones that are linked
to Starpharma’s business areas. For the 3-year performance period to 30 June 2024, these were:
• the monetisation of the VIRALEZE™, VivaGel® and DEP® drug delivery portfolios represented
by the generation of revenue, or value from assets sales(s), through the completion of a number
of commercial deals that build shareholder value; and
• optimisation of returns from VIRALEZE™ and VivaGel® revenue, development of new DEP®
candidates, completion of specified DEP® clinical trials, and/or the licensing (and/or asset
sales) of DEP® candidates.
Due to the commercially sensitive nature of the specific performance metrics within these
KPIs, Starpharma will retrospectively disclose the achievement of corporate KPIs to the extent
commercially practicable in the Annual Report.
In maintaining the link between executive remuneration outcomes and the returns to shareholders,
relative total shareholder return (TSR) is considered a relevant performance condition with
respect to LTIs. The relative TSR hurdle reflects Starpharma’s TSR compared to the S&P/ASX300
Accumulation Index (Index) and includes share price growth and any dividends and capital returns.
The Board has chosen this Index for the TSR comparator group as it provides an external, market-
based performance measure to which the company’s performance can be compared in relative
terms. The Index is considered appropriate as it provides a comparison of shareholder returns that
is relevant to investors and reflects the aspiration of the company.
37
Annual Report 2024
Starpharma Holdings Limited
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4. Executive Remuneration Policy continued
(c) Details of executive equity incentive plans continued
Starpharma Long-Term Incentives (LTI) – Equity continued
What are the LTI
performance conditions
for the performance
period to 30 June 2024?
continued
The Board considers that the Index is a more appropriate comparator than a customised group
of peer companies due to the inherent volatility of each of these companies, typical within the
biotechnology industry. In the past, the performance of Starpharma’s industry peers has been
particularly volatile, with a number of companies experiencing significant decreases in market
capitalisation, and a number going through some type of corporate activity (e.g. takeovers) or
are no longer ASX listed. Given that the relative TSR is measured over a 3-year period, the Index
is favoured as a more stable and appropriate comparator. The published S&P/ASX 200
Healthcare Index was also considered as a possible comparator, however, it was determined to be
inappropriate given its concentrated composition, including CSL Limited and other large service
oriented companies, such as private hospitals. Each year, the Remuneration and Nomination
Committee and the Board review the suitability of the Index as a comparator.
To achieve the full relative TSR performance condition, Starpharma’s TSR must achieve 10%
per annum (or 30% over 3 years) above the Index, which is considered a realistic stretch target.
The table below sets out the percentage of performance rights that will vest depending on the
company’s TSR compared to the Index over the relevant period.
Annualised Starpharma TSR compared
with the Index
Percentage of rights subject to the relative
TSR performance condition which vest
Below Index
0%
Equal to Index
50%
Between Index and Index + 9.99%
Pro rata basis from 51% to 99%
At least 10% per annum above Index
(or ≥ 30% over 3 years)
100%
For example, if the TSR of the Index is 10% per annum, then Starpharma would need to achieve
a TSR of 20% per annum or more for all of the relative TSR-related performance rights to vest.
The above hurdle recognises the return that investors expect when investing in the biotechnology
sector. The Board considers an additional return of 10% per annum (or 30% over 3 years) above
the Index to be a realistic stretch target for all relative TSR rights to vest.
The performance measures applicable in determining LTI awards for the CEO and other executives
and the relative proportions are noted in the table below.
Corporate KPIs
TSR
Business unit KPIs
CEO
70%
30%
N/A
Other executives
15%
15%
70%
For FY24, the Board considered 30% and 15% of LTI equity as the appropriate portion for relative
TSR for the CEO and other executives, respectively. In determining the percentages for FY24, the
Board considered input from investors and proxy advisers to arrive at a level that was considered
meaningful as a measure of performance, and sufficient to be relevant. Following a review of
the performance pay framework in FY24, the Board will increase the proportion of incentives
allocated to TSR in FY25 to further strengthen the alignment between executive performance pay
and shareholder returns.
The relative TSR performance measure does not allow for a portion of the award to vest at below
median performance, which is consistent with good market practice. Additionally, the Board
maintains absolute discretion in finalising remuneration outcomes for incentive-based awards to
the CEO and other executives. The Board may exercise its discretion (either up or down) to take into
account the impacts of external market conditions outside the control of management. The Board
is cognisant of ensuring fairness and that any exercise of discretion reinforces Starpharma’s strategy
and remuneration policy. Accordingly, in the event that the Index has performed particularly poorly,
the Board may exercise its discretion to prevent excessive executive awards in years of poor
shareholder returns.
Remuneration Report continued
38
Annual Report 2024
Starpharma Holdings Limited
How is performance
assessed?
At the end of each performance period, after consideration of actual performance against
KPIs, the Remuneration and Nomination Committee recommends the amount of LTIs to vest
to the CEO for approval by the Board. For executives other than the CEO, the Remuneration and
Nomination Committee seeks recommendations from the CEO and then makes recommendations
to the Board.
Relative TSR is calculated independently by a professional services firm with specialist expertise.
When is performance
assessed and when are
awards paid or vest?
The performance period aligns with the financial year. Performance is assessed following the end
of the financial year to allow for the timely disclosure of performance-related awards in the annual
remuneration report. This is usually within two months of the end of the financial year.
For LTI equity, the rights will vest on 30 September following the performance assessment.
Once vested, executives can elect to convert vested rights into shares during prescribed exercise
windows throughout future periods. Following changes to the company Performance Rights Plan
at the 2023 AGM, the maximum period for the exercise of vested rights is now 5 years from the
grant date.
Is performance against
KPIs disclosed?
Same as for STI.
Contractual entitlement?
There are no predetermined LTI equity entitlements.
What happens if an
executive leaves?
Same as for STI.
What happens on
a change of control?
Same as for STI.
What happens in the case
of fraud/dishonesty?
Same as for STI.
Re-testing
Same as for STI.
How is the conversion
of performance rights
to shares satisfied?
Same as for STI.
Are performance rights
eligible for dividends?
Same as for STI.
39
Annual Report 2024
Starpharma Holdings Limited
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Declaration
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Notes to the Consolidated
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Directors’
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Independent
Auditor’s Report
Shareholder
Information
Intellectual
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Corporate
Directory
4. Executive Remuneration Policy continued
(d) Grant of equity incentives to KMP executives in FY24
In FY24, the Board determined the number of rights granted for STI and LTI equity based on the face value of rights (see below)
and the target remuneration mix as set out on page 34.
Starpharma uses and reports face value for determining the allocation of equity as it provides transparency on the value of
the allocations compared with fair value. This practice reflects the increasingly accepted view by industry that presenting
remuneration equity at face value provides a more accurate representation of the true value of that equity and for users to
understand the value of these awards.
The face value of each right is based on the volume weighted average price (“VWAP”) of the company’s shares traded on the ASX
over the 3-month period to the beginning of the performance period. The 3-month period has been determined to be the appropriate
duration for the calculation of the VWAP as it limits any unintended consequences of short-term volatility in the company’s share price
and is consistent with the duration used in the calculation of TSR for the relative TSR performance condition.
The below table summarises the equity incentives granted to KMP executives in FY24:
KMP
executive
STI/LTI
Equity
Performance period
Performance
condition
Vesting date
Number
of rights
granted
Face value
of rights
granted1
Fair value
of rights
granted2,3
C Maley
STI equity
8 Jan 2024 – 30 Jun 2024
Corporate KPIs
30 Jun 2025
398,725
$58,134
$61,802
LTI equity
8 Jan 2024 – 30 Jun 2026
Corporate KPIs
30 Sep 2026
1,315,792
$191,842
$203,948
LTI equity
8 Jan 2024 – 30 Jun 2026
TSR
30 Sep 2026
563,911
$82,218
$64,063
J K Fairley
STI equity
1 Jul 2023 – 8 Jan 2024
Corporate KPIs
30 Jun 2025
667,441
$246,820
$90,105
J W Cahill
STI equity
5 Sep 2023 – 30 Jun 2025
Business unit and
corporate KPIs
30 Jun 2025
50,000
$10,680
$7,000
STI equity
1 Jul 2023 – 30 Jun 2024
Business unit and
corporate KPIs
30 Jun 2025
139,750
$51,680
$19,565
LTI equity
1 Jul 2023 – 30 Jun 2026
Business unit and
corporate KPIs
30 Sep 2026
475,150
$175,710
$66,521
LTI equity
1 Jul 2023 – 30 Jun 2026
TSR
30 Sep 2026
83,850
$31,008
$6,742
J R Paull
STI equity
5 Sep 2023 – 30 Jun 2025
Business unit and
corporate KPIs
30 Jun 2025
120,000
$25,632
$16,800
STI equity
1 Jul 2023 – 30 Jun 2024
Business unit and
corporate KPIs
30 Jun 2025
139,750
$51,680
$19,565
LTI equity
1 Jul 2023 – 30 Jun 2026
Business unit and
corporate KPIs
30 Sep 2026
475,150
$175,710
$66,521
LTI equity
1 Jul 2023 – 30 Jun 2026
TSR
30 Sep 2026
83,850
$31,008
$6,742
A Eglezos
STI equity
5 Sep 2023 – 30 Jun 2025
Business unit and
corporate KPIs
30 Jun 2025
120,000
$25,632
$16,800
STI equity
1 Jul 2023 – 30 Jun 2024
Business unit and
corporate KPIs
30 Jun 2025
139,750
$51,680
$19,565
LTI equity
1 Jul 2023 – 30 Jun 2026
Business unit and
corporate KPIs
30 Sep 2026
475,150
$175,710
$66,521
LTI equity
1 Jul 2023 – 30 Jun 2026
TSR
30 Sep 2026
83,850
$31,008
$6,742
1. Based on 3-month VWAP to the beginning of the performance period.
2. The grant date to calculate the fair value of the award under AASB2 is the AGM date when shareholders approved the grant of the rights.
3. The grant date to calculate the fair value of the award under AASB2 is the date when the performance rights were granted.
Remuneration Report continued
40
Annual Report 2024
Starpharma Holdings Limited
5. KMP Executive Remuneration Outcomes, Including Link to Performance
Given the company’s stage of development, financial metrics (such as profitability) are not necessarily an appropriate measure
of executive performance. The company’s remuneration policy aligns executive rewards with the interests of shareholders.
The primary focus is on growth in shareholder value through the achievement of development, regulatory and commercial
milestones, and therefore performance goals are not necessarily linked to typical financial performance measures utilised
by companies operating in other market segments. However, the Board recognises that share price performance is clearly
relevant to the extent that it reflects shareholder returns, and as such, Starpharma’s TSR relative to the S&P/ASX300 Index is
used as a relevant metric for portions of executive equity awards. Details of share price, earnings and the impact of share price
performance on the vesting of certain performance rights over the last 5 years are detailed in the table below. No dividends have
been paid in the last 5 years.
FY24
FY23
FY22
FY21
FY20
Closing share price 30 June
$0.10
$0.31
$0.74
$1.50
$1.13
Share price high
$0.43
$0.85
$1.55
$2.52
$1.43
Share price low
$0.09
$0.27
$0.62
$1.02
$0.62
Profit/(Loss) for the year ($M)
(8.2)
(15.6)
(16.2)
(19.7)
(14.7)
Number of performance rights forfeited by CEO based on
share price performance for the period ending 30 June (or
otherwise in the FY)
118,406
191,152
161,039
22,293
–
% of performance rights forfeited by CEO based on share
price performance (as a percentage of total performance
rights) for the period ending 30 June (or otherwise in the FY)
15%
22%
25%
3%
0%
Fixed remuneration
The increases in the total fixed remuneration package for individual KMP executives were between 2% and 5% for the year.
Performance-related pay
In the assessment of STI and LTI KPIs for the performance period ended 30 June 2024, the Board took into account the significant
achievements obtained in the performance periods and the effort and dedication required to accomplish these milestones.
The percentages of STI and LTI award for Dr Fairley and Ms Maley are different due to the transitional nature of the roles, the
difference in remuneration package for Ms Maley, and the emphasis the Board placed on achievement of certain objectives
noted on page 42. These achievements include those listed on pages 43 and 45. The summaries of STI and LTI awards in the
sections below exclude J R Paull and A Eglezos, who are no longer classified as KMP from January 2024.
Short-term incentives (STI)
Summary of STI performance pay related to FY24:
STI cash awarded
Performance period
Performance
condition
Maximum cash
bonus available
Cash bonus
awarded
% awarded
C Maley1
8 Jan 2024 – 30 Jun 2024
KPIs
$70,000
$56,000
80%
J K Fairley
1 Jul 2023 – 8 Jan 2024
KPIs
$183,9952
$103,037
56%
J W Cahill3
1 Jul 2023 – 30 Jun 2024
KPIs
N/A4
$67,000
N/A4
1. C Maley also received a $45,000 sign-on cash bonus in FY24.
2. J K Fairley retired as CEO on 8 January 2024. Her maximum cash bonus available to be awarded was prorated for FY24, based on period of service.
3. In addition to the performance-based cash bonus of $67,000, J Cahill is eligible for a cash-based retention payment of $50,000, payable
in October 2024, on the condition of continued employment.
4. Executives other than the CEO do not have a pre-specified maximum cash bonus entitlement for FY24; however, bonuses are awarded from
a target shared pool for executives. A maximum cash bonus is applicable for all executives for FY25.
41
Annual Report 2024
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5. KMP Executive Remuneration Outcomes, Including Link to Performance continued
Short-term incentives (STI) continued
STI equity
awarded
Performance period
Performance
condition
Maximum STI
rights available
STI rights
awarded
% awarded
C Maley
8 Jan 2024 – 30 Jun 2024
KPIs
398,725
318,980
80%
J K Fairley
1 Jul 2023 – 8 Jan 2024
KPIs
762,7891
427,162
56%
J W Cahill
1 Jul 2023 – 30 Jun 2024
KPIs
139,750
112,583
81%
1. J K Fairley retired as CEO on 8 January 2024. Her maximum STI rights available to be awarded was prorated based on period of service.
The Remuneration and Nomination Committee and the Board determined the above STI performance assessment for the
performance period 1 July 2023 to 30 June 2024, based on the annual review of actual performance against predetermined
corporate and business unit KPIs. These targets were set by the Remuneration and Nomination Committee and the Board
at the beginning of the performance period and align with the company’s strategic, operational and financial objectives.
STI equity awards for the CEO in FY24 were based on the assessed scorecard measures and weightings as disclosed below.
STI performance assessment
Performance period
1 July 2023 to
30 June 2024
Performance category
Metric
Weighting
Development, registration
and commercialisation
of VIRALEZE™
Continue commercial roll-out of VIRALEZE™ and further development
activities to support regulatory and marketing activities and sales, including
completing the post-market study.
9%
Regulatory and
commercialisation
activities for VivaGel® BV
Secure distribution rights from Mundipharma, sign distribution agreements
for new and existing markets, and optimise returns.
11%
Development and
commercialisation of
internal DEP® assets
Progress internal clinical DEP® programs through Phase II clinical
development (or sign a licence, as appropriate) with a focus on expediting
outcomes and building value, which may be through additional indications
and/or combinations.
Identify and advance additional internal DEP® product candidates through
preclinical development.
Secure new DEP® partnered programs and support and further develop
existing partnered DEP® programs and/or expanded field/products
and/or progress with new partnering deals/licences.
41%
Strategy Review, Capital
management, culture
and leadership
Undertake a forensic review of Company Strategy and update strategic
direction of the organisation. Manage the company’s finances in a prudent
manner to create value, increase recurrent revenues, maintain and enhance
the reputation for corporate responsibility and effectively manage
organisational culture and people to achieve superior performance.
39%
100%
Remuneration Report continued
42
Annual Report 2024
Starpharma Holdings Limited
In making this STI assessment, the Remuneration and Nomination Committee and the Board considered the following factors,
with other commercially sensitive matters also taken into account.
• VIRALEZE™ regulatory and commercial activities, including:
– Completed the post-market clinical study of VIRALEZE™ in COVID-19-positive patients in November 2023, generating
valuable clinical data to support the requirements for the transition to the new European Medical Device Regulations
(EU MDR), which will come into full effect in 2029, as well as ongoing marketing efforts.
– Advanced the application process for marketing authorisation in Australia.
– Continued to market VIRALEZE™ online through dedicated product webstores and Amazon UK in regions where the product
has already achieved registration.
• VivaGel® BV regulatory and commercial activities, including:
– Successfully achieved regulatory certification of VivaGel® BV under the new EU MDR in June 2024. Certification under
the EU MDR gives renewed certainty about the status of VivaGel® BV in Europe and is an important factor for potential
commercial partners in this region.
– Successfully negotiated an exit from the VivaGel® BV license with Mundipharma. Under the settlement agreement,
Starpharma regained commercial distribution rights to Mundipharma’s licensed territories and received a one-time cash
payment of $6.6M AUD from Mundipharma.
– Secured a sales and distribution agreement for the Middle East and North Africa Region with ITROM Pharmaceutical Group,
following the reversion of distribution rights from Mundipharma.
– Outcome of the VivaGel® BV formal dispute resolution process with the US Food and Drug Administration (FDA).
• Internal clinical-stage DEP® assets, including:
– Completed all three Phase II DEP® clinical programs, generating clinical validation of Starpharma’s DEP® technology
in drug delivery and cancer treatment.
– Reported the final results from the DEP® SN38 (DEP® irinotecan) clinical program in May 2024. These clinical results were
presented as an oral presentation at the highly competitive and world-renowned American Society of Clinical Oncology
(ASCO) Annual Meeting in June 2024. Earlier, in September 2023, interim data from the DEP® SN38 clinical study were
presented at the International Conference on Molecular Targets and Cancer Therapeutics, co-hosted by the American
Association of Cancer Research (AACR), National Cancer Institute (NCI) and European Organisation for Research and
Treatment of Cancer (EORTC).
– Reported the final results from the Phase II DEP® cabazitaxel study in October 2023. These results were presented in an oral
presentation at the ASCO Annual Meeting in June 2024. Data on the efficacy of DEP® cabazitaxel in gastro-oesophageal
cancers were also presented at the ASCO Gastrointestinal Cancers Symposium in January 2024.
– Reported the final results from the DEP® docetaxel clinical program, which involved monotherapy and combination therapy
arms, in December 2023.
• Develop the preclinical DEP® pipeline:
– Progressed internal DEP® development candidates, including DEP® radiopharmaceuticals and DEP® antibody-drug
conjugates (ADCs), through preclinical research.
– Reported the results of a preclinical study showing the benefits of Starpharma’s DEP® technology in radiodiagnostics
for cancer imaging applications in July 2023, and in May 2024, announced plans to advance the radiodiagnostic candidate
towards a first-in-human clinical study.
– Delivered presentations on the advantages of Starpharma’s dendrimer technology in radiopharmaceuticals at multiple
international industry conferences, including the AACR-NCI-EORTC International Conference of Molecular Targets and
Cancer Therapeutics in October 2023, the Targeted Radiopharmaceuticals Summit in Berlin in December 2023, and the
Society of Nuclear Medicine and Molecular Imaging (SNMMI) Annual Meeting in June 2024.
43
Annual Report 2024
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5. KMP Executive Remuneration Outcomes, Including Link to Performance continued
Short-term incentives (STI) continued
• Progressed existing and cultivated new partnered DEP® programs, including:
– Executed a new strategic partnership with Medicxi, a leading life sciences investment firm, to form Petalion Therapeutics.
This partnership is focused on developing a novel cancer therapy leveraging Starpharma’s dendrimer technology and
dendrimer science expertise.
– Continued existing partnered DEP® research programs, including MSD and Genentech. In these partnerships, Starpharma
provides dendrimer chemistry expertise and develops functionalised dendrimers for its partners to test.
– Partnered with the University of Queensland’s Hub for Advanced Manufacture of Targeted Radiopharmaceuticals
(AMTAR Hub) in July 2023, to advance the research and development of Starpharma’s targeted DEP® radiopharmaceuticals.
– Undertook business development activities and commercial discussions with new potential partners for DEP® drug delivery
programs in a number of research areas, including oncology and non-oncology areas, ADCs, and radiotheranostics.
Long-term incentives (LTI)
Summary of LTI performance pay related to FY24:
LTI equity
awarded
Performance period
Performance
condition
Maximum LTI
rights available
LTI rights
awarded
% awarded
J K Fairley1
1 Jul 2021 – 30 Jun 2024
KPIs
245,614
73,684
30%
1 Jul 2021 – 30 Jun 2024
TSR
105,263
–
0%
1 Jul 2022 – 30 Jun 2025
KPIs
354,203
35,420
10%
1 Jul 2022 – 30 Jun 2025
TSR
151,803
–
0%
1. J K Fairley retired as CEO on 8 January 2024. Her maximum LTI rights available to be awarded was prorated based on period of service.
The Remuneration and Nomination Committee and the Board determined the above award of LTI incentives for the performance
period 1 July 2021 to 30 June 2024 and 1 July 2022 to 30 June 2025, based on the annual review of actual performance against
predetermined corporate KPIs and TSR performance. These targets were set by the Remuneration and Nomination Committee
and the Board at the beginning of the performance period and align with the company’s strategic, operational and financial
objectives. LTI equity awards for the CEO in FY24 were based on the assessed scorecard measures, weightings and TSR,
as disclosed below.
LTI performance assessment
Performance period
1 July 2021 to
30 June 2024
Performance category
Metric
Weighting
Financial KPIs for
VIRALEZE™, VivaGel®
BV and DEP®
Monetisation of the VIRALEZE™, VivaGel® and DEP® Drug Delivery portfolios
represented by the generation of revenue, or value from asset sale(s), through
the completion of a number of commercial deals that build shareholder value.
40%
Business KPIs for
VIRALEZE™, VivaGel®
and DEP®
Optimisation of returns from VIRALEZE™ and VivaGel® revenue, represented
by programs to maximise product returns to Starpharma; development of new
DEP® candidates; completion of specified DEP® clinical trials; and/or licensing
(and/or asset sales) of DEP® candidates.
30%
Relative TSR
Starpharma’s TSR compared to the performance of the S&P/ASX300 Index over
a 3-year period.
30%
100%
Remuneration Report continued
44
Annual Report 2024
Starpharma Holdings Limited
In making this LTI assessment, the Remuneration and Nomination Committee and the Board considered the following factors,
with other commercially sensitive matters not disclosed also taken into account.
– Expanded the commercial availability of VIRALEZE™ nasal spray in Europe, Vietnam, the UK, Hong Kong and Macau, including
through online and retail channels.
– Signed sales and distribution arrangements for VIRALEZE™ nasal spray with commercial partners in the UK, Italy, Vietnam,
the Middle East, Hong Kong and Macau.
– Commenced and completed the VIRALEZE™ post-marketing study in the UK, generating valuable clinical data to support
the transition to the new EU MDR, which will come into effect in 2029.
– Generated additional preclinical data on SPL7013 and VIRALEZE™, demonstrating their effects in multiple strains of
SARS-CoV-2 in laboratory studies.
– Generated and reported tolerability data on VIRALEZE™ from a clinical study completed in Australia.
– Achieved new registrations of both VIRALEZE™ and VivaGel® BV.
– Successfully achieved regulatory certification of VivaGel® BV under the new EU MDR in June 2024. Certification under
the EU MDR gives renewed certainty about the status of VivaGel® BV in Europe and is an important factor for potential
commercial partners in this region.
– Successfully negotiated an exit from the VivaGel® BV license with Mundipharma. Under the settlement agreement,
Starpharma regained commercial distribution rights to Mundipharma’s licensed territories and received a one-time cash
payment of $6.6M AUD from Mundipharma.
– Secured a sales and distribution agreement for the Middle East and North Africa Region with ITROM Pharmaceutical Group,
following the reversion of distribution rights from Mundipharma.
– Completed the VivaGel® BV formal dispute resolution process with the US Food and Drug Administration (FDA).
– VivaGel® BV commercialisation expanded with new product launches in additional countries in Asia and Africa. A new VivaGel®
condom range was launched by Okamoto in Japan, targeting youth demographics.
– Completed all three in-house Phase II DEP® clinical trials of DEP® SN38, DEP® cabazitaxel, and DEP® docetaxel, and
reported the final results from all programs. Undertook ongoing commercial discussions with potential licensees
for each product.
– Presented the Phase II clinical trial results of DEP® SN38 and DEP® cabazitaxel at notable industry conferences, including
ASCO and AACR.
– Expanded the market potential for all internal clinical-stage DEP® candidates by adding new indications and progressing
value-adding combination studies to Phase II trials for: DEP® docetaxel plus gemcitabine and DEP® SN38 plus 5-FU/
leucovorin (‘FOLFIRI’).
– Developed and progressed DEP® radiotheranostic candidates, targeted and untargeted, including DEP® lutetium, DEP®
HER2-lutetium and DEP® zirconium, through preclinical research. Generated and released data highlighting the benefits
of DEP® applied to radiotheranostics.
– Developed and progressed DEP® ADCs candidates. Generated and reported data showcasing the benefits afforded
by DEP® in ADCs.
– Completed the preclinical development activities for DEP® gemcitabine.
– Partnered with Medicxi, a leading life sciences investment firm, to form Petalion Therapeutics. Starpharma will license
background intellectual property (IP) to develop a DEP® cancer therapy. Medicxi will contribute up to £20M to fund the
development of the asset, and in return for licensing its background IP, Starpharma will receive a 22.5% equity position
in Petalion.
– Signed and commenced two DEP® Research Agreements with MSD whereby Starpharma designs and synthesises
dendrimer-based ADCs and DEP® dendrimer conjugates and provides them to MSD for testing and characterisation.
– Signed and commenced a new DEP® Research Agreement with Genentech to evaluate DEP® drug conjugates and
expanded the DEP® Agreement within six months to include an additional DEP® program.
– Supported AstraZeneca’s development of AZD0466. AstraZeneca significantly expanded the clinical program for its
DEP® product, AZD0466, during the period. However, on 31 July 2023, Starpharma announced that AstraZeneca had made
the decision to discontinue the development of AZD0466, following an internal review of their haematology portfolio.
AstraZeneca confirmed the asymptomatic events leading to these decisions were not related to the dendrimer component
of AZD0466. Starpharma’s DEP® Licence Agreement with AstraZeneca remains in place.
45
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
5. KMP Executive Remuneration Outcomes, Including Link to Performance continued
Short-term incentives (STI) continued
TSR Assessment
The company’s total shareholder return (TSR) was benchmarked against the performance of the S&P/ASX300 Index for the
three-year performance period ending 30 June 2024. The company’s annualised TSR for the period was (60.2%) compared to
the S&P/ASX300 Index’s annualised TSR of 2.0%. As a result, 0% of rights subject to the TSR performance condition vested based
on the prescribed sliding scale on page 38. The TSR calculations were performed by an independent professional services firm.
The table below provides a summary of the achievement of annualised TSR performance.
Performance period
3 years to
30 June 2024
3 years to
30 June 2023
Starpharma annualised TSR
(60.2%)
(29.9%)
Index annualised TSR
2.0%
6.7%
Starpharma over/(under) performance of Index (annualised over 3 years)
(62.2%)
(36.6%)
% of relative TSR awarded
0%
0%
6. Details of Remuneration
Non-executive director remuneration
The below table details the remuneration for the non-executive directors in FY24 and FY23.
Non-executive directors
Financial Year
Base and
committee
fees (excluding
superannuation)
$
Superannuation
$
Total
$
R B Thomas
Chairman
2024
123,377
13,571
136,948
2023
121,267
12,733
134,000
R Basser1
2024
69,405
7,635
77,040
2023
24,442
2,566
27,008
D J McIntyre
2024
83,039
–
83,039
2023
81,000
–
81,000
L Cheng
2024
79,765
8,774
88,539
2023
75,581
7,936
83,517
J R Davies
2024
69,405
7,635
77,040
2023
67,873
7,127
75,000
Z Peach2
2024
–
–
–
2023
32,212
3,382
35,594
Total non-executive directors
2024
424,991
37,615
462,606
2023
402,375
33,744
436,119
1. Z Peach resigned from the Board on 29 November 2022.
2. R Basser was appointed to the Board on 20 February 2023.
Remuneration Report continued
46
Annual Report 2024
Starpharma Holdings Limited
KMP executive remuneration (statutory disclosure)
The below table details of the remuneration for the KMP executives in FY24 and FY23.
Short-term benefits
Post-
employ-
ment
Termi-
nation
benefits6
Long
service
leave7
Share-
based
payments
KMP executives1
Financial
Year
Salary
and fees2
$
Cash
bonus3,4
$
Non-
monetary
benefits5
$
Super-
annuation
$
$
$
Perfor-
mance
rights3
$
Total
$
C Maley8
CEO & Managing
Director
2024
244,086
101,000
53,735
13,700
–
422
62,821
475,764
2023
–
–
–
–
–
–
–
–
J K Fairley9
CEO & Managing
Director
2024
287,889
103,037
22,797
14,215
155,607
4,023
(75,529)
512,039
2023
534,289
140,850
41,115
25,296
–
15,593
313,601
1,070,744
J W Cahill10
CFO & Company
Secretary
2024
288,478
117,000
–
27,399
–
513
30,768
464,158
2023
71,250
50,000
–
6,324
–
123
–
127,697
N J Baade11
CFO & Company
Secretary
2024
–
–
–
–
–
–
–
–
2023
186,699
–
18,294
18,972
109,353
–
5
333,323
A Eglezos
VP Business
Development
2024
140,902
30,000
3,467
13,700
–
5,542
56,089
249,700
2023
266,873
73,000
7,260
25,296
–
7,091
141,895
521,415
J R Paull
VP Development &
Regulatory Affairs
2024
144,475
21,500
10,111
13,700
–
7,394
63,503
260,683
2023
229,994
75,000
44,909
34,296
–
9,298
167,099
560,596
Total KMP executives
2024
1,105,830
372,537
90,110
82,714
155,607
17,894
137,652
1,962,344
2023
1,289,105
338,850
111,578
110,184
109,353
32,105
622,600
2,613,775
1.
For the reasons explained in Section 1 of the Remuneration Report, the Board has assessed J R Paull and A Eglezos as no longer being KMP from
January 2024. Accordingly, the above table presents their remuneration for H1 FY24.
2. Executives may elect to salary sacrifice part of their total fixed remuneration package. Cash salary and fees represents gross salary earned less
any salary sacrifice amounts. The two forms of salary sacrifice in FY24 were leasing a motor vehicle under a novation arrangement, and the use
of a car park. These amounts are reported in non-monetary benefits, and these amounts for cash salary and fees may vary from one year to the
next, depending on the elections chosen.
3. All performance-related remuneration, including cash bonuses and performance rights granted, are determined to be an ‘at risk’ component
of total remuneration. As required by the Accounting Standards, share-based payments relate to the fair value of the performance rights
(which may include performance rights granted in prior years), rather than their face value. Where share-based payments expense is a negative
number, this reflects the reversal of prior year expensing on the forfeiture of performance rights.
4. The cash bonus reported includes FY24 performance related bonuses, and a retention payment of $50,000 for J W Cahill (to be paid in FY25),
as well as a $45,000 sign-on bonus (already paid to C Maley on commencement). For J R Paull and A Eglezos the cash bonus reported relates
to FY24 performance accrued during H1 FY24.
5. In addition to any salary sacrifice amounts for KMP executives, non-monetary benefits include one-off relocation and temporary
accommodation costs of $52,688 for C Maley, who relocated from Sydney for the role in FY24.
6. After a CEO transition period between January and March 2024, J K Fairley remained available until June 2024 (end of notice period) in an
as-needed advisory capacity. Services during the as-needed advisory period were not deemed substantive, and therefore payments
to the end of the notice period have been disclosed as termination benefits in FY24.
Termination benefits in FY23 relate to N J Baade’s annual leave and long service leave entitlements upon resignation.
7. Long service leave relates to amounts accrued during the year.
8. C Maley was appointed as Chief Executive Officer and Managing Director on 8 January 2024.
9. J K Fairley retired as Chief Executive Officer and Managing Director on 8 January 2024.
10. J W Cahill commenced employment on 3 April 2023.
11. N J Baade resigned on 31 March 2023.
47
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
6. Details of Remuneration continued
Details of KMP executive remuneration mix
The relative proportions of KMP executive remuneration for FY24 that are linked to performance and those that are fixed are
as follows:
Fixed
remuneration
At risk –
STI cash
At risk –
STI equity
At risk –
STI total
At risk –
LTI equity
CEO
Target
35%
25%
40%
C Maley
Actual
72%
13%
4%
17%
11%
J K Fairley
Actual
64%
20%
16%
36%
0%
Other KMP executives
Target
50%
20%
30%
J W Cahill
Actual
76%
16%
2%
18%
6%
J R Paull
Actual
68%
8%
6%
14%
18%
T Egelzos
Actual
65%
12%
6%
18%
17%
Details of remuneration: cash bonuses, shares, and performance rights
For each cash bonus and grant of equity included in the tables on pages 47 to 51, the percentage of the available bonus or grant
that was paid, or that vested, in the financial year, and the percentage that was forfeited because the person did not meet the
service and performance objectives, is set out below. Performance rights vest over the specified periods provided vesting
criteria are met. No rights will vest if the conditions are not satisfied, hence, the minimum value of the rights yet to vest is nil. The
maximum value of the rights yet to vest has been determined as the amount of the grant date fair value of the rights that is yet to
be expensed. KMP Executives were awarded a percentage of their maximum cash bonus entitlement as per the table on page 41.
Performance rights
Name
Grant date
fair value of
rights granted
during 20241,2
$
Financial year
granted
Vested
%
Forfeited
%
Financial years
in which rights
may vest
Maximum
fair value
yet to vest
$
C Maley
330,036
2024
0%
20%
FY25
33,481
2024
0%
0%
FY27
221,374
J K Fairley
90,105
2024
0%
36%
FY25
7,053
2023
0%
47%
FY24
–
2023
0%
96%
FY25
1,204
2022
0%
81%
FY25
9,074
2021
36%
64%
FY24
–
J W Cahill
99,828
2024
0%
19%
FY25
10,673
Remuneration Report continued
48
Annual Report 2024
Starpharma Holdings Limited
Performance rights
Name
Grant date
fair value of
rights granted
during 20241,2
$
Financial year
granted
Vested
%
Forfeited
%
Financial years
in which rights
may vest
Maximum
fair value
yet to vest
$
2024
0%
0%
FY27
50,734
2024
0%
0%
FY25
3,848
J R Paull
109,628
2024
0%
32%
FY25
3,514
2024
0%
0%
FY27
50,734
2024
0%
0%
FY25
9,235
2023
0%
30%
FY24
–
2023
0%
0%
FY26
62,115
2022
0%
43%
FY25
7,147
2021
66%
34%
FY24
–
A Eglezos
109,628
2024
0%
43%
FY25
1,460
2024
0%
0%
FY27
50,734
2024
0%
0%
FY25
9,235
2023
0%
39%
FY24
–
2023
0%
0%
FY26
56,866
2022
0%
47%
FY25
6,130
2021
63%
37%
FY24
–
1. The value at grant date calculated in accordance with AASB 2 Share-based Payments of performance rights granted during the year as part
of remuneration.
2. The maximum value of performance rights is determined at grant date and is amortised over the applicable vesting period. The amount which will
be included in a given KMP executive’s remuneration for a given year is consistent with this amortised amount. No performance rights will vest if
the conditions are not satisfied, hence the minimum value yet to vest is nil.
Details of related party transactions
Subsidiary, Starpharma Pty Ltd, paid $9,028 for consulting services in FY24 to Centre for Biopharmaceutical Excellence Pty Ltd,
which Starpharma non-executive director Dr Jeff Davies is also a director and shareholder. The consulting services were provided
by principals other than Dr Jeff Davies and were on normal commercial terms.
There are no other related party transactions with KMP that are not otherwise disclosed within this remuneration report.
49
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
7. KMP Executive Employment Agreements
Major provisions of the agreements relating to remuneration are set out below for KMP executives who are employed at the date
of this report.
C Maley
J W Cahill
Agreement term
No fixed term
No fixed term
Base salary per annum,
inclusive of superannuation
$550,000
$315,877
STI cash bonus
Up to $70,000 for FY24, on the
achievement of predetermined KPIs
$45,000 sign-on bonus payable upon
commencement on 8 January 2024
STI cash bonus payable subject to personal
and company achievement against Board
approved performance objectives
STI and LTI equity
Participates in STI and LTI equity plan,
subject to receiving any required or
appropriate shareholder approval
Participates in STI and LTI equity plan
The termination provisions for C Maley and J W Cahill are as follows:
Notice period
Payment in
lieu of notice
Treatment of equity STI
Treatment of LTI
Resignation
CEO – 6 Months
CFO – 3 months
Yes
Unvested awards forfeited
Unvested awards forfeited
Termination
for cause
None
None
Unvested awards forfeited
Unvested awards forfeited
Termination
without cause,
including
redundancy
CEO – 6 months
CFO – 3 months
CEO – 6 months
payment in lieu
of notice
CFO – 3 months
payment in lieu
of notice
Unvested awards lapse unless
the Board determines otherwise
after considering the portion of
the performance period that has
elapsed and the extent to which
performance conditions have
been met. Vesting of the rights
may be accelerated in this case.
Unvested awards lapse unless
the Board determines otherwise
after considering the portion of
the performance period that has
elapsed and the extent to which
performance conditions have
been met. Vesting of the rights
may be accelerated in this case.
Termination in
cases of death,
disablement
or other cause
approved by
the Board
N/A
N/A
Unvested awards lapse, unless
the Board determines otherwise
after considering the portion of
the performance period that has
elapsed and the extent to which
performance conditions have
been met. Vesting of the rights
may be accelerated in this case.
Unvested awards lapse, unless
the Board determines otherwise
after considering the portion of
the performance period that has
elapsed and the extent to which
performance conditions have
been met. Vesting of the rights
may be accelerated in this case.
There are no loans or other transactions to the KMP executives.
Remuneration Report continued
50
Annual Report 2024
Starpharma Holdings Limited
8. KMP Equity Holdings
Ordinary shares
The table below sets out the movements in shares held directly or indirectly by KMP during the year.
2024
Name
Balance at the
start of the year
Granted during
the year as
compensation
On exercise of
performance
rights during
the year
Other changes
during the year1
Balance at the
end of the year
Non-executive directors
R B Thomas
950,000
–
–
950,000
1,900,000
D J McIntyre
16,240
–
–
–
16,240
L Cheng
60,000
–
–
110,555
170,555
J R Davies
50,000
–
–
879,687
929,687
R Basser
–
–
–
71,428
71,428
KMP executives
C Maley2
–
–
–
125,000
125,000
J K Fairley3
4,055,434
–
–
–
4,055,434
J W Cahill4
–
–
–
–
–
J R Paull5
41,106
–
–
–
41,106
A Eglezos5
267,542
–
–
18,285
285,827
1. Other changes relate to purchases of shares on-market.
2. C Maley was appointed as Chief Executive Officer and Managing Director on 8 January 2024.
3. J K Fairley retired as Chief Executive Officer and Managing Director on 8 January 2024.
4. J W Cahill commenced as Chief Financial Officer and Company Secretary on 3 April 2023.
5. For the reasons explained in Section 1 of the Remuneration Report, J R Paul and A Eglezos are no longer assessed as KMP from January 2024.
Performance rights
The table below sets out the movements in rights over ordinary shares held by KMP during the year.
2024
Name
Balance at
the start of
the year
Granted
during the
year as
compensation
Exercised
during the
year
Other
changes
during the
year1
Balance at
the end of
the year
Vested and
exercisable
at the end
of the year
Total
unvested
KMP executives
C Maley2
–
2,278,428
–
–
2,278,428
–
2,278,428
J K Fairley3
6,280,125
667,441
–
(514,918)
6,432,648
4,458,798
1,973,850
J W Cahill4
–
748,750
–
–
748,750
–
748,750
J R Paull5
2,026,224
818,750
–
(88,994)
2,755,980
1,530,030
1,225,950
A Eglezos5
1,787,290
818,750
–
(93,740)
2,512,300
1,320,750
1,191,550
1. Other changes during the year relate to the forfeiture of rights.
2. C Maley was appointed as Chief Executive Officer and Managing Director on 8 January 2024.
3. J K Fairley retired as Chief Executive Officer and Managing Director on 8 January 2024.
4. J W Cahill commenced as Chief Financial Officer and Company Secretary on 3 April 2023.
5. For the reasons explained in Section 1 of the Remuneration Report, J R Paul and A Eglezos are no longer assessed as KMP from January 2024.
51
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
8. KMP Equity Holdings continued
The market value at vesting date of performance rights that vested during 2024 was $99,951 (2023: $338,461). The market value
is calculated using the opening share price on the respective vesting/exercise date or forfeit date.
No other shares were issued on the vesting of performance rights provided as remuneration to any of the groups’ directors
or KMP in the current year.
Dilutionary impact of performance rights on issue
As at 30 June 2024, there were 25,498,545 performance rights on issue, representing 6.2% of the 412,372,598 shares on issue.
As at 30 June 2024, there were 3,027,178 performance rights held by KMP, representing 0.7% of the 412,372,598 shares on issue.
9. Details of equity incentives affecting current and future remuneration
The terms and conditions of the grant of performance rights to the key management personnel of the group in the current year
or which impact future years are as follows:
Grant date
Vesting date
Number of
rights granted
Performance
measure1
Fair value
per right at
grant date
% vested
5 September 2023
30 June 2025
290,000
KPIs
$0.14
0
27 October 2023
30 June 2025
419,250
KPIs
$0.14
0
27 October 2023
30 September 2026
1,425,450
KPIs
$0.14
0
27 October 2023
30 September 2026
251,550
TSR
$0.08
0
29 November 2023
30 June 2025
667,441
KPIs
$0.14
64%
10 January 2024
30 June 2025
398,725
KPIs
$0.16
0
10 January 2024
30 September 2026
1,315,792
KPIs
$0.16
0
10 January 2024
30 September 2026
563,911
TSR
$0.11
0
1. Achievement of KPIs: The achievement of certain key business performance indicators linked to matters which the Board believes are key
drivers of shareholder value. Relative TSR (TSR): As set out on page 37 of the remuneration report.
End of remuneration report
Remuneration Report continued
52
Annual Report 2024
Starpharma Holdings Limited
Directors’ Report continued
Shares Under Rights
Unissued ordinary shares
There were 25,498,545 unissued ordinary shares of Starpharma Holdings Limited under the Employee Performance Rights Plan
as at 30 June 2024 and the date of this report. Please refer to Note 27(b) for a summary. Performance rights and the resultant
shares are granted for nil consideration. Performance rights and the resultant shares are granted for nil consideration.
Shares Issued on the exercise of vested rights
There were 11,098,655 ordinary shares of Starpharma Holdings Limited issued during the year ended 30 June 2024. No further
shares have been issued since that date. Please refer to Note 27(b) for a summary. The shares are issued for nil consideration.
Insurance of Officers
During the financial year, Starpharma Holdings Limited paid a premium to insure the company’s directors, executive officers and
related bodies corporate against certain liabilities and expenses.
In accordance with normal commercial practice, the disclosure of the amount of premium payable, and the nature of the liabilities
and expenses covered by the policy, is prohibited by a confidentiality clause in the relevant insurance contract.
Audit and Non-Audit Services
Details of the amounts paid or payable to the auditor (PricewaterhouseCoopers) for audit services provided during the year
are set out below. There were no non-audit services provided by the auditor during the financial year.
During the year, the following fees were paid or payable for services provided by the auditor (PricewaterhouseCoopers)
of the company, its related practices and non-related audit firms.
Assurance services
2024
$
2023
$
Audit or review of financial reports of the entity or any entity in the group under
the Corporations Act 2001
158,100
169,218
No other taxation or advisory services have been provided by the auditor in either the current or prior year.
53
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
Directors’ Report continued
Auditor’s Independence Declaration
A copy of the auditor’s independence declaration as required under section 307C of the Corporations Act 2001 is set out
on page 55.
Rounding of Amounts
The company is of a kind referred to in ASIC Corporations (Rounding Financial/Directors’ Reports) Instrument 2016/191, issued by
the Australian Securities and Investments Commission, relating to the “rounding off’’ of amounts in the directors’ report. Amounts in
the directors’ report have been rounded off in accordance with that Instrument to the nearest thousand dollars, or in certain cases,
the nearest dollar.
Auditor
PricewaterhouseCoopers continues in office in accordance with section 327 of the Corporations Act 2001.
This report is made in accordance with a resolution of the directors.
Robert B Thomas AO
Chairman
Melbourne, 22 August 2024
54
Annual Report 2024
Starpharma Holdings Limited
Auditor’s Independence Declaration
PricewaterhouseCoopers, ABN 52 780 433 757
2 Riverside Quay, SOUTHBANK VIC 3006, GPO Box 1331, MELBOURNE VIC 3001
T: 61 3 8603 1000, F: 61 3 8603 1999, www.pwc.com.au
Liability limited by a scheme approved under Professional Standards Legislation.
Auditor’s Independence Declaration
As lead auditor for the audit of Starpharma Holdings Limited for the year ended 30 June 2024, I
declare that to the best of my knowledge and belief, there have been:
(a)
no contraventions of the auditor independence requirements of the Corporations Act 2001 in
relation to the audit; and
(b)
no contraventions of any applicable code of professional conduct in relation to the audit.
This declaration is in respect of Starpharma Holdings Limited and the entities it controlled during the
period.
Brad Peake
Melbourne
Partner
PricewaterhouseCoopers
22 August 2024
55
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
Annual Financial Report
FOR THE YEAR ENDED 30 JUNE 2024
These financial statements are the consolidated financial statements for the consolidated entity consisting of Starpharma
Holdings Limited and its subsidiaries (collectively, “the group”). The financial statements are presented in dollars denominated
in Australian currency. Starpharma Holdings Limited is a public company limited by shares, incorporated and domiciled in the
state of Victoria, Australia.
Its registered office and principal place of business is:
Starpharma Holdings Limited
4-6 Southampton Crescent
Abbotsford, Victoria, 3067
Australia
A description of the nature of the group’s operations and its principal activities is included in pages 20 to 24, which are not part
of this financial report.
The financial statements were authorised for issue by the directors on 22 August 2024. The directors have the power to amend
and reissue the financial report.
Through the use of the internet, Starpharma ensures that corporate reporting is timely and complete. All recent press
releases, financial reports and other information are available on the group’s website ), as well as ASX announcements and
releases available via the Australian Securities Exchange (www2.asx.com.au/markets/trade-our-cash-market/historical-
announcements).
Consolidated Income Statement
57
Consolidated Balance Sheet
58
Consolidated Statement of Changes in Equity
59
Consolidated Statement of Cash Flows
60
Notes to the Consolidated Financial Statements
61
Consolidated Entity Disclosure Statement
85
Directors’ Declaration
86
Independent Audit Report
87
56
Annual Report 2024
Starpharma Holdings Limited
Consolidated Income Statement
FOR THE YEAR ENDED 30 JUNE 2024
Notes
30 June 2024
$’000
30 June 2023
$’000
Continuing operations
Revenue
5
9,756
4,208
Cost of goods sold
(632)
(1,120)
Other income
5
–
135
Research and product development expense
(net of R&D tax incentive)
6
(10,053)
(11,239)
Commercial and regulatory operating expense
6
(3,664)
(3,854)
Corporate, administration and finance expense
6
(3,572)
(3,768)
Loss before income tax
(8,165)
(15,638)
Income tax expense
7
–
–
Loss from continuing operations attributable to equity holders of the company
(8,165)
(15,638)
Other comprehensive income (loss)
–
–
Total comprehensive income (loss) for the period
(8,165)
(15,638)
Loss per share for loss from continuing operations attributable
to the ordinary equity holders of the company
$
$
Basic loss per share
26
($0.02)
($0.04)
Diluted loss per share
26
($0.02)
($0.04)
The above consolidated income statement should be read in conjunction with the accompanying notes.
57
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
Consolidated Balance Sheet
AS AT 30 JUNE 2024
Notes
30 June 2024
$’000
30 June 2023
$’000
Current assets
Cash and cash equivalents
8
23,360
35,180
Trade and other receivables
9
7,151
9,169
Inventories
10
2,408
2,773
Total current assets
32,919
47,122
Non-current assets
Property, plant and equipment
11
1,314
1,584
Right-of-use assets
14
2,581
3,380
Total non-current assets
3,895
4,964
Total assets
36,814
52,086
Current liabilities
Trade and other payables
12
4,013
7,667
Borrowings
13
775
4,778
Lease liabilities
14
796
744
Provision for employee benefits
15
1,050
1,281
Deferred income
5
28
3
Total current liabilities
6,662
14,473
Non-current liabilities
Lease liabilities
14
1,957
2,750
Provision for employee benefits
15
79
48
Total non-current liabilities
2,036
2,798
Total liabilities
8,698
17,271
Net assets
28,116
34,815
Equity
Contributed capital
16
240,750
240,715
Reserves
17
29,730
28,299
Accumulated losses
18
(242,364)
(234,199)
Total equity
28,116
34,815
The above consolidated balance sheet should be read in conjunction with the accompanying notes.
58
Annual Report 2024
Starpharma Holdings Limited
Consolidated Statement of Changes in Equity
FOR THE YEAR ENDED 30 JUNE 2024
Notes
Contributed
capital
$’000
Reserves
$’000
Accumulated
losses
$’000
Total equity
$’000
Balance at 1 July 2022
240,669
26,285
(218,561)
48,393
Loss for the year
–
–
(15,638)
(15,638)
Other comprehensive income (loss)
–
–
–
–
Total comprehensive income (loss)
for the year
–
–
(15,638)
(15,638)
Transactions with owners,
recorded directly in equity:
Employee share plans
16
46
–
–
46
Employee performance rights plan
17
–
2,014
–
2,014
Total transactions with owners
46
2,014
–
2,060
Balance at 30 June 2023
240,715
28,299
(234,199)
34,815
Loss for the year
–
–
(8,165)
(8,165)
Other comprehensive income (loss)
–
–
–
–
Total comprehensive income (loss) for the year
–
–
(8,165)
(8,165)
Transactions with owners,
recorded directly in equity:
Employee share plans
16
35
–
–
35
Employee performance rights plan
17
–
1,431
–
1,431
Total transactions with owners
35
1,431
–
1,466
Balance at 30 June 2024
240,750
29,730
(242,364)
28,116
The above consolidated statement of changes in equity should be read in conjunction with the accompanying notes.
59
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
Consolidated Statement of Cash Flows
FOR THE YEAR ENDED 30 JUNE 2024
Notes
30 June 2024
$’000
30 June 2023
(restated)
$’000
Cash flows from operating activities
Receipts from trade and other debtors (inclusive of GST)
8,412
3,085
Grant income and R&D tax incentives (inclusive of GST)
7,244
7,146
Payments to suppliers and employees (inclusive of GST)
(23,941)
(25,459)*
Interest received
1,532
1,194
Interest paid
(224)
(277)
Net cash outflows from operating activities
25
(6,977)
(14,311)
Cash flow from investing activities
Payments for property, plant and equipment
(89)
(621)
Proceeds from sale of financial assets
–
11
Net cash outflows from investing activities
(89)
(610)
Cash flow from financing activities
Proceeds from borrowings
886
1,037*
Repayment of borrowings
(4,888)
(259)*
Lease repayments
(745)
(695)
Net cash outflows from financing activities
(4,747)
83
Net increase (decrease) in cash and cash equivalents held
(11,813)
(14,838)
Cash and cash equivalents at the beginning of the year
35,180
49,918
Effects of exchange rate changes on cash and cash equivalents
(7)
100
Cash and cash equivalents at the end of the year
23,360
35,180
* The prior year cashflows from financing activities have been restated to reflect $1,037,000 proceeds from borrowings from an insurance
premium loan (premiums paid directly by the lender to the insurer) and $259,000 subsequent repayments of those borrowings. There is
a corresponding $778,000 increase in payments to suppliers due to the misclassification.
The above consolidated statement of cash flows should be read in conjunction with the accompanying notes.
60
Annual Report 2024
Starpharma Holdings Limited
Notes to the Consolidated Financial Statements
30 JUNE 2024
1. Material Accounting Policies
The principal accounting policies adopted in the preparation of these consolidated financial statements are set out below.
These policies have been consistently applied to all the years presented unless otherwise stated. The financial statements
are for the consolidated entity consisting of Starpharma Holdings Limited (“the company” or “parent entity”) and its subsidiaries
(collectively, “the group” or “the consolidated entity”).
(a) Basis of preparation
These general purpose financial statements have been prepared in accordance with Australian Accounting Standards and
Interpretations issued by the Australian Accounting Standards Board and the Corporations Act 2001. Starpharma Holdings
Limited is a for-profit entity for the purpose of preparing the financial statements.
(i) Compliance with IFRS
The consolidated financial statements of the group also comply with International Financial Reporting Standards (IFRS) as issued
by the International Accounting Standards Board (IASB).
(ii) New and amended standards adopted by the group
The group has adopted all standards which became effective for the annual reporting period commencing 1 July 2023. The
adoption of these standards did not have any impact on the amounts recognised in prior periods and are not expected to
significantly affect the current or future periods. The group has not elected to apply any pronouncements before their operative
date in the annual reporting period beginning 1 July 2023.
(iii) Historical cost convention
These financial statements have been prepared under the historical cost convention basis.
(iv) Critical accounting estimates
The preparation of financial statements requires the use of certain critical accounting estimates. It also requires management to
exercise its judgement in the process of applying the group’s accounting policies. The areas involving a higher degree of judgement
or complexity, or areas where assumptions and estimates are significant to the financial statements, are disclosed in note 3.
(v) Going concern
For the year ended 30 June 2024, the consolidated group has incurred losses from continuing operations of $8,165,000
(2023: $15,638,000) and experienced net cash outflows of $6,977,000 from operations (2023: $14,311,000), as disclosed in
the income statement and statement of cash flows, respectively. The consolidated group is in the development and early
commercialisation phase, and given the entity’s strategic plans, the directors are satisfied regarding the availability of working
capital for the period up to at least 31 August 2025. Accordingly, the directors have prepared the financial report on a going
concern basis in the belief that the consolidated entity will realise its assets and settle its liabilities and commitments in the
normal course of business and for at least the amounts stated in the financial report.
(b) Principles of consolidation and equity accounting
(i) Subsidiaries
Subsidiaries are all entities (including structured entities) over which the group has control. The group controls an entity when
the group is exposed to, or has rights to, variable returns from its involvement with the entity and has the ability to affect those
returns through its power to direct the activities of the entity. Subsidiaries are fully consolidated from the date on which
control is transferred to the group. They are deconsolidated from the date that control ceases. The group has one subsidiary,
Starpharma Pty Limited.
Intercompany transactions, balances and unrealised gains on transactions between group companies are eliminated. Unrealised
losses are also eliminated unless the transaction provides evidence of the impairment of the asset transferred. Accounting
policies of subsidiaries have been changed where necessary to ensure consistency with the policies adopted by the group.
(ii) Associates
Associates are all entities over which the group has significant influence but not control or joint control. This is generally the case
where the group holds between 20% and 50% of the voting rights. Investments in associates are accounted for using the equity
method of accounting after initially being recognised at cost. Details of associates are disclosed in note 24.
(c) Segment reporting
Operating segments are reported in a manner consistent with the internal reporting provided to the chief operating decision
maker. The chief operating decision maker, who is responsible for allocating resources and assessing performance of the
operating segments, has been identified as the Chief Executive Officer.
61
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
1. Material Accounting Policies continued
(d) Foreign currency translation
(i) Functional and presentation currency
Items included in the financial statements of each of the group’s entities are measured using the currency of the primary
economic environment in which the entity operates (‘the functional currency’). The consolidated financial statements are
presented in Australian dollars, which is the company’s functional and presentation currency.
(ii) Transactions and balances
Foreign currency transactions are translated into the functional currency using the exchange rates prevailing at the dates of the
transactions. Foreign exchange gains and losses resulting from the settlement of such transactions and from the translation at
year-end exchange rates of monetary assets and liabilities denominated in foreign currencies are recognised in profit or loss.
(e) Revenue recognition
The accounting policies for the group’s revenue from contracts with customers are explained in note 5.
(f) Leases
The group’s leasing policy is described in note 14.
(g) Cash and cash equivalents
For the purpose of presentation in the consolidated statement of cash flows, cash and cash equivalents include cash on hand,
deposits held with financial institutions, and other short-term, highly liquid investments that are readily convertible to known
amounts of cash and which are subject to an insignificant risk of changes in value. The amount of significant cash and cash
equivalents not available for use is disclosed in note 8.
(h) Trade receivables
Trade receivables are recognised initially at fair value and subsequently measured at amortised cost using the effective interest
method, less any allowance for expected credit loss. Trade receivables are generally due for settlement within 30 to 60 days.
They are presented as current assets unless collection is not expected for more than 12 months after the reporting date.
Collectability of trade receivables is reviewed on an ongoing basis. The group applies the AASB 9 simplified approach
to measuring expected credit losses which uses a lifetime expected loss allowance for all trade receivables and contract
assets. To measure the expected credit losses, trade receivables and contract assets are grouped based on shared credit risk
characteristics and the days past due. An expected credit loss is recognised when there is objective evidence that the group
will not be able to collect the relevant receivable.
(i) Inventories
Raw materials, work in progress and finished goods are stated at the lower of cost and net realisable value. Cost includes
expenditure incurred in acquiring the inventories and bringing them to their existing condition and location. Costs are assigned
to individual items of inventory on the basis of weighted average costs. Costs of purchased inventory are determined after
deducting rebates and discounts. Net realisable value is the estimated selling price in the ordinary course of business less the
estimated costs of completion and the estimated costs necessary to make the sale.
(j) Property, plant and equipment and leasehold improvements
Property, plant and equipment is stated at historical cost less depreciation. Historical cost includes expenditure that is directly
attributable to the acquisition of the items. Subsequent costs are included in the asset’s carrying amount or recognised as a
separate asset, as appropriate, only when it is probable that future economic benefits associated with the item will flow to the
group and the cost of the item can be measured reliably. The carrying amount of any component accounted for as a separate
asset is derecognised when replaced. All other repairs and maintenance are charged to profit or loss during the financial period
in which they are incurred. Depreciation is calculated using the straight-line method to allocate their cost or revalued amounts,
net of the residual values, over their estimated useful lives. The expected useful lives are two to 20 years. The assets’ residual
values and useful lives are reviewed, and adjusted if appropriate, at each balance sheet 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 are included
in profit or loss.
The cost of improvements to or on leasehold properties is amortised over the remaining term of the premises lease (being 3.5 years
at the reporting date) or the estimated useful life of the improvement to the group, whichever is shorter.
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
62
Annual Report 2024
Starpharma Holdings Limited
(k) Intangible assets
(i) Patents and licences
Costs associated with patents are expensed as incurred. Licences and acquired patents with a finite useful life are carried at cost
less accumulated amortisation and impairment losses. Amortisation is calculated using the straight-line method to allocate the
cost of licences and patents over the period of the expected benefit, which is up to 20 years. As at the reporting date no patents
or licences are recognised as intangible assets.
(ii) Research and development
Research and development expenditure is expensed as incurred, except that costs incurred on development projects, relating
to the design and testing of new or improved products, are recognised as intangible assets when it is probable that the project
will, after considering its commercial and technical feasibility, be completed and generate future economic benefits and its costs
can be measured reliably. To date, no research and development costs have been recognised as intangible assets.
(l) Trade and other payables
These amounts represent liabilities for goods and services provided to the group prior to the end of the financial year which
are unpaid. The amounts are unsecured and are usually paid within 30 to 45 days of recognition. Trade and other payables are
presented as current liabilities unless payment is not due within 12 months from the reporting date.
(m) Provisions
Provisions for legal claims, service claims, and make good obligations are recognised when the group has a present legal or
constructive obligation as a result of past events, and it is more probable than not that an outflow of resources will be required
to settle the obligation and the amount has been reliably estimated. Provisions are not recognised for future operating losses.
Where there are a number of similar obligations, the likelihood that an outflow will be required in settlement is determined by
considering the class of obligations as a whole. A provision is recognised even if the likelihood of an outflow with respect to
any one item in the same class of obligations may be small. Provisions are measured at the present value of management’s best
estimate for the expenditure required to settle the present obligation at the balance date. The discount rate used to determine
the present value reflects current market assessment of the time, value of money, and the risks specific to the liability. The increase
of the provision due to the passage of time is recognised as interest expense.
(n) Employee benefits
(i) Short-term obligations
Liabilities for wages and salaries, including non-monetary benefits, annual and long service leave expected to be settled within
12 months after the end of the period in which the employees render the related service are recognised in respect of employees’
services up to the period and are measured at the amounts expected to be paid when the liabilities are settled. The liability for
annual and long service leave is recognised in the provision for employee benefits. All other short-term employee benefit obligations
are presented as payables.
(ii) Superannuation benefits
Group companies make the statutory superannuation guarantee contribution in respect of each employee to their nominated
complying superannuation fund. In certain circumstances, pursuant to an employee’s employment contract, the group companies
may also be required to make additional superannuation contributions and/or agree to make salary sacrifice superannuation or
pension contributions in addition to the statutory guarantee contribution. The relevant entities’ legal or constructive obligation
is limited to the above contributions. Contributions to the employees’ superannuation are recognised as an expense as they
become payable.
63
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
1. Material Accounting Policies continued
(n) Employee benefits continued
(iii) Share-based payments
Share-based compensation benefits are offered to employees via an Employee Performance Rights Plan and an Employee
Share Plan ($1,000 Plan). Information relating to these plans is set out in note 27 and in the remuneration report under the
directors’ report.
The fair value of performance rights granted is recognised as an employee benefit expense with a corresponding increase in equity.
The fair value of employee services received, measured by reference to the grant date fair value, is recognised over the vesting
period. Depending on the performance measure of the right vesting, the fair value at grant date represents either a volume weighted
average price (VWAP) of shares leading up to the grant date, or a value calculated using a hybrid Monte-Carlo-trinomial option
pricing model taking into account the absolute total shareholder return (TSR) target, the term of the right, the share price at grant
date, the risk-free rate, the expected dividend yield, expected share price volatility, the volatility of the relevant index, and the
correlation between the share price and that index. The fair value excludes the impact of any non-market vesting conditions
(for example, profitability and sales growth targets). Non-market vesting conditions are included in assumptions about the number
of performance rights that are expected to become exercisable. At each reporting date, the entity revises its estimate of the
number of performance rights that are expected to become exercisable. The employee benefit expense recognised in each
period takes into account the most recent estimate. The impact of the revision to original estimates, if any, is recognised in
the consolidated income statement with a corresponding adjustment to equity.
Under the Employee Share Plan ($1,000 Plan), shares are issued to employees for no cash consideration and vest at the earlier
of three years or cessation of employment. On this date, the market value of the shares issued is recognised as an employee
benefits expense with a corresponding increase in equity.
(iv) Bonus payments
The group recognises a liability and an expense for employee bonuses based on a formula that takes into consideration
performance criteria that have been set. The group recognises a provision where contractually obliged or where there is a past
practice that has created a constructive obligation.
For non-cash incentives where equity is granted, refer to note 27 and the remuneration report under the directors’ report.
(o) Borrowings
Borrowings are initially recognised at fair value, net of transaction costs incurred. Borrowings are subsequently measured at
amortised cost. Any difference between the proceeds (net of transaction costs) and the redemption amount is recognised
in profit or loss over the period of the borrowings using the effective interest method.
Borrowings are removed from the balance sheet when the obligation specified in the contract is discharged, cancelled or
expired. The difference between the carrying amount of a financial liability that has been extinguished or transferred to another
party and the consideration paid, including any non-cash assets transferred or liabilities assumed, is recognised in profit or loss
as other income or finance costs.
Borrowings are classified as current liabilities unless the group has an unconditional right to defer settlement of the liability for
at least 12 months after the reporting period.
(p) Contributed equity
Ordinary shares are classified as equity. Incremental costs directly attributable to the issue of new shares or performance
rights are shown in equity as a deduction, net of tax, from the proceeds. Incremental costs directly attributable to the issue of
new shares or performance rights for the acquisition of a business are not included in the cost of the acquisition as part of the
purchase consideration.
(q) Dividends
Provision is made for the amount of any dividend declared, being appropriately authorised and no longer at the discretion
of the entity, on or before the end of the reporting period but not distributed at the end of the reporting period.
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
64
Annual Report 2024
Starpharma Holdings Limited
(r) Earnings per share
(i) Basic earnings per share
Basic earnings per share is calculated by dividing the profit attributable to owners of the company, excluding any costs of servicing
equity other than ordinary shares, by the weighted average number of ordinary shares outstanding during the financial year,
adjusted for bonus elements in ordinary shares issued during the year and excluding treasury shares.
(ii) Diluted earnings per share
Diluted earnings per share adjusts the figures used in the determination of basic earnings per share to take into account the
after income tax effect of interest and other financing costs associated with dilutive potential ordinary shares and the weighted
average number of additional ordinary shares that would have been outstanding assuming the conversion of all dilutive potential
ordinary shares.
(s) Goods and services tax (GST)
Revenues, expenses and assets are recognised net of the amount of associated GST unless the GST incurred is not recoverable
from the taxation authority. In this case, it is recognised as part of the cost of acquisition of the asset or as part of the expense.
Receivables and payables are stated inclusive of the amount of GST receivable from, or payable to, the taxation authority and are
included with other receivables or payables in the balance sheet. Cash flows are presented on a gross basis. The GST components
of cash flows arising from investing or financing activities which are recoverable from, or payable to, the taxation authority are
presented as operating cash flows.
(t) Rounding of amounts
The company is of a kind referred to in ASIC Corporations (Rounding Financial/Directors’ Reports) Instrument 2016/191, issued
by the Australian Securities and Investments Commission, relating to the ‘rounding off’ of amounts in the financial statements.
Amounts in the financial statements have been rounded off in accordance with that Instrument to the nearest thousand dollars,
or in certain cases, the nearest dollar.
(u) Parent entity financial information
The financial information for the parent entity disclosed in note 28 has been prepared on the same basis as the consolidated
financial statements, except as set out below.
(i) Investments in subsidiaries, associates and joint venture entities
Investments in subsidiaries, associates and joint venture entities are accounted for at cost in the financial statements of the
parent entity. Dividends received from associates are recognised in the parent entity’s profit or loss when its right to receive
the dividend is established.
(ii) Share-based payments
The grant by the parent entity of rights over its equity instruments to the employees of subsidiary undertakings in the group
is treated as a capital contribution to that subsidiary undertaking. The fair value of employee services received, measured
by reference to the grant date fair value, is recognised over the vesting period as an increase to investment in subsidiary
undertakings, with a corresponding credit to equity.
65
Annual Report 2024
Starpharma Holdings Limited
Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
2. Financial Risk Management
The group’s activities expose it to a variety of financial risks; including market risk, credit risk and liquidity risk. The group’s overall
financial risk management program focuses on the unpredictability of financial markets and seeks to minimise potential adverse
effects on the financial performance of the group. The Chief Executive Officer, and Chief Financial Officer & Company Secretary,
under the guidance of the Audit and Risk Committee and the Board, have responsibility for the financial risk management program.
(a) Market risk
(i) Foreign exchange risk
Foreign exchange risk arises when future commercial transactions and recognised assets and liabilities are denominated in a
currency that is not the entity’s functional currency. The group operates internationally and is exposed to foreign exchange risk
arising from currency exposures to major currencies including United States dollars (US$) and Great British pounds (£).
On the basis of the nature of these transactions, the group does not use derivative financial instruments to hedge such
exposures but maintains cash and deposits in Australian dollars, United States dollars and Great British pounds. The directors
regularly monitor the potential impact of movements in foreign exchange exposure.
The exposure to foreign currency risk at the reporting date calculated using the closing exchange rate as at 30 June 2024 for
US$ of $0.6651 and for £ of $0.5262 was as follows:
30 June 2024
US$
$’000
30 June 2023
US$
$’000
30 June 2024
£
£’000
30 June 2023
£
£’000
Cash and cash equivalents
26
328
21
510
Trade and other receivables
340
382
1
–
Trade and other payables
46
171
778
2,363
Group sensitivity
The group is mainly exposed to US$ and £ on foreign currencies held, receivable and payable. The following table details the
group’s sensitivity to a 10% increase and decrease in the Australian dollar against the US$ or £. A positive number indicates
a favourable movement; that is an increase in profit or reduction in the loss.
Impact on profit/(loss) on a movement of
30 June 2024
$’000
US$
30 June 2023
$’000
US$
30 June 2024
£’000
£
30 June 2023
£’000
£
Australian dollar strengthens (increases)
against the foreign currency by 10%
(44)
(74)
131
321
Australian dollar weakens (decreases)
against the foreign currency by 10%
54
90
(160)
(393)
(ii) Cash flow interest rate risk
The group holds interest bearing assets and therefore the income and operating cash flows are exposed to market interest rates.
At the end of the reporting period, the group had the following value of term and at call deposits. Refer to note 8 for
additional information.
30 June 2024
$’000
30 June 2023
$’000
Term deposits and deposits at call
22,829
33,519
Group sensitivity
At 30 June 2024, if interest rates changed by 50 basis points (0.50%) either higher or lower from the year end rates with all other
variables held constant, group profit for the year would have been $114,000 higher or lower (2023 – change of 50 bps: $168,000
higher/lower) due to either higher or lower interest income from cash or cash equivalents.
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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(b) Credit risk
Credit risk is managed on a group basis. Credit risk arises from cash and cash equivalents with banks and financial institutions,
as well as credit exposures from sales and distribution, product supply, licensing and royalty agreements. Credit risk for cash and
deposits with banks and financial institutions is managed by maximising deposits held under major Australian banks. All cash and
deposits are held with the National Australia Bank and Commonwealth Bank of Australia. Other than government grants, tax incentives
and taxes receivable, third party receivables largely consist of customer receivables from leading multinational organisations.
(c) Liquidity risk
Prudent liquidity risk management implies maintaining sufficient cash reserves and marketable securities. The directors regularly
monitor the cash position of the group, giving consideration to the level of expenditure and future capital commitments.
(d) Fair value estimation
The fair value of financial assets and financial liabilities must be estimated for recognition and measurement for disclosure
purposes. The carrying value less impairment provision of trade receivables and payables are assumed to approximate their fair
values due to their short-term nature. The fair value of financial liabilities for disclosure purposes is estimated by discounting the
future contractual cash flows at the current market interest rate that is available to the group for similar financial instruments.
3. Critical Accounting Estimates and Judgements
Estimates and judgements are continually evaluated and are based on historical experience and other factors, including expectations
of future events that may have a financial impact on the entity and that are believed to be reasonable under the circumstances.
The group makes estimates and assumptions concerning the future. The resulting accounting estimates will, by definition,
seldom equal the related actual results. The estimates and assumptions that have a significant risk of causing material
adjustment to the carrying amounts of assets and liabilities within the next financial year are discussed below.
(i) Australian Government Research & Development Tax Incentive
The group’s eligible research and development activities qualify for the Australian Government R&D Tax Incentive. Management has
assessed these activities and expenditure to determine which are likely to be eligible under the incentive scheme. For the period
to 30 June 2024, the group has recorded a contra research and development expense of $5,527,000 (2023: $7,631,000). The total
R&D Tax Incentive receivable recorded at 30 June 2024 is $5,527,000 (2023: $7,244,000).
4. Segment Information
The group has determined that on the basis of internal reporting and monitoring to the Chief Executive Officer, who is the chief
operating decision maker, the group operates in one business segment, being the discovery, development and commercialisation
of dendrimers for pharmaceutical, life science and other applications.
5. Revenue and Other Income
30 June 2024
$’000
30 June 2023
$’000
Revenue from contracts with customers
8,289
2,939
Interest revenue
1,467
1,269
Total revenue from continuing operations
9,756
4,208
Other income
–
135
Total revenue and other income from continuing operations
9,756
4,343
Disaggregation of revenue from contracts with customers
Total revenue from contracts with customers for the year was $8,289,000 (2023: $2,939,000) and included a nonrecurring
$6,553,000 from the commercial settlement and termination of the VivaGel® BV license and supply agreement with Mundipharma
in August 2023. Revenue from contracts with customers also includes product sales, royalty, and research revenue from
commercial partners.
67
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Directors’
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Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
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Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
5. Revenue and Other Income continued
Assets and liabilities related to contracts with customers
The group has recognised the following current assets and current liabilities related to contracts with customers:
30 June 2024
$’000
30 June 2023
$’000
Trade and other receivables
588
604
Contract liabilities
(28)
(3)
Customer trade and other receivables as at 30 June 2024 are $588,000.
Performance obligations
Revenue is recognised when the company satisfies a performance obligation by transferring control of the promised good or
service to a customer at an amount that reflects the consideration to which the company expects to be entitled in exchange
for the goods or services. Information about the company’s performance obligations is summarised below:
(i) Licensing revenue and royalties
Typically, a licence granted by the company provides the customer with the right to use, but not own, the company’s intellectual
property as it exists at the point in time the licence is granted. The company may receive signature payments, milestone payments
for specific development (such as clinical or regulatory) or commercial-based outcomes and/or sales-based royalties as
consideration for the licence. The performance obligation(s) for a licence are usually satisfied upon, or soon after, the granting
of the licence to the partner. Signature payments are normally fixed, where-as development and commercial milestones are
variable consideration as they are dependent on the achievement of certain events in the future. The company’s estimate of
variable consideration will only be recognised to the extent it is highly probable that a significant revenue reversal will not occur
in future periods.
Royalties based on sales of product are recognised when the customer’s sales of product occur. Where consideration includes
guaranteed minimum royalties, they are recognised when the licence is granted or when they are no longer subject to constraint.
Milestones payments are generally due within 30 to 60 days from timing of the milestone event. Royalties are generally due
30 to 60 days after the end of the defined royalty reporting period.
(ii) Product sales
The performance obligation is satisfied upon delivery of the goods. Payment is on normal commercial terms, which may include
prepayment and/or payment within 30 to 60 days from delivery. Some contracts provide customers with a right of return for product
non-conformance, or discounts based on product shelf-life, which may give rise to variable consideration subject to constraint.
(iii) Research revenue
The performance obligation is satisfied over time upon completion of outlined deliverables and payment is generally due within
30 to 60 days of achievement of each deliverable.
6. Expenses
30 June 2024
$’000
30 June 2023
$’000
Loss from continuing operations before income tax expense includes the following items:
R&D tax incentive (contra expense)1
(5,527)
(7,631)
Employee benefits expenses (including share-based payments)
9,659
10,334
Depreciation of property, plant and equipment
316
392
Depreciation of right-of-use assets
799
802
1. Included within the research and product development expense line item in the consolidated income statement.
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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7. Income Tax Expense
30 June 2024
$’000
30 June 2023
(restated*)
$’000
(a) Income tax expense/(credit)
Current tax/deferred tax
–
–
Total income tax expense
–
–
Income tax attributable to continuing operations
–
–
(b) Numerical reconciliation of income tax expense to prima facie tax payable
Loss from continuing operations before income tax expense
(8,165)
(15,638)
Tax at the Australian tax rate of 25% (2023: 25%)
(2,041)
(3,909)
Tax effect of amounts which are not deductible (taxable) in calculating taxable income:
Eligible expenses claimed under R&D tax incentive
1,795
2,255
Share-based payments
367
515
Taxable capital gains
3,141
–
Sundry items
145
(53)
Future income tax benefits not brought to account
(3,407)
1,192
Income tax expense
–
–
(c) Tax losses
Unused tax losses for which no deferred tax asset has been recognised
(as recovery is currently not probable)
121,875
135,502
Potential tax benefit
30,469
33,875
(d) Unrecognised temporary differences
Temporary differences for which no deferred tax asset has been recognised
(as recovery is currently not probable)
17,950
5,068
Unrecognised deferred tax relating to the temporary differences
4,487
1,267
(e) Deferred tax liabilities
Unrecognised deferred tax liabilities relating to the above temporary differences:
Lease right-of-use assets
645
845
Property, plant and equipment
258
297
Sundry items
3
4
Total deferred tax liabilities
906
1,146
Set-off of deferred tax assets pursuant to set-off provisions
(906)
(1,146)
Net deferred tax liabilities
–
–
* The prior year has been restated to reflect a 25% (previously 30%) Australian tax rate. The 25% “base rate entity company tax rate” is applicable
as the group’s current aggregated turnover and passive income is below the prescribed level.
Deferred tax assets and deferred tax liabilities have been set off as there is a legally recognised right to set off current tax assets
and liabilities, and the deferred tax assets and liabilities relate to income taxes levied by the relevant tax authority. Deferred tax
assets are mainly attributable to unused tax losses. Potential future income tax benefits attributable to tax losses carried forward
have not been brought to account at 30 June 2024 because the directors do not presently believe that it is appropriate to regard
realisation of the future income tax benefit as probable. Similarly, future benefits attributable to net temporary differences have
not been brought to account as the directors do not regard the realisation of such benefits as probable.
Realisation of the benefit of tax losses would be subject to the group satisfying the conditions for deductibility imposed by tax
legislation and no subsequent changes in tax legislation adversely affecting the group. The group has made an assessment
as to the satisfaction of deductibility conditions at 30 June 2024, which it believes will be satisfied.
69
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Notes to the Consolidated
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Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
8. Current Assets – Cash and Cash Equivalents
30 June 2024
$’000
30 June 2023
$’000
Cash at bank and on hand
531
1,661
Term deposits and deposits at call
22,829
33,519
23,360
35,180
Cash at bank and on hand
The cash at bank and on hand is non-interest bearing, and includes foreign currencies held.
Term deposits and deposits at call
The term deposits have maturities of three months or less. Funds in deposits at call allow the group to withdraw funds
on demand.
Deposits not available
There is $1,256,000 (2023: $1,198,000) of term deposits not available for use due to funds being utilised as security for a bank
guarantee on the company’s property lease, and for a finance lease facility.
Interest rate risk
Current receivables are non-interest bearing.
Floating
interest
rate
Fixed interest maturing
Non-
interest
bearing
30 June 2024
Notes
$’000
1 year
or less
$’000
1 to 5 years
$’000
More than
5 years
$’000
$’000
Total
$’000
Contractual
cash flows
Financial assets
Cash and deposits
8
2,220
20,609
–
–
531
23,360
–
Receivables
9
–
–
–
–
7,151
7,151
7,151
2,220
20,609
–
–
7,682
30,511
7,151
Weighted average
interest rate
4.5%
5.0%
–%
–%
–%
Financial liabilities
Payables
12
–
–
–
–
4,012
4,012
4,012
Lease liabilities
14
–
796
1,957
–
–
2,753
2,753
Borrowings
13
–
775
–
–
–
775
775
–
1,571
1,957
–
4,012
7,540
7,540
Weighted average
interest rate
–%
3.5%
4.3%
–%
–%
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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Floating
interest
rate
Fixed interest maturing
Non-
interest
bearing
30 June 2023
Notes
$’000
1 year
or less
$’000
1 to 5 years
$’000
More than
5 years
$’000
$’000
Total
$’000
Contractual
cash flows
Financial assets
Cash and deposits
8
3,022
30,498
–
–
1,660
35,180
N/A
Receivables
9
–
–
–
–
9,169
9,169
9,169
3,022
30,498
–
–
10,829
44,349
9,169
Weighted average
interest rate
4.3%
4.7%
–%
–%
–%
Financial liabilities
Payables
12
–
–
–
–
7,667
7,667
7,667
Lease liabilities
14
–
744
2,750
–
–
3,494
3,494
Borrowings
13
4,000
778
–
–
–
4,778
4,778
4,000
1,522
2,750
–
7,667
15,939
15,939
Weighted average
interest rate
4.3%
3.6%
4.2%
–%
–%
9. Current Assets – Trade and Other Receivables
30 June 2024
$’000
30 June 2023
$’000
Trade and grant receivables
6,095
7,857
Interest receivables
64
128
Prepayments
811
934
Other receivables
181
250
7,151
9,169
Trade and grant receivables
Trade and grant receivables primarily comprise of $5,527,000 (2023: $7,244,000) of eligible expenditure reimbursable under
the Australian Government’s R&D tax incentive scheme, with the balance related to customer receivables. Customer receivables
are subject to normal terms of settlement within 30 to 60 days.
Prepayments
Prepayments primarily relate to insurance premiums paid in advance.
Other receivables
Other receivables comprise GST/VAT and other taxes refundable and sundry debtors, and are subject to normal terms
of settlement within 30 to 90 days.
71
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Consolidated Financial
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Notes to the Consolidated
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Directors’
Declaration
Independent
Auditor’s Report
Shareholder
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Property Report
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9. Current Assets – Trade and Other Receivables continued
Credit risk
The group considers that there is no significant credit risk with respect to trade and other receivables. Grant receivables are with
government bodies and trade receivables are from large companies.
Impaired receivables
As at 30 June 2024, there were no material trade and grant receivables that were past due (2023: nil). The group applies the
accounting policy in note 1(h) to trade receivables. Under the expected credit loss model, no receivables are considered
impaired at 30 June 2024 (2023: nil).
10. Inventories
Current assets
30 June 2024
$’000
30 June 2023
$’000
Raw materials
2,317
2,578
Finished goods
91
195
2,408
2,773
Assigning costs to inventories
The costs of individual items of inventory are determined using the weighted average cost method. See note 1(i) for detail
on the group’s accounting policy for inventories.
Amounts recognised in profit or loss
Inventories recognised as an expense during the year ended 30 June 2024 amounted to $632,000 (2023: $1,120,000). These were
included in cost of goods sold.
Write-downs of inventories to net realisable value amounted to $21,000 (2023: $16,000). These were included in cost of
goods sold.
Raw materials
Raw materials consist of the key raw materials and components used in the manufacture of commercial products, including
VIRALEZE™ and VivaGel®.
Finished goods
Finished goods are products that are subject to a customer purchase order, have completed production, or are awaiting
delivery to the customer.
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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11. Non-Current Assets – Property, Plant and Equipment
Plant and
equipment
$’000
Leasehold
improvements
$’000
Total
$’000
At 30 June 2022
Cost
4,623
691
5,314
Accumulated depreciation
(3,326)
(652)
(3,978)
Net book amount
1,297
39
1,336
Year ended 30 June 2023
Opening net book amount
1,297
39
1,336
Additions
558
84
642
Disposals
(3)
–
(3)
Depreciation
(349)
(42)
(391)
Closing net book amount
1,503
81
1,584
At 30 June 2023
Cost
3,936
776
4,712
Accumulated depreciation
(2,433)
(695)
(3,128)
Net book amount
1,503
81
1,584
Year ended 30 June 2024
Opening net book amount
1,503
81
1,584
Additions
46
–
46
Disposals
(52)
–
(52)
Depreciation
(247)
(18)
(264)
Closing net book amount
1,251
63
1,314
At 30 June 2024
Cost
3,930
776
4,706
Accumulated depreciation
(2,679)
(713)
(3,392)
Net book amount
1,251
63
1,314
12. Current Liabilities – Trade and Other Payables
30 June 2024
$’000
30 June 2023
$’000
Trade payables and accruals
2,725
6,615
Other payables
1,288
1,052
4,013
7,667
Trade payables and accruals
The majority of trade payables are related to expenditure associated with the group’s research and product development programs.
73
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Directors’
Declaration
Independent
Auditor’s Report
Shareholder
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Intellectual
Property Report
Corporate
Directory
13. Current Liabilities – Borrowings
Borrowings of $775,000 (2023: $4,778,000) relate to an insurance premium loan maturing January 2025, interest rate 2.9%.
Borrowings at 30 June 2023 included the $4,000,000 Invest Victoria R&D cash flow loan with Treasury Corporation of Victoria
(TCV) which was repaid in October 2023.
14. Current and Non-Current Assets/Liabilities – Leases
The balance sheet shows the following amounts relating to leases:
30 June 2024
$’000
30 June 2023
$’000
Right-of-use assets
Premises
2,298
2,950
Plant and equipment
283
430
2,581
3,380
Lease liabilities
Current
796
744
Non-current
1,957
2,750
2,753
3,494
The group leases premises (laboratory and offices space) until 19 December 2027. The group also leases scientific equipment
generally over a three to five year term.
The consolidated income statement includes the following amounts relating to leases:
30 June 2024
$’000
30 June 2023
$’000
Depreciation charge of right-of-use assets
Premises
657
655
Plant and equipment
146
146
Total depreciation charge of right-of-use assets
803
801
Interest expense on lease liabilities
128
156
Expense relating to leases of low-value assets
6
7
Expense relating to variable lease payments not included in lease liabilities
70
91
Total cash outflow for leases
873
851
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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Starpharma Holdings Limited
15. Current and Non-Current Liabilities – Provision for Employee Benefits
Leave obligations
30 June 2024
$’000
30 June 2023
$’000
Current
1,050
1,281
Non-current
79
48
1,129
1,329
The leave obligations represent the group’s liability for employee long service leave and annual leave. The current portion
of this liability includes all of the accrued annual leave, and the unconditional entitlements to long service leave where
employees have completed the required period of service. However, based on past experience, the group does not expect
all employees to take the full amount of current accrued leave or require payment of the entire amount within 12 months from
the reporting date. Current leave obligations expected to be settled after the date which is 12 months from the reporting date
is $710,000 (2023: $919,000).
Refer to note 1(n) for further information.
16. Contributed Equity
(a) Share capital
2024
Shares
2023
Shares
2024
$’000
2023
$’000
Share capital
Ordinary shares – fully paid
412,372,598
410,493,077
240,750
240,715
(b) Movements in ordinary share capital
Date
Details
Number
of shares
Issue price
$’000
1 Jul 2023
410,493,077
240,715
6 Oct 2023
Employee performance rights plan share issue
121,082
$ –
–
9 Nov 2023
Employee performance rights plan share issue
1,089,805
18 Dec 2023
Employee performance rights plan share issue
93,794
31 Jan 2024
Employee share plan ($1,000) issue
242,862
$0.14
34
28 Jun 2024
Employee share plan ($1,000) issue
7,143
$0.14
1
28 Jun 2024
Employee performance rights plan share issue
324,835
$ –
–
Balance at 30 June 2024
412,372,598
240,750
Date
Details
Number
of shares
Issue price
$’000
1 Jul 2022
408,443,407
240,669
27 Oct 2022
Employee performance rights plan share issue
409,040
$ –
–
1 Feb 2023
Employee share plan ($1,000) issue
67,620
$ 0.68
46
17 Mar 2023
Employee performance rights plan share issue
339,710
$ –
–
5 May 2023
Employee performance rights plan share issue
1,233,300
$ –
–
Balance at 30 June 2023
410,493,077
240,715
75
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Property Report
Corporate
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16. Contributed Equity continued
(c) Ordinary shares
As at 30 June 2024 there were 412,372,598 issued ordinary shares. Ordinary shares entitle the holder to participate in dividends
and the proceeds on winding up of the company in proportion to the number of, and amounts paid on, the shares held. On a
show of hands every holder of ordinary shares present at a duly convened shareholder meeting in person or by proxy is entitled
to one vote, and upon a poll each share is entitled to one vote. Ordinary shares have no par value and the company does not have
authorised capital. There is no current on-market share buy-back.
(d) Employee Share Plan ($1,000 Plan)
Information relating to the Employee Share Plan, including details of shares issued under the plan, is set out in note 27.
(e) Employee Performance Rights Plan
Information relating to the Employee Performance Rights Plan, including details of rights issued under the plan, is set out in note 27.
(f) Capital risk management
The group’s and the parent entity’s objectives when managing capital are to safeguard their ability to continue as a going concern,
so that they can continue to provide returns for shareholders and benefits for other stakeholders. In order to maintain or adjust
the capital structure, the group may adjust the amount of dividends paid to shareholders, return capital to shareholders, issue
new shares or sell assets.
17. Reserves
(a) Reserves
30 June 2024
$’000
30 June 2023
$’000
Share-based payments reserve
29,730
28,299
29,730
28,299
(b) Movement in reserves
Share-based payments reserve
30 June 2024
$’000
30 June 2023
$’000
Balance at 1 July
28,299
26,285
Performance right expense
1,431
2,014
Balance at 30 June
29,730
28,299
(c) Nature and purpose of reserves
The share-based payments reserve is used to recognise the fair value of options and performance rights granted.
18. Accumulated Losses
30 June 2024
$’000
30 June 2023
$’000
Accumulated losses balance at 1 July
(234,199)
(218,561)
Net loss for the year
(8,165)
(15,638)
Accumulated losses balance at 30 June
(242,364)
(234,199)
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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19. Related Party Transactions
(a) Subsidiaries and associates
Interests in subsidiaries and associates are set out in note 24.
(b) Key management personnel compensation
30 June 2024
$
30 June 2023
$
Short-term employee benefits
1,993,469
2,141,908
Post-employment benefits
120,327
143,928
Other long-term benefits
17,894
32,105
Termination benefits
155,607
109,353
Share-based payments
137,652
622,600
2,424,949
3,049,894
Detailed remuneration disclosures are provided in the Section 6 of the remuneration report.
(c) Transactions with group entities
There are related party transactions within the group between the parent and subsidiaries. Transactions include funds advanced
to/from entities and the associated interest charge, and management and services fees. All transactions were made on an arm’s
length basis.
(d) Transactions with associates
There are related party transactions with the associate, Petalion Therapeutics Ltd (Petalion). Starpharma provides R&D services
to Petalion on a fee for service basis. Total service fees for FY24 were $514,412. All transactions were made on an arm’s length basis.
(e) Transactions with other related parties
The group paid $9,028 for consulting services to Centre for Biopharmaceutical Excellence Pty Ltd, which Starpharma non-executive
director Dr Jeff Davies is also a director and shareholder. The consulting services were provided by principals other than Dr Jeff Davies
and were on normal commercial terms.
20. Remuneration of Auditors
During the year the following fees were paid or payable for services provided by PricewaterhouseCoopers Australia (PwC) as auditor
of the parent entity, its related practices and non-related audit firms:
30 June 2024
$
30 June 2023
$
Auditors of the group – PwC
Audit and review of financial reports of the entity or any entity in the consolidated entity
158,100
169,218
Other assurance services
–
–
Total services provided by PwC
158,100
169,218
21. Events Occurring After the Balance Sheet Date
No matters or circumstances have arisen since 30 June 2024 that have significantly affected, or may significantly affect:
(a) the consolidated entity’s operations in future financial years; or
(b) the results of those operations in future financial years; or
(c) the consolidated entity’s state of affairs in future financial years.
77
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Independent
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22. Commitments
(a) Capital commitments
There is no material capital expenditure contracted not recognised as liabilities at the reporting date (2023: nil).
(b) Termination commitments
The service contracts of key management personnel include benefits payable by the group on termination of the employee’s
contract. Refer to the remuneration report for details of these commitments.
23. Contingencies
Following the completion of the US FDA dispute resolution process in February 2024, Starpharma terminated its VivaGel® BV
product licence with ITF Pharma (now “EDW Pharma”) in May 2024. The previously reported contingent liability (2023:
US$1.35 million) to pay a proportion of license receipts to an investment bank, which advised on the competitive licence
process, is no longer applicable. Accordingly, the company has no contingent liabilities at 30 June 2024.
The company has no contingent assets at 30 June 2024 (2023: nil).
24. Interests in Other Entities
(a) Subsidiaries
The consolidated financial statements incorporate the assets, liabilities and results of the following subsidiaries in accordance
with the accounting policy described in note 1(b).
Ownership interest
held by the group
Name of entity
Place of business/country of incorporation
2024
%
2023
%
Starpharma Pty Limited
Australia
100%
100%
(b) Interests in associates
Set out below are the associates of the group.
Ownership interest
held by the group
Name of entity
Place of business/country of incorporation
2024
%
2023
%
Petalion Therapeutics Limited
United Kingdom
22.5%
N/A
On 6 April 2024, Starpharma licensed intellectual property in exchange for a 22.5% shareholding in the newly formed UK entity,
Petalion Therapeutics Limited (Petalion). Petalion is now developing a new dendrimer-drug oncology candidate, and the controlling
shareholder, Medicxi, will fund the development program with an investment of up to £20 million based on the achievement of
project milestones. Starpharma will provide R&D services to Petalion on a fee for service basis. A Starpharma representative
holds 1 of the 4 Petalion Board seats.
The carrying amount of the investment in associate is $Nil, as no cash consideration was paid for the shareholding, and the
carrying value of the intellectual property licensed to the associate in exchange for shares was $Nil. The class of shareholding and
associated liquidation preferences do not currently provide Starpharma with rights to the assets of the associate. The share of the
profit or loss of the associate will not be recognised in the group’s income statement.
If the associates’ dendrimer-drug oncology candidate is successfully developed and advanced, the associate may be acquired
via a trade sale or possible IPO where Starpharma may realise a return from a share sale of its equity investment.
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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25. Reconciliation of Profit After Income Tax to Net Cash Inflow from Operating Activities
30 June 2024
$’000
30 June 2023
(restated)
$’000
Operating profit/(loss) after tax
(8,165)
(15,638)
Adjustments for:
Depreciation and amortisation
1,115
1,193
Foreign exchange (gain)/loss
7
(100)
Non-cash employee benefits: share-based payments
1,466
2,060
Net gain/(loss) on sale of property, plant and equipment
–
(6)
Change in operating assets and liabilities, net of effects of acquisitions
and disposals of entities:
Decrease/(increase) in receivables and other assets
2,065
(1,257)
(Increase)/decrease in inventories
365
51
Increase/(decrease) increase in trade creditors
(3,655)
(84)
Increase/(decrease) in employee provisions
(200)
(67)
Increase/(decrease) in deferred income
25
(463)
Net cash outflows from operating activities*
(6,977)
(14,311)
* The prior year cashflow statement was restated. See the Consolidated Statement of Cash Flows for information.
26. Earnings Per Share
30 June 2024
30 June 2023
Basic earnings/(loss) per share/Diluted earnings/(loss) per share
Total earnings/(loss) per share attributable to the ordinary equity holders of the company ($)
(0.02)
(0.04)
Reconciliations of earnings/(loss) used in calculating earnings per share
Profit/(loss) attributable to the ordinary equity holders of the company used in calculating
basic earnings/(loss) per share: ($’000)
(8,165)
(15,638)
Weighted average number of ordinary shares used as the denominator in calculating
basic earnings/(loss) per share
411,433,050
409,035,257
As at 30 June 2024 the company had on issue 25,498,545 (30 June 2023: 17,548,885) performance rights. The rights are not included
in the determination of basic earnings per share. The rights are also not included in the determination of diluted earnings per share.
They are not considered dilutive as their conversion would not increase loss per share from continuing operations.
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Directors’
Report
Remuneration
Report
Auditor’s Independence
Declaration
Consolidated Financial
Statements
Notes to the Consolidated
Financial Statements
Directors’
Declaration
Independent
Auditor’s Report
Shareholder
Information
Intellectual
Property Report
Corporate
Directory
27. Share-Based Payments
Performance rights
(a) Employee Performance Rights Plan
The Employee Performance Rights Plan (Plan) was most recently approved by shareholders at the 2023 Annual General Meeting.
All executives and staff, including the Chief Executive Officer, are eligible to participate in the Plan. The Plan allows for the issue
of performance rights (being rights to receive fully paid ordinary shares subject to continued employment with the company
and the satisfaction of certain performance hurdles over a specified period). Performance rights are granted under the Plan
for no consideration. The objective of the Plan is to assist in the recruitment, reward, retention and motivation of employees
of the company.
(b) Fair value of performance rights granted
The weighted average assessed fair value at grant date of performance rights granted during the year ended 30 June 2024
was $0.14 per right (2023: $0.57). There were 11,098,655 performance rights granted in the current year (2023: 5,189,084).
The estimated fair value at grant date of rights with a total shareholder return (TSR) performance measure has been valued using
a hybrid Monte-Carlo-trinomial option pricing model taking into account the absolute TSR target, the term of the right, the share
price at grant date, the risk-free rate, the expected dividend yield, expected share price volatility, the volatility of the relevant
index, and the correlation between the share price and that index. All other rights incorporate Key Performance Indicator (KPI)
measures, and the fair value at grant date of these rights, represents a volume weighted average price (VWAP) of shares leading
up to the grant date.
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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Set out below is a summary of performance rights:
2024
Grant date
Vesting date
Balance at start
of the year
Number
Granted during
the year
Number
Converted
during the year
Number
Forfeited
during the year
Number
Balance at end
of the year1
Number
11 Nov 2015
30 Jun 2017
127,625
–
16,000
–
111,625
11 Nov 2015
30 Sep 2018
539,347
–
64,000
–
475,347
19 Nov 2015
30 Jun 2017
181,001
–
–
–
181,001
19 Nov 2015
30 Sep 2018
836,260
–
–
–
836,260
13 Oct 2016
30 Jun 2018
148,438
–
16,000
–
132,438
13 Oct 2016
30 Sep 2019
651,823
–
152,000
–
499,823
29 Nov 2016
30 Jun 2018
172,842
–
–
–
172,842
29 Nov 2016
30 Sep 2019
846,281
–
–
–
846,281
10 Aug 2017
30 Jun 2019
246,396
–
45,400
–
200,996
10 Aug 2017
30 Sep 2020
966,339
–
259,978
–
706,361
29 Nov 2017
30 Jun 2019
197,226
–
–
–
197,226
29 Nov 2017
30 Sep 2020
736,665
–
–
–
736,665
16 Aug 2018
30 Jun 2020
82,931
–
–
–
82,931
16 Aug 2018
30 Sep 2021
314,651
–
–
–
314,651
2 Nov 2018
30 Jun 2020
87,200
–
28,800
–
58,400
2 Nov 2018
30 Sep 2021
323,016
–
89,416
–
233,600
29 Nov 2018
30 Jun 2020
112,708
–
–
–
112,708
29 Nov 2018
30 Sep 2021
350,253
–
–
–
350,253
17 Oct 2019
30 Jun 2021
168,514
–
13,915
–
154,599
17 Oct 2019
30 Sep 2022
758,002
–
194,677
–
563,325
21 Nov 2019
30 Jun 2021
101,320
–
–
–
101,320
21 Nov 2019
30 Sep 2022
203,983
–
–
–
203,983
30 Oct 2020
30 Jun 2021
287,288
–
16,405
–
270,883
30 Oct 2020
30 Jun 2022
271,246
–
57,196
–
214,050
30 Oct 2020
30 Sep 2023
1,500,400
–
469,245
194,409
836,746
20 Nov 2020
30 Jun 2021
176,755
–
–
–
176,755
20 Nov 2020
30 Jun 2022
124,249
–
–
–
124,249
20 Nov 2020
30 Sep 2023
637,173
–
–
407,791
229,382
25 Oct 2021
30 Jun 2023
244,157
–
85,040
3,220
155,897
25 Oct 2021
30 Sep 2024
1,053,014
–
20,896
65,242
966,876
30 Nov 2021
30 Jun 2023
69,070
–
–
–
69,070
30 Nov 2021
30 Sep 2024
394,688
–
–
–
394,688
27 Oct 2022
30 Jun 2024
699,675
–
43,092
103,458
553,125
27 Oct 2022
30 Sep 2025
2,798,698
–
57,456
302,832
2,438,410
29 Nov 2022
30 Jun 2024
227,930
–
–
107,127
120,803
29 Nov 2022
30 Sep 2025
911,721
–
–
–
911,721
5 Sep 2023
30 Jun 2025
–
315,000
–
–
315,000
27 Oct 2023
30 Jun 2025
–
1,533,557
–
67,080
1,466,477
27 Oct 2023
30 Sep 2026
–
6,134,229
–
268,320
5,865,909
29 Nov 2023
30 Jun 2025
–
667,441
–
–
667,441
10 Jan 2024
30 Jun 2025
–
398,725
–
–
398,725
10 Jan 2024
30 Sep 2026
–
1,879,703
–
–
1,879,703
4 Jun 2024
31 Jan 2025
–
170,000
–
–
170,000
Total
17,548,885
11,098,655
1,629,516
1,519,479
25,498,545
1. Unvested rights at the end of the year are not available for employees to exercise into shares.
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27. Share-Based Payments continued
Performance rights continued
(b) Fair value of performance rights granted continued
Information used in assessing the fair value of 11,098,655 performance rights granted during the year ended 30 June 2024
is as follows:
Right grant date
5 September 2023
27 October 2023
27 October 2023
Number of rights granted
315,000
1,533,557
5,837,013
Vesting date
30 June 2025
30 June 2025
30 September 2026
Performance measure
KPIs
KPIs
KPIs
Expected price volatility of the company’s shares
70%
70%
70%
Risk-free interest rate
3.91%
4.32%
4.32%
Expected dividend yield
–
–
–
Share price at grant date
$0.14
$0.14
$0.14
Assessed fair value
$0.14
$0.14
$0.14
Right grant date
27 October 2023
29 November 2023
10 January 2024
Number of rights granted
297,216
667,441
398,725
Vesting date
30 September 2026
30 June 2025
30 June 2025
Performance measure
TSR
KPIs
KPIs
Expected price volatility of the company’s shares
70%
70%
70%
Risk-free interest rate
4.32%
4.21%
3.95%
Expected dividend yield
–
–
–
Share price at grant date
$0.14
$0.14
$0.16
Assessed fair value
$0.08
$0.14
$0.16
Right grant date
10 January 2024
10 January 2024
4 June 2024
Number of rights granted
1,315,792
563,911
170,000
Vesting date
30 September 2026
30 September 2026
31 January 2025
Performance measure
KPIs
TSR
KPIs
Expected price volatility of the company’s shares
70%
70%
70%
Risk-free interest rate
3.70%
3.70%
4.19%
Expected dividend yield
–
–
–
Share price at grant date
$0.16
$0.16
$0.10
Assessed fair value
$0.16
$0.11
$0.10
Share price volatility and the risk-free interest rate are obtained through an independent valuation.
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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Information used in assessing the fair value of 5,189,084 performance rights granted during the year ended 30 June 2023
is as follows:
Right grant date
27 October 2022
27 October 2022
27 October 2022
Number of rights granted
809,887
3,097,706
141,840
Vesting date
30 June 2024
30 September 2025
30 September 2025
Performance measure
KPIs
KPIs
TSR
Expected price volatility of the company’s shares
60%
60%
60%
Risk-free interest rate
3.49%
3.33%
3.33%
Expected dividend yield
–
–
–
Share price at grant date
$0.61
$0.61
$0.61
Assessed fair value
$0.61
$0.61
$0.36
Right grant date
29 November 2022
29 November 2022
29 November 2022
Number of rights granted
227,930
638,205
273,516
Vesting date
30 June 2024
30 September 2025
30 September 2025
Performance measure
KPIs
KPIs
TSR
Expected price volatility of the company’s shares
60%
60%
60%
Risk-free interest rate
3.40%
3.22%
3.22%
Expected dividend yield
–
–
–
Share price at grant date
$0.52
$0.52
$0.52
Assessed fair value
$0.52
$0.52
$0.28
Share price volatility and the risk-free interest rate are obtained through an independent valuation.
Shares
(a) Employee Share Plan ($1,000 Plan)
All staff are eligible to participate in the Starpharma Employee Share Plan ($1,000 Plan). The objective of the $1,000 Plan is to
assist in the reward, retention and motivation of employees of the group. An annual allocation of up to $1,000 of shares may be
granted and taxed on a concessional basis. Shares are granted under the $1,000 Plan for no consideration and are escrowed
for three years whilst participants are employed by the group.
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27. Share-Based Payments continued
(b) Fair value of shares granted
The weighted average fair value at grant date of shares granted under the $1,000 Plan during the year ended 30 June 2024
was $0.14 per share (2023: $0.68 per share). The fair value at grant date is determined by the share price on the date of grant.
These shares were granted for no consideration. There was no allocation of shares under the plan to key management personnel.
30 June 2024
30 June 2023
Share grant date
31 January 2024
1 February 2023
Number of shares granted
250,005
67,620
Share price at grant date/Assessed fair value
$0.14
$0.68
Expenses arising from share-based payment transactions
Total expenses arising from share-based payment transactions recognised during the period were as follows:
30 June 2024
$’000
30 June 2023
$’000
Employee shares issued
35
46
Employee performance rights
1,431
2,014
1,466
2,060
28. Parent Entity Financial Information
(a) Summary financial information
The individual financial statements for the parent entity (Starpharma Holdings Ltd) show the following aggregate amounts:
Parent entity
30 June 2024
$’000
30 June 2023
$’000
Balance sheet
Current assets
22,359
33,374
Total assets
22,359
33,374
Current liabilities
1,656
1,744
Total liabilities
1,656
1,744
Shareholders’ equity
Contributed equity
240,750
240,715
Reserves
29,221
27,790
Accumulated losses
(249,269)
(236,875)
Loss for the year
(12,394)
(14,541)
Total comprehensive income
(12,394)
(14,541)
(b) Contingencies of the parent entity
The parent entity has no contingent assets or liabilities at 30 June 2024 (2023: nil).
Notes to the Consolidated Financial Statements continued
30 JUNE 2024
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Consolidated Entity Disclosure Statement
FOR THE YEAR ENDED 30 JUNE 2024
Name of entity
Type of entity
% of share capital
Place of
business/country
of incorporation
Australian resident
or foreign resident
Starpharma Holdings Ltd
Body Corporate
N/A
Australia
Australian
Starpharma Pty Ltd
Body Corporate
100
Australia
Australian
Basis of preparation
This consolidated entity disclosure statement (CEDS) has been prepared in accordance with the Corporations Act 2001 and
includes information for each entity that was part of the consolidated entity as at the end of the financial year in accordance
with AASB 10 Consolidated Financial Statements.
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Statements
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Financial Statements
Directors’
Declaration
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Property Report
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Directory
Directors’ Declaration
FOR THE YEAR ENDED 30 JUNE 2024
In the directors’ opinion:
(a) the financial statements and notes set out on pages 56 to 84 are in accordance with the Corporations Act 2001, including:
(i)
complying with accounting standards, the Corporations Regulations 2001 and other mandatory professional reporting
requirements, and
(ii) giving a true and fair view of the consolidated entity’s financial position as at 30 June 2024 and of its performance for
the financial year ended on that date, and
(b) there are reasonable grounds to believe that the company will be able to pay its debts as and when they become due
and payable, and
(c) the consolidated entity disclosure statement on page 85 is true and correct.
Note 1(a) confirms that the financial statements also comply with International Financial Reporting Standards as issued by the
International Accounting Standards Board.
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.
This declaration is made in accordance with a resolution of the directors.
Robert B Thomas AO
Chairman
Melbourne, 22 August 2024
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Independent Audit Report
TO THE MEMBERS OF STARPHARMA HOLDINGS LIMITED
PricewaterhouseCoopers, ABN 52 780 433 757
2 Riverside Quay, SOUTHBANK VIC 3006, GPO Box 1331, MELBOURNE VIC 3001
T: 61 3 8603 1000, F: 61 3 8603 1999
Liability limited by a scheme approved under Professional Standards Legislation.
Independent auditor’s report
To the members of Starpharma Holdings Limited
Report on the audit of the financial report
Our opinion
In our opinion:
The accompanying financial report of Starpharma Holdings Limited (the Company) and its controlled
entities (together the Group) is in accordance with the Corporations Act 2001, including:
(a)
giving a true and fair view of the Group's financial position as at 30 June 2024 and of its
financial performance for the year then ended
(b)
complying with Australian Accounting Standards and the Corporations Regulations 2001.
What we have audited
The financial report comprises:
the consolidated balance sheet as at 30 June 2024
the consolidated statement of changes in equity for the year then ended
the consolidated statement of cash flows for the year then ended
the consolidated income statement for the year then ended
the notes to the consolidated financial statements, including material accounting policy
information and other explanatory information
the consolidated entity disclosure statement as at 30 June 2024
the directors’ declaration.
Basis for opinion
We conducted our audit in accordance with Australian Auditing Standards. Our responsibilities under
those standards are further described in the Auditor’s responsibilities for the audit of the financial
report section of our report.
We believe that the audit evidence we have obtained is sufficient and appropriate to provide a basis
for our opinion.
Independence
We are independent of the Group in accordance with the auditor independence requirements of the
Corporations Act 2001 and the ethical requirements of the Accounting Professional & Ethical
Standards Board’s APES 110 Code of Ethics for Professional Accountants (including Independence
Standards) (the Code) that are relevant to our audit of the financial report in Australia. We have also
fulfilled our other ethical responsibilities in accordance with the Code.
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Statements
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Financial Statements
Directors’
Declaration
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Our audit approach
An audit is designed to provide reasonable assurance about whether the financial report is free from
material misstatement. Misstatements may arise due to fraud or error. They are considered material if
individually or in aggregate, they could reasonably be expected to influence the economic decisions of
users taken on the basis of the financial report.
We tailored the scope of our audit to ensure that we performed enough work to be able to give an
opinion on the financial report as a whole, taking into account the geographic and management
structure of the Group, its accounting processes and controls and the industry in which it operates.
Audit scope
Key audit matters
Our audit focused on where the Group made
subjective judgements; for example, significant
accounting estimates involving assumptions and
inherently uncertain future events.
Audit procedures are predominantly performed by
PwC Australia, consistent with the location of
Group management and financial records.
Amongst other relevant topics, we communicated
the Research and Development Tax Incentive key
audit matter to the Audit and Risk Committee.
This is further described in the Key audit matters
section of our report.
Key audit matters
Key audit matters are those matters that, in our professional judgement, were of most significance in
our audit of the financial report for the current period. The key audit matter was addressed in the
context of our audit of the financial report as a whole, and in forming our opinion thereon, and we do
not provide a separate opinion on this matter. Further, any commentary on the outcomes of a
particular audit procedure is made in that context.
Key audit matter
How our audit addressed the key audit matter
Research and Development Tax Incentive
Receivable
(Refer to note 3 critical accounting estimates and
judgements, note 6 expenses and note 9 current
assets - trade and other receivables)
The Group undertakes research and development
(R&D) activities, some of which, could qualify for a
refundable tax offset under the Australian Government
R&D Tax Incentive scheme. The Group has assessed
these activities and related expenditure to determine
their eligibility under the incentive scheme.
The R&D Tax Incentive receivable recorded as at 30
June 2024 was $5.52 million and $5.52 million was
recognised as a contra R&D expense in the
consolidated income statement for the year ended 30
June 2024.
We performed the following procedures, amongst
others, to assess the Group’s estimate of the R&D Tax
Incentive receivable as at 30 June 2024:
compared the estimate recorded in the
consolidated financial statements as at 30
June 2023 to the amount of cash received
after lodgement of the R&D Tax Incentive
claim to assess historical accuracy of the
Group’s estimate.
compared the nature of the underlying R&D
expenditure included in the current year
estimate to the nature of expenditure included
in the prior year estimate.
assessed the nature of a sample of expenses
against the eligibility criteria of the R&D Tax
Incentive programme.
Independent Audit Report continued
TO THE MEMBERS OF STARPHARMA HOLDINGS LIMITED
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Key audit matter
How our audit addressed the key audit matter
This is a key audit matter due to:
the financial significance of the amount
receivable as at 30 June 2024; and
the degree of judgement and interpretation of
the R&D tax legislation required by the Group
to assess the eligibility of the R&D
expenditure under the scheme.
agreed a sample of eligible expenditure in the
estimate to the general ledger, supporting
documentation or other underlying accounting
records.
obtained copies of correspondence with the
company’s external tax advisor and agreed
relevant advice to the Group’s R&D Tax
Incentive Receivable calculation for the
current financial year.
evaluated the reasonableness of the
disclosures against the requirements of
Australian Accounting Standards.
Other information
The directors are responsible for the other information. The other information comprises the
information included in the annual report for the year ended 30 June 2024, but does not include the
financial report and our auditor’s report thereon.
Our opinion on the financial report does not cover the other information and accordingly we do not
express any form of assurance conclusion thereon through our opinion on the financial report. We
have issued a separate opinion on the remuneration report.
In connection with our audit of the financial report, our responsibility is to read the other information
and, in doing so, consider whether the other information is materially inconsistent with the financial
report or our knowledge obtained in the audit, or otherwise appears to be materially misstated.
If, based on the work we have performed on the other information that we obtained prior to the date of
this auditor’s report, we conclude that there is a material misstatement of this other information, we are
required to report that fact. We have nothing to report in this regard.
Responsibilities of the directors for the financial report
The directors of the Company are responsible for the preparation of the financial report in accordance
with Australian Accounting Standards and the Corporations Act 2001, including giving a true and fair
view, and for such internal control as the directors determine is necessary to enable the preparation of
the financial report that is free from material misstatement, whether due to fraud or error.
In preparing the financial report, the directors are responsible for assessing the ability of the Group to
continue as a going concern, disclosing, as applicable, matters related to going concern and using the
going concern basis of accounting unless the directors either intend to liquidate the Group or to cease
operations, or have no realistic alternative but to do so.
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Independent
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Auditor’s responsibilities for the audit of the financial report
Our objectives are to obtain reasonable assurance about whether the financial report as a whole is
free from material misstatement, whether due to fraud or error, and to issue an auditor’s report that
includes our opinion. Reasonable assurance is a high level of assurance, but is not a guarantee that
an audit conducted in accordance with the Australian Auditing Standards will always detect a material
misstatement when it exists. Misstatements can arise from fraud or error and are considered material
if, individually or in the aggregate, they could reasonably be expected to influence the economic
decisions of users taken on the basis of the financial report.
A further description of our responsibilities for the audit of the financial report is located at the Auditing
and Assurance Standards Board website at:
https://www.auasb.gov.au/admin/file/content102/c3/ar1_2020.pdf. This description forms part of our
auditor's report.
Report on the remuneration report
Our opinion on the remuneration report
We have audited the remuneration report included in the directors’ report for the year ended 30 June
2024.
In our opinion, the remuneration report of Starpharma Holdings Limited for the year ended 30 June
2024 complies with section 300A of the Corporations Act 2001.
Responsibilities
The directors of the Company are responsible for the preparation and presentation of the
remuneration report in accordance with section 300A of the Corporations Act 2001. Our responsibility
is to express an opinion on the remuneration report, based on our audit conducted in accordance with
Australian Auditing Standards.
PricewaterhouseCoopers
Brad Peake
Melbourne
Partner
22 August 2024
Independent Audit Report continued
TO THE MEMBERS OF STARPHARMA HOLDINGS LIMITED
90
Annual Report 2024
Starpharma Holdings Limited
Shareholder Information
Supplementary information as required by ASX listing requirements.
A. Distribution of Equity Shareholders
Equity security holders by size of holding, as at 14 August 2024:
Class of equity security
Shares
Performance
rights
1 –1,000
2,046
–
1,001–5,000
2,332
–
5,001–10,000
1,021
–
10,001–100,000
1,688
3
100,001 and over
382
38
Total
7,469
41
There were 4,471 holders of less than a marketable parcel of ordinary shares.
B. Equity Security Holders
The names of the 20 largest holders of quoted equity securities as at 14 August 2024:
Ordinary shares
Name
Number held
Percentage of
issued shares
1.
HSBC Custody Nominees (Australia) Limited
81,247,474
19.70
2.
JP Morgan Nominees Australia Pty Limited
31,174,308
7.56
3.
Citicorp Nominees Pty Limited
15,203,959
3.69
4.
BNP Paribas Noms Pty Ltd
14,494,331
3.51
5.
Bell Potter Nominees Ltd
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