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FY2024 Annual Report · Santander Bank Polska
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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  
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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
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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
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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
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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
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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
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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
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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

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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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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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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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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Remuneration 
Report
Auditor’s Independence 
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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
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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
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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
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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
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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
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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

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
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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
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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

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
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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

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
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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
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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
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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

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
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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
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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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Starpharma Holdings Limited

(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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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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Starpharma Holdings Limited

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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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
70
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Starpharma Holdings Limited

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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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
72
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Starpharma Holdings Limited

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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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
74
Annual Report 2024
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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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.
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Declaration
Consolidated Financial 
Statements
Notes to the Consolidated 
Financial Statements
Directors’ 
Declaration
Independent 
Auditor’s Report
Shareholder 
Information
Intellectual  
Property Report
Corporate 
Directory

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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Starpharma Holdings Limited

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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Consolidated Financial 
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Notes to the Consolidated 
Financial Statements
Directors’ 
Declaration
Independent 
Auditor’s Report
Shareholder 
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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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Property Report
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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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Financial Statements
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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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Financial Statements
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Independent 
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Intellectual  
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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
88
Annual Report 2024
Starpharma Holdings Limited

 
 
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. 
89
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

 
 
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
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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 
9,000,000
2.18
6.
Ingot Capital Investments Pty Ltd
8,705,000
2.11
7.
T & N Argyrides Investments P/L 
5,060,000
1.23
8.
BNP Paribas Nominees Pty Ltd 
4,866,370
1.18
9.
Mr Kingsley Bryan Bartholomew
4,612,025
1.12
10.
Lavya Pty Ltd 
4,344,628
1.05
11.
BNP Paribas Nominees Pty Ltd 
4,267,008
1.03
12.
HSBC Custody Nominees (Australia) Limited – A/C 2
4,141,107
1.00
13.
Mr Peter Murray Jackson 
3,921,959
0.95
14.
E Equities Pty Ltd
3,700,000
0.90
15.
All-States Finance Pty Limited
3,500,000
0.85
16.
Applecross Secretarial Services Pty Ltd 
3,361,550
0.82
17.
Ms Jacinth Fairley
3,252,386
0.79
18.
Charles & Cornelia Goode Foundation Pty Ltd 
3,200,000
0.78
19.
Mr Thomas Argyrou
3,000,000
0.73
20.
BNP Paribas Nominees Pty Ltd  
2,739,822
0.66
213,791,927
51.84
91
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

Shareholder Information continued
B. Equity Security Holders continued
Unquoted equity securities  
over ordinary shares
Name
Number 
on issue
Number 
of holders
Employee performance rights
25,498,545
41
C. Substantial Holders
Substantial shareholders with a shareholding greater than 5% as shown in substantial shareholder notices received by the 
company as at 16 August 2024:
Ordinary shares
Name
Number held
Percentage of 
issue shares
Allianz SE
48,480,000
11.8
ICM Investment Management Ltd
33,066,682
8.0
Allan Gray Australia Pty Ltd
27,938,497
6.8
D. Voting Rights
The voting rights attached to each class of equity securities are set out below:
(a)	 Ordinary shares	
On a show of hands every member present at a meeting in person or by proxy shall have one vote 
and on a poll each share shall have one vote.
(b)	 Performance rights	
No voting rights.
92
Annual Report 2024
Starpharma Holdings Limited

Intellectual Property Report
The Starpharma patent portfolio currently has 19 active patent families with over 150 granted patents and more than 40 patent 
applications pending.
Key patents within the Starpharma portfolio as at 31 July 2024:
Title
Priority date and 
publication number
Patents granted
Applications pending
VivaGel® patent portfolio
Agents for the Prevention 
& Treatment of Sexually 
Transmitted Diseases
30 March 2001  
WO02/079299
USA
Microbicidal Dendrimer 
Composition Delivery System 
(Condom related)
18 October 2005  
WO2007/045009
Hong Kong, Japan, Malaysia,  
South Korea, Taiwan, USA
Method of Treatment or 
Prophylaxis of Bacterial 
Vaginosis
16 May 2011  
WO2012/000891
Australia, Canada, China, Europe, 
Hong Kong, Israel, Japan, Mexico, 
Russia, South Korea, USA
Method of Treatment or 
Prophylaxis of Infection of the Eye
13 September 2012  
WO2014/043576
Canada, China, Europe,  
Hong Kong, India, Japan, USA
Drug Delivery patent portfolio (includes DEP® patents)
Macromolecules Compounds 
having Controlled Stoichiometry
25 October 2005  
WO2007/048190
Australia, Canada, Europe, USA
Modified Macromolecules
20 January 2006  
WO2007/082331
Australia, Canada, China, Europe, 
Hong Kong, India, Japan, USA
Targeted Polylysine Dendrimer 
Therapeutic Agent
11 August 2006  
WO2008/017125
China, Europe, India, USA
Macromolecules  
(Drug linkers)
6 June 2011  
WO2012/167309
Australia, Brazil, Canada, China, 
Europe, Hong Kong, Japan, South 
Korea, USA
USA
Dendrimer Drug Conjugates 
(DEP-Insulin/GLP1)
6 June 2014  
WO 2015/184510
Europe, India, USA
Therapeutic Dendrimer  
(DEP-Cabazitaxel)
19 July 2018  
WO2020/014750
USA
Australia, Canada, China, Europe, 
Japan, South Korea 
Dendrimer for Therapy and 
Imaging (DEP-radiotheranostic)
29 November 2018 
WO2020/107078
Australia, Japan
Canada, China, Europe,  
South Korea, USA
Therapeutic Dendrimer  
(DEP-Irinotecan)
20 November 2018 
WO2020/102852
India
Australia, Canada, China, Europe, 
Japan, South Korea, USA
Therapeutic Dendrimer  
(DEP-GEM)
26 September 2019  
WO2021/056077
Australia, Canada, China, Europe, 
Japan, South Korea, USA
Targeted Dendrimer 
Conjugates (DEP-targeted)
28 August 2019 
WO2021/035310
Australia, Canada, China, Europe, 
Japan, South Korea, USA
Method of Prophylaxis 
of Coronavirus Infection
15 April 2020  
WO/2021/207790
Australia, Singapore, Taiwan, 
United Kingdom
China, Europe, Hong Kong, Japan, 
Saudi Arabia, USA
Dendrimer-drug conjugates 
(Remdesivir)
31 August 2020  
WO2022/040761
Europe, USA
93
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

Intellectual Property Report continued
Title
Priority date and 
publication number
Patents granted
Applications pending
Drug Delivery patent portfolio (includes DEP® patents) continued
Targeted Dendrimer Therapy 
(Targeted DxD)
24 April 2024 
PCT/AU2024/050397
International Patent  
Cooperation Treaty (PCT)
Targeted Dendrimer Conjugates 
(Targeted FAP/Multi-targeted)
26 March 2024 
AU2024900811
Australia (provisional)
Targeting Agent-Dendrimer 
Conjugates (Combined 
Targeting Agent/PK Modifier)
26 March 2024 
AU2024900816
Australia (provisional)
Starpharma actively protects its trademark rights with filings and registrations in key markets. The primary marks protected  
are STARPHARMA, VIVAGEL and VIRALEZE. 
94
Annual Report 2024
Starpharma Holdings Limited

Corporate Directory
Company Name
Starpharma Holdings Limited 
ABN 20 078 532 180
Directors
R B Thomas AO – Chairman
C Maley – Chief Executive Officer and Managing Director
D J McIntyre
L Cheng
J R Davies
R Basser
Company Secretary
Justin Cahill
Registered Office and Postal Address
4-6 Southampton Crescent 
Abbotsford VIC 3067 Australia
Telephone +61 3 8532 2700
Share Register 
Computershare Investor Services Pty Limited 
452 Johnston Street  
Abbotsford VIC 3067
GPO Box 2975 
Melbourne VIC 3001
1300 850 505 (within Australia) 
+613 9415 4000 (outside Australia) 
www.computershare.com
Auditor
PricewaterhouseCoopers 
2 Riverside Quay 
Southbank VIC 3006 Australia
Solicitors
DLA Piper  
80 Collins Street 
Melbourne VIC 3000 Australia
Stock Exchange Listing
ASX Limited  
Level 4, North Tower, Rialto,  
525 Collins Street 
Melbourne VIC 3000 Australia
ASX Code: SPL
Starpharma’s American Depositary Receipts (ADRs) 
trade under the code SPHRY (CUSIP number 855563102). 
Each Starpharma ADR is equivalent to 10 ordinary shares 
of Starpharma as traded on the ASX. The Bank of New York 
Mellon is the depositary bank.
Starpharma’s ADRs are listed on OTCQX International 
(www.otcmarkets.com), a premium market tier in the US 
for international exchange-listed companies operated 
by OTC Markets Group.
Website 
www.starpharma.com
95
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

Starpharma Holdings Limited
ABN 20 078 532 180
4-6 Southampton Crescent 
Abbotsford VIC 3067 Australia
Telephone +61 3 8532 2700
www.starpharma.com