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Faron

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FY2024 Annual Report · Faron
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LEADING THE WAY IN
BREAKTHROUGH
IMMUNOTHERAPIES
2024
ANNUAL REPORT

FARON PHARMACEUTICALS OY
ANNUAL REPORT 2024
Faron (AIM: FARN, First North: FARON) is a global, 
clinical-stage biopharmaceutical company, focused 
on tackling cancers via novel immunotherapies. Its 
mission is to bring the promise of immunotherapy to 
a broader population  by uncovering novel ways to 
control and harness the power of the immune system. 
The Company’s lead asset is bexmarilimab, a Faron’s 
wholly owned, investigational immunotherapy designed to 
overcome resistance to existing treatments and optimize 
Faron Pharmaceuticals in brief
2024 was a year of success and transformation for the company, with 
the positive clinical development of bexmarilimab solidifying our position 
in the field of immunotherapy. Faron’s progress, from both a clinical and 
regulatory perspective, only strengthens our confidence in the potential 
of bexmarilimab to address critical unmet needs in oncology and unlock 
significant value creation for the company and shareholders. We remain 
steadfast in our mission to bring life-changing immunotherapies to patients 
who need them most and the exceptional progress we’ve achieved this year 
brings us closer to achieving that goal.”
Dr. Juho Jalkanen | Chief Executive Officer 
For further information on Faron’s progress, development programs and pipeline, please visit Faron´s website www.faron.com.
clinical outcomes, by targeting myeloid cell function 
and igniting the immune system. Bexmarilimab is being 
investigated in Phase I/II clinical trials as a potential 
therapy for patients with hematological cancers in 
combination with other standard treatments. Faron is 
also progressing plans to investigate bexmarilimab in 
combination with anti-PD-1 therapy in selected advanced 
solid tumors. Faron is headquartered in Turku, Finland.
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FARON PHARMACEUTICALS OY
ANNUAL REPORT 2024
CONTENTS
Our Pipeline 	
4
Highlights 2024 	
7
Statement of Comprehensive Income 	
41
Balance Sheet 	
42 
Parent Company Statement of Changes in Equity 	
43
Group Statement of Changes in Equity 	
44 
Statement of Cash Flows 	
45
Notes to the Financial Statements 	
46
Results and Dividends	
65
Auditor’s Report	
67
Chairman’s Introduction to Governance 	
22
Compliance with the Principles of the QCA Code 	
23
Board of Directors 	
24
Remuneration Report 	
30
Corporate Governance Statement 	
35 
Directors’ Report 	
39
Chairman’s Statement 	
11
Chief Executive Officer’s Review 	
13
Financial Review 	
15
Risks and Uncertainties 	
18
FARON PHARMACEUTICALS
STRATEGIC REPORT
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FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT

FARON PHARMACEUTICALS OY
ANNUAL REPORT 2024
OUR PIPELINE
Building the future of immunotherapy
TREATMENT
INDICATION(S)
PHASE OF DEVELOPMENT
ANTICIPATED KEY MILESTONES
Preclinical
Phase I
Phase II
Phase III
Single-Agent 
Bexmarilimab 
Advanced solid tumors 
FARON SPONSORED
• Completed. Bex can modulate the TME which 
leads to improved survival
Bexmarilimab
+ Azacitidine
r/r MDS
FARON SPONSORED
• Phase II topline readout in April’ 25
• Phase II will be the registrational population for r/r 
MDS. Confirmatory Phase III in 1st line HR MDS
1st Line MDS
FARON SPONSORED
• Phase I/II topline readount in April’25
• Phase III preparations expected in H2’25
Bexmarilimab 
+ PD-1
PD-1 Blockade Basket trial in Solid Tumors 
FARON SPONSORED
• First-patient-in expected in Q1 ‘26
PD-1 resistant NSCLC and Melanoma 
INVESTIGATOR INITIATED
• First-patient-in expected in Q2 ‘25
Soft Tissue Sarcomas 
INVESTIGATOR INITIATED
• First-patient-in expected in Q4’25
TBC
Lymphomas (DLBCL and TCL)
FARON SPONSORED
• Preclinical expected to complete Q2’25
Company pipeline
MATINS (First in Human, single agent)
BEXMAB
BEXMAB
MATINS-02
BLAZE
BEXAR
MATINS-03
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THE TARGET AND PROGRAMME
Bexmarilimab is Faron’s wholly owned, investigational 
precision immunotherapy. Tumor-associated 
macrophages (TAM) are considered a key source of 
resistance to current standard of care. Bexmarilimab is 
a novel humanised anti-CLEVER-1 antibody, that targets 
a subpopulation of TAMs, and converts the highly 
immunosuppressive M2-like macrophages to a more 
pro-inflammatory state to promote immune activation. 
Bexmarilimab has been shown to successfully alter the 
scavenging functions of CLEVER-1 in macrophages, which 
leads to increased antigen presentation and promotion 
of interferon gamma secretion by leukocytes. Additional 
preclinical studies have proven that CLEVER-1, encoded by 
the Stabilin-1 or STAB-1 gene, is a major source of T cell 
exhaustion and involved in cancer growth and spread. 
Observations from clinical studies to date indicate that 
CLEVER-1 has the capacity to control T cell activation 
directly. This suggests the inactivation of CLEVER-1 
as an immune suppressive molecule could be more 
important than previously thought. Certain blood cancer 
cells carry significant amounts of cell surface CLEVER-1, 
which may limit the body’s ability to mount an immune 
response, and research has shown a clear survival 
benefit among certain blood cancer patients with low 
CLEVER-1 expression. As an immuno-oncology therapy, 
bexmarilimab is designed to downregulate CLEVER-1 
expression, thereby increasing antigen presentation 
and allowing the immune system to better identify and 
kill cancer cells. This could result in a deeper and more 
durable clinical benefit compared to what most patients 
experience with currently approved treatments. 
CLINICAL DEVELOPMENT
Bexmarilimab is currently being studied in combination 
with standard of care in patients with hypomethylating 
agents (HMAs)-refractory or -relapsed myelodysplastic 
Bexmarilimab –  
a CLEVER approach to fight cancer 
syndrome (MDS), an aggressive myeloid leukemia with 
very few treatment options with focus on hematological 
malignancies. The Company is also exploring the 
immunotherapy’s potential in low risk MDS as well as 
chronic myelomonocytic leukaemia (CMML) patients, 
who are currently treated with HMA-based therapies 
treatment upon worsening of disease. 
Faron’s current priority is its Phase I/II BEXMAB trial, 
investigating the safety, tolerability and preliminary 
efficacy of bexmarilimab in combination with standard 
of care therapies, azacitidine and other hypomethylating 
agents in relapsed/refractory myelodysplastic syndromes 
(MDS) and relapsed/refractory acute myeloid leukemia 
(AML) and chronic myelomonocytic leukemia (CMML). 
The BEXMAB Phase II Interim results presented at the 
66th American Society of Hematology (ASH) Annual 
Meeting in December 2024 showed a high objective 
response rate (ORR) at 80% (16/20) and estimated 
median overall survival of the 20 r/r MDS patients were 
13.4 months. Beyond Hematological malignancies, 
the Company has planned Bexmarilimab combination 
studies in solid tumours.
BEXMARILIMAB MANUFACTURING
At the end of 2023, Faron, with its partner AGC Biologics, 
produced the first commercial scale 2000L batch of the 
active pharmaceutical ingredient (API) of bexmarilimab. 
During 2024, activities with AGC were paused as a 
cash saving measure at the end of Q1 2024 but then 
reactivated after securing finances in Q3 2024. The API 
is now being manufactured into final drug product to 
undergo stability and quality testing in order to be ready 
to be used in confirmatory registrational trials in leading 
to marketing approval. Final clinical testing needs to be 
done using the product that is produced using a tightly 
regulated commercial manufacturing process.
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FARON PHARMACEUTICALS OY
ANNUAL REPORT 2024
THE TARGET AND PROGRAMME
Traumakine® is Faron’s investigational intravenous (IV) 
interferon beta-1a (IFN beta-1a) therapy for the prevention 
of complications from cytokine release syndrome (CRS), 
or ischemia and hyperinflammatory conditions. The 
body’s own, natural production of IFN beta-1a, a key anti-
inflammatory signalling protein produced in response to 
viral infections, is one of the main defense mechanisms 
of the immune system against viruses and vital for 
cell integrity.  
Traumakine® – enhancing the endothelial 
barrier, organ protection in ischemia  
and inflammation
CLINICAL DEVELOPMENT 
Faron joined a research consortium which received 
a U.S. Department of Defense grant to investigate 
the use of intravenous interferon beta (Traumakine®) 
for the prevention of ischemia-reperfusion injury in 
battlefield victims when using a lifesaving torniquet 
for the prevention of excessive blood loss. The Study 
is named Resuscitation by Endothelial Stabilization 
and Targeted Oxygen Rescue (RESTOR) Platform 
for Battlefield Applications. Participating institutions 
are Duquesne University School of Pharmacy and Wake 
Forest Medical University Health Sciences.   
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FARON PHARMACEUTICALS OY
ANNUAL REPORT 2024
Hematological cancer with  
standard of care (SOC) - BEXMAB
•	 The Company announced Positive Phase II Interim data 
from the BEXMAB trial confirming earlier positive Phase 
I and II findings in MDS patients with prior HMA failure.  
•	 	Overall response rate of 80% (16 out of 20) in refractory 
or relapsed HMA failed MDS patient population 
(r/r MDS). 
•	 Observed responses were primarily deep and durable 
with 70% (14 out of 20) r/r MDS patients achieving 
complete response (CR) / marrow complete remission 
(mCR) / partial response (PR). 
•	 	Four patients have moved on to receive a bone 
marrow transplant.
•	 Estimated mOS of approximately 13.4 months in 
r/r MDS population. 
•	 	The combination of bexmarilimab and azacitidine 
remains well tolerated.
•	 	Clever-1 target engagement and expression in the 
bone marrow with an increased antigen presentation 
capacity and presence of CD8 T and NK cells 
supports bexmarilimab mechanism-of-action. 
•	 The FDA granted bexmarilimab Fast Track Designation 
for the treatment of r/r MDS in combination with 
azacitidine. 
•	 Faron received positive feedback from its formal 
Type D Scientific Advice Meeting with the FDA 
regarding the registrational clinical development plan 
for bexmarilimab in the treatment of HR MDS. The FDA 
acknowledged the difficulties of running a randomized 
study with a comparator in the r/r setting and instead 
proposed that Faron conduct a confirmatory phase III 
trial in frontline high-risk MDS (HR MDS), that would 
not require a separate phase III in r/r MDS. Accelerated 
approval for r/r MDS could possibly be obtained with 
the existing phase II trial in addition to an interim 
read-out from the confirmatory phase III trial as per the 
FDA’s Project FrontRunner. 
•	 The Company received regulatory approval from 
the MHRA to conduct the BEXMAB trial in the UK. 
This approval allows Faron to recruit UK hematology 
patients directly, accelerating its research efforts by 
increasing recruitment and enhancing the study’s 
diversity and scope by expanding the participant pool. 
•	 Bexmarilimab received an Innovation Passport, under 
the Innovative Licensing and Access Pathway (ILAP) 
from the MHRA, for the treatment of r/r MDS. 
•	 Further analysis of the patient profiles of those 
treated in the completed Phase I part of the BEXMAB 
trial confirmed that patients had experienced 
disease progression following previous treatment 
with azacitidine monotherapy or combinations of 
up to four therapies that included azacitidine or 
decitabine combined with magrolimab, venetoclax 
and sabatolimab. 
HIGHLIGHTS
Operational (including post period):
BEXMARILIMAB – Faron’s wholly owned, novel 
precision cancer immunotherapy candidate, 
in Phase I/II development for difficult-to-treat 
hematological and solid tumor cancers.
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FARON PHARMACEUTICALS
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FARON PHARMACEUTICALS OY
ANNUAL REPORT 2024
•	 Full analysis of the positive Phase II interim data from 
BEXMAB trial was presented at the 66th American 
Society of Hematology (ASH) Annual Meeting and 
Exposition. 
Combination potential with solid tumours - 
and further expansion
Preparations are ongoing for the initiation of three 
proof-of-concept studies in solid tumours.  
•	 BLAZE – Can bexmarilimab overcome resistance to 
PD-1 inhibitors? Resistance to first-line immunotherapy 
in NSCLC and melanoma is common. Targeting 
tumor-associated macrophages may overcome this 
resistance. The response to bexmarilimab combined 
with anti-PD-1 antibody will serve as proof-of-concept 
for reversing resistance. The study involves initial 
priming with bexmarilimab seven days before the 
combination treatment. Biomarker analysis will 
provide translational correlations of macrophage 
switch and immune activation. Blaze is an Investigator 
Initiated Trial.
•	 BEXAR – Can bexmarilimab turn cold tumors hot in 
soft-tissue sarcomas? Early clinical trials with immune 
checkpoint inhibitors (ICIs) in soft tissue sarcoma 
(STS) have been disappointing, as these tumors are 
often “cold” due to an immunosuppressive tumor 
microenvironment rich in M2-like macrophages and 
Clever-1 expression. Studies show that Clever-1-positive 
macrophages are associated with poor chemotherapy 
response. In vitro, Clever-1 inhibition induces anti-tumor 
macrophages, and combining chemotherapy with an 
anti-Clever-1 antibody significantly increases survival in 
mice models. Targeting Clever-1 in immune cells may 
improve chemotherapy response in cancer patients by 
making primary refractory STS tumors more sensitive 
to treatment. Bexar is an Investigator Initiated Trial. 
•	 MATINS-02 – Can bexmarilimab overcome PD-1 
primary resistance and expand the population of PD-1 
responders? PD-1 inhibitors have shown disappointing 
results in immunologically cold tumors like gastric, 
gallbladder, cholangiocarcinoma, and ER+ breast 
cancer. Bexmarilimab has the potential to make 
these primary refractory (cold) tumors sensitive to 
PD-1. The study will also prospectively validate the 
use of intratumoral Clever-1 positivity as a predictive 
biomarker for treatment benefit. Matins-02 is a Faron 
Sponsored Trial.
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FARON PHARMACEUTICALS OY
ANNUAL REPORT 2024
•	 The Company filed a patent application around the 
use of soluble Clever-1 for inactivating T-cells and the 
treatment of autoimmune diseases and inflammatory 
disorders. The Company will take the identified part 
of soluble Clever-1 and design the optimal drug 
composition with the desired characteristics for treating 
autoimmune diseases
FINANCIAL
•	 On December 31, 2024, Faron held cash balances of 
EUR 9.5 million (2023: EUR 6.9 million).   
•	 Loss for the period for the financial year ended 
December 31, 2024, was EUR -25.9 million 
(2023: EUR -30.9 million).   
•	 Net assets on December 31, 2024, were 
EUR –9.8 million (2023: EUR -15.2 million). 
•	 In February 2024, Faron announced that it was in 
breach of several undertakings agreed in the facilities 
agreement entered into on 28 February 2022 between 
IPF Fund II SCA, SICAV-FIAR (“IPF”) as Lender and 
Faron Pharmaceuticals Ltd as Borrower (“Facilities 
Agreement”) and subsequent waiver letters provided by 
IPF, and therefore was in several Events of Default, as 
defined in the Facilities Agreement. 
•	 In March 2024, Faron successfully raised a total 
of EUR 3.2 million in subordinated convertible loan 
arrangements with certain existing shareholders 
allowing the Company to make critical payments to 
third parties under agreed waivers with IPF.   
•	 In April 2024 the Company conducted a private 
placement directed to a limited number of institutional 
and other investors to raise EUR 4.8 million which, 
together with the EUR 3.2 million convertible loan 
announced on 4 March 2024, secured the required 
short-term bridge financing totaling EUR 8 million. 
•	 In June 2024, the Company raised a total 
of approximately EUR 30.7 million, of which 
approximately EUR 3.7 million was paid by converting 
the convertible loan and related arrangement fees and 
interests into shares in the Company. 
•	 The primary reason for conducting the placings were 
to accelerate and expand the clinical development of 
the Company’s main drug candidate, bexmarilimab, 
advance bexmarilimab’s commercial scale production, 
support general corporate purposes and other pipeline 
development, and to strengthen the Company’s 
balance sheet. 
CORPORATE HIGHLIGHTS 
•	 The cash position was significantly strengthened 
through a combination of a convertible note issuance, 
private placements directed to institutional and other 
investors, a public offering to Finnish retail investors and 
an open offering to UK retail and institutional investors 
to raise a total of EUR 35.5 million (gross). 
•	 In May 2024, Dr. Juho Jalkanen was appointed as the 
Company’s new Chief Executive Officer (CEO), taking 
over from Dr. Markku Jalkanen, who retired as CEO, 
but who is continuing as a member of the Board of 
Directors of Faron. Dr. Juho Jalkanen has worked at 
Faron in various roles since 2006, most recently serving 
as its Chief Operating Officer. 
•	 Mr. Tuomo Pätsi was elected as the Chair of the 
Board, following the departure of Dr. Frank Armstrong 
who did not stand for re-election. Mr. Pätsi was the 
President of the EMEA region and Worldwide Markets 
for Celgene Corporation, a global pharmaceutical 
company and currently wholly owned subsidiary of 
Bristol Myers Squibb, engaged primarily in the discovery, 
development, and commercialization of therapies for 
the treatment of cancer. He is an experienced biotech 
and pharmaceutical executive who was, until recently, 
the Executive Vice President for Seagen Inc., a US-
based, cancer-focused biotechnology company. 
•	 In April 2024, Mr. Yrjö Wichmann was appointed as the 
Company’s interim Chief Financial Officer (CFO) and in 
August as the permanent CFO. Mr. Wichmann previously 
served as the Company’s CFO between 2014 and 2019 
and as Senior Vice President, Financing & IR from 2019 
to April 2024. Mr. Wichmann is an accomplished biotech 
and financial executive with over 20 years’ experience in 
financing and investment banking.  
•	 In August 2024, Dr. Petri Bono was appointed as the 
Company’s Chief Medical Officer (CMO), succeeding 
Dr. Birge Berns, who will continue her role as part 
of Faron’s medical leadership team involved in 
developing bexmarilimab. Dr. Bono is an oncologist 
and has served as the CMO and member of the Group 
executive team of Terveystalo, the largest private 
healthcare service provider in Finland. Prior to joining 
Terveystalo he was the CMO at Helsinki University 
Hospital. He brings leading expertise in immunology, 
with his own research focusing on molecular and 
immunological oncology. 
•	 In May 2024, Dr. Markku Jalkanen, co-founder, Board 
member and former CEO of Faron, and Dr. Sirpa 
Jalkanen, co-founder and member of Faron’s Scientific 
Advisory Board, were selected as finalists for the 
European Inventor Award 2024, in recognition of their 
research developing Faron’s wholly owned precision 
cancer immunotherapy candidate, bexmarilimab. 
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FARON PHARMACEUTICALS OY
ANNUAL REPORT 2024
CONSOLIDATED KEY FIGURES, IFRS
€’000
Unaudited 
7–12/2024 
months
Unaudited 
7–12/2023 
months
1–12/2024
12 months
1–12/2023
12 months
Other operating income
0
0
0
0
Research and Development expenses
(5,082)
(11,024)
(11,744)
(19,542)
General and Administrative expenses
(2,301)
(4,732)
(6,929)
(9,026)
Operative Loss for the period
(7,383)
(15,756)
(18,673)
(28,568)
Loss per share, EUR
(0.11)
(0.26)
(0.29)
(0.48)
Number of shares at end of period
104,624,864
68,786,699
104,624,864
68,786,699 
Average number of shares
104,624,864
67,137,790
88,518,654
65,055,036 
€’000
Unaudited 
30 Jun 2024
Unaudited 
30 Jun 2023
31 Dec 2024
31 Dec 2023
Cash and cash equivalents
29,979
6,315
9,503
6,875
Equity
1,379
(9,483)
(9,762)
(15,160)
Balance sheet total
35,460
12,836 
12,521
10,220
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FINANCIAL REPORT

CHAIRMAN’S  
STATEMENT
Year 2024 has seen us achieve significant clinical 
milestones and strategic advancements, showcasing 
our resilience in a challenging biotechnology landscape. 
Despite the obstacles encountered, we conclude the year 
in our strongest position to date. 
Faron has continued to make significant strides in the 
clinical development of bexmarilimab, its wholly owned, 
investigational immunotherapy, through the progression 
of our BEXMAB trial. We were very pleased to dose the 
first patient in Phase II part of that trial at the start of the 
year, evaluating the safety and efficacy of bexmarilimab in 
combination with standard of care (SoC) in patients with 
hypomethylating agents (HMAs)-refractory or relapsed 
myelodysplastic syndrome (r/r MDS). Data generated 
continue to be highly encouraging with the latest 
positive interim Phase II data, presented at the American 
Society of Hematology (ASH) Annual Meeting, showing 
a remarkable 80% overall response rate. In July 2024, 
we received positive feedback from the FDA regarding 
the registrational study plan for bexmarilimab, providing 
clear guidance on the path to approval. Their proposal 
significantly reduces the devolvement costs and timelines 
to bring this promising therapy to a broader group of 
patients and is a significant achievement for Faron.  
The financial landscape for biotechnology companies 
has been challenging but, despite this, Faron has 
demonstrated remarkable resilience. We successfully 
raised €35.5 million (gross) through an oversubscribed 
combined share offering, supported by both existing 
and new shareholders. This financial achievement not 
only provides critical funding for our BEXMAB trial but 
also reflects the confidence of our investors in our 
scientific approach and further validates the potential of 
bexmarilimab. 
In 2024 we had notable changes in our leadership and 
governance. We welcomed Juho Jalkanen (previously 
our COO) as our new CEO, while retaining the invaluable 
guidance of former CEO, Markku Jalkanen, as a member 
of the Board. We also appointed Yrjö Wichmann as 
our CFO, Dr. Petri Bono as Chief Medical Officer and I 
We will continue to explore the 
best options to commercialize 
bexmarilimab in the combination 
setting and, as we move to 
next year, we are looking to 
have substantial interactions 
with the US FDA about the best 
path to market in our chosen 
indications.”
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Tuomo Pätsi 
Chairman
February 27, 2025
assumed the position of Chairman from Frank Armstong. 
I’d particularly like to thank both Markku and Frank for 
their support and guidance during their tenure at Faron. 
Their contributions have helped enormously in bringing 
Faron to the strong position that we find ourselves 
in today. Additionally, we established a Shareholders’ 
Nomination Board, comprised of representatives from our 
top five shareholders, which will provide direct input into 
our Board nominations and strategic direction.  
One highlight of the year was the international recognition 
received by our founders, Dr. Markku Jalkanen and Prof. 
Sirpa Jalkanen, as finalists at the 2024 European Inventor 
Awards, underscoring the innovative spirit that continues 
to drive Faron. 
Looking forward to 2025, we remain excited about the 
potential of our bexmarilimab program. We expect topline 
efficacy readouts from our Phase II trial in the first half 
of the year, which will be crucial in determining our next 
steps. The Board is optimistic about potentially initiating 
preparations for Phase III development in the second half 
of 2025, a significant milestone that would bring us ever 
closer to bringing this innovative therapy to patients who 
desperately need new treatment options. 
I would like to extend my gratitude to our dedicated 
team, our invaluable shareholders, the physicians and 
patients, and all other stakeholders who have made our 
continued progress possible. We look forward to 2025 
with optimism. 
Amongst other things, these 
funds have allowed us to 
accelerate our bexmarilimab 
program, bringing this much 
needed potential treatment one 
step closer to patients.”
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2024 was a year of success and transformation for Faron 
Pharmaceuticals, marking a new chapter in Faron’s story 
and solidifying our position as a leader in the field of 
immunotherapy.  
With fresh leadership and renewed focus, we reinforced 
our organisational structure. We welcomed Tuomo Pätsi 
as the new Chairman of our Board, taking over from 
Dr. Frank Armstrong, alongside Yrjö Wichmann as our 
new CFO and Dr. Petri Bono as Chief Medical Officer, all 
of whose extensive expertise and fresh perspectives 
have invigorated our renewed strategy. I was also proud 
to assume the role of CEO this year, taking over from 
Dr. Markku Jalkanen. These changes, coupled with the 
strong foundation built by our predecessors, have enabled 
us to refine our mission and approach, making us well-
equipped to navigate the complexities of a competitive 
and rapidly evolving sector and I would like to thank 
Markku and Frank for their commitment to Faron and for 
their support during this transition. Their contributions 
thus far, combined with the dedication of our entire team, 
have enabled us to sustain momentum even amidst 
challenging market conditions, setting a clear course for 
sustainable growth and innovation at Faron.  
The theme of transformation has continued through 
the clinical development program for our lead asset, 
bexmarilimab. We have made significant progress, from 
both a clinical and regulatory perspective, further cementing 
our believe in the potential of bexmarilimab to address 
critical unmet needs in oncology. We had numerous 
positive interactions with regulatory authorities resulting in 
key milestones including Fast Track Designation (FTD) for 
bexmarilimab from the FDA for the treatment of relapsed 
or refractory myelodysplastic syndrome (r/r MDS) patients, 
underscoring the urgency for novel therapies in treating this 
aggressive blood cancer. 
We also received positive feedback from our formal Type 
D Scientific Advice Meeting with the FDA regarding the 
registrational clinical development plan for bexmarilimab in 
the treatment of high-risk MDS (HR MDS). The FDA 
acknowledged the difficulties of running a randomized 
study with a comparator in the r/r setting and instead 
proposed that Faron conduct a confirmatory phase III trial in 
frontline HR MDS, that would not require a separate phase 
III in r/r MDS.   
CHIEF EXECUTIVE 
OFFICER’S REVIEW
2024 was a year of success 
and transformation for Faron 
Pharmaceuticals.”
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These two milestones significantly enhance our ability 
to advance bexmarilimab through the regulatory 
process, also allowing for frequent FDA interactions 
and streamlined development pathways, which will 
be invaluable as we prepare for pivotal studies and 
market approval.  
In parallel, the Phase II interim data from our BEXMAB 
trial, presented at the 66th American Society of 
Hematology (ASH) Annual Meeting, demonstrated 
remarkable efficacy. The trial achieved an 80% overall 
response rate in r/r MDS patients, with 70% achieving 
deep and durable responses, including complete and 
partial remissions. Importantly, four patients progressed 
to potentially curative bone marrow transplants, and the 
combination therapy with azacitidine continued to show a 
favourable safety profile.  
The regulatory recognition and the robust clinical 
results achieved to date highlight bexmarilimab’s ability 
to reprogram myeloid cells by engaging the Clever-1 
receptor, overcoming resistance to hypomethylating 
agents (HMAs), and activating the immune system, 
demonstrating its potential as a transformative therapy 
for an underserved population. As we advance to pivotal 
efficacy readouts and prepare for the initiation of Phase 
III development in the second half of 2025 after having an 
end-of-phase 2 (EOP2) meeting with the FDA. We remain 
focused on our mission to bring this innovative therapy to 
patients facing significant unmet medical needs.   
Also in 2024, we considerably strengthened our financial 
position, successfully raising €35.5 million (gross) 
through an oversubscribed combined share offering, 
a strong reflection of our investors’ confidence in the 
potential of bexmarilimab. This additional financing 
played an essential role in the acceleration of our clinical 
programs – particularly our BEXMAB trial and provided a 
stronger foundation for advancing bexmarilimab towards 
commercialisation.  
Looking ahead, 2025 promises to be a pivotal year as 
we aim to deliver crucial clinical data and engage in 
meaningful discussions with regulatory authorities. We 
remain steadfast in our mission to bring life-changing 
immunotherapies to patients who need them most and 
the exceptional progress we’ve achieved this year brings 
us closer to achieving that goal. I would like to extend my 
gratitude to our shareholders, partners, and the Faron team 
for their continuous support and commitment this year 
and I look forward to what 2025 brings.  
Dr Juho Jalkanen 
Chief Executive Officer  
 
February 27, 2025
Looking ahead, 2025 
promises to be a pivotal year.”
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14

Despite continuing challenging market conditions in 2024, 
the Company significantly strengthened its cash position 
through a combination of a convertible note issuance, 
private placements directed to institutional and other 
investors, a public offering to Finnish retail investors and 
an open offering to UK retail and institutional investors 
to raise a total of EUR 35.5 million (gross). As a result of 
these fundraising efforts, the net cash increased from 
financing activities of EUR 25.8 million compared to 
EUR 24.0 million in 2023.  
Faron places a strategic emphasis on capital efficiency, 
a key element of efforts to extend our cash runway, 
without compromising the ability to advance our clinical 
development program. This capital efficiency has allowed 
us to achieve more with available resources, while 
focusing on clinical outcomes.
RESEARCH AND DEVELOPMENT COSTS
R&D costs were EUR 11.7 million in 2024 compared 
to 19.5 million in 2023, a decrease of EUR 7.8 million. 
These costs are attributable to advancing our clinical 
programs including completion of BEXMAB Phase I and 
the initiation of Phase II. Clinical trial costs include the 
cost of patient and site enrollment, CRO service costs 
including monitoring, investigator fees, and compensation 
and benefits for personnel directly responsible for 
R&D activities, and product supply costs. The costs of 
outsourced clinical trial services were EUR 3.3 million in 
2024 compared to EUR 4.0 million in 2023. Compensation 
and benefits were EUR 1.4 million in 2024 and EUR 3.2 
million in 2023 and included stock compensation expense 
of EUR 0.02 million and EUR 0.7 million in 2024 and 2023, 
respectively.  
GENERAL AND ADMINISTRATION COSTS
G&A expenses were EUR 6.9 million in 2024 compared to 
EUR 9.0 million in 2023, and decrease of EUR 2.1 million. 
The decrease was mainly due to the recognition of the 
incremental fair value of amending the terms of 2015 
option plan of EUR 1.1 million.  Compensation and 
benefits were EUR 3.3 million in 2024 and EUR 5.7 million 
in 2023 and included stock compensation expense of 
EUR 0.7 million and EUR 1.7 million in 2024 and 2023, 
respectively.  
TAXATION
The Company’s tax credit for the fiscal year 2024 can 
be recorded only after the Finnish tax authorities have 
approved the tax report and confirmed the amount of 
tax-deductible expenses. The total amount of cumulative 
tax losses carried forward approved by tax authorities 
on 31 December 2024 was EUR 57.7 million (2023: 
EUR 51.6 million). The Company can utilize these losses 
against potential taxable profits generated during the 
years 2025 to 2034. In addition, the Company has 
FINANCIAL 
REVIEW
FARON PHARMACEUTICALS
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FARON PHARMACEUTICALS LTD  |  ANNUAL REPORT 2024
15

EUR 117.2 million of R&D costs incurred in the financial 
years 2010 - 2023 that have not yet been deducted from 
taxation. This amount can be deducted over an indefinite 
period at the Company’s discretion. 
LOSSES
Loss before income tax and total comprehensive income in 
2024 was EUR 25.9 million compared to EUR 30.9 million 
in 2023, which represents a loss of EUR 0.29 per share and 
EUR 0.48 per share in 2024 and 2023, respectively.  
CASH FLOWS
Net cash flow 2024 and 2023 was essentially flat. Cash 
used for operating activities in 2024 was EUR 23.0 million 
compared to 2023 of EUR 23.8 million. Net cash inflow 
from financing activities in 2024 was EUR 25.8 million 
compared to 2023 of EUR 24.0 million. 
FUNDRAISING 
On 19 February 2024 the Company announced that 
it was in breach of several undertakings agreed in 
the secured debt agreement dated 28 February 2022, 
between IPF Fund II SCA, SICAV-FIAR (“IPF”) as Lender 
and Faron Pharmaceuticals Ltd as Borrower and 
subsequent waiver letters provided by IPF, and was 
therefore in several events of default. Faron’s bank 
accounts are pledged to IPF and IPF notified Faron’s 
banks of the blocking of the pledged accounts due to 
the above-mentioned breaches. After successful funding 
arrangements, the bank accounts were released in the 
beginning of March 2024. 
On 4 March 2024 the Company raised a total of EUR 3.2 
million through convertible loan instruments subscribed 
by a limited number of the Company’s existing 
shareholders. The Convertible loans and related interest 
and fees were converted into shares in the June offering. 
On 4 April 2024 the Company conducted a private 
placement directed to a limited number of institutional 
and other investors to raise EUR 4.8 million which, 
together with the EUR 3.2 million convertible loan 
announced on 4 March 2024, secured the required short-
term bridge financing totaling EUR 8 million. 
On 4 June 2024, Faron announced an offering of 
approximately EUR 30.7 million in total by offering for 
subscription preliminarily a maximum of 30,714,592 
new and/or treasury shares at a subscription price 
of EUR 1.00 per Offer Share. The Offering was conducted 
as a directed share issue by way of 
i.	 a public offering to private individuals and legal 
entities in Finland, 
ii.	 an institutional offering to institutional investors in 
the European Economic Area. 
iii.	a separate open offer to qualifying holders of 
depositary interests in the United Kingdom and 
elsewhere and 
iv.	a separate retail offer to retail investors in 
the United Kingdom on the “REX” platform.  
The results of the offering were announced on 
20 June 2024, and it attracted significant interest 
from both existing shareholders and new investors 
and was oversubscribed. The Company raised a 
total of approximately EUR 30.7 million, of which 
approximately EUR 3.7 million was paid by converting 
the convertible loan and related arrangement fees 
and interests into shares in the Company. As a result 
of the share offering, with the gross proceeds of 
approximately EUR 27 million the Company believes 
it will have sufficient resources to execute its core 
business and deliver on its key milestones of the year 
2024 under the current business plan and in compliance 
with the financial covenants of the IPF Fund. The Board 
of Directors of the Company decided to issue of a 
total of 30,709,056 newly issued treasury shares and 
new shares in the Company. As set out in the terms 
and conditions of the Offering, existing shareholders 
and DI (depositary interest) holders were given an 
allocation preference. Carnegie Investment Bank 
AB, Finland Branch (“Carnegie”) and Peel Hunt LLP (“Peel 
Hunt”) acted as lead managers (the “Lead Managers”) 
and bookrunners for the Offering. On 20 June 2024 the 
Company entered into 90-day lock-up agreement with 
Lead Managers. 
As a post-period event, Faron conducted in early 
February 2025 a private placement directed to a 
limited number of institutional and other investors 
raising EUR 12.0 million.  
FINANCIAL POSITION  
As of 31 December 2024, total cash and cash equivalents 
held were EUR 9.5 million compared to 2023 of 
EUR 6.9 million.  
GOING CONCERN
As part of their going concern review, the Directors have 
followed the Finnish Limited Liability Companies Act, the 
Finnish Accounting Act and the guidelines published by 
the Financial Reporting Council entitled “Guidance on 
the Going Concern Basis of Accounting and Reporting 
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16

on Solvency and Liquidity Risks – Guidance for directors 
of companies that do not apply the UK Corporate 
Governance Code”. Faron is subject to a number of 
risks similar to those of other development stage 
pharmaceutical companies.  
These risks include, amongst others, generation of 
revenues in due course from the development portfolio 
and risks associated with research, development, 
testing and obtaining related regulatory approvals of its 
pipeline products. Ultimately, the attainment of profitable 
operations is dependent on future uncertain events which 
include obtaining adequate financing to fulfil Faron’s 
commercial and development activities and generating 
a level of revenue adequate to support Faron’s cost 
structure.  
Faron made a net loss of EUR 25.9 million during the 
year ended 31 December 2024. It had a negative equity 
of EUR 9.8 million including an accumulated deficit of 
EUR 197.4 million. As 31 December 2024, Faron had cash 
and cash equivalents of EUR 9.5 million. As a post-period 
event Faron conducted In early February 2025 a private 
placement directed to a limited number of institutional 
and other investors to raise EUR 12.0 million, which 
significantly strengthened its financial position.  
The Directors have prepared detailed financial forecasts 
and cash flows looking beyond 12 months from the 
date of the approval of these financial statements. In 
developing these forecasts, the Directors have made 
assumptions based upon their view of the current and 
future economic conditions that are expected to prevail 
over the forecast period. Directors estimate that the 
cash held by Faron at 31 December 2024 together with 
the EUR 12.0 million funds raised post-period as well 
as known receivables will be sufficient to support the 
current level of activities into the third quarter of 2025. 
Despite this the Directors are continuing to explore 
sources of additional financing and they believe they have 
a reasonable expectation that they will be able to secure 
additional cash inflows that are sufficient for Faron to 
continue its activities for not less than 12 months from 
the date of approval of these financial statements; they 
have therefore prepared the financial statements on a 
going concern basis. Because the additional finance is 
not committed at the date of issuance of these financial 
statements, these circumstances represent a material 
uncertainty that may cast significant doubt on Faron’s 
ability to continue as going concern. Should Faron be 
unable to obtain additional financing such that the going 
concern basis of preparation were no longer appropriate, 
adjustments would be required, including to reduce 
balance sheet values of assets to their recoverable 
amounts, to provide for further liabilities that might arise.   
HEADCOUNT
Faron’s headcount at the end of year was 25 (2023: 34).
SHARES AND SHARE CAPITAL
During the period 1 January to 31 December 2024, the 
Company, using the share authorities granted at the 
Extraordinary General Meeting held on 22 September 
2023 issued a total of 3,200,298 new ordinary shares 
at an issuance price of EUR 1.5 per share to investors. 
During the same period, the Company, using the share 
authorities granted at the Annual General Meeting held 
on 5 April 2024, issued a total of 30,709,056 shares at 
an issuance price of EUR 1.0 per share to investors. The 
subscription price net of costs was credited in full to the 
Company’s reserve for invested unrestricted equity, and 
the share capital of the Company was not increased. 
The Company has no shares in treasury; therefore, at 
the end of 2024 the total number of voting rights was 
104,624,864.  
Yrjö Wichmann 
Chief Financial Officer
February 27, 2025 
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17

RESEARCH AND DEVELOPMENT
Faron’s main products are in clinical development 
however, they may not be successful in clinical trials 
and the Company may not be able to develop approved 
or marketable products. Technical risk is also present 
at each stage of the discovery and development 
process of other, earlier stage products with challenges 
in biology (including the ability to produce candidate 
drugs with appropriate safety, efficacy and usability 
characteristics). Conversion of cutting-edge scientific 
research into clinical development programmes of novel 
compounds and drugs where there is a limited amount 
of guidance, and no previous examples involves a high 
degree of uncertainty. This uncertainty, combined with 
Faron’s lean organisation, could result in situations 
where the Company needs to make rapid alterations 
to its development projects without full visibility of all 
of the downstream consequences. Additionally, drug 
development is a highly regulated environment which 
presents technical risk through the need for study 
designs and data to be accepted by regulatory agencies. 
As part of the development risk, the manufacturing of  
the Company’s intended products could become 
impossible or products would be supplied in lower 
quantities than needed. 
COMMERCIAL PRODUCTS 
AND MANUFACTURING
The biotechnology and pharmaceutical industries in 
which Faron operates are very competitive. Faron is a 
clinical stage biopharmaceutical company and, similar 
to other companies operating in this field, is subject 
to a number of risks and uncertainties. Competitors 
include major multinational pharmaceutical companies, 
biotechnology companies and research institutions. 
Many of these companies have substantially greater 
financial, technical, and operational resources, such as 
larger research and development resources and staff. 
It may have a material adverse impact on the Company 
if its competitors succeed in developing, acquiring, or 
licensing drug product candidates that are more effective 
or less costly than any of the product candidates which 
the Company is currently developing or which it may 
develop. Furthermore, there can be no guarantee that 
the Company will be able, or that it will be commercially 
advantageous for the Company, to monetise the value of 
its intellectual property through entering into licensing or 
other cooperation deals with pharmaceutical companies. 
There can be no assurance that the Company’s proposed 
products will be capable of being manufactured in 
sufficient quantities and standards for clinical trials or 
in commercial quantities, in compliance with regulatory 
requirements and at an acceptable cost or within an 
acceptable timeframe.
RISKS AND 
UNCERTAINTIES
Faron is a clinical stage biopharmaceutical company and, similar to other 
companies operating in this field, is subject to a number of risks and 
uncertainties. The principal risks and uncertainties identified by Faron for 
the year ended December 31, 2024 are below.
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18

DEPENDENCE ON KEY PERSONNEL AND 
SCIENTIFIC AND CLINICAL COLLABORATORS
The Company’s success is highly dependent on the 
expertise and experience of the Directors and key 
management. Whilst the Company has entered into 
employment and other agreements with each of these 
key personnel, the retention of such personnel cannot be 
guaranteed. Should key personnel leave or no longer be 
party to agreements or collaborations with the Company, 
the Company’s business prospects, financial conditions 
and/or results of operations may be materially adversely 
affected. To develop new products and commercialise 
its current pipeline, the Company relies, in part, on 
the recruitment of appropriately qualified personnel, 
including personnel with a high level of scientific and 
technical expertise. There is currently a shortage of such 
personnel in the pharmaceutical industry, meaning that 
the Company is likely to face significant competition 
in recruitment. The Company may be unable to find 
a sufficient number of appropriately highly trained 
individuals to satisfy its growth rate, which could affect its 
ability to develop as planned. Furthermore, the Company’s 
development and prospects depend to a significant 
degree on the experience, performance and continued 
service of its senior management team including the 
Directors. The Company has invested in its management 
team and has entered into contractual arrangements 
with these individuals with the aim of securing their 
services. Retention of these services or the identification 
of suitable replacements, however, cannot be guaranteed. 
The loss of the services of any of the Directors or other 
members of the senior management team and the costs 
of recruiting replacements may have a material adverse 
effect on the Company and its commercial and financial 
performance and reduce the value of an investment in 
the shares of the Company. The Company’s financial 
situation may require savings measures that result in 
reduction of staff.  
REGULATORY ENVIRONMENT
The Company operates in a highly regulated environment. 
Whilst the Company will take every effort to ensure that 
the Company and its partners comply with all applicable 
regulations and reporting requirements, there can be 
no guarantee of this. Failure to comply with applicable 
regulations could result in the Company being unable to 
successfully commercialise its products and/or result 
in legal action being taken against the Company, which 
could have a material adverse effect on the Company. 
The Company will need to obtain various regulatory 
approvals (including from the FDA and the EMA) and 
comply with extensive regulations regarding safety, 
quality and efficacy standards in order to market its 
products. While efforts have been and will be made to 
ensure compliance with governmental standards and 
regulations, there is no guarantee that any product will 
be able to achieve the necessary regulatory approvals 
to promote that product in any of the targeted markets 
The Company’s success 
is highly dependent on the 
expertise and experience of the 
Directors and key management.”
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19

and any such regulatory approval may include significant 
restrictions for which the Company’s products can be 
used. In addition, the Company may be required to incur 
significant costs in obtaining or maintaining its regulatory 
approvals. Delays or failure in obtaining regulatory 
approval for products would likely have a serious 
adverse effect on the value of the Company and have 
a consequent impact on its financial performance. 
INTELLECTUAL PROPERTY AND 
PROPRIETARY TECHNOLOGY
The Company relies and will rely on intellectual property 
laws and third-party non-disclosure agreements to protect 
its patents and other proprietary rights. The Intellectual 
Property Rights (IPRs) on which the Company’s business 
is based is a combination of patents, patent applications, 
confidential business knowhow and trade secrets, 
and trademarks. No assurance can be given that any 
currently pending patent applications or any future 
patent applications will result in patents being granted. In 
addition, there can be no guarantee that the patents will 
be granted on a timely basis, that the scope of any patent 
protection will exclude competitors or provide competitive 
advantages to the Company, that any of the Company’s 
patents will be held valid if challenged, or that third parties 
will not claim rights in, or ownership of, the patents and 
other proprietary rights held by the Company. 
Despite precautions taken by the Company to protect its 
products, unauthorised third parties may attempt to copy, 
or obtain and use, the Company’s IPR and other technology 
that is incorporated into its pharmaceutical products. 
In addition, alternative technological solutions similar 
to the Company’s products may become available to 
competitors or prospective competitors of the Company. 
It should be noted that once granted, a patent could be 
challenged both in the relevant patent office and in the 
courts by third parties. Third parties can bring material and 
arguments which the patent office granting the patent may 
not have seen at the time of granting the patent. Therefore, 
whilst a patent may be granted to the Company, it could 
in the future be found by a court of law or by the patent 
office to be invalid or unenforceable or in need of further 
restriction. Should the Company be required to assert its 
IPR, including any patents, against third parties it is likely to 
use a significant amount of the Company’s resources as 
patent litigation can be both costly and time consuming. 
No assurance can be given that the Company will be in 
a position to devote sufficient resources to pursue such 
litigation. Any unfavourable outcomes in respect of patent 
litigation could limit the Company’s IPR and activities 
moving forward.
The Directors do not believe that the Company’s lead 
pharmaceutical drug candidates, future drug candidates 
in development, and proprietary processes for generating 
those candidate compounds infringe the IPR of any 
third parties. However, it is impossible to be aware of all 
third party intellectual property. The Company’s research 
has included searching and reviewing certain publicly 
available resources, which are examined by senior 
levels of management to keep abreast of developments 
in the field.
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20

FINANCIAL
The Company has incurred significant losses since its 
inception and does not have any approved or revenue 
generating products. The Company expects to incur 
losses for the foreseeable future, and there is no 
certainty that the business will generate a profit. The 
Company is highly dependent on equity, public grants 
and loan financing. The Company may not be able to 
raise additional funds that will be needed to support its 
product development programmes or commercialisation 
efforts, and any additional funds that are raised could 
cause dilution to existing investors. The Company 
operates internationally, and it is thus exposed in various 
currencies and fluctuation in their relative values. Even 
though the Company seeks to hedge currency positions 
there is no guarantee that it will be successful. The 
Company has a loan from IPF Fund II SCA, SICAV-FIAR in 
the principal amount of EUR 8.69 million. The said loan 
contains many financial covenants, and it is not certain 
that the company can comply with the said financial 
covenants at all times (see Note 25.). Certain covenants 
are in the control of the Company (e.g. the Minimum Cash 
Covenant) whereas certain are dependent on external 
events (e.g. Gearing covenant which is calculated using 
the Company stock price). Furthermore, the Company 
may not be able to repay the loan, as agreed with the 
lender. The Company’s IPR, business mortgages and 
bank accounts are pledged to the lender, giving the 
lender operational control of the Company in an Event 
of Default, if the Company is in breach of its obligations 
towards the lender. 
OTHER RISKS RELATED TO OPERATIONS
Operating with multiple vendors and other external 
suppliers means that the Company regularly delivers and 
receives information and data through multiple channels. 
Some of these are trade secrets or of confidential nature. 
Even though the Company uses all reasonably available 
means to secure the data and the channels used, there 
is no certainty that full data security can be obtained. 
As was seen with the COVID-19 pandemic, unexpected 
external reasons may have significant inpact on the 
market we are operating and indirectly affect or even 
directly affect also our operations, including our ability 
to conduct clinical trials. Additionally, military conflicts 
like the one currently taking place in Ukraine, have the 
potential to disrupt operations and negatively impact the 
debt and equity markets. The Company is publicly listed 
and as such subject to various securities laws in multiple 
jurisdictions. The Company uses significant amount of 
both internal and external resources to secure that all its 
operations and external communication are conducted in 
accordance with these regulations. Whilst the Company 
will take every effort to ensure that the Company and its 
partners comply with all applicable securities laws and 
requirements, there can be no guarantee of this. 
This report was approved by the Board on 27 February, 2025.
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21

CORPORATE 
GOVERNANCE
CHAIRMAN’S INTRODUCTION TO GOVERNANCE
The Board of the Company emphasises the importance 
of good corporate governance and is aware of its 
responsibility for overall corporate governance and for 
supervising the general affairs and business of Faron.
As Chairman of the Board, I oversee the adoption, 
delivery and communication of Faron’s corporate 
governance model. In this role, I endeavour to foster 
a positive governance culture throughout Faron, seeing 
that ultimate responsibility for the quality of, and Faron’s 
approach to, corporate governance lies with me.
Faron is not required to comply with the UK Corporate 
Governance Code by virtue of being an AIM and Nasdaq 
First North Growth Market quoted company. The 
Board does, however, seek to apply the QCA Corporate 
Governance Code (as devised by the Quoted Companies 
Alliance in consultation with a number of significant 
institutional small company investors) in its updated 
form. After the year end 2020 and the UK leaving the 
European Union, Faron has to follow applicable domestic 
laws of the UK in addition to Finnish national and 
European Union’s legislation. 
No significant changes in governance arrangements 
occurred during the year.
As described below, the Board continues to promote 
a healthy corporate culture that is based on ethical 
values and behaviours consistent with Faron’s objectives, 
strategy and business model described on Faron’s 
website and with the description of principal risks and 
uncertainties set out in this document. As good corporate 
governance is fundamentally about culture, rather than 
procedure, Faron’s corporate culture is monitored on 
a regular basis, and appropriate action is taken if, and to 
the extent, deemed necessary.
Tuomo Pätsi 
Non-Executive Chairman
 27 February 2025
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COMPLIANCE WITH THE PRINCIPLES OF THE QCA CODE
Compliance
The Principles of the QCA Code
Comply/Explain
Disclosure in the 2024 Report
1.	 Establish a strategy and business  
model which promote long-term
Comply
Pages 4, to 7 and 12 to 19
2.	 Seek to understand and meet  
shareholder needs and expectations
Comply
Pages 38 to 41
3.	 Take into account wider stakeholder  
and social responsibilities and their  
implications for long-term success
Comply
Pages 38  to 41
4.	 Embed effective risk management,  
considering both opportunities and threats,  
throughout the organisation
Comply
Pages 20 to 23
5.	 Maintain the board as a well-functioning,  
balanced team led by the chair
Comply
Pages 26 to 30 and 42 to 43
6.	 Ensure that between them the directors  
have the necessary up-to-date experience,  
skills and capabilities
Comply
Pages 26 to 30
7.	 Evaluate board performance based on  
clear and relevant objectives, seeking  
continuous improvement
Comply
Page 31 
8.	 Promote a corporate culture that is  
based on ethical values and behaviours
Comply
Page 24
9.	 Maintain governance structures and  
processes that are fit for purpose and support  
good decision-making by the board
Comply
Pages 24 and 26
10.	Communicate how the company is governed 
and is performing by maintaining a dialogue with 
shareholders and other relevant stakeholders
Comply
Pages 24 to 43
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FARON PHARMACEUTICALS
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On 5 April 2024, the Company held its Annual General 
Meeting (AGM). At the AGM the number of Directors was 
confirmed as five. Markku Jalkanen,  John Poulos, Christine 
Roth, Marie-Louise Fjällskog and Tuomo Pätsi were re-
elected to the Board for a term that ends at the end of the 
next AGM. After the AGM Tuomo Pätsi was elected as the 
Chairman of the Board. The longterm Chairman of the 
Board, Frank Armstrong, had decided to step down from 
his position. 
At the end of year 2024, the Board comprised of five 
non-executive directors. Brief biographical details for the 
Directors can be found on the following pages. During 2024, 
the Board held 26 meetings. 
The Board is responsible to the shareholders for the proper 
management of the Company and meets regularly to set the 
overall direction and strategy of Faron, to review scientific, 
operational and financial performance, to review the strategy 
and activities of the business, and to advise on management 
appointments. The Board sees to the administration 
of Faron and the organisation of its operations, being 
responsible for the appropriate arrangement of the control 
of Faron’s  accounts and finances. 
All key operational and investment decisions are subject 
to full Board approval. The management of the Company 
prepares a monthly management and financial accounts 
pack of the Group, which is distributed to the Board every 
month and in advance of Board meetings. In individual 
cases the Board may decide in a matter falling within the 
general competence of the Chief Executive Officer.  
The roles of Chief Executive Officer and Non-Executive 
Chairman are well defined and clearly separated. 
The Chairman oversees the Board’s work, ensures that 
the Board’s decision-making is balanced and that the 
Non-Executive Directors have all relevant information on 
matters to be decided. The Chairman sees to it that the 
Board meets when necessary.
The Chief Executive Officer is responsible for implementing 
the strategy of the Board and managing Faron’s day-to-day 
business activities. The Chief Executive Officer, reviewing 
the operating results regularly to make decisions about the 
allocation of resources and to assess overall performance, 
is the chief operating decision-maker.
The Board considers there to be sufficient independence 
of the Board and that all the non-executive Directors 
are of sufficient competence and calibre to add 
strength and objectivity to the Board, and to bring 
considerable experience in terms of their knowledge 
of the scientific, operational and financial development 
of biopharmaceutical products and companies. Where 
necessary, the Company facilitates that non-executive 
Directors obtain specialist external advice from 
appropriate advisers.
The term of office of each Director expires on the closing 
of the AGM immediately following their appointment to 
the Board. Under the Finnish Limited Liability Companies 
Act and the Company’s Articles of Association, the 
Directors are elected by the shareholders at general 
meetings annually. Under the Act, Directors may be 
removed from office at any time, with or without 
cause, by a majority of votes cast at a general meeting. 
Vacancies on the Board may only be filled by a majority of 
shareholder votes cast at a general meeting.   
BOARD OF
DIRECTORS
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Dr. Jalkanen is the previous Chief Executive Officer of 
Faron Pharmaceuticals Ltd. a role he has served since 
2007 and was a founding member of the Company. 
He has more than 40 years of experience within 
biomedical research, biotech development and the 
biopharmaceutical industry and has published over 130 
peer reviewed scientific publications in various highly 
ranked international journals.
Between 1996 and 2002, Dr. Jalkanen was the founding 
CEO and President of BioTie Therapies Corp, which 
became the first publicly traded Finnish biotech company 
to be listed on NASDAQ. BioTie was sold to Acorda 
Therapeutics in January 2016 for $363 million. Over his 
career, Dr. Jalkanen has held several board memberships 
for both public and private companies including Inveni 
Capital Management, Meddia Ltd and Priaxon AG. He is 
also an advisor for the only active Finnish life sciences 
fund – Inveni Capital.
Dr. Jalkanen obtained a Masters in Medical Biochemistry 
from the University of Kuopio and subsequently received 
a PhD in Medical Biochemistry from the University 
of Turku. He completed a side-laudatur examination 
in Molecular Biology from the University of Turku 
and completed his post-doctoral training at Stanford 
University, California between 1983 and 1986. Dr. 
Jalkanen obtained the position of docent in Biochemistry 
from University of Helsinki and the same qualification in 
Molecular and Cell Biology from the University of Turku. 
He became a Professor at the University of Turku in 1992
Holdings in the Company: 3,413,434 shares (directly and 
with his spouse) and 570,000 stock options, entitling to 
same amount of shares in the Company.
MARKKU JALKANEN
Non-Executive Director
b. 1954
Mr. Tuomo Pätsi (b. 1964) is a Non-Executive Chairman 
of Faron Pharmaceuticals Ltd., a role he has served since 
April 2024 prior joining the Board in March 2023 as a Non-
Executive Director.
Mr. Tuomo Pätsi was the President of the EMEA region 
and Worldwide Markets for Celgene Corporation, a global 
pharmaceutical company and currently wholly owned 
subsidiary of Bristol Myers Squibb, engaged primarily 
in the discovery, development and commercialization 
of therapies for the treatment of cancer. He is an 
experienced biotech and pharmaceutical executive who 
was until recently the Executive Vice President for Seagen 
Inc., a US-based cancer-focused biotechnology company.
Mr. Pätsi has over 30 years’ experience working in biotech 
and pharmaceuticals, with more than 10 years working 
at Celgene in various senior management roles, including 
as President of European and International Operations 
and President of the EMEA region and Worldwide 
Markets. Prior to this, he served as Vice President of 
Europe for Human Genome Science, a specialty pharma 
organization in Europe. Earlier in his career, he held roles 
of increasing responsibility in pharmaceutical companies, 
including more than ten years at Amgen Inc. Mr. Pätsi 
began his career as a Biomedical Research Scientist 
in Finland. He is a registered pharmacist and holds an 
MSc in pharmacology from the School of Pharmacy, 
Helsinki University.
Holdings in the company: 31,765 shares and 130,000 
stock options, entitling him to the same amount of shares 
in the company.
TUOMO PÄTSI
Non-Executive Chairman
b. 1964
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Mr. Poulos is a Non-Executive Director of Faron 
Pharmaceuticals Ltd., a role he has served since joining 
the board in May 2017. He has extensive experience in 
the global pharmaceutical industry having spent nearly 
40 years at AbbVie and Abbott.
Mr. Poulos served as Vice President, Head of Business 
Development and Acquisitions for AbbVie from 2013 
until 2016. He was also Group Vice President, Head of 
Pharmaceutical Licensing and Acquisitions for Abbott 
from 2005 until 2012. During his career with AbbVie and 
Abbott, Mr. Poulos was instrumental in the negotiation 
of numerous acquisitions, including Knoll/BASF Pharma 
(Humira) in 2001 for $6.9 billion, Kos Pharmaceuticals in 
2006 for $3.7 billion, Solvay in 2010 for $6.2 billion and 
Pharmacyclics (Imbruvica) in 2015 for $21 billion.
Mr. Poulos is currently President GNK Advisors Inc.,  
a Pharmaceutical Business Development firm, and is  
a member of the Board of Memgen, Inc. Mr. Poulos also 
serves as a advisor at Nucleome Therapetics.
Mr. Poulos holds a B.S. in Marketing and M.B.A in Finance 
from Indiana University.
Holdings in the Company: no shares and 170,000 
stock options, entitling to same amount of shares in 
the Company.
JOHN POULOS 
Non-Executive Director
b. 1954
Dr. Marie-Louise Fjällskog (b. 1964) is a Non-Executive 
Director of Faron Pharmaceuticals Ltd., joining the Board 
in September 2023. She is an experienced life sciences 
leader who has held senior leadership positions at large 
pharmaceutical, biotech and specialty pharma companies.
Dr. Marie-Louise Fjällskog is a professional with extensive 
experience in the pharmaceutical and biopharmaceutical 
industry, particularly in the field of clinical oncology, 
translational research, and drug development. She holds 
an MD degree and a Ph.D. from Uppsala University, 
Sweden, and is an Associate Professor of Oncology at the 
same institution. With over 25 years of clinical experience, 
Dr. Fjällskog has made significant contributions to the 
development of targeted therapies for cancer. She has 
held key roles in various pharmaceutical companies, 
such as Sensei Biotherapeutics, Merus, and Infinity 
Pharmaceuticals, where she led clinical development 
programs and played instrumental roles in their success, 
including Sensei’s $152 million IPO in 2021. Her extensive 
expertise and leadership have also earned her a position 
on the board of Biovica International AB, a prominent 
biotech company in Sweden and in the US, respectively. 
She is also on the board of Norwegian company Lytix 
Biopharma.
In January 2022, Dr. Fjällskog assumed the role of Chief 
Medical Officer at Faron where she leads Faron’s clinical 
development programs, particularly the bexmarilimab 
program. Dr. Fjällskog stepped down from the CMO role 
on September 21, 2023. Currently Dr. Fjällskog serves as 
a Interim CMO at Excientia.
Holdings in the company: No shares and 210,000 stock 
options, entitling her to the same amount of shares in 
the company.
MARIE-LOUISE FJÄLLSKOG
Non-Ececutive Director
b. 1964
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Ms. Christine Roth (b. 1963) is a Non-Executive Director 
of Faron Pharmaceuticals Ltd., joining the Board in 
September 2023. She is an experienced life sciences 
leader who has held senior leadership positions at large 
pharmaceutical companies.
Ms. Christine Roth is a pharmaceutical executive with 
over three decades of experience in the industry. She 
has played key roles in the development and launch of 
several therapies, including the first immune-oncology 
therapy and intentionally designed targeted therapy 
combinations. Her career includes leadership positions 
at major pharmaceutical companies, such as Novartis, 
Bristol-Myers Squibb, GlaxoSmithKline (GSK), and most 
recently, Bayer AG, where she serves as the Executive 
Vice President of the Oncology Strategic Business 
Unit focussing on precision molecular oncology, next-
generation immuno-oncology medicines, and radioligand 
therapies. At GSK, she was responsible for the rebuild of 
the oncology business, including the integration of assets 
following the acquisition of Tesaro. Ms. Roth’s expertise 
extends across various therapy areas, including Oncology, 
Cardiovascular, Metabolic, and Infectious Diseases. She 
is actively involved in industry associations, such as the 
American Society of Clinical Oncology and the American 
Society of Hematology. She holds a Bachelor’s degree 
in Chemistry from the University of North Carolina at 
Chapel Hill.
Holdings in the company: 46,075 shares and 60,000 stock 
options, entitling her to the same amount of shares in 
the company.
CHRISTINE ROTH
Non-Executive Director
b. 1963
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BOARD COMMITTEES
The Company has established audit, nomination, 
business development and remuneration committees 
of the Board with formally delegated duties and 
responsibilities.
Under the Finnish Limited Liability Companies Act, Board 
committees do not, generally speaking, have a formal 
legal status or independent decision-making powers; 
rather, their role is to provide support in the preparation of 
the decision-making. The responsibility for the decisions 
remains with the Board even if the matter has been 
delegated to a committee.
Members of the Board committees were first elected 
at the Board meeting held following the AGM on 
5 April 2024.
During 2024, the Remuneration and Business 
Development Committee did not formally convene. 
REMUNERATION COMMITTEE
The remuneration committee has the task of advising on 
and making recommendations to the Board in relation to 
the remuneration paid to the Directors and supervising 
the development of any other remuneration or reward 
systems of Faron. In the beginning of year 2024, the 
Remuneration Committee comprised of John Poulos as 
Chair together with Christine Roth and Frank Armstrong.
As of 5 April 2024, the Remuneration Committee 
comprises of John Poulos as Chair together with 
Christine Roth and Tuomo Pätsi. 
AUDIT COMMITTEE
In the beginning of year 2024, the Audit Committee 
comprised Erik Ostrowski as Chair together with Frank 
Armstrong, Marie-Louise Fjällskog and Tuomo Pätsi. 
As of 5 April 2024, the Committee comprises Markku 
Jalkanen as Chair together with Marie-Louise Fjällskog 
and John Poulos. The Audit Committee meets not less 
than twice a year. The audit committee has the task 
of supervising and developing the internal audit of the 
Group, monitoring of financial reporting, and advising and 
making recommendations to the Board on related issues. 
NOMINATION COMMITTEE
In the beginning of year 2024, the nomination committee 
comprised Frank Armstrong as Chair together with 
Erik Ostrowski and Tuomo Pätsi. As of 5 April 2024, the 
Committee comprises Tuomo Pätsi as a chair together 
with Markku Jalkanen and Christine Roth. The nomination 
committee has the task, in co-operation with the Board, of 
advising on and making recommendations to the Board 
on issues relating to the composition and nomination of 
the Board.
The nomination committee considers succession 
planning for senior executives in the course of its work.
BUSINESS DEVELOPMENT COMMITTEE
The Business Development committee has the task of 
evaluating and identifying new business opportunities 
and strategic partners that align with the company’s 
mission and vision. In 2024, the business development 
committee has comprised of John Poulos as a chair 
together with Markku Jalkanen and Juho Jalkanen as the 
other members, and Leopoldo Zambeletti as a consultant 
to the committee.
SHAREHOLDERS’ NOMINATION BOARD
The Annual General Meeting decided on 5 April 2024 to 
establish a Shareholders’ Nomination Board, a corporate 
body of the Company’s shareholders, responsible for 
preparing and submitting proposals to the Annual 
General Meeting for the election and remuneration of the 
members of the Board of Directors and the remuneration 
of any committees of the Board of Directors. The 
members of the Board are selected by the five biggest 
shareholders. Starting 29 October 2024, the Nomination 
Board comprised of Timo Syrjälä as Chair together with 
Erkka Kohonen and Joonas Haakana. Chairman of the 
Board of Directors Tuomo Pätsi acts as an expert to the 
Nomination Board. During 2024, the Nomination Board 
held two meetings.
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During 2024, the Board held 26 meetings. The table below lists the Directors’ 
attendance at the Board and Committee meetings during the year:
THE DIRECTORS’ ATTENDANCE DURING THE YEAR ENDED 31 DECEMBER 2024
Attendance at Board Meetings
Board 
meetings
Audit 
Committee
Nomination 
Committee
Executive Directors
Jalkanen Markku*
26
1
3
Non-Executive Directors
Armstrong Frank**
11
1
3
Ostrowski Erik**
12
1
3
Poulos John
24
1
3
Pätsi Tuomo
25
3
Fjällskog Marie-Louise
24
2
Roth Christine
26
(*) Executive Director until May 2024
(**) Board Member until April 2024
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FINANCIAL REPORT

BASIC SALARY
Executive Directors’ basic salaries are reviewed annually. 
The review process is managed by the Remuneration 
Committee with reference to market salary data, the 
Executive Director’s performance and contribution to 
Faron during the year.
BONUSES
Executive Directors’ annual bonuses are based on the 
achievement of Faron’s strategic and financial targets 
and personal performance objectives. The Non-Executive 
Directors believe that bonuses are an incentive to achieve 
the targets and objectives and represent an important 
element of the total compensation of the Executive 
Directors; they have established that the annual bonus 
potential will be up to 50% for the Executive Directors.
LONGER TERM INCENTIVES
In order to further incentivise the Executive Directors and 
employees, and align their interests with shareholders, 
the Extraordinary General Meeting of the Company on 
15 September 2015 approved a share option plan and 
granted share options to the members of the Board 
under this option plan. At the AGM held on 28 May 2019, 
The Remuneration Committee sets the remuneration policy that aims to align Director remuneration with shareholders’ 
interests and attract and retain the best talent for the benefit of Faron. No Director is involved in discussions relating to 
their own remuneration. This report sets out Faron’s remuneration policy for the Executive and Non-Executive Directors. 
The remuneration of the Directors during the year ended 31 December 2024 is set out below:
the Company authorised the Board to implement a new 
share option plan for the employees and Directors of, 
and persons providing services to the Group. Rules of 
that new option plan were approved by the Board on 
20 November 2019. The most recent versions of the 
amendment Option plans 2015 and 2019 were resolved 
by the general meetings during 2023. Details of these 
option plans are on pages 33 to 34.
PENSION
Faron has a law-defined contribution plans under which it 
pays fixed contributions into a separate entity. The plans 
cover all the employees of Faron including the Executive 
Directors. Faron has no legal or constructive obligations 
to pay further contributions if the fund does not hold 
sufficient assets to pay all employees the benefits relating 
to employee service in the current and prior periods.
OTHER BENEFITS
The Chief Executive Officer and some employees have the 
possibility to take a company car allowance, which is part 
of their gross salary. All employees including Executive 
Directors have a company mobile phone that constitutes 
a company mobile phone allowance.
REMUNERATION 
REPORT
Remuneration Policy for Directors
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FINANCIAL REPORT

EXECUTIVE DIRECTORS’ SERVICE CONTRACTS 
AND TERMINATION PROVISIONS
The service contracts of Executive Directors are approved 
by the Board and are concluded for an indefinite term.
The details of the Executive Directors’ contracts are 
summarised below:
Date of contract
Notice period
Jalkanen Juho, CEO
1.5.2024
6 months
NON-EXECUTIVE DIRECTORS’ SERVICE 
CONTRACTS AND REMUNERATION
The remuneration and compensation payable to the 
members of the Board including the Non-Executive 
Directors is approved by the shareholders at the AGM. 
Any Non-Executive Director who, by request, goes 
or resides abroad for any purposes of Faron or who 
performs services which in the opinion of the Board go 
beyond the ordinary duties of a Director may be paid extra 
remuneration or may receive such other benefits as the 
Remuneration Committee may approve. Non-Executive 
Directors are entitled to be reimbursed in respect 
of their reasonably and properly incurred travelling, 
accommodation and incidental expenses for attending 
and returning from meetings of the Board, Committee 
meetings or the general meetings of shareholders.
With the exception of share options disclosed below, 
the Non-Executive Directors do not receive any pension, 
bonus or benefit from the Company. The contracts of 
the Non-Executive Directors, excluding remuneration and 
compensation, are reviewed by the Board annually.
Current contracts are summarised below:
Non-Executive Directors
Independence
Contract
Date of Contract
Tuomo Pätsi
Independent
Chairman
27.03.2023
Markku Jalkanen
Not independent
Member
16.09.2015
Poulos John
Independent
Member
16.05.2017
Roth Christine
Independent
Member
25.09.2023
Fjällskog Marie-Louise
Not independent
Member
25.09.2023
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FINANCIAL REPORT

The appointments of Non-Executive Directors are 
terminable with immediate effect, in accordance with 
the Company’s Articles of Association and pursuant to 
the Finnish Limited Liability Companies Act, through 
a resolution of shareholders at a general meeting on 
any grounds. The Non-Executive Directors may resign 
(*) Executive Director until May 2024
(**) Executive Director starting 1.5.2024
(***) Board member until April 2024
€
Salaries and fees
Bonus
Taxable benefits
Total
Executive Directors
Jalkanen Markku*
131,442
117,548
120
249,110
   Jalkanen Juho**
220,350
160
220,510
Non-Executive Directors
Armstrong Frank***
43,500
43,500
Tuomo Pätsi
62,500
62,500
Fjällskog Marie-Louise
42,000
42,000
Jalkanen Markku
20,462
20,462
Poulos John
48,000
48,000
Roth Christine
42,500
42,500
Ostrowski Erik***
24,500
24,500
as a director by delivering three months’ notice to the 
registered office of the Company or through tendering 
such resignation at a meeting of the Board.
The Directors received the following remuneration 
during the year: 
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FINANCIAL REPORT

THE COMPANY’S OPTION PLANS AND  
DIRECTORS’ SHARE OPTIONS
Aggregate remunerations disclosed on the previous page 
exclude any amounts for the value of options to acquire 
ordinary shares in the Company granted to or held by 
the Directors.
Option Plan 2015 was adopted by the Company at the 
Extraordinary General Meeting held on 15 September 
2015 and amended in the Annual General Meetings 
of 16 May 2017, 18 May 2020, 23 April 2021 and 22 
September 2023, respectively. Option Plan 2015 allowed 
the Company to offer options for subscription free of 
charge to members of the Board and to such officers 
and employees of the Company as the Board sees fit. 
Each option entitles the holder of the option to subscribe 
for one ordinary share in the Company. Under the terms 
of Option Plan 2015, an aggregate maximum number 
of 1,800,000 options could be granted, such aggregate 
being made up of a maximum of 400,000 “2015A” 
options, the subscription period for which ended on 9 
June 2016, a maximum of 400,000 “2015B” options, the 
subscription period for which ended on 30 September 
2019, a maximum of 500,000 “2015C” options, the 
subscription period for which ended on 30 September 
2019, and a maximum of 500,000 “2015D” options, the 
subscription period for which ended on 30 September 
2019, all such options being exercisable until 30 
September 2025.
The exercise price for ordinary shares based on “2015A” 
options is €3.71. The exercise price for ordinary shares 
based on “2015B” options is €2.90. The exercise price 
for ordinary shares based on “2015C” options is €8.39. 
The exercise price for ordinary shares based on “2015D” 
options is €1.09.  All options granted under 2015 Option 
plan are visible on the next pages.
Share Option Plan 2019 was adopted by the Board on 
20 November 2019 and amended on 19 March 2020 
based on an authorisation by the Annual General Meeting 
of 28 May 2019, as amended in the Annual General 
Meeting of 18 May 2020. During 2023 the Option Plan 
2019 was amended at the Annual General Meeting on 
24 March 2023. Share Option Plan 2019 allows the 
Company to offer options for subscription free of charge 
to employees and directors of the Group (including any 
non-executive members of the Board) and any eligible 
person who provides services to the Group. Each option 
entitles the holder of the option to subscribe for one 
ordinary share in the Company. Under the amended rules 
of the Share Option Plan 2019, an aggregate maximum 
number of 4,350,000 options can be granted. The number 
of granted options under the Option Plan 2019 and their 
exercise period and prices is described in the table below.
Option tranches under  
Option Plans 2015 and 2019
Total number 
of options
Grant date
Exercised period, 
vesting 25% per annum
Exercise price, €
2015 A options
400,000
16.09.2015
02.11.2015–30.09.2025
3.67
2015 B options
400,000
18.11.2016
08.10.2016–30.09.2025
2.90
2015 C options
500,000
16.11.2017
08.10.2017–30.09.2025
8.39
2015 D options
500,000
21.05.2019
08.10.2018–30.09.2025
1.09
2019 A options
554,333
23.07.2020
23.07.2021–23.07.2025
3.80 
2019 B options
590,583 
24.03.2021
24.03.2022–24.03.2026
3.99 
2019 B bis options
0 
05.07.2021
05.07.2022–05.07.2026
4.40 
2019 B tertiary options
147,000 
17.11.2021
17.11.2022–17.11.2026
4.47 
(4.04€ under US plan)
2019 C options
440,000
24.03.2022
24.03.2023–24.03.2027
3.09 
(2.91€ under US plan)
2019 C bis options
129,000
24.08.2022
24.08.2023–24.08.2027
2.50
(2.38€ under US plan)
2019 C tertiary options
16,000
17.11.2022
17.11.2023–17.11.2027
2.06
2019 D options
779,000
08.06.2023
08.06.2024–08.06.2028
3.57 
(3.36€ under US plan)
2019 D bis options
34,000
09.11.2023
09.11.2024–9.11.2028
3.53
(3.35€ under US plan)
2019 E options
645,000
25.06.2024
25.06.2025-25.06.2029
1.00
(1.35€ under US plan)
2019 E bis options
100,000
26.08.2024
26.08.2025-26.08.2029
1.48
2019 E tertiary options
50,000
04.12.2024
04.12.2025-04.12.2029
2.28
(2.01€ under US plan)
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(*) of which 2,225,266 are held by Markku Jalkanen directly and 1,188,168 are held by Markku Jalkanen’s wife Sirpa Jalkanen
Issued Share Capital
Share Options
At 31 December 2024
Ordinary shares 
Percentage held
Options
Average exercise price, €
Non-Executive Directors
Jalkanen Markku
3,413,434*
3.26
570,000
4.17
Poulos John
0
0.00 
170,000
3.71
Pätsi Tuomo
31,765 
0.03
130,000
1.59
Fjällskog Marie-Louise
0
0.00
210,000
3.31
Roth Christine
46,075
0.04
60,000
2.35
(*) Board member until April 2024 
Total options under 2015 and 2019 
Option Plans
At 1
January
2024
Granted
during  the
 period
Exercised
during
the period:
At 31
December
2024
Average exerc. 
price per 2024 
options, €
Jalkanen Markku
540,000
30,000
0
570,000
1.00
Armstrong Frank*
340,000
0
0
340,000
-
Ostrowski Erik*
60,000
0
0
60,000
-
Poulos John
140,000
30,000
0
170,000
1.35
Pätsi Tuomo
30,000
100,000
0
130,000
1.00
Fjällskog Marie-Louise
180,000
30,000
0
210,000
1.35
Roth Christine
30,000
30,000
0
60,000
1.35
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FINANCIAL REPORT

COMMUNICATING WITH SHAREHOLDERS
The Company acknowledges that effective communication 
with its shareholders on strategy and governance is an 
important part of its responsibilities. Interim and final 
results are communicated via formal meetings with 
investor roadshows, participation in conferences and 
additional dialogue with key investor representatives held 
in the intervening periods. Faron recognises the Annual 
General Meeting as an opportunity to meet shareholders.
As an AIM and First North listed company, Faron 
complies the Market Abuse Regulation (both EU and UK 
domestic laws after year end 2020), the AIM Rules for 
Companies and the Nasdaq First North Growth Market 
Rulebook. Faron complies with other relevant legislation 
in all its corporate communications issues. 
Faron speaks to the financial community and 
shareholders only through authorised representatives. 
In accordance with Faron’s disclosure policy, the Chief 
Executive Officer is the designated person to make public 
statements. The Chief Executive Officer may delegate this 
authority to other members of the management team.  
In addition to the CEO, the CFO is able to communicate 
externally on behalf of Faron on financial matters.
The contact details are below: 
email: investor.relations@faron.com
Media and investor relations: 
Consilium Strategic Communications 
email: faron@consilium-comms.com
SHARE DEALING
The Company has established a share dealing code 
appropriate to an AIM and First North listed company, 
and all the Directors understand the importance of 
compliance to that code.
ETHICAL VALUES AND CORPORATE CULTURE
Faron is strongly committed to conducting its business 
affairs with honesty and integrity and in full compliance 
with all applicable laws, rules and regulations. 
All employees and Directors are required to comply 
with all laws, rules and regulations applicable to Faron 
wherever it does business. 
Employees and Directors should endeavour to deal 
honestly, ethically and fairly with Faron’s collaborators, 
licensors, licensees, business partners, suppliers, 
customers, competitors and other employees. 
Statements regarding Faron’s therapies and services 
must not be untrue, misleading, deceptive or fraudulent.
Employees and Directors act in the best interests of 
Faron and use its assets and services solely for legitimate 
business purposes and not for any personal benefit or the 
personal benefit of anyone else.
RISK MANAGEMENT AND INTERNAL CONTROL
The principal risks and uncertainties identified by the 
Board are set out on pages 18-21 of the 2024 Report. 
The Board has put in place internal controls and systems 
which are designed to manage rather than eliminate 
CORPORATE 
GOVERNANCE 
STATEMENT
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35
FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT

risk and provide reasonable but not absolute assurance 
against material misstatement or loss. A key element of 
delivering Faron’s strategy and managing the risks facing 
Faron is the employment of a skilled workforce and use 
of appropriate vendors. The Board reviews the risks and 
uncertainties facing Faron and the effectiveness of its 
systems annually.
At present, Faron does not consider it necessary to have 
an internal audit function due to the small size of the 
administrative function, the frequent interaction with the 
auditors and the supervision of the audit committee. The 
Board is, however, closely following both regulatory and 
operational developments in this realm and plans to react 
appropriately if, and to the extent, considered necessary.
There is a monthly review and authorisation of 
transactions by the Chief Financial Officer and Chief 
Executive Officer. A comprehensive budgeting process 
is completed once a year and is reviewed and approved 
by the Board. The Group’s results, compared with the 
budget, are reported to the Board on a monthly basis and 
discussed in detail.
Faron maintains appropriate insurance cover in respect of 
actions taken against the Directors because of their roles, 
as well as against material loss or claims against Faron. 
The insured values and type of cover are comprehensively 
reviewed on a periodic basis.
REGULATED ADVISORS  
The shares of the Company  are listed for trading on the 
London Stock Exchange AIM and Nasdaq First North 
Growth Market marketplaces, which require the nominating 
of advisors. Cairn Financial Advisers LLP is the Company´s 
nominated advisor and broker on AIM and Sisu Partners 
Oy is the Company’s certified advisor on First North.
RESPONSIBILITY
At Faron we embrace the responsibility we have to 
patients, our employees, the communities where we 
work and the planet. We set ambitious goals for our own 
operations, high expectations for our suppliers and serve 
as an example of leadership for our industry.
In the same way that it drives the development of 
our transformational medicines, innovation fuels our 
approach to practices related to environmental, social and 
governance (ESG) matters. We are focused on enhancing 
patient access to medicines, being an employer of choice 
and prioritizing environmental sustainability, all while 
operating with the highest levels of quality, integrity and 
ethics. Our strong governance profile includes board 
oversight and active participation and reporting from 
leadership and team members across functions and 
geographies.
Faron is committed to maintaining and promoting 
high standards of business integrity. Faron’s values, 
which incorporate the principles of corporate social 
responsibility and sustainability, guide its relationships 
with clients, employees and the communities and 
environment in which it operates. Faron’s approach to 
sustainability addresses both its environmental and social 
impacts, supporting its vision to remain an employer 
of choice, while meeting client demands for socially 
responsible partners. 
By putting ESG into practice, Faron is committed, 
wherever possible, to:
•	 developing treatments for medical conditions  
with significant unmet needs 
•	 conducting itself responsibly and in an ethical manner
•	 creating a positive and supportive working environment
•	 acting fairly in its dealings with suppliers and  
other third parties
•	 minimising the impact on its environment 
Environmental – Prioritizing Sustainability  
The well-being of our communities is enriched by 
a safe, clean and healthy environment. Faron is 
committed to behaving responsibly and to minimizing 
its impact on the world around us. In considering 
the environment, Faron has resolved to include 
environmental factors in its business travel practices 
and to minimise its consumption of natural resources 
and manage waste through responsible disposal and 
reuse and recycling. Faron endeavours also, through its 
suppliers, to make environment-friendly choices where 
possible, for example when selecting packages for our 
drug substances.
Social – Patients, Employees and Inventions
Unmet medical needs and enhancing patient access 
Faron exists to help patients overcome serious medical 
conditions and diseases. Bexmarilimab has been used for 
cancer patients for which all available treatments have 
been tested and which were not bringing help for them.
FARON PHARMACEUTICALS LTD  |  ANNUAL REPORT 2024
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STRATEGIC REPORT
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FINANCIAL REPORT

Inventions from academia to patients 
We are a pioneer in partnering with academia to bring 
scientific advancements from the laboratory to patients in 
the clinic. All three of Faron’s pipeline candidates originate 
from academic laboratories. 
Be an Employer of Choice 
Driving everything we do is a team of dedicated and 
talented professionals who share a commitment to 
working every day to deliver innovative medicines for 
patients with serious and life-threatening diseases. 
Not only do we hire the best and brightest people, but 
we also provide them with a work environment that 
places a premium on diversity, integrity, collaboration, 
community involvement and personal development. 
We have created an inclusive and empowering culture 
that embraces diverse experiences and perspectives of 
all our employees to drive innovation and transformative 
scientific and business results. Faron considers all staff 
members to be equal and aims to create a working 
environment which is free of unlawful discrimination. 
In this regard, Faron maintain an internal code of conduct 
based on professionalism and respect.
Governance 
Accountability is fundamental to our business. Faron 
respects local laws and customs while supporting 
international laws and regulations. Faron aims to adopt 
the highest professional standards and not to act in 
such a way as to compromise its integrity. Faron is also 
committed to eliminating unlawful discrimination and 
to promoting equality and diversity in its professional 
dealings, which includes a commitment to enter into clear 
and fair contracts with its suppliers. 
The cornerstone for Faron’s internal policies is its Code 
of Business Conduct and Ethics, which embodies the 
standards and policies under which Faron operates. The 
code combines the values and corporate responsibility 
commitments to provide the framework and guidance 
for its employees to operate in an open, honest, ethical, 
and principled way. The code is supported by a set of 
internal policies varying from information security to 
anti-corruption. Faron continuously trains its employees 
on e.g., business ethics, securities regulations, and data 
privacy. We have also engaged with external providers 
to test IT security, the results of which identified no 
major vulnerabilities. 
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FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT

The Board has overall responsibility and plays a key role 
in ensuring the appropriate systems and controls are in 
place and effective. As described in this Annual Report, 
the Company complies QCA’s Corporate Governance 
Code for Small and Medium Sized Companies. Faron 
is fully committed to the highest possible standards 
of openness, honesty, and accountability. In line with 
that commitment, Faron actively encourages all staff 
members who have serious concerns about any real or 
perceived departure from the high ethical standard that it 
sets to voice those concerns openly.
STATEMENT OF RESPONSIBILITIES
Under the Finnish Limited Liability Companies Act and 
the Finnish Accounting Act, the Company must prepare 
financial statements in accordance with applicable law 
and regulations.
The Board and the CEO are responsible for the 
preparation of financial statements that give a true and 
fair view in accordance with International Financial 
Reporting Standards (IFRS) as adopted by the EU, as 
well as for the preparation of financial statements and 
the report of the Board that give a true and fair view in 
accordance with the laws and regulations governing the 
preparation of the financial statements and the report 
of the Board in Finland. The Board is responsible for 
the appropriate arrangement of the control of Faron’s 
accounts and finances, and the CEO shall see to it that 
the accounts of Faron are in compliance with the law and 
that its financial affairs have been arranged in a reliable 
manner. In accordance with the rules of the London Stock 
Exchange for companies trading securities on AIM, the 
Company is also required to prepare annual accounts and 
financial statements under IFRS.
In preparing these financial statements, the Board of 
Directors is required to: 
•	 select suitable accounting policies and then  
apply them consistently;
•	 make judgements and accounting estimates  
that are reasonable and prudent;
•	 state whether they have been prepared in accordance 
with IFRS as adopted by the EU,  
subject to any material departures disclosed and 
explained in the financial statements;
•	 prepare the financial statements on the going concern 
basis unless it is inappropriate to presume that the 
Company will continue in business.
The Board and the CEO are responsible for keeping 
adequate accounting records that are sufficient to 
show and explain Faron’s transactions and disclose 
with reasonable accuracy at any time the financial 
position of Faron and enable them to ensure that the 
financial statement comply with the requirements of the 
Finnish Accounting Act. They are also responsible for 
safeguarding the assets of Faron and hence for taking 
reasonable steps for the prevention and detection of 
fraud and other irregularities.
WEBSITE PUBLICATION
The Directors are responsible for ensuring that the 
financial statements are made available on a website. 
Financial statements are published on Faron’s website in 
accordance with AIM Rule 26, Nasdaq First North Growth 
Market Rulebook and the recommendations of the QCA’s 
Corporate Governance Code for Small and Medium 
Sized Companies.
On behalf of the Board
Tuomo Pätsi 
Non-Executive Chairman 
 
27 February 2025
FARON PHARMACEUTICALS LTD  |  ANNUAL REPORT 2024
38
FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT

DIRECTORS
During the year ended 31 December 2024 the following 
persons have been members of the Board of 
the Company:
Executive  
Dr Markku Jalkanen, PhD | Chief Executive Officer until 
30.4.2024
Non-executive   
Dr. Frank Armstrong | Chairman* 
Mr. Tuomo Pätsi | Non-Executive Director, Chairman**
Dr. Markku Jalkanen | Non-Executive Director*** 
Mr John Poulos | Non-Executive Director 
Mr Leopoldo Zambeletti | Non-Executive Director 
Mr Erik Ostrowski | Non-Executive Director**** 
Dr. Marie-LouiseFjällskog | Non-Executive Director 
Mrs. Christine Roth | Non-Executive Director
*Chairman and a member until April 2024 
** Chairman starting April 2024 
***Executive director until April 2024 
**** A member until April 2024
The Directors present their report together with the audited financial statements for the year ended 31 December 2024. 
PRINCIPAL RISKS AND UNCERTAINTIES
For a discussion of the principal risks and uncertainties 
which face Faron please see pages 18 to 21 of this 
document.
RESULTS AND DIVIDENDS
The Consolidated Statement of Comprehensive Income 
for the year is set out here.
The Group’s loss of the financial year after taxation 
and other comprehensive losses was 25.9 million 
(2023: €30.9 million).
The Company has no distributable equity and thus the 
Directors do not recommend the payment of a dividend 
(2023: nil).
FINANCIAL INFORMATION
The Group produces budgets and cash flow projections 
on an annual basis for approval by the Board. These are 
reviewed during the year and updated if needed to reflect 
any changes in the business. Detailed management 
accounts are produced on a monthly basis, with 
all significant variances investigated promptly. The 
management accounts are reviewed and commented 
on by the Board at Board meetings and are reviewed and 
reported to the Directors on a monthly basis by the Chief 
Financial Officer.
DIRECTORS’
REPORT
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FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT

FINANCIAL KEY PERFORMANCE INDICATORS 
(KPIS)
For a review of the Group’s KPIs please see pages 15-17 
Financial Review.
RESEARCH AND DEVELOPMENT
Details of the Group’s key research and development 
programmes can be found in the Strategic Report and the 
detailed programme sections. See also notes 2.7 and 5. 
Further information is also available on Faron’s website, 
www.faron.com.
FINANCIAL INSTRUMENTS AND MANAGEMENT 
OF LIQUID RESOURCES
The Group’s principal financial instrument comprises 
cash, and this is used to finance the Group’s operations. 
The Group has also other financial instruments such as 
leasing facilities that arise directly from its operations.
The Group has a policy, which has been consistently 
followed, of not trading in financial instruments and 
to minimise currency exposure by actively matching 
currency expenses and income to the extent possible. 
The Group’s cash is held on bank accounts in reputable 
banks in Finland, Switzerland and US. See note 2.16 
‘Financial assets’, note 19 ‘Financial assets and liabilities’ 
and note 20, ‘Financial risk management’ in the notes to 
the Financial Statements for IFRS disclosure regarding 
financial instruments.
SUBSTANTIAL SHAREHOLDINGS 
On 31 December 2024, the Company had been notified of 
the following holdings of 3% or more of the issued share 
capital of the Company.
The information presented in the below table is 
consistent with the Company’s best knowledge as at  
31 December 2024.
Timo Syrjälä*
16,024,023
15.32 %
Varma Mutual Pension Fund
4,498,869
4.30%
The European Investment Council 
Fund, EIC
3,630,437
3.47%
A&B (HK) Company Limited
3,559,893
3.40%
Fjärde AP Fonden
3,490,405
3.34%
Markku Jalkanen**
3,413,434
3.26%
(*) of which 4,944,614 are held directly by Timo Syrjälä and 11,079,409 are 
held by Acme Investments SPF S.à.r.l., an entity which is wholly owned by 
Timo Syrjälä / (**) of which 2,256,266 are held by Markku Jalkanen directly 
and 1,188,168 are held by Markku Jalkanen’s wife Sirpa Jalkanen 
GENERAL MEETINGS
The Company held the Annual General Meeting on 5 April 
2024. In 2025, the Annual General Meeting will be held 
on 21 March 2025. Further details will be provided to 
shareholders in advance of the meeting.
INDEPENDENT AUDITORS
PricewaterhouseCoopers have expressed their 
willingness to continue in office as auditors for the year. 
A resolution to reappoint them will be proposed at the 
forthcoming Annual General Meeting.
DISCLOSURE AND INFORMATION TO AUDITORS
Each of the current Directors hereby confirms that: 
(a) So far as he/she is aware, there is no relevant audit 
information of which the auditors are unaware; and
(b) He/she has taken all reasonable steps to ascertain 
any relevant audit information and to ensure that the 
auditors are aware of such information
On behalf of the Board
Tuomo Pätsi 
Chairman
27 February 2025
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FARON PHARMACEUTICALS
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FINANCIAL REPORT

Statement of Comprehensive Income
FINANCIAL
STATEMENTS 2024
For the year ended 31 December
Group
Parent
€’000 (except per share information)
Note
2024
2023
2024
2023
Revenue
3
-
- 
-
Other operating income
4
-
-
3
65
Research and development expenses
5, 6, 7
(11,744)
(19,542)
(11,735)
(19,019)
General and administrative expenses
5, 6, 7
(6,929)
(9,026)
(7,046)
(9,792)
Operating loss
 
(18,673)
(28,568)
(18,778)
(28,746)
Financial income
8
434
233
455
317
Financial expenses 
8
(7,676)
(2 609)
(7,673)
(2,664)
Loss before tax
 
(25,915)
(30,944)
(25,995)
(31,094)
Tax expense
9
(5)
-
(5)
-
Loss for the period
 
(25,920)
(30,944)
(26,000)
(31,094)
Other comprehensive income (loss) 
9
2
-
-
Total comprehensive loss for the period
(25,911)
(30,942)
(26,000)
(31,094)
Loss per ordinary share
Basic and diluted loss per share, EUR
 10
(0.29)
(0.48)
(0.29)
(0.48)
FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT
FARON PHARMACEUTICALS LTD  |  ANNUAL REPORT 2024
41

Balance Sheet
As at December 31
Group
Parent
€’000
Note
2024
2023
2024
2023
Assets
Non-current assets
Machinery and equipment
11
1
6
1
6
Right-of-use-assets
13
296
198
296
198
Subsidiary shares
23
-
-
18
18
Intangible assets
11
1,112
1,088
1,112
1,088
Prepayments and other receivables
12
46
60
551
544
Total non-current assets
1,456
1,352
1,979
1,854
Current assets
Prepayments and other receivables
14
1,563
1,992
1,682
2,317
Cash and cash equivalents
15
9,503
6,875
9,462
6,842
Total current assets
 
11,065
8,868
11,143
9,159
 
 
Total assets
12,521
10,220
13,122
11,013
Equity and liabilities
Capital and reserves attributable to  
the equity holders of Faron
Share capital
2,691
2,691
2,691
2,691
Reserve for invested unrestricted equity
184,955
154,352
184,955
154,346
Accumulated deficit
(197,421)
(172,208)
(197,955)
(172,649)
Translation difference
13
4
0
0
Total equity
16, 17
(9,762)
(15,160)
(10,308)
(15,611)
Provisions
Other provisions
0
0
0
0
Total provisions
 
0
0
0
0
Non-current liabilities
Borrowings
18
8,088
9,423
8,093
9,428
Lease liabilities
13
186
50
186
50
Other liabilities
20
3,839
895
3,839
895
Total non-current liabilities
 
12,113
10,369
12,117
10,373
Current liabilities
Borrowings
18
3,722
3,475
3,718
3 475
Lease liabilities
13
117
163
117
163
Trade payables
21
4,876
8,971
5,996
10,585
Accruals and other current liabilities
21
1,456
2,403
1,482
2,028
Total current liabilities
 
10,171
15,012
11,313
16,251
Total liabilities
 
22,284
25,380
23,430
26,624
Total equity and liabilities
 
12,521
10,220
13,122
11,013
FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT
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42

Parent Company Statement 
of Changes in Equity
€’000
Note
Share 
capital
Reserve for 
invested 
unrestricted 
equity
Accumulated 
deficit
Total 
equity
Balance as at 31 December 2022
2,691
129,539
(144,008)
(11,778)
Comprehensive loss for the period
-
-
(31,094)
(31,094)
 
Transactions with equity holders of the Company
Issue of ordinary shares, net of transaction costs 
16
-
24,808
-
24,808
Share-based compensation
6,17
-
-
2,450
2,450
Other movements
-
-
2
2
-
24,808
(28,641)
(3,833)
 
Balance as at 31 December 2023
2,691
154,346
(172,649)
(15,611)
Comprehensive loss for the period
-
-
(26,000)
(26,000)
Transactions with equity holders of the Company
Issue of ordinary shares, net of transaction costs
-
30,609
-
30,609
Share-based compensation
-
-
694
694
Other movements
-
-
-
-
-
30,609
(25,306)
5,303
Balance as at 31 December 2024
2,691
184,955
(197,955)
(10,308)
FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT
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43

Group Statement of Changes in Equity
€’000
Note
Share 
capital
Reserve for 
invested 
unrestricted 
equity
Translation 
difference
Accumulated
 deficit
Total 
equity
Balance as at 31 December 2022
2,691
129,544
2
(143,713)
(11,476)
Comprehensive loss for the period
-
-
2
(30,944)
(30,942)
Transactions with equity holders of the Group
Issue of ordinary shares, net of transaction costs
-
24,808
-
-
24,808
Share-based compensation
-
-
-
2,450
2,450
-
24,808
2
(28,494)
(3,684)
Balance as at 31 December 2023
2,691
154,352
4
(172,208)
(15,160)
Comprehensive loss for the period
-
-
9
(25,920)
(25,911)
Transactions with equity holders of the Group
Issue of ordinary shares,  
net of transaction costs
16
-
30,609
-
-
30,609
Share-based compensation
6,17
-
-
-
694
694
Reserve on retained earning for legal
(5)
11
6
30,603
9
(25,215)
5,398
Balance as at 31 December 2024
2,691
184,955
13
(197,421)
(9,762)
FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT
FARON PHARMACEUTICALS LTD  |  ANNUAL REPORT 2024
44

Statement of Cash Flows
As at 31 December
Group
Parent
€’000
Note
2024
2023
2024
2023
Cash flow from operating activities
Loss before tax
(25,915)
(30,944)
(25,995)
(31,094)
Adjustments for:
Received grants
4
-
(33)
-
(33)
Depreciation and amortisation
7
314
346
314
346
Change in provision
-
(158)
-
(158)
Financial items
8
7,242
2,376
7,217
2,348
Share-based compensation
17
694
2,450
694
2,450
Operating cash flows before movements in 
working capital
(17,665)
(25,963)
(17,770)
(26,141)
Change in net working capital:
Prepayments and other receivables
444
300
627
59
Trade payables
(4,095)
2,994
(4,589)
3,253
Other liabilities
(947)
(50)
(545)
50
Cash used in operations
(22,263)
(22,719)
(22,277)
(22,779)
Income taxes paid
(41)
-
(5)
-
Interest received
361
243
361
243
Interest paid
(1,028)
(1,330)
(1,028)
(1,330)
Net cash used in operating activities
(22,971)
(23,806)
(22,949)
(23,866)
Cash flow from investing activities
Payments for intangible assets
11
(225)
(123)
(225)
(123)
Payments for tangible assets
11
(1)
-
(1)
-
Net cash used in investing activities
(226)
(123)
(226)
(123)
Cash flow from financing activities
Proceeds from issue of shares
16
31,850
26,031
31,850
26,031
Share issue transaction cost
16
(4,951)
(1,190)
(4,951)
(1,190)
Proceeds from borrowings
18
3,200
64
3,200
64
Repayment of borrowings
18
(3,371)
(861)
(3,371)
(861)
Transaction and structuring fees of borrowings
18
(750)
(400)
(750)
(400)
Proceeds from grants
4, 21
-
481
-
481
Payment of lease liabilities
2, 18
(162)
(142)
(162)
(142)
Net cash from financing activities
25,816
23,983
25,816
23,983
Net increase (+) / decrease (-) 
in cash and cash equivalents
2,627
(114)
2,620
(41)
Effect of exchange rate changes on  
cash and cash equivalents
(8)
(168)
(22)
(35)
Cash and cash equivalents at 1 January
15
6,876
6,990
6,842
6,884
Cash and cash equivalents at 31 December
15
9,503
6,876
9,462
6,842
FARON PHARMACEUTICALS
STRATEGIC REPORT
CORPORATE GOVERNANCE
FINANCIAL REPORT
FARON PHARMACEUTICALS LTD  |  ANNUAL REPORT 2024
45

Notes to the Financial Statements
1. CORPORATE INFORMATION
Faron Pharmaceuticals Oy (“Company”), a clinical stage 
biopharmaceutical company incorporated and domiciled 
in Finland, with its headquarters at Joukahaisenkatu 6 
B, 20520 Turku, Finland, is the parent company for all 
its subsidiaries (“Faron” or “Group”). The Group has a 
pipeline based on the receptors involved in regulation 
of immune response in oncology, organ damage and 
bone marrow regeneration. Faron Pharmaceuticals Oy is 
listed on the London Stock Exchange’s AIM market since 
17 November 2015 and Nasdaq First North Growth 
Market since 21 November 2019. The Board of Directors 
of the Company approved the financial statements on 
26 February 2025.
2. SUMMARY OF MATERIAL ACCOUNTING  
POLICIES
2.1. Basis of Preparation
The financial statements incude both the group and 
the Company which have been prepared in accordance 
with the IFRS Accounting Standards as adopted 
by the European Union and the interpretations of 
the International Financial Reporting Standards 
Interpretations Committee (IFRIC). The financial 
statements have been prepared on a historical cost 
basis, unless otherwise stated. The parent company 
bears vast majority of the costs in the Group. 
The intercompany items are recognized by the Parent 
which make the Group figures differ.
The principal accounting policies applied in the 
preparation of these financial statements are set out 
below. These policies have been applied consistently to all 
the periods presented, unless otherwise stated. The areas 
of the financial statements involving a higher degree of 
judgment or complexity, or areas where assumptions and 
estimates are significant to the financial statements are 
disclosed in note 2.21.
The Consolidated Financial Statements incorporate 
the parent company, Faron Pharmaceuticals Oy, and 
all subsidiaries in which it holds over 50% of the voting 
rights. The subsidiaries established during the financial 
period are consolidated from the date that control was 
obtained by the Group.The subsidiaries are consolidated 
by using the purchase method. All intragroup 
transactions, receivables, liabilities and unrealized gains 
are eliminated in the Consolidated Financial Statements. 
Faron Pharmaceuticals Oy holds 100% ownership of all 
its subsidiaries.
The Consolidated Financial Statements and parent 
company financial statemetnts are presented in euro 
which is the functional currency of the parent company. 
The statements of comprehensive income and statements 
of cash flows of foreign subsidiaries, whose functional 
currency is not euro, are translated into euro each month at 
the average monthly exchange rates, while the statements 
of financial position of such subsidiaries are translated 
at the exchange rate prevailing at the reporting date. 
Translation differences resulting from the translation of 
profit for the period and other items of comprehensive 
income in the statement of comprehensive income 
and statement of financial position are recognized as a 
separate component in equity and in other comprehensive 
income. Also, the translation differences arising from 
the application of the purchase method and from the 
translation of equity items cumulated subsequent to 
acquisition are recognized in other comprehensive income.
All figures presented in notes are group figures if not 
else stated. Where the numbers for the Group and the 
Company differ significantly those are explained in the 
notes. The differences are mainly caused by employee 
related costs at subsidiaries and compensation of the 
services subsidiaries provide to the Company.All amounts 
are presented in thousands of euros, unless otherwise 
indicated, rounded to the nearest euro thousand.
2.2. Going Concern 
As part of their going concern review, the Directors 
have followed International Accounting Standard 1, 
Presentation of Financial Statements (IAS 1). The 
Company and its subsidiaries are subject to a number 
of risks similar to those of other development state 
pharmaceutical companies. These risks include, 
amongst others, generation of revenues in due course 
from the development portfolio and risks associated 
with research, development, testing and obtaining 
related regulatory approvals of its pipeline products. 
The subsidiaries have limited economic activities and 
have immaterial assets and liabilities and thus Group’s 
ability to continue as going concern is dependent on 
the Company. Ultimately, the attainment of profitable 
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operations is dependent on future uncertain events which 
include obtaining adequate financing to fulfill the Group’s 
commercial and development activities and generate a 
level of revenue adequate to support the Group’s cost 
structure.
The Group generated a net loss of EUR -25.9 million and 
recorded a EUR 23.0 million cash outflow from operating 
activities during the year ended 31 December 2024. At 
the end of the financial year, it had total negative equity of 
EUR -9.8 million including an accumulated deficit of EUR 
197.4 million. As of that date, the Group had cash and 
cash equivalents of EUR 9.5 million.
During the financial period ended 31, December 2024, 
the Group raised 35.5 million (gross) in three fundraising 
rounds. Subsequent to 31 December 2024, the Group has 
conducted in early February 2025 a private placement 
directed to a limited number of institutional and other 
investors raising EUR 12.0 million. 
The Directors have prepared the detailed financial 
forecasts and cash flows looking beyond 12 months 
from the date of these financial statements. In developing 
these forecasts, the Directors have made assumptions 
based upon their view of the current and future economic 
conditionsto the Company and the Group that are 
expected to prevail over the forecast period. The Director’s 
estimate that the cash held by the Group, together with 
the EUR 12.0 million funds raised post-period as well as 
with known receivables will be sufficient to support the 
current level of activities until Q3 2025. 
Despite this the Directors are continuing to explore 
sources of additional financinge available to Faron and 
they believe they have a reasonable expectation that they 
will be able to secure additionalsufficient cash inflows 
that are sufficient for Faron to continue its activities for 
not less than 12 months from the date of approval of 
these financial statements; they have therefore prepared 
the financial statements on a going concern basis. 
Because the additional finance is not committed at 
the date of issuance of these financial statements, 
these circumstances represent a [material] uncertainty 
that may cast significant doubt on Faron’s ability to 
continue as going concern. Should Faron be unable to 
obtain additionalfurther financinge such that the going 
concern basis of preparation were no longer appropriate, 
adjustments would be required, including to reduce 
balance sheet values of assets to their recoverable 
amounts, to provide for further liabilities that might arise. 
2.3. Foreign Currency Transactions and Balances
Functional and Presentation Currency 
The financial statements are presented in euro, which is 
the Company’s functional and presentation currency.
Transaction Currency  
Transactions in foreign currencies are translated at the 
exchange rates ruling at the date of the transaction. 
Monetary assets and liabilities denominated in foreign 
currencies are translated at the exchange rates ruling 
at the reporting date. Foreign exchange differences 
arising on translation are recognized in the statement 
of comprehensive income. Non-monetary assets and 
liabilities denominated in foreign currencies are translated 
at the foreign exchange rate ruling at the date of the 
transaction. 
2.4. Segment Reporting
Operating segments are reported in a manner consistent 
with the internal reporting provided to the chief operating 
decision maker. The Chief Executive Officer, reviewing 
the operating results regularly to make decisions 
about the allocation of resources and to assess overall 
performance, is identified as the chief operating decision 
maker. The Chief Executive Officer manages the Group 
as one integrated business and hence, the Group has one 
operating and reportable segment.
2.5. Revenue Recognition
The Group uses IFRS 15 standard for Revenue from 
Contracts with Customers and applies the single, 
principles based five-step model to all contracts with 
customers provided by IFRS 15 as follows: 
1.	Identify the contract with a customer
2.	Identify the performance obligations in the contract
3.	Determine the transaction price
4.	Allocate the transaction price to the performance 
obligations in the contract
5.	Recognize revenue when (or as) the entity  
satisfies a performance obligation (over time  
or at a point in time). 
Revenue from Licensing Agreements 
According to IFRS 15, performance obligation is a promise 
to provide a distinct good or service or a series of distinct 
goods or services. Goods and services that are not 
distinct are bundled with other goods or services in the 
contract until a bundle of goods or services that is distinct 
is created. A good or service promised to a customer 
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is distinct if the customer can benefit from the good or 
service either on its own or together with other resources 
that are readily available to the customer and the entity’s 
promise to transfer the good or service to the customer is 
separately identifiable from other promises in the contract.
2.6. Recognition of Government Grants
The direct government grants are recognized as other 
operating income at the same time as the underlying 
expenditure is incurred, provided that there is reasonable 
assurance that the Group will receive the grant and it 
complies with the conditions of such grant. Direct grant 
payments received in advance of the incurrence of the 
expenditure that the grant is intended to compensate 
are deferred at the reporting date and presented under 
advances received on the balance sheet.
The indirect government assistance in the form of below-
market interest government loans is recognized as grant 
income and recorded as other operating income in the 
same period in which the Group recognizes the expenses 
for which the benefit is intended to compensate. Grant 
income is measured as the difference between the initial 
fair value of the loan and the proceeds received.
2.7. Research and Development Expenses
Research and development costs are expensed as incurred 
and presented under research and development expenses 
in the statement of comprehensive income. Research 
and development expenses include costs for outsourced 
clinical trial services, materials and services, employee 
benefits and other expenditure directly attributable to the 
Group’s research and development activities. The Group’s 
research and development expenses are directly related 
to the Group’s development projects and may therefore 
fluctuate strongly from year to year. 
Capitalization of expenditure on the development of the 
Group’s products commences from the point at which 
technical and commercial feasibility of the product can 
be demonstrated and it is probable that future economic 
benefits will result from the product once completed. As 
at 31 December 2024, considering the development stage 
of the Group’s drug candidates, no internally developed 
assets related to Group’s development activities had met 
these criteria and had therefore not been recognized. 
The uncertainties inherent in developing pharmaceutical 
products prohibits the capitalization of internal 
development expenses as an intangible asset until the 
marketing approval has been received from the relevant 
regulatory agencies. 
2.8. Employee Benefits
The Group’s employee benefits consist of short-
term employee benefits, post-employment benefits 
(defined contribution pension plans) and share-based 
compensation. Short-term employee benefits are 
charged to the statement of comprehensive income in 
the year in which the related service is provided. Under 
defined contribution plans, the Group’s contributions 
are recorded as an expense in the accounting period to 
which they relate and the Group does not have any further 
obligations once the contributions have been paid. 
2.9. Share-based Compensation
The options granted under share-based incentive 
programs are measured at fair value at earlier of the 
grant date or the service commencement date, using the 
Black-Scholes valuation model. The options, for which 
the option exercise price is determined later, right before 
the vesting, an estimate is used to determine the fair 
value at service commencement date and the estimate is 
subsequently revised until the options become granted. 
The share-based compensation expense is recognized on 
a straight-line basis over the vesting period together with 
a corresponding increase in equity, based on the Group’s 
estimate of equity instruments that will eventually vest. 
At each reporting date, the Group revises its estimate of 
the number of equity instruments that are expected to 
vest and its estimate of the grant date fair value for the 
options with earlier service commencement date. The 
exercise price paid by the option or warrant holder to 
subscribe the Group’s shares is recognized in the reserve 
for invested unrestricted equity.
2.10. Loss per Share
Basic loss per share is calculated by dividing the loss for 
the period with the weighted average number of ordinary 
shares during the period.
Since the Group and parent company have reported 
losses, inclusion of unexercised options would decrease 
the loss per share and therefore they are not taken into 
account in diluted loss per share calculation. 
2.11. Income Tax
Income tax expense for the period consists of current 
and deferred taxes. Tax is recognized in the statement of 
comprehensive income, except for the income tax effects 
of items recognized in other comprehensive income or 
directly in equity, which is similarly recognized in other 
comprehensive income or equity. 
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Deferred taxes are recognized using the liability method 
on temporary differences arising between the tax bases 
of assets and liabilities and their carrying amounts in the 
financial statements. Deferred taxes are determined using 
tax rates enacted or substantively enacted by the balance 
sheet date in the respective countries and are expected 
to apply when the related deferred tax asset is realised or 
the deferred tax liability is settled. 
Deferred income tax assets are recognized only to the 
extent that it is probable that future taxable income will 
be available, against which the temporary differences, tax 
losses and tax credit can be utilized. 
2.12. Machinery and Equipment
The Group’s machinery and equipment comprise of 
office furniture and equipment, which is stated at 
historical cost less depreciation and any impairment 
losses. The historical cost includes expenditure that is 
directly attributable to the acquisition of the machinery 
and equipment.
Depreciation is calculated using the straight-line method 
over the asset’s estimated useful life of four years. 
Depreciation is recorded to the costs of the asset function.
2.13. Intangible Assets
The Group’s intangible assets comprise of capitalized 
patent costs arising in connection with the preparation, 
filing and obtaining of patents. Patent costs are 
amortized on a straight-line basis over the useful lives of 
the patents of ten years. 
2.14. Impairment of Non-financial Assets
Assets that are subject to depreciation or amortisation are 
reviewed for impairment whenever there are indications 
that the carrying amount may not be recoverable. 
An impairment loss is recognized for the amount by 
which the asset’s carrying amount exceeds its recoverable 
amount. The recoverable amount is the higher of an asset’s 
fair value less costs of disposal and value in use. The value 
in use represents the discounted future net cash flows 
expected to be derived from the asset. 
2.15. Inventories
Inventories are stated at the lower of cost and net 
realizable value. The cost includes all costs of direct 
materials and external services associated with the 
process of manufacturing of the goods sellable upon 
obtaining the regulatory marketing approval. The cost of 
inventories is fully written down.
2.16. Financial Assets
The Group’s financial assets comprise of other 
receivables and cash and cash equivalents, which are all 
classified to the category “financial assets measured at 
amortised cost”. These are non-derivative financial assets 
with fixed or determinable payments that are not quoted 
in an active market. They are included in current assets, 
except for maturities greater than 12 months after the 
reporting date, which are classified as non-current assets. 
Other receivables consist mainly of VAT refund and 
restricted cash in the form of security deposits for rental 
agreements. Cash and cash equivalents comprise cash 
at banks.
2.17. Financial Liabilities
The Group’s financial liabilities comprise of interest-
bearing borrowings, trade payables, other non-current 
and current liabilities. The Group’s financial liabilities are 
divided into two groups: the ones measured at amortized 
cost using the effective interest method and the ones at 
fair value through profit and loss.
Borrowings are initially recognized at fair value, less any 
directly attributable transaction costs. Subsequently 
borrowings are carried at amortized cost using the 
effective interest method (EIR). Amortized cost is 
calculated by taking into account any discount or 
premium on acquisition and fees or costs that are an 
integral part of the EIR. The EIR amortization is included 
as finance costs in the statement of profit or loss. 
Borrowings are presented as current liabilities unless 
the Group has an unconditional right to defer settlement 
of the liability for at least 12 months after the end of 
the reporting period. Borrowings are not derecognized 
until the liability has ceased to exist, that is, when the 
obligation identified in a contract has been fulfilled or 
cancelled or is no longer effective. When an existing 
financial liability is replaced by another from the same 
lender on substantially different terms, or the terms of 
an existing liability are substantially modified, such an 
exchange or modification is treated as the derecognition 
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of the original liability and the recognition of a new 
liability. The difference in the respective carrying amounts 
is recognized in the statement of profit or loss.
Borrowings comprise of a secured debt by IPF partners 
and four government loans with a below-market rate of 
interest from The Finnish Funding Agency for Technology 
and Innovation (“Business Finland”). 
The grant component of the gorvernment loans, which is 
the benefit of the below-market interest rate, is measured 
as the difference between the initial fair value of the loan 
and the proceeds received.
Other liabilities consist of warrants issued as part of 
the IPF loan agreement for no consideration paid. 
The warrants meet the definition of a derivative and are 
therefore recognized at fair value through profit or loss. 
In estimating the fair value of the liability, the Group uses 
market-observable data to the extent it is available.
Fair value hierarchy levels 1 to 3 are based on the degree 
to which the fair value is observable:
•	 Level 1 fair value measurements are those  
derived from quoted prices (unadjusted) in  
active markets for identical assets or liabilities;
•	 Level 2 fair value measurements are those  
derived from inputs other than quoted prices included 
within Level 1 that are observable for  
the asset or liability, either directly (i.e. as prices)  
or indirectly (i.e. derived from prices); and
•	 Level 3 fair value measurements are those  
derived from valuation techniques that include inputs 
for the asset or liability that are not based  
on observable market data (unobservable inputs).
Where Level 1 inputs are not available, the Group engages 
third party qualified valuers to assist in preparing the 
valuation models. 
Trade payables and other liabilities 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 end of the reporting period, in which 
case they are classified as non-current liabilities. The 
carrying amount of trade payables and other current 
liabilities are considered to be the same as their fair 
values, due to their short-term nature. 
2.18. Equity
The Group’s equity comprises of share capital, reserve 
for invested unrestricted equity and accumulated deficit. 
The proceeds from issuance of new ordinary shares, 
less incremental costs directly attributable to the issue, 
are credited to the reserve for invested unrestricted 
equity, in accordance with the terms and conditions of 
the share issue. The accumulated deficit comprises of 
the accumulated profits and losses of the Group since 
the inception. 
Under the Finnish Limited Liability Companies Act 
(624/2006, as amended), if the board of directors of a 
company notices that the company has negative equity, 
the board must make a register notification on the loss 
of share capital. However, if the fair value of the assets 
of the Company is otherwise than temporarily notably 
higher than their book value, the difference between the 
probable current price and the book value may be taken 
into account as an addition to equity. During Financial 
Period 2024, the Board notified that the equity of the 
Company turned negative. After having notified this, the 
Board decided to further assess the equity amount. In 
this regard, the Board, exercising special caution, noted 
that the fair value of the intangible assets related to 
Traumakine and Bexmarilimab is significantly higher 
than their respective book values. When making the 
calculations mandated by the Finnish Limited Liability 
Companies Act, the difference of the book and fair value 
of the assets was taken into account, thus the registration 
has not been filed.
2.19. Leases
The Group as Lessee 
The Group recognizes all leases, with the exception of 
short-term (i.e. lease term less than 12 months) and low 
value leases, in line with IFRS 16 Leases as right-of-use 
assets with a corresponding lease liability at the date at 
which the leased asset is available for use by the Group. 
A contract is or contains a lease if the Group has the right 
to control the use of an identified asset for a period of 
time in exchange for consideration. When determining 
the lease term, the Group assesses the probability of 
exercising extension and termination options over the 
non-cancellable period by considering all relevant facts 
and circumstances. Right-of-use assets and lease 
liabilities are initially recognized on the consolidated 
balance sheet at future fixed lease payments over the 
lease term. Lease payments are discounted to present 
value using an effective interest rate. Right-of-use 
assets are depreciated on a straight-line basis over 
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the lease term and reviewed periodically for indication 
of impairment. When the future lease payments are 
revised due to changes in index-linked considerations 
or the lease term changes, the right-of-use asset and 
the corresponding lease liability is remeasured. Any 
differences arising on reassessments are recognized in 
the consolidated income statement. Interest expense on 
lease liabilities is presented within Interest expense in the 
consolidated income statement. In the consolidated cash 
flow statement, the principal portion of the lease payment 
is presented in the cash flow from financing activities. 
2.20. Provisions and Contingent Liabilities
Provisions are recognized when the Group has a 
present legal or constructive obligation as a result of 
past events, it is probable that an outflow of resources 
will be required to settle the obligation, and a reliable 
estimate of the amount can be made. A contingent 
liability is a possible obligation that arises from past 
events and whose existence will be confirmed only by 
the occurrence of uncertain future events not wholly 
within the control of the entity. Such present obligation 
that probably does not require settlement of a payment 
obligation and the amount of which cannot be reliably 
measured is also considered to be a contingent liability. 
Contingent liabilities are disclosed in the notes to the 
financial statements. 
2.21. Critical Accounting Estimates and Significant 
Management Judgements in Applying Accounting 
Policies
Share-based Compensation 
The Group and the Company recognizes expenses for 
share-based compensation. For share options management 
estimates certain factors used in the option pricing model, 
including volatility, vesting date of options and number of 
options likely to vest. If these estimates vary from actual 
occurrence, this will impact the value of the share-based 
compensation. Further details of the Group’s estimation of 
share-based compensation are disclosed in note 17.
Clinical Trial Accruals 
Quantification of the accruals related the clinical trials 
require a lot of detailed information about the services 
performed. The services invoiced by Contract Research 
Organizations consist of contributions of various 
independent subcontractors and the actual tasks 
completed may be reported with significant delays. Also 
the clinical study sites, may invoice their costs with long 
delays. These factors combined result in a complicated 
task of defining on which period the cost belongs to and 
the Group has implemented a detailed tracking process to 
minimize any judgement needed. 
2.22. New and Amended Standards and  
Interpretations Adopted by the Group
The effect of changes required by the adoption of new 
standards, interpretations and amendments to existing 
standards and interpretations on 1 January 2024 were 
considered immaterial for the group. 
New standards not yet implemented by the Group: 
Certain new accounting standards, amendments to 
accounting standards and interpretations have been 
published that are not mandatory for 31 December 2024 
reporting periods and have not been early adopted by the 
group. Those include:
•	 IFRS 18, ‘Presentation and Disclosure in Financial 
Statements’
•	 Amendments to IAS 21 - Lack of Exchangeability
•	 Amendments to the Classification and Measurement 
of Financial Instruments – Amendments to IFRS 9 and 
IFRS 7
•	 These standards, amendments or interpretations 
are not expected to have a material impact on the 
entity in the current or future reporting periods and on 
foreseeable future transactions
•	 The group is monitoring potential changes in  
future accounting standards and assessing any impact 
thereof on a continuing basis.
3. SEGMENT REPORTING
Faron is a late clinical stage drug discovery and 
development Group. Its operations have been focused on 
the development of its main drug candidates Traumakine 
and Bexmarilimab. The Group’s chief operating decision 
maker has been identified as the Chief Executive Officer 
(CEO). The CEO manages the Group as one integrated 
business and hence the Group has one operating and 
reportable segment. The Group had no revenue in 2024 
(EUR 0 thousand in 2023). All of the Group’s non-current 
assets are located in Finland.
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4. OTHER OPERATING INCOME
The Group had no operating income in year 2024 or 2023.
The Company had EUR 3,42 thousand operating income 
in 2024 and EUR 65 thousand operating income in 2023 
related to intra-group transactions.
5. BREAKDOWN OF EXPENSES BY FUNCTION
Research and Development Expenses
Year ended 31 December
€’000
2024
2023
Materials and services
(505)
(134)
Employee benefits
(1,363)
(3,230)
Outsourced clinical trials services
(3,277)
(3,997)
Drug production
(3,633)
(8,095)
Analytics
(655)
(1,288)
Data management
(233)
(260)
Legal and consulting
(1,382)
(1,731)
IT expenses
(143)
(246)
IPR expenses
(188)
(200)
Travelling
(70)
(74)
Depreciation and amortization
(170)
(129)
Short term rent and premises
-
(26)
Other R&D costs
(126)
(133)
Total research and  
development expenses
(11,744)
(19,542)
The significant decrease of R&D costs was mainly caused 
by lower costs in drug production and analytics. Also the 
cost of employee benefits/option programs were lower 
due to changes in share price as well as lower number of 
employees. Third main contributor was lower usage of 
external legal and consulting services.
 The Company had lower research and development 
expenses than the group mainly due to employee benefits 
at subsidiaries.
General and Administration Expenses 
Year ended 31 December
€’000
2024
2023
Employee benefits
(3,314)
(5,686)
Communication
(395)
(481)
Audit fees
(120)
(46)
Legal and consulting
(1,918)
(1,167)
IT expenses
(205)
(276)
Travelling
(118)
(225)
Depreciation and amortization
(144)
(217)
Short term rent and premises
(246)
(320)
Other G&A
(469)
(607)
Total general and  
administrative expenses
(6,929)
(9,026)
The sizable decrease in G&A costs was due to lower 
costs of employee benefits/option programs due to 
changes in share price as well as lower number of 
employees. The legal and consulting costs however were 
much higher due to the complex financing arrangements 
in spring 2024. 
The Company had higher general and administration 
expenses than the group mainly due to compensation of 
services subsidiaries has provided to the Company.
6. EMPLOYEE BENEFITS
Year ended 31 December
€’000
2024
2023
Salaries
(3,407)
(5,540)
Pension expenses – 
contribution-based plans
(499)
(758)
Social security contributions
(77)
(165)
Share-based compensation
(694)
(2,453)
Total employee benefit expenses
(4,676)
(8,916)
Employee benefit expenses by function
Research and development expenses
(1,363)
 (3,230)
General and administrative expenses 
(3,314)
(5,686)
Total employee benefit expenses
(4,676)
(8,916)
The headcount of personnel at the end of 2024 was 
25 (2023: 34). Share-based compensation information 
is included in note 17 and management remuneration 
information in note 23.
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The foreign exchange gains mainly relate to the cash 
balance denominated in US Dollars which strengthened 
against the EUR. Unrealised foreign exchange gain, net is 
EUR 67 thousand for 2024 and EUR 7 thousand for 2023.
9. TAX EXPENSE 
Year ended 31 December
€’000
2024
2023
Tax expense
5
-
Total tax expense
5
-
The difference between income taxes at the statutory 
tax rate in Finland (20%) and income taxes recognised 
in the statement of comprehensive income is reconciled 
as follows:
Year ended 31 December
€’000
2024
2023
Loss before tax
(25,915)
(30,944)
Income tax calculated at Finnish 
tax rate 20%
5,183
6,189
Tax losses and temporary 
differences for which no deferred 
tax asset is recognised
(5,919)
(5,950)
Non-deductible expenses, 
tax-exempt income and other 
permanent items
736
(239)
Foreign income taxes
(5)
-
Taxes in the statement of  
comprehensive income
(5)
-
Tax losses and deductible temporary differences for 
which no deferred assets have been recognised, are 
as follows:
Year ended 31 December
€’000
2024
2023
R&D expenses not yet deducted  
in taxation (1)
117,625
95,179
Tax losses carried forward (2)
57,679
51,633
Total
175,304
146,812
(1) The Group has incurred research and development 
costs, which have not yet been deducted in its taxation 
in Finland. The amount deferred for tax purposes can be 
deducted over an indefinite period. 
(2) Tax losses carried forward relate to Finland and expire 
over the period of 10 years. The tax losses will expire as 
follows:
7. DEPRECIATION AND AMORTISATION
Year ended 31 December
€’000
2024
2023
Depreciation and amortisation  
by type of asset 
Depreciation for right-of-use-assets
(110)
(149)
Intangible assets - patents
(170)
(129)
Intangible assets
(31)
(61)
Machinery and equipment
(4)
 (7)
Total depreciation and amortisation
(314)
(346)
Depreciation and amortisation  
by function
Research and development expenses
(170)
(129)
General and administrative expenses
(144)
(217)
Total depreciation and amortisation
(314)
(346)
8. FINANCIAL INCOME AND EXPENSES
Year ended 31 December
€’000
2024
2023
Financial income
Interest income
93
230
Other financial income
268
-
Gains from foreign exchange
72
3
Total financial income
434
233
Financial expenses
Interest expenses
(3,943)
(2,124)
Warrant value change
(2,944)
(42)
Losses from foreign exchange
(5)
4
Interest expenses from lease 
liabilities
(1)
(1)
Transaction and structuring fees of 
borrowings
(750)
(400)
Other financial expenses
(33)
(46)
Total financial expenses
(7,676)
(2,609)
Total financial income and  
expenses, net
(7,242)
(2,376)
Interest expenses consist of paid and accrued interest 
expenses. The interest expense relates mainly to the IPF 
loan, Business of Finland loans and interest expenses 
recognised from lease liabilities.  
 
The single most important factor in the increase of 
financial expenses was the value change of the IPF 
warrants due to a new lower strike price of the warrants. 
The interest expenses related to the complex financing 
arrangements in spring 2024 caused an sizable increase 
in the interest expenses
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€’000
2024
2023
Expiry within five years
34,060
30,911
Expiry within 6-10 years
23,619
20,722
Total
57,679
51,633
The related deferred tax assets have not been recognised 
in the balance sheet due to the uncertainty as to whether 
they can be utilized. The Group has a loss history, which 
is considered a significant factor in the consideration of 
not recognizing deferred tax assets. The total tax value of 
unrecognized deferred tax assets is EUR 35,061 thousand 
(2023: EUR 29,362 thousand).
The Group does not have any other material deductible 
or taxable temporary differences. Therefore, no deferred 
tax assets or liabilities have been recognised in the 
balance sheet and thus the itemization of deferred taxes 
is not provided.
10. LOSS PER SHARE
Loss per share is calculated by dividing the net loss by 
the weighted average number of ordinary shares in issue 
during the year. 
Year ended 31 December
€’000
2024
2023
Loss for the period
(25,911)
(30,942)
Weighted average number of 
ordinary shares in issue
88,518,654
65,055,036
Basic and dilutive loss  
per share (in €)
(0.29)
(0.48)
As of 31 December 2024, Faron Pharmaceuticals Oy had 
only share options outstanding. Number of potentially 
dilutive instruments currently outstanding totaled 
4,617,816 as of 31 December 2024 (31 December 2023: 
4,007,066, comparative number was revised to match 
with the calculation method of 2024). Since the Group 
and the Company has reported a net loss, the share 
options would have a further dilutive effect and are 
therefore not taken into account in diluted loss per share-
calculation. As such, there is no difference between basic 
and diluted loss per share.
11. INTANGIBLE ASSETS AND MACHINERY  
AND EQUIPMENT
€’000
Intangible 
assets
Machinery
and equipment
Book value on 1 January 2024
1,088
6
Additions
225
-
Disposals
-
-
Depreciation/amortisation
(200)
(5)
Book value 31 December 2024
1,112
1
As at 31 December 2024
Acquisition cost
2,245
27
Accumulated disposals
-
-
Accumulated depreciation/
amortisation
(1,132)
(25)
Book value 31 December 2024
1,112
1
Book value on 1 January 2023
1,154
13
Additions
122
-
Disposals
-
- 
Depreciation/amortisation
(188)
(7)
Book value 31 December 2023
1,088
6
As at 31 December 2023
Acquisition cost
2,031
27
Accumulated disposals
-
- 
Accumulated depreciation/
amortisation
(943)
(21)
Book value 31 December 2023
1,088
6
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12. NON-CURRENT PREPAYMENTS AND OTHER 
RECEIVABLES
As at 31 December
€’000
2024
2023
Other receivables
46
60
Total non-current 
prepayments and other 
receivables
46
60
Other receivables consist mainly of restricted cash in the 
form of security deposits for rental agreements.
For the parent company, the other receivables (2024 EUR 
551 thousand) consist of intercompany loans that are 
eliminated at the group level.
13. RIGHT-OF-USE-ASSETS AND LEASING 
LIABILITIES
€’000
31 December 
2024
31 Dec
2023
Right-of-use assets
 
Office & parking places
296
198
Total right-of-use assets
296
198
Lease liabilities
Long-term leasing liability
117
50
Short-term leasing liability
186
163
Total leasing liabilities
303
213
New lease contracts were done in 2024. The new lease 
for office space is valid until 31st of July 2027. New 
contract for parking places is valid until further notice and 
thus lease term is estimated reflecting same period as 
the office lease.
14. CURRENT PREPAYMENTS AND OTHER RECEIVABLES
As at 31 December
Group
Parent
€’000
2024
2023
2024
2023
Prepayments
1,280
1,764
1,279
1,761
Other accrued incomes and other receivables
201
196
321
524
Prepayment for product testing
-
-
-
-
VAT receivable
82
32
82
32
Total current prepayments and other receivables
1,563
1,992
1,682
2,317
15. CASH AND CASH EQUIVALENTS
As at 31 December
Group
Parent
€’000
2024
2023
2024
2023
Bank accounts
9,503
6,875
9,462
6,842
Total cash and cash equivalents
9,503
6,875
9,462
6,842
The majority of prepayments consist of the Clinical Service 
Agreements with Contract Research Organizations, which 
are current service providers in different clinical trials. 
The decrease of the prepayments, other accrued incomes 
and other receivables is due to the recognition of those 
costs as those costs accrued during the period.
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The subscription price for the shares is recorded to 
the share capital, unless the Board has made a resolution 
to record the subscription price in the reserve for 
invested unrestricted equity. If the shares of a Finnish 
limited liability company have no par value according to 
its articles of association, the Finnish Limited Liability 
Companies Act allows companies the recognition of the 
proceeds from share issuance to the reserve for invested 
unrestricted equity. In such situations the board of 
a company can choose on a subscription-by-subscription 
basis, how much of the issue, if anything, is recorded in 
share capital and how much to the reserve for invested 
unrestricted equity that is distributable. During 2023 and 
2024, the Company recognised all relevant transactions  
in the invested unrestricted equity reserve.
16. SHAREHOLDERS’ EQUITY
Movements in number of shares, share capital and 
reserve for invested unrestricted equity were as follows:
€’000
Total registered 
shares (pcs)
Share 
capital
Reserve for 
unrestricted equity
1 January 2023
59,805,383
2,691
129,544
Issue of new shares, net of transaction costs
8,981,316
-
24,808
31 December 2023
68,786,699
2,691
154,352
1 January 2024
68,786,699
2,691
154,352
Issue of new shares, net of transaction costs
35,838,165
-
30,609
Accumulated deficit, legal reserve
-
-
(5)
31 December 2024
104,624,864
2691
184,955
On 19 January 2024, the number of shares was increased 
to 68,807,199 shares following the issue of 20,500 new 
shares. On 4 April 2024, the number of shares was 
increased to 72,007,497 shares following the issue of 
3,200,298 new shares. On 20 June 2024, the number of 
shares was increased to 104,624,864 shares following 
the issue of 32,617,367 new shares. At the year end 2024 
authorization to issuance of shares, options or other 
special rights entitling to shares and conveyance of up 
to the same maximum number of treasury shares was 
19,113,496.
Faron Pharmaceuticals Ltd has one class of ordinary 
shares. The shares have no par value. Each share entitles 
the holder to one vote at the Annual General Meeting and 
equal dividend. All shares are fully paid. 
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56

17. SHARE OPTIONS 
Option Plan 2015
The Option Plan 2015 was approved at the Company’s 
extraordinary shareholders’ meeting on 15 September 
2015 as part of the Group’s incentive scheme determined 
by the Board of Directors. The share options are 
granted to the members of the Board of Directors and 
the management team and other management and 
employees for no consideration. The annual general 
meeting on 16 May 2017 resolved to amend, due to the 
increase in the number of employees in the Group and 
the increase in the number of members of the Board 
of Directors, the Option Plan so that a maximum total 
of 500,000 C options and a maximum total of 500,000 
D options may be offered under initial Option Plan 
terms and conditions. The share options have a service 
condition and are forfeited in case the employee leaves 
the Company before the share options vest, unless the 
Board of Directors approves otherwise. After the beginning 
of the share subscription period, the vested options may 
be freely transferred or exercised. Grant dates for the 
share options may vary depending on the date when the 
Company and the employees agree to the key terms and 
conditions of the Option Plan. The maximum number of 
share options that can be awarded under the Option Plan 
is 1,800,000 in four different tranches designated as A 
options, B options, C options and D options. Each share 
option entitles the holder of the option to subscribe for 
one ordinary share of the Company.
The exercise price for ordinary shares based on A 
options is euro equivalent of the Company’s share 
subscription price in the Company’s initial public offering 
on the AIM marketplace of the London Stock Exchange 
on 17 November 2015. The exercise price for ordinary 
shares based on B options, C options and D options is 
euro equivalent of the exercise price determined based 
on the Company’s average share price on the AIM 
marketplace during 1 July - 30 September 2016, 2017 and 
2018, respectively.
The extraordinary general meeting 2023 resolved to 
amend the terms and conditions of the Option Plan 
2015 so that the subscription period for shares based 
on the options is extended by two (2) years, i.e., until 30 
September 2025. The amendment is expected to enhance 
the usability of the options and thereby significantly 
increase the desired benefits of the incentivisation 
system for the management and personnel of the 
Company. The management has determined the 
incremental fair value related to the extension of the 
subscription window of the 2015 Option Plan. This 
valuation is based on a comparison of the fair value of 
the instruments before and after the modification, using 
Black-Scholes-Merton model. Notably, as the modification 
occurred post-vesting date, the incremental fair value was 
promptly recognized in the financial statements.
Key characteristics and terms of the option plan are listed 
in the table below. 
2015 Option Plan
A options
B options
C options
D options
Maximum number of share options
400,000
400,000
500,000 
500,000
Exercise price, EUR
3.71
2.90
8.39 
1.09
Dividend adjustment
No
No
No
No
Beginning of
subscription period
2 November 2015
8 October 2016
8 October 2017
8 October 2018
End of subscription period
30 September 2025*
30 September 2025*
30 September 2025*
30 September 2025*
Vesting conditions
Service until the beginning of the subscription period
* The extraordinary general meeting, held on 22 September 2023, resolved to amend the terms and conditions of the Option Plan 2015 so that the subscription period for shares 
based on the options is extended by two (2) years, i.e., until 30 September 2025. 
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2024 
2015 Option Plan
2023 
2015 Option Plan
Number of share options
A
B
C
D
A
B
C
D
Outstanding at 1 January
385,000
338,400
500,000
170,000
385,000
383,900
500,000
320,000
Granted
-
-
-
-
-
-
-
-
Forfeited
-
-
-
-
-
-
-
-
Exercised
-
5,000
-
8,000
-
45,500
-
150,000
Outstanding at 31 December
385,000
333,400
500,000
162,000
385,000
338,400
500,000
170,000
Exercisable at 31 December
385,000
333,400
500,000
162,000
385,000
338,400
500,000
170,000
The weighted average fair value of the share 
options granted, EUR
-
-
-
-
-
-
-
-
The weighted average share price 
at the date of exercise, EUR
-
1,73
-
1,73
-
3.19
3.19
Option Plan 2019
The Option Plan 2019 was approved at the Company’s 
board of directors meeting on 20 November 2019. The 
Annual General Meeting on 24 March 2023 resolved to 
amend the terms and conditions of the Option Plan 2019, 
so that a maximum total under the 2019 Option Plan is 
4,350,000 options. The share options are granted to the 
members of the Board of Directors, Scientific Advisory 
Board, the management team and other management 
and employees for no consideration. 
The share options have a service condition and are 
forfeited in case the employee leaves the Group before 
the share options vest, unless the Board of Directors 
approves otherwise. After the beginning of the share 
subscription period, the vested options may be freely 
transferred or exercised. The fair value of the options 
has been determined using the Black & Scholes option 
valuation model and expensed over the vesting period. 
Grant dates for the share options may vary depending 
on the date when the Company and the employees 
agree to the key terms and conditions of the Option Plan. 
The maximum number of share options has certain 
maximum limits per certain person. The details of the 
plan are available on www.faron.com. Each share option 
entitles the holder of the option to subscribe for one 
ordinary share of the Company.
The exercise price for ordinary shares based on 2019 
grant options is euro equivalent of the average share price 
at the London AIM list for the past 90 or 30 days prior to 
the grant date. For the GBP to EUR price conversion, the 
exchange rate of the European Central bank on the grant 
date is used. The weighted average exercise price for 
ordinary shares based on Plan 2019 granted options in 
2024 is EUR 1.16 
The Company’s Board has confirmed the grant of a total 
of 785,000 options under the Option plan 2019 during 
2024. The Options have been allocated under the Share 
Option Plan 2019 and will be released in 25% per annum 
over a period of 4 years starting on the first anniversary 
after grant. Key characteristics and terms of the option 
plan are listed in the table below. 
2019 Option Plan
2024
2023*
Maximum number of 
share options
4,350,000
4,350,000
Exercise price, EUR 
(weighted average if 
several grant during 
the year)
1.16
3.45
Dividend adjustment
No
No
Beginning of first 
subscription period
17 November 
2022
17 November 
2022
End of the last 
subscription period
9 November 
2028
9 November 
2028
Vesting conditions
Service 
until the 
beginning 
of each 
subscription 
period
Service 
until the 
beginning 
of each 
subscription 
period
* In There were two grants, in both 2024 and 2023
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2023–2024 
2019 Option Plan
Number of share options
2024
2023
Outstanding at 1 January
2,613,666
1,876,916
Granted
785,000
813,000
Forfeited
153,750
76,250
Exercised
7,500
-
Outstanding at 31 December
3,237,416
2,613,666
Exercisable at 31 December
1,477,957
904,040
2023–2024 
2019 Option Plan
Valuation inputs for instruments 
granted during period 
(weighted average)
2024
2023
Share price at grant date, EUR
1.18 - 2.36
2.96 - 3.50
Subscription price, EUR 
1.00 - 2.28
3.35 - 3.77
Volatility, % *
76.5
65.4
Risk free rate, %
2.8
3.1
Expected dividends yield, %
0
0
Option fair value, EUR
0.87
1.31
* Expected volatility was determined by calculating the historical volatility of the 
Company`s share using monthly observations over corresponding maturity.
The share-based compensation expense for the Option 
Plan 2019 was EUR 694 thousand (EUR 1,259 thousand 
in 2023).
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18. FINANCIAL ASSETS AND LIABILITIES
As at 31 December
Group
Parent
€’000
2024
2023
2024
2023
Financial assets measured at amortised cost
Other receivables*
121
72
121
169
Cash and cash equivalents
9,503
6,875
9,462
6,842
Total financial assets measured at amortised cost
9,624
6,948
9,583
7,011
Financial liabilities measured at amortised cost
Lease liabilities
303
213
303
213
Account payables
4,876
8,971
5,996
10,585
Borrowings in form of Business Finland R&D loans
3,124
3,520
3,124
3,520
Borrowings in form of IPF Tranche A
8,686
9,383
8,686
9,383
Total financial liabilities measured at amortised cost
16,990
22,087
18,109
23,701
Financial liabilities measured at FVTPL (category 2)
Other non-current liabilities**
3,839
895
3,839
895
Total financial liabilities measured at FVTPL
3,839
895
3,839
895
* Prepayments are excluded as they are not considered to be financial instruments.
**see note 21
Borrowings in the Form of Business  
Finland R&D Loans
Fair value for the Business Finland R&D loans is 
calculated by discounting estimated future cash flows 
for the loans using appropriate interest rates at the 
reporting date. The discount rate considers the risk-free 
interest rate and estimated margin for the Company’s 
own credit risk. Discounted future cash flows are derived 
from the terms containing the repayment amounts 
and repayment dates for the principal and the cash 
payments for interest. Given that some of the inputs to 
the valuation technique rely on unobservable market 
data, loan fair values are classified in Level 3. The 
carrying amount of all the Business Finland loans was 
EUR 3,124 thousand (2023 EUR 3,520 thousand).
Business Finland R&D loans are granted to a defined 
product development project and cover a contractually 
defined portion of the underlying development projects’ 
R&D expenses. The below-market interest rate for these 
loans is the base rate set by the Ministry of Finance 
minus three (3) percentage points, subject to a minimum 
rate of 1%. Repayment of these loans shall be initiated 
after 5 years, thereafter loan principals shall be paid 
back in equal instalments over a 5-year period, unless 
otherwise agreed with Business Finland. Requesting 
accord to the loan(s) is also a possibility. For more 
information on contractual maturities of the Business 
Finland R&D loans and interests is provided in the 
note 19. The interest on Business Finland R&D loans 
amounted to EUR 83 thousand (2023 EUR 329 thousand).
Loan facilities and related warrant  
agreements with IPF 
On 28 February 2022, Faron entered into agreement  
with IPF Fund II SCA (IPF), which contained
•	 a Euro term loan facility (Tranche A) of up to  
EUR 10 million,
•	 a Euro term loan facility (Tranche B) of up to  
EUR 5 million,
•	 the possibility of Faron to request up to an additional 
EUR 15 million facility (Tranche C), subject to IPFs 
approval process and certain conditions to be met,
•	 Faron to issue warrants to IPF as part of the loan 
agreement, based on the amount drawn in the above 
facilities.
The first tranche (Tranche A) of EUR 10 million was drawn 
down upon signing the agreements in 2022. Faron pays 
cash interest on drawn amounts of the above facilities 
plus a pay-in-kind interest (PIK) for drawn amounts in 
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Tranche A. In addition, Faron has paid a structuring 
fee of the committed facility on the utilization date of 
the respective facility. Tranche A has been measured 
at amortised cost using the effective interest method. 
The carrying amount of the Tranche A was EUR 8,686 
thousand. With respect to the availability of additional 
funding from IPF, the respective term allowing the Group 
to draw on Tranche B and Tranche C has expired. The 
Group does not anticipate, at this time, having the ability to 
draw further funding from IPF. The interest on Tranche A 
facility amounted to EUR 945 thousand. The loan facility 
is subject to financial covenants. The covenants measure 
the Group’s gearing ratio and cash runway. Given that 
some of the inputs to the valuation technique rely on 
unobservable market data, loan fair values are classified 
in Level 3. 
Liabilities designated at fair value through profit or 
loss primarily represent warrants which entitle IPF to 
subscribe for new ordinary shares in the Company. 
The subscription price per share is the lower of EUR 1,85 
or the subscription price per share in any subsequent 
share offering undertaken by the Company. The warrants 
were issued as part of the loan agreement in 2022 
for no consideration paid and have been treated as a 
separate financial instrument. On initial recognition of the 
agreement, the fair value of the loan facility was reduced 
by the structuring fee and other fees that are integral 
part of the loan and by the implicit costs of the warrants. 
On subsequent reporting dates the changes in fair value 
of warrants have been accounted separately through 
profit and loss. The warrants are classified as Level 2 
instruments and their fair value is determined using 
techniques whose inputs are based on observable market 
data. Total warrants issued in 2024 were 1.5 million.
This section sets out an analysis of net debt and 
the movements in net debt (calculated as cash and 
cash equivalents less borrowings) for each of the 
periods presented.
As at 31 December
Group
Parent
€’000
2024
2023
2024
2023
Cash and cash equivalents
9,503
6,875
9,462
6,842
Lease liabilities
(303)
(213)
(303)
(213)
IPF Tranche A
(8,686)
(9,383)
(8,686)
(9,383)
Business Finland R&D loans
(3,124)
(3,520)
(3,124)
(3,520)
Net debt
(2,610)
(6,241)
(2,651)
(6,274)
€’000
Borrowings
Lease 
liabilities
Other 
liabilities
Total
Opening balance as at 1 Jan 2023
12,953
316
853
14,123
Financing cash flows
(692)
(142)
(834)
Fair value adjustments
42
42
Other movements (*)
637
39
676
Balance as at 31 Dec 2023
12,898
213
895
14,006
Financing cash flows
3,200
(162)
(4,033)
New lease liability
239
239
Fair value adjustments
2,944
2,944
Other movements (*)
(4,288)
13
2,792
Balance as at 31 Dec 2024
11,810
303
3,839
15,952
*) Other changes include reversals, interest accruals and payments.
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19. FINANCIAL RISK MANAGEMENT 
This section applies to The Group and the Company. The 
operations of the Group expose it to financial risks. The 
main risk that the Group is exposed to is liquidity risk, with 
capital management being another important area given 
the nature of the Group’s operations and its financing 
structure. The Group’s financial risk management 
principles focus on obtaining funding and managing 
capital taking into consideration the unpredictability of 
the financial markets with the aim at minimizing any 
undesired impacts on the Group’s financial performance 
and position. The Board of Directors define the general 
risk management principles and approve operational 
guidelines concerning specific areas including but not 
limited to liquidity risk, foreign exchange risk, interest rate 
risk, credit risk, the use of any derivatives and investment 
of the Group’s liquid assets. 
(a) Capital Management and Liquidity Risks 
The Group’s objective when managing capital is to 
safeguard the Group’s ability to continue as a going 
concern (refer to note 2.2). 
Significant financial resources are required to advance 
the drug development programs into commercialized 
pharmaceutical products. The Group relies on its ability 
to fund the operations of the Group through three 
major sources of financing – equity financing, research 
and development grants and loans, venture debt and 
licensing agreements. 
The Company has been able to fund its operations with 
equity, grants, debt and R&D loans. While equity financing 
has generally been available in the past, there can be no 
assurance that sufficient funds can be secured in order 
to permit the Group to carry out its planned activities. 
In general, capital market conditions are volatile. 
The prevailing financial market situation and overall 
investor sentiment dictate whether the Group is able to 
secure additional financing in the future, which can be 
considered a risk. To partly manage this risk, the Group 
and its management is in constant dialogue with financial 
investors, investment banks, debt providers and other 
market participants.
The Group also relies on different sources of financing 
and research and development grants and loans. These 
funds, which are provided through regional, national or EU 
level institutions, have been historically available to the 
Group. The Group strictly complies with all rules and legal 
obligations pertaining to these funding programs and is 
in regular contact with the funding agencies providing 
these. Availability of such funds in the future cannot be 
guaranteed and thus this poses a potential risk to the 
Group’s funding in the future.
Finally entering into potential commercialization, 
collaboration and licensing agreements with larger 
pharmaceutical companies entitles the Group to receive 
up-front and milestone payments related to agreed 
regulatory or commercial points, as well as royalty 
payments once commercialization has been successful. 
Activities in the area of business development are 
targeted at securing such agreements. Consideration of 
these activities is part of the management’s duties and 
is monitored by the Board of Directors, which ultimately 
decides on entering into such agreements. 
There can be no assurance that sufficient financing can 
be secured in order to permit the Group to carry out 
its planned activities. To protect the continuity of the 
Group’s operations, sufficient liquidity and capital has to 
be maintained. The Group aims to have funds to finance 
its operations for the foreseeable future. The Group can 
influence “somewhat” as the ability to impact on cash 
runway with cost management is limited the amount of 
capital by adapting its cost basis considering available 
financing. Management monitors liquidity on the basis of 
the amount of funds. These are reported to the Board of 
Directors on a monthly basis. 
The Company’s Board of Directors approves the 
operational plans and budget and monitors the 
implementation of these plans and the financial status of 
the Group on a monthly basis. 
As at 31 December 2024, the contractual maturity of non-
derivative liabilities excluding other payables and accruals 
was as follows. The Company had additional EUR 1,124 
thousand (EUR 1,464 thousand as at 31 December 2023) 
trade payables to subsidiaries:
€’000
2025
2026
2027
2028 - thereafter
Total
Borrowings
4,644
4,182
5,094
476
14,396
Trade payables
4,876
-
-
-
4,876
Lease liabilities
117
109
76
-
303
Total
9,638
4,292
5,170
476
19,575
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As at 31 December 2023, the contractual maturity of non-
derivative liabilities and interests excluding other payables 
€’000
2024
2025
2026
2027 - thereafter
Total
Borrowings
4,371
4,177
4,277
4,132
16,958
Trade payables
8,971
-
-
-
8,971
Lease liabilities
163
50
-
-
213
Total
13,505
4,227
4,277
4,132
26,141
(b) Market Risk 
i. Foreign Exchange Risk  
The Group operates internationally but is mainly exposed 
to translation risk in respect of US Dollar (“USD”) 
denominated cash and cash equivalents balances. 
The Group’s policy is not to hedge translation risk. As 
of 31 December 2024, the Group had cash and cash 
equivalents of EUR 6,752 thousand, USD 205 thousand, 
CHF 20 thousand and GBP 2,100 thousand (2023: EUR 
6,460 thousand, GBP 90 thousand, CHF 2 thousand 
and USD 342 thousand) and the foreign exchange 
gains and losses recorded arise mainly from the USD 
cash balances. The Group is not exposed to significant 
transaction risk, as the Group mainly operates in EUR. 
ii. Interest Rate Risk  
The Group’s interest rate risk arises from the IPF Tranche 
A loan and Business Finland R&D loans. IPF Tranche A 
interest consists of cash interest (margin and 3 months 
EURIBOR) and payment in kind interest accrued over the 
repayment period. 
Business Finland R&D loans, which interest is the base 
rate defined by the Finnish Ministry of Finance minus 
three (3) percentage points, is subject to a minimum rate 
of 1%. During the periods presented, the interest has been 
below the minimum level and the Group has paid the 
minimum interest of 1% on the loans. During the periods 
presented, the Group has not been exposed to material 
variable interest rate risk and accordingly the Group has 
not entered into derivative contracts.
(c) Credit and Counterparty Risk 
The Group works with partners and financial institutions 
with good credit ratings. Management monitors credit 
ratings of the financial institutions that hold the Group’s 
bank deposits regularly. 
20. OTHER NON-CURRENT LIABILITIES
As at 31 December
€’000
2024 
2023
FV of warrants 
3,839
895
Total non-current liabilities
3,839
895
The fair value of warrants issued to IPF (see note 18) is 
recognized in Other liabilities.
and accruals was as follows. Trade payable are presented 
to align with 2024 presentation:
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21. TRADE PAYABLES AND OTHER CURRENT LIABILITIES
As at 31 December
Group
Parent
€’000
2024
2023
2024
2023
Trade payables
3,703
8,177
4,823
9,791
Clinical trial site fees (included in trade payables in BS)
1,173
794
1,173
794
Accrued payroll
1,208
1,718
1,208
1,567
Accrued general and administration
166
114
166
109
Other liabilities and accruals
96
550
109
352
Total
6,336
12,147
7,478
13,407
22. CONTINGENCIES AND COMMITMENTS
Operating Lease – Faron as a Lessee 
The future aggregate minimum lease payments under 
non-cancellable operating leases are as follows:
Year ended 31 December
€’000
2024 
2023
No later than 1 year
9
54
Later than 1 year and  
no later than 5 years
2
-
Later than 5 years
-
-
The Group’s operating lease commitments comprise of 
lease commitments for machines and equipment with 
low value leases of 3 to 4 years. The Group’s operating 
leases are non-cancellable and they do not include 
redemption or extension options. Contingencies and 
commitments liabilities do not include lease liabilities that 
are recognised as lease liabilities on the balance sheet.
Contractual Contingencies 
The Group has a contingent contractual liability to a 
development party for Bexmarilimab to pay additional 
milestone payments. The remaining milestone becomes 
payable upon the Group receiving a certain amount of Net 
Sales for Bexmarilimab.
23. RELATED PARTY TRANSACTIONS
Parent and subsidiary relations of Faron Pharmaceuticals 
Group on 31 December 2024:
Country
Group
holding 
%
Group 
voting
%
Companies owned 
by the parent 
company
Faron Europe GmbH  
Switzerland
100
100
Faron USA LLC      
USA
100
100
At the end of period, the Company has EUR 512 thousand 
in long term receivables from subsidiaries, which contains 
intercompany loans and the interests associated with 
them. The transactions are at arm’s length. The parent 
Company trade payables to subsidiaries at the end of the 
period were EUR 1,124 thousand. 
During the period the profit and loss relevant bookings 
are EUR 22 thousand for the interest of the intercompany 
loans, management fee charges to subsidiaries of EUR 3 
thousand and the invoices for administrative services by 
the subsidiaries of EUR 413 thousand.
The Group identifies the following related parties: 
•	 Members of the Board of Directors, and their close 
family members; and 
•	 Company’s key Management team and their close 
family members
The Company has not had interests in other entities as at, 
and for the years ended, December 31, 2024 and 2023. 
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Transactions with Related Parties 
There are no additional related party transactions during 
2024 and 2023 than already disclosed.
24. SUBSEQUENT EVENTS
In January 2025, Faron announced that the final MDS 
patient was identified for the BEXMAB Phase II trial and 
that topline readout is expected in April 2025. 
In early February 2025, Faron conducted a private 
placement directed to a limited number of institutional 
and other investors raising EUR 12.0 million. 
Result and Dividends
The Company’s comprehensive loss for the period was 
EUR 25,999,608 (2023: EUR 31,093, 581). The Board of 
Directors proposes to the Annual General Meeting 2024 
not to pay dividend.
Key Management Personnel 
The Company’s key management personnel consist of 
the following: 
•	 Members of the Board of Directors 
•	 Management team, including CEO 
Year ended 31 December
€’000
2024
2023
Compensation of key  
management personnel*
Salaries and other short-term 
employee benefits
1,685
2,929
Post-employment benefits
118
134
Share-based payments 
576
1,409
Total
2,378
4,472
* Presented information for the Management includes the executive directors of 
the Board
The Management team was awarded 396,000 share 
options during 2024 (2023: 211,000 share options). At the 
end of the 2024 the number of outstanding options and 
shares granted to the Management team amounted to 
860,270 share options (at the end of 2023: 888,270 share 
options). 
Non-executive Directors were awarded 580,000 share 
options during 2024, (2023: 220,000 share options). 
At the end of 2024, the number of outstanding options 
and share options granted to the non-executive directors 
amounted to 1,900,000 share options (at the end of 2023: 
800,000 share options). 
Management and Board Shareholding 
Management* shareholding
31 December 
2024
Number of shares (pcs)
2,104,062
Shareholding, percentage
2.01
Board** shareholding, 31 December 2024  
(excluding the shareholding of CEO)
Number of shares (pcs)
3,491,274
Shareholding, percentage
3,34
Total number of shares outstanding at  
31 December 2024 (pcs)
104,624,864
* Presented information for the Management includes the executive directors of 
the Board 
** Presented information for the Board includes only non-executive directors.
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THE AUDITOR’S NOTE
A report on the audit performed has been issued today
Helsinki, 26 February 2025 
PricewaterhouseCoopers Oy 
Authorised Public Accountants
Tuomo Pätsi 
Chairman
Markku Jalkanen
Christine Roth
Panu Vänskä
Authorised Public Accountant (KHT)  
Juho Jalkanen 
CEO
John Poulos
Marie-Louise Fjällskog
BOARD SIGNATURES
Turku, 26 February 2025
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1 (3) 
 
 
 
PricewaterhouseCoopers Oy, Authorised Public Accountants, P.O. Box 1015 (Itämerentori 2), FI-00101 HELSINKI 
Phone +358 20 787 7000,  www.pwc.fi   
Reg. Domicile Helsinki, Business ID 0486406-8 
 
Auditor’s Report (Translation of the Finnish Original) 
To the Annual General Meeting of Faron Pharmaceuticals Oy 
Report on the Audit of the Financial Statements  
Opinion 
In our opinion the financial statements give a true and fair view of the group’s and the parent company’s financial 
position, financial performance and cash flows in accordance with IFRS Accounting Standards as adopted by the 
EU and comply with statutory requirements. 
What we have audited 
We have audited the financial statements of Faron Pharmaceuticals Oy (business identity code 2068285-4) for 
the year ended 31 December 2024. The financial statements comprise the balance sheets, statements of 
comprehensive income, statements of changes in equity, statements of cash flows and notes, which include 
material accounting policy information and other explanatory information for the group as well as for the parent 
company. 
Basis for Opinion  
We conducted our audit in accordance with good auditing practice in Finland. Our responsibilities under good 
auditing practice are further described in the Auditor’s Responsibilities for the Audit of the Financial Statements 
section of our report. 
We believe that the audit evidence we have obtained is sufficient and appropriate to provide a basis for our 
opinion.  
Independence 
We are independent of the parent company and of the group companies in accordance with the ethical 
requirements that are applicable in Finland and are relevant to our audit, and we have fulfilled our other ethical 
responsibilities in accordance with these requirements. 
Material Uncertainty Related to Going Concern 
We draw attention to note 2.2 Going concern in the financial statements. Because the additional finance is not 
committed at the date of issuance of these financial statements, this fact together with other matters stated in the 
notes, indicates that a material uncertainty exists that may cast significant doubt on the group’s and the parent 
company’s ability to continue as a going concern. Our opinion has not been modified in respect of this matter. 
Responsibilities of the Board of Directors and the Managing Director for the Financial 
Statements 
The Board of Directors and the Managing Director are responsible for the preparation of consolidated financial 
statements that give a true and fair view in accordance with IFRS Accounting Standards as adopted by the EU, 
and of financial statements that give a true and fair view in accordance with the laws and regulations governing 
the preparation of financial statements in Finland and comply with statutory requirements. The Board of Directors 
and the Managing Director are also responsible for such internal control as they determine is necessary to enable 
the preparation of financial statements that are free from material misstatement, whether due to fraud or error.  
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2 (3) 
 
In preparing the financial statements, the Board of Directors and the Managing Director are responsible for 
assessing the parent company’s and the group’s ability to continue as a going concern, disclosing, as applicable, 
matters relating to going concern and using the going concern basis of accounting. The financial statements are 
prepared using the going concern basis of accounting unless there is an intention to liquidate the parent company 
or the group or to cease operations, or there is no realistic alternative but to do so.  
Auditor’s Responsibilities for the Audit of the Financial Statements 
Our objectives are to obtain reasonable assurance about whether the financial statements as a whole are 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 good auditing practice 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 these financial 
statements. 
As part of an audit in accordance with good auditing practice, we exercise professional judgment and maintain 
professional skepticism throughout the audit. We also: 
• 
Identify and assess the risks of material misstatement of the financial statements, whether due to fraud or 
error, design and perform audit procedures responsive to those risks, and obtain audit evidence that is 
sufficient and appropriate to provide a basis for our opinion. The risk of not detecting a material misstatement 
resulting from fraud is higher than for one resulting from error, as fraud may involve collusion, forgery, 
intentional omissions, misrepresentations, or the override of internal control. 
• 
Obtain an understanding of internal control relevant to the audit in order to design audit procedures that are 
appropriate in the circumstances, but not for the purpose of expressing an opinion on the effectiveness of the 
parent company’s or the group’s internal control.  
• 
Evaluate the appropriateness of accounting policies used and the reasonableness of accounting estimates 
and related disclosures made by management. 
• 
Conclude on the appropriateness of the Board of Directors’ and the Managing Director’s use of the going 
concern basis of accounting and based on the audit evidence obtained, whether a material uncertainty exists 
related to events or conditions that may cast significant doubt on the parent company’s or the group’s ability 
to continue as a going concern. If we conclude that a material uncertainty exists, we are required to draw 
attention in our auditor’s report to the related disclosures in the financial statements or, if such disclosures 
are inadequate, to modify our opinion. Our conclusions are based on the audit evidence obtained up to the 
date of our auditor’s report. However, future events or conditions may cause the parent company or the 
group to cease to continue as a going concern. 
• 
Evaluate the overall presentation, structure and content of the financial statements, including the disclosures, 
and whether the financial statements represent the underlying transactions and events so that the financial 
statements give a true and fair view. 
• 
Plan and perform the group audit to obtain sufficient appropriate audit evidence regarding the financial 
information of the entities or business units within the group as a basis for forming an opinion on the group 
financial statements. We are responsible for the direction, supervision and review of the audit work performed 
for purposes of the group audit. We remain solely responsible for our audit opinion. 
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3 (3) 
 
We communicate with those charged with governance regarding, among other matters, the planned scope and 
timing of the audit and significant audit findings, including any significant deficiencies in internal control that we 
identify during our audit. 
Other Reporting Requirements  
Other Information  
The Board of Directors and the Managing Director are responsible for the other information. The other 
information comprises the information included in the Annual Report 2024, but does not include the financial 
statements and our auditor’s report thereon.  
Our opinion on the financial statements does not cover the other information and we do not express any form of 
assurance conclusion thereon. 
In connection with our audit of the financial statements, our responsibility is to read the other information and, in 
doing so, consider whether the other information is materially inconsistent with the financial statements or our 
knowledge obtained in the audit, or otherwise appears to be materially misstated.  
If, based on the work we have performed, we conclude that there is a material misstatement of the other 
information, we are required to report that fact. We have nothing to report in this regard. 
 
Helsinki 26.2.2025 
PricewaterhouseCoopers Oy 
Authorised Public Accountants 
 
Panu Vänskä 
Authorised Public Accountant (KHT) 
 
 
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Faron Pharmaceuticals Ltd 
Joukahaisenkatu 6, 20520 Turku Finland 
Phone: +358 2 469 5151 
Fax: +358 2 469 5152 
Email: info@faron.com