Sareum
Holdings PLC
("Sareum"
or the "Company")
Final
Results for the Year Ended 30 June 2024
Cambridge, UK,
29 October 2024 - Sareum Holdings plc (AIM:
SAR), a biotechnology company developing next generation kinase
inhibitors for autoimmune disease and cancer, announces its audited
financial results for the year ended 30 June 2024.
Sareum also provides a broader update on
operational activities and pipeline progress, highlighting the
successful completion of the Phase 1 clinical trial for SDC-1801, a
TYK2/JAK1 inhibitor being developed for a range of autoimmune
diseases with an initial focus on psoriasis, several successful
fundraises, providing sufficient cash runway to advance the
development of SDC-1801, including longer-term
toxicology studies, to prepare the asset for Phase 2 clinical
trials.
Sareum announces that the Annual Report
detailing these financial results will be made available and posted
in the coming weeks.
OPERATIONAL
HIGHLIGHTS - INCLUDING POST-PERIOD
UPDATES
SDC-1801 (autoimmune
disease)
·
After the period end, Sareum announced the
successful completion of its Phase 1 clinical trial for SDC-1801,
including both single ascending dose ("SAD") and multiple ascending
dose ("MAD") stages.
·
Positive topline data revealed that blood plasma levels of
SDC-1801 significantly exceeded the predicted therapeutic exposure,
with a half-life of 17-20 hours, suggesting once-daily dosing will
be possible.
· No
deaths or serious adverse events due to SDC-1801 were reported
and the frequency of adverse events (all
mild or moderate) were similar in the active and placebo
groups.
·
Post-period, the Company secured funding of £3.4 million
through share subscriptions and received a A$1.9 million (c. £1
million) Australian R&D tax credit. This funding will enable further development of SDC-1801, including
required longer term toxicology studies, to prepare the asset for
Phase 2 clinical trials and undertake further translation and
preclinical development on its SDC-1802 cancer immunotherapy
programme.
·
IP position has been strengthened with patent
allowances in China for certain crystalline forms of SDC-1801 and
in the US for the chemical structure, for the use in treating
inflammatory diseases, and for certain methods of chemical
synthesis.
SDC-1802 (cancer
immunotherapy)
SDC-1802 is a
TYK2/JAK1 inhibitor being developed for cancer
immunotherapy.
Funds from the recent share subscriptions will
accelerate the translational studies needed to support
development of SDC-1802, defining the optimal cancer
application before completing toxicology and manufacturing
studies
FINANCIAL
HIGHLIGHTS
• Cash at 30
June 2024 of £1.5 million (£1.0 million as of 30 June
2023).
•
Loss on ordinary activities after taxation for the
year ended 30 June 2024 of £3.4 million (£3.2 million loss for the
year ended 30 June 2023), which reflects the increased R&D
investment required for the conduct of the clinical trial and
higher level of activity.
•
R&D tax credits of £0.8 million received in the
year.
• Funding
facility provided by RiverFort Global Opportunities PCC Ltd
("Riverfort") was fully settled in April 2024. The Company raised
net funds of £4.4 million via share issues during the
period.
• Post
period end, the Company completed fundraises totalling £3.4 million
(before expenses), from certain high net worth individuals,
corporates and institutions, via subscriptions for a total of
16,264,444 new ordinary shares of 1.25 pence each in the capital of
the Company ("Ordinary Shares") at an aggregate price of 20.7 pence
per new Ordinary Share. An Australian R&D tax credit of AS1.9
million (c£1.0 million) was also received in October
2024.
Dr Stephen Parker, Executive Chairman of Sareum,
commented:
"2024 has been an important year for Sareum. We have reported
positive topline data from our completed Phase 1 trial of SDC-1801,
which demonstrated a favourable safety profile and achieved blood
plasma levels significantly exceeding the predicted therapeutic
exposure. These results, along with our strengthened financial
position and IP portfolio, position us well to advance SDC-1801
towards Phase 2 clinical trials and accelerate the preclinical
development of SDC-1802. The Clinical Study Report from the Phase 1
trial is expected to be available later in 2024. We look forward to
building on this momentum in the coming year."
For further
information, please contact:
Sareum Holdings plc
Stephen Parker, Executive
Chairman
|
01223 497700
ir@sareum.co.uk
|
Strand Hanson Limited (Nominated
Adviser)
James Dance / James
Bellman
|
020 7409 3494
|
Hybridan LLP (Corporate
Broker)
Claire Noyce
|
020 3764 2341
|
ICR Healthcare (Financial
PR)
Jessica Hodgson / Davide Salvi /
Kumail Waljee
|
020 3709 5700
|
About
Sareum
Sareum (AIM: SAR) is a
biotechnology company developing next generation
kinase inhibitors for autoimmune disease and cancer.
The Company is focused on developing
next generation small molecules which modify the activity of the
JAK kinase family and have best-in-class potential. Its lead
candidate, SDC-1801, simultaneously inhibits TYK2 and JAK1.
SDC-1801 is a potential treatment for a range of
autoimmune diseases, including psoriasis, and has completed Phase 1
clinical development.
Sareum is also developing SDC-1802,
a TYK2/JAK1 inhibitor with a potential application for cancer
immunotherapy.
Sareum Holdings plc is based in
Cambridge, UK, and is quoted on the AIM market of the London Stock
Exchange, trading under the ticker SAR. For further information,
please visit the Company's website at www.sareum.com.
CHAIRMAN'S
STATEMENT
Sareum has made excellent progress during and
after this period, successfully completing the Phase 1 clinical
trial of our lead asset, SDC-1801. We are delighted to report
positive topline data from this study, which demonstrated that
SDC-1801 achieved blood plasma levels well above the predicted
therapeutic exposure, with a long half life indicating that
once-daily dosing can be possible. Importantly, no deaths or
serious adverse events due to SDC-1801 were reported.
The success of this trial highlights that high
blood levels of our dual TYK2/JAK1 kinase inhibitor can be achieved
without serious side effects. Moreover, based on the unblinded data
now available, we are pleased to note that the frequency of adverse
events (all mild or moderate) was similar in the active and placebo
groups. No clinically significant effects on any component of
blood, which have been affected by earlier generation JAK
inhibitors, were observed. The observed favourable safety and
pharmacokinetic profiles may give SDC-1801 significant advantage
over competitors.
The TYK2/JAK1 inhibitor class is increasingly
proving its promise for the treatment of autoimmune disease, and we
believe SDC-1801 has the potential to be a best-in-class. The
positive Phase 1 results have reinforced our confidence as we look
to advance SDC-1801 further through clinical
development.
In addition, post the financial year end, we
secured £3.4 million before expenses in funding through
subscriptions, and received a A$1.9 million (c. £1 million)
Australian tax credit . These funds will enable us to conduct
further development of SDC-1801, including longer-term toxicology
studies, to prepare the asset for Phase 2 clinical trials
and also undertake further translation and
preclinical development of the SDC-1802 cancer immunotherapy
programme, thereby enhancing their potential
values.
Our intellectual property position for SDC-1801
has also been strengthened. We've received patent allowances in
China for certain crystalline forms and in the US for the chemical
structure, its use in treating inflammatory diseases, and certain
methods of chemical synthesis. These complement existing approvals
in other major territories.
After the period end, we announced some
management changes. Dr. Tim Mitchell, co-founder and CEO, has
transitioned to the part-time role of Chief Operating Officer while
remaining on the Board. I have assumed the position of Executive
Chairman, and we intend to appoint a new CEO at the appropriate
time as the Company progresses with its strategy.
We're excited about the future of SDC-1801 and
are committed to building a strong data package to advance to the
next stage of its development and will be presenting the clinical
data at upcoming partnering and scientific conferences, with the
aim of further engaging with potential licensing and
commercialisation partners. We look forward to sharing further
updates in due course.
PROGRAMME
UPDATES
SDC-1801
SDC-1801 is a TYK2/JAK1 inhibitor
being developed as a potential new therapeutic for a range of
autoimmune diseases with an initial focus on psoriasis, an
autoimmune condition affecting the skin.
Sareum has successfully completed
the Phase 1 trial of SDC-1801 (trial ID
ACTRN12623000416695p), including both
single ascending dose (SAD) and multiple ascending dose (MAD)
stages. This was a randomised, placebo-controlled
trial investigating the safety, tolerability,
pharmacokinetics and pharmacodynamics of an oral formulation of
SDC-1801 in healthy subjects, conducted at a clinical unit in
Melbourne, Australia.
The trial demonstrated that SDC-1801 achieved
blood plasma levels well above the predicted therapeutic exposure,
with a half-life of 17-20 hours, suggesting that once-daily dosing
will be possible. Importantly, no deaths or serious adverse events
due to SDC-1801 were reported, and the frequency of adverse
events (all mild or moderate) was similar in the active and placebo
groups. No clinically significant effects were observed on any
component of blood (including red blood cells, haemoglobin,
reticulocytes, platelets or neutrophils) which have been affected
by earlier generation JAK inhibitors.
Analysis of blood samples from trial participants who
received SDC-1801 for 10 days in the MAD cohorts demonstrated
clear, dose-responsive reductions in three biomarkers of JAK1
and/or TYK2 activity. This provides strong evidence that safe blood
levels of SDC-1801 were able to significantly inhibit major
inflammatory pathways.
The additional funding of £3.4
million through share subscriptions and receipt of a A$1.9 million
(c. £1 million) Australian tax credit will enable further
development of SDC-1801 to prepare the asset for Phase 2 clinical
trials. This will include additional drug product synthesis and
toxicology studies, of up to four months and in two species, which
are required to match the intended duration of the dosing of
patients in these Phase 2 studies. It is the intention to complete
these preclinical studies by mid-2025.
SDC-1802
SDC-1802 is a TYK2/JAK1 inhibitor being
developed for cancer and cancer immunotherapy
applications.
The funding received from the October 2024
share subscriptions will enable further translational and
preclinical development studies on SDC-1802, which we look forward
to reporting in the current period.
SRA737
(cancer)
SRA737 is a clinical-stage oral, selective
Checkpoint kinase 1 inhibitor that targets cancer cell replication
and DNA damage repair mechanisms.
· On
2 January 2024, Sareum announced the Company's
co-development partner, the CRT Pioneer Fund ("CPF"), entered into
a development and commercialisation licence agreement for SRA737
with a private biopharma company (the "Licensee Company") based
in the United States.
·
Sareum received US$137,500 from the upfront fee payable under
the Licensing Agreement,
· An
additional fee made up of up to US$1.0 million cash and 500,000
shares in the Licensee Company may be payable to CPF, of which
Sareum is entitled to a 27.5% share, upon the sooner of 12 months
following the signing of the Licensing Agreement, or the event of
the Licensee Company achieving certain commercial and material
financing objectives.
·
Sareum is also entitled to 27.5% of any future payments
payable by the Licensee Company , under the terms of Sareum's
co-development agreements with CPF and Cancer Research Technology
Ltd.
FINANCIAL
REVIEW
At 30 June 2024, Sareum had cash of
£1.5 million (£1.0 million as of 30 June 2023).
The loss on ordinary activities
after taxation for the year ended 30 June 2024 was £3.4 million
(£3.2 million loss for the year ended 30 June 2023), which reflects
the increased R&D investment required for the conduct of the
clinical trial. R&D tax credits
of £0.8m were received in the year.
During the year, Sareum made use of a funding
facility provided by RiverFort Global Opportunities PCC Ltd
("Riverfort") which was fully settled in April 2024. The Company
raised net funds of £4.4 million via share issues.
Subsequent to the year end, in October 2024,
the Company completed two fundraises totalling £3.4million (before
expenses), from certain high net worth individuals and
institutions, via subscriptions for a total of 11,820,000 new
Ordinary Shares at a price of 20 pence per new Ordinary Share and
subscriptions for a total of 4,444,444 new Ordinary Shares at a
price of 22.5 pence per new Ordinary Share. An Australian
R&D tax credit of AS1.9 million (c£1.0 million) was also
received in October 2024.
OUTLOOK
Sareum has successfully completed its Phase 1
clinical trial for SDC-1801, including both single ascending dose
(SAD) and multiple ascending dose (MAD) stages. The positive
topline data from this trial have significantly bolstered the
Company's confidence in SDC-1801's potential as a best-in-class
TYK2/JAK1 inhibitor for autoimmune diseases.
The Clinical Study Report from the Phase 1
trial is expected to be available later in 2024. Sareum plans to
conduct the preparatory work required to obtain regulatory approval
for a Phase 2 clinical trial. We look forward to
presenting this data at upcoming partnering and scientific
conferences, including discussing the data with potential licensing
and commercialisation partners.
The recent funding, will enable the Group to
conduct further development of SDC-1801, including the longer-term
toxicology studies required to prepare the asset for Phase 2
clinical trials and also undertake further translational and
preclinical development on its SDC-1802 cancer immunotherapy
programme thereby enhancing their potential values.
The Board of Sareum continues to apply a rigorous
approach to capital allocation in the development of the Company's
assets. The Company maintains a clear focus on advancing these
potential medicines to patients as efficiently as possible while
maximizing value for shareholders.
With the recent management changes, including
Dr. Stephen Parker's transition to Executive Chairman and Dr. Tim
Mitchell's move to a part-time Chief Operating Officer role, Sareum
is well-positioned to navigate through this exciting phase of
development.
CONSOLIDATED STATEMENT OF
COMPREHENSIVE INCOME
FOR THE YEAR ENDED 30 JUNE
2024
|
|
Note
|
|
|
2024
£'000
|
2023
£'000
|
|
|
|
|
|
|
|
|
CONTINUING OPERATIONS
|
|
|
|
|
|
|
Revenue
|
|
|
|
-
|
-
|
|
|
|
|
|
|
|
|
Administrative expenses
|
|
|
|
(4,596)
|
(4,048)
|
|
Share of loss of
associates
|
|
|
|
(60)
|
(18)
|
|
Other operating income
|
|
|
|
22
|
-
|
|
|
|
|
|
--------------
|
--------------
|
|
OPERATING LOSS
|
|
|
|
(4,634)
|
(4,066)
|
|
|
|
|
|
|
|
|
Finance income
|
4
|
|
|
32
|
41
|
|
|
|
|
|
|
|
|
LOSS BEFORE TAXATION
|
5
|
|
|
(4,602)
|
(4,025)
|
|
|
|
|
|
|
|
|
Taxation
|
6
|
|
|
1,182
|
833
|
|
|
|
|
|
|
|
|
LOSS FOR THE YEAR
|
|
|
|
(3,420)
|
(3,192)
|
|
|
|
|
|
|
|
|
TOTAL COMPREHENSIVE EXPENSE FOR THE YEAR
|
|
|
|
(3,420)
|
(3,192)
|
|
|
|
|
|
|
|
|
Loss attributable to owners of the
parent
|
|
|
|
(3,420)
|
(3,192)
|
|
|
|
|
|
|
|
Total comprehensive income
attributable to owners of the parent
|
|
|
|
(3,420)
|
(3,192)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic and diluted loss per share
(pence per share)
|
7
|
|
|
(4.2)
|
(4.7)
|
|
|
|
|
|
|
|
|
|
|
|
|
| |
The accompanying notes form part of these
financial statements.
CONSOLIDATED BALANCE
SHEET
30 JUNE 2024
|
Note
|
|
|
2024
£'000
|
2023
£'000
|
ASSETS
|
|
|
|
|
|
NON-CURRENT ASSETS
|
|
|
|
|
|
Property, plant and
equipment
|
8
|
|
|
-
|
1
|
Investment in associate
|
9
|
|
|
9
|
46
|
|
|
|
|
|
|
|
|
|
|
9
|
47
|
|
|
|
|
|
|
CURRENT ASSETS
|
|
|
|
|
|
Trade and other
receivables
|
10
|
|
|
1,299
|
979
|
Cash and cash equivalents
|
11
|
|
|
1,459
|
994
|
|
|
|
|
|
|
|
|
|
|
2,758
|
1,973
|
CURRENT LIABILITIES
|
|
|
|
|
|
Trade and other payables
|
12
|
|
|
(653)
|
(867)
|
|
|
|
|
|
|
NET
CURRENT ASSETS
|
|
|
|
2,105
|
1,106
|
|
|
|
|
|
|
NET
ASSETS
|
|
|
|
2,114
|
1,153
|
|
|
|
|
|
|
SHAREHOLDERS' EQUITY
|
|
|
|
|
|
Called up share capital
|
15
|
|
|
1,349
|
851
|
Share premium
|
17
|
|
|
24,802
|
20,925
|
Share-based compensation
reserve
|
17
|
|
|
312
|
325
|
Foreign exchange reserve
|
17
|
|
|
20
|
14
|
Retained earnings
|
17
|
|
|
(24,369)
|
(20,962)
|
|
|
|
|
|
|
TOTAL EQUITY
|
|
|
|
2,114
|
1,153
|
|
|
|
|
|
|
The accompanying notes form part of these
financial statements.
CONSOLIDATED
STATEMENT OF CHANGES IN EQUITY
FOR THE YEAR
ENDED 30 JUNE 2024
|
Called up share capital
£'000
|
Share premium
£'000
|
Share-based compensation
reserve
£'000
|
|
|
|
|
Balance at 1 July 2022
|
851
|
20,925
|
325
|
|
|
|
|
Issue of share capital
|
-
|
-
|
-
|
Transfer for options exercised /
expired
|
-
|
-
|
-
|
Total comprehensive
income
|
-
|
-
|
-
|
|
|
|
|
Balance at 30 June 2023
|
851
|
20,925
|
325
|
|
|
|
|
Issue of share capital
|
498
|
3,877
|
-
|
Total comprehensive
income
|
-
|
-
|
-
|
Transfer for options exercised /
expired
|
-
|
-
|
(13)
|
|
|
|
|
Balance at 30 June 2024
|
1,349
|
24,802
|
312
|
|
|
|
|
|
Foreign exchange reserve
£'000
|
Retained earnings
£'000
|
Total equity
£'000
|
|
|
|
|
Balance at 1 July 2022
|
-
|
(17,770)
|
4,331
|
|
|
|
|
Issue of share capital
|
-
|
-
|
-
|
Transfer for options exercised /
expired
|
-
|
-
|
-
|
Arising on consolidation
|
14
|
-
|
14
|
Total comprehensive
income
|
-
|
(3,192)
|
(3,192)
|
|
|
|
|
Balance at 30 June 2023
|
14
|
(20,962)
|
1,153
|
|
|
|
|
Issue of share capital
|
-
|
-
|
4,375
|
Transfer for options exercised /
expired
|
-
|
13
|
-
|
Arising on consolidation
|
6
|
-
|
6
|
Total comprehensive
income
|
-
|
(3,420)
|
(3,420)
|
|
|
|
|
Balance at 30 June 2024
|
20
|
(24,369)
|
2,114
|
|
|
|
|
The accompanying notes form part of these
financial statements.
CONSOLIDATED
CASH FLOW STATEMENT
FOR THE YEAR
ENDED 30 JUNE 2024
|
|
Note
|
|
2024
£'000
|
2023
£'000
|
|
|
|
|
|
|
Cash flows from operating activities
|
|
|
|
|
|
Cash used in operations
|
|
19
|
|
(4,739)
|
(3,676)
|
Tax received
|
|
|
|
820
|
409
|
|
|
|
|
|
|
Net
cash outflow from operating activities
|
|
|
|
(3,919)
|
(3,267)
|
|
|
|
|
|
|
Cash flows from investing activities
|
|
|
|
|
|
Purchase of tangible fixed
assets
|
|
|
|
-
|
-
|
Investment in associate
|
|
|
|
(23)
|
(41)
|
Interest received
|
|
|
|
32
|
41
|
|
|
|
|
|
|
Net
cash inflow from investing activities
|
|
|
|
9
|
-
|
|
|
|
|
|
|
Cash flows from financing activities
|
|
|
|
|
|
Share issues
|
|
|
|
4,375
|
-
|
|
|
|
|
|
|
Net
cash inflow from financing activities
|
|
|
|
4,375
|
-
|
|
|
|
|
-------------
|
-------------
|
(Decrease)/increase in cash and cash
equivalents
|
|
|
|
465
|
(3,267)
|
Cash and cash equivalents at
beginning of year
|
|
|
|
994
|
4,261
|
|
|
|
|
------------
|
------------
|
Cash and cash equivalents at end of year
|
|
|
|
1,459
|
994
|
|
|
|
|
=======
|
=======
|
The accompanying notes form part of these
financial statements.
1.
BASIS OF PREPARATION
The financial statements of Sareum Holdings plc
(the "Company") have been prepared in accordance with
UK-adopted international accounting standards, and
in accordance with international accounting standards
in conformity with the requirements of the Companies Act
2006, with IFRIC interpretations.
The financial statements have been prepared
under the historical cost convention.
Going
concern
The Group made a loss after tax of £3.4 million
(2022: £3.2 million), as it continued to progress research and
development activities. These activities, and the related
expenditure, are in line with the budgets previously set and are
funded by regular cash fundraises.
The Directors consider that the cash held at
the year-end, together with that received after the year end and
projected to be received, will be sufficient for the Group to meet
its forecast expenditure for at least one year from the date of
signing the financial statements. If there is a shortfall the
Directors will implement cost savings to ensure that the cash
resources last for this period of time.
For these reasons the financial statements have
been prepared on a going concern basis.
Basis of
consolidation
The consolidated financial statements
incorporate the financial statements of the Company and entities
controlled by the Company (its subsidiaries and an associate,
together, the "Group") made up to 30 June each year. Control is
achieved where the Company has the power to govern the financial
and operating policies of another entity or business, so as to
obtain benefits from its activities. The consolidated financial
statements present the results of the Company and its subsidiary as
if they formed a single entity. Inter-company transactions and
balances between group companies are eliminated on
consolidation.
2. ACCOUNTING
POLICIES
The principal accounting policies applied are
set out below.
Property,
plant and equipment
Depreciation is provided on a straight-line
basis over three years in order to write off each asset over its
estimated useful life.
Financial
instruments
Financial instruments are classified and
accounted for, according to the substance of the contractual
arrangement, as either financial assets, financial liabilities or
equity instruments. An equity instrument is any contract that
evidences a residual interest in the assets of the Company after
deducting all of its liabilities.
Cash and cash
equivalents
Cash and cash equivalents comprise cash in hand
and demand deposits and other short term highly liquid investments
that are readily convertible to a known amount of cash and are
subject to insignificant risk of change in value.
Pension
contributions
The Group does not operate a pension scheme for
the benefit of its employees but instead makes contributions to
their personal pension plans. The contributions due for the period
are charged to the profit and loss account.
Employee share
schemes
The Group has in place a share option scheme
for employees, which allows them to acquire shares in the Company.
Equity settled share-based payments are measured at fair value at
the date of grant. The fair value of options granted is recognised
as an expense spread over the estimated vesting period of the
options granted. Fair value is measured using the Black-Scholes
model, taking into account the terms and conditions upon which the
options were granted.
Research and
development
Expenditure on research and development is
written off in the year in which it is incurred. Research
expenditure is written off in the period in which it is incurred.
Development expenditure incurred is capitalised as an intangible
asset only when all of the following criteria are met:
-
It is technically feasible to complete the intangible asset
so that it will be available for use or sale;
-
There is the intention to complete the intangible asset and
use or sell it;
-
There is the ability to use or sell the intangible
asset;
-
The use or sale of the intangible asset will generate
probable future economic benefits;
-
There are adequate technical, financial and other resources
available to complete the development and to use or sell the
intangible asset; and
-
The expenditure attributable to the intangible asset during
its development can be measured reliably.
Expenditure that does not meet the above
criteria is expensed as incurred.
Taxation
Current taxes are based on the results shown in
the financial statements and are calculated according to local tax
rules, using tax rates enacted or substantially enacted by the
balance sheet date.
Deferred tax is recognised in respect of all
timing differences that have originated but not reversed at the
balance sheet date where transactions or events have occurred at
that date that will result in an obligation to pay more, or a right
to pay less or to receive more tax, with the following
exception:
Deferred tax is measured on an undiscounted
basis at the tax rates that are expected to apply in the periods in
which timing differences reverse, based on the tax rates and laws
enacted or substantively enacted at the balance sheet date.
Deferred tax assets are recognised only to the extent that the
Directors consider that it is more likely than not that there will
be suitable taxable profits from which the future reversal of the
underlying timing differences can be deducted.
Revenue
recognition
Revenue is measured as the fair value of the
consideration received or receivable in the normal course of
business, net of discounts, VAT and other sales related taxes and
is recognised to the extent that it is probable that the economic
benefits associated with the transaction will flow to the Group.
Revenues from licensing agreements are recognised in line with the
performance obligations being met, as outlined in the terms of the
agreement. Grant income is recognised as earned based on
contractual conditions, generally as expenses are incurred. Such
income is recognised as Other Operating Income.
Critical
accounting estimates and areas of judgement
Estimates and judgements are continually
evaluated and are based on historical experience and other factors,
including expectations of future events that are believed to be
reasonable under the circumstances. Actual results may differ from
these estimates. The estimates and assumptions that have the most
significant effects on the carrying amounts of the assets and
liabilities in the financial information are considered to be
research and development costs and equity settled share-based
payments.
Investment in
associates
An associate is an entity over which the
Company has significant influence. Significant influence is the
power to participate in the financial and operating policy
decisions of the Investee but is not control or joint control over
those policies. Investments in associates are accounted for using
the equity method, whereby the investment is initially recognised
at cost and adjusted thereafter for the post-acquisition change in
the associate's net assets with recognition in the profit and loss
of the share of the associate's profit or loss.
Impairment of
assets
At the date of the statement of financial
position, the Group reviews the carrying amounts of its non-current
assets to determine whether there is any indication that those
assets have suffered an impairment loss. If any such indication
exists, the recoverable amount of the asset is estimated in order
to determine the extent of the impairment loss (if any).
Recoverable amount is the higher of fair value
less cost to sell and value in use. In assessing value in use, the
estimated future cash flows are discounted to their present value
using a pre-tax discount rate that reflects current market
assessments of the time value of money and the risks specific to
the asset for which the estimates of future cash flows have not
been adjusted. If the recoverable amount of an asset is estimated
to be less than its carrying amount, the carrying amount of the
asset is reduced to its recoverable amount. An impairment loss is
recognised as an expense immediately, unless the relevant asset is
carried at a revalued amount, in which case the impairment loss is
treated as a revaluation decrease.
New or revised
accounting standards
Certain new accounting standards and
interpretations have been published that are not mandatory for 30
June 2024 reporting periods and have not been early adopted by the
Company or the Group. These standards are not expected to have a
material impact on the entity in the current or future reporting
periods and on foreseeable future transactions.
3. EMPLOYEES
AND DIRECTORS
|
|
|
2024
£'000
|
2023
£'000
|
Directors' remuneration
|
|
|
|
|
Directors' emoluments
|
|
|
530
|
523
|
Directors' pension contributions to
money purchase schemes
|
|
|
28
|
29
|
|
|
|
|
|
|
|
|
£'000
|
£'000
|
Remuneration of the highest paid Director
|
|
|
|
|
Directors' emoluments
|
|
|
193
|
193
|
Director's pension contributions to
money purchase schemes
|
|
|
14
|
15
|
|
|
|
|
|
|
|
|
|
| |
There are two (2022: two) Directors
who are members of third party held money purchase retirement
benefit schemes.
Average monthly number of persons employed
|
|
|
Number
|
Number
|
Office and management
|
|
|
4
|
4
|
Research
|
|
|
1
|
1
|
|
|
|
|
|
|
|
|
5
|
5
|
|
|
|
|
|
|
|
|
£'000
|
£'000
|
Staff costs during the year
|
|
|
|
|
Wages and salaries
|
|
|
530
|
523
|
Social security costs
|
|
|
59
|
58
|
Pension costs
|
|
|
28
|
29
|
|
|
|
|
|
|
|
|
617
|
610
|
|
|
|
|
|
4. NET FINANCE
INCOME
|
|
|
2024
£'000
|
2023
£'000
|
|
|
|
|
|
Deposit account
interest
|
|
|
32
|
41
|
|
|
|
|
|
|
|
|
|
| |
5. LOSS BEFORE
INCOME TAX
The loss before income tax is stated
after charging:
|
|
|
2024
£'000
|
2023
£'000
|
Depreciation - owned
assets
|
|
|
1
|
1
|
Research and development
Other operating leases
Foreign exchange
differences
Auditor's remuneration
|
|
|
3,591
21
(37)
17
|
2,909
21
24
16
|
|
|
|
|
|
|
|
|
|
| |
6. INCOME
TAX
|
2024
|
2023
|
|
£'000
|
£'000
|
Current tax
|
|
|
Adjustment to prior years
|
(3)
|
-
|
Overseas taxation credit
|
1,031
|
395
|
UK corporation tax credit on losses
for the period
|
154
|
438
|
|
------------
|
------------
|
|
1,182
|
833
|
|
|
|
The credit for the year can be
reconciled to the accounting loss as follows:
|
|
2024
£'000
|
2023
£'000
|
Loss before tax
|
|
(3,420)
|
(4,025)
|
|
|
|
|
Notional tax credit at average rate
of 20.5% (2022: 19%)
|
|
|
1,150
|
825
|
Effects of:
Expenses not deductible for tax
purposes
Adjustment to tax charge in respect
of prior periods
Other timing differences
Unutilised tax losses
Losses surrendered for research and
development tax credits
Research and development tax credits
claimed
|
|
|
(44)
(3)
(629)
(271)
(206)
1,185
|
-
-
(234)
(293)
(298)
833
|
|
|
|
|
|
Actual current tax credit in the year
|
|
|
1,182
|
833
|
|
|
|
|
|
The tax rate of 25% used above is the average
corporation tax rate applicable in the United Kingdom.
A potential deferred tax asset as at 30 June
2024 of £3.2 million (2023: £2.8 million) calculated using the
expected corporation tax rate of 25% (2022: 25%), has not been
recognised, as there remains a significant degree of uncertainty
that the Group will make sufficient profits in the foreseeable
future to justify recognition.
7
EARNINGS PER SHARE
The calculation of loss per share is
based on the following data:
|
|
|
2024
|
2023
|
Loss on ordinary activities after
tax
Weighted average number of shares in
issue
Basic and diluted loss per share
(pence)
|
|
|
£3,420,000
80,992,566
(4.2)
|
£3,192,000
68,069,416
(4.7)
|
|
|
|
|
|
As the Group has generated a loss for the
period, there is no dilutive effect in respect of share
options.
8. PROPERTY
PLANT & EQUIPMENT
|
|
Fixtures and computers
£'000
|
Cost
|
|
|
At
1 July 2023 and 30 June 2024
|
|
13
|
|
|
|
Depreciation
|
|
|
At 1 July 2023
|
|
12
|
Charge for the year
|
|
1
|
|
|
|
At
30 June 2024
|
|
13
|
|
|
|
Carrying amount
|
|
|
At 30 June 2023
|
|
1
|
|
|
=======
|
At
30 June 2024
|
|
-
|
|
|
|
9.
INVESTMENTS
|
|
|
Interest in associate
£'000
|
Cost
|
|
|
|
At 1 July 2023
|
|
|
1,217
|
Additions
|
|
|
23
|
|
|
|
|
At
30 June 2024
|
|
|
1,240
|
|
|
|
|
Provision for impairment
|
|
|
|
At 1 July 2023
|
|
|
1,171
|
Impairment for year
|
|
|
60
|
|
|
|
|
At
30 June 2024
|
|
|
1,231
|
|
|
|
|
Net
book value
|
|
|
|
At 30 June 2023
|
|
|
46
|
|
|
|
|
At
30 June 2024
|
|
|
23
|
|
|
|
|
The investment in associate represents the
investment by the Group in the partnership with the Cancer Research
Technology Pioneer Fund to advance the SRA737 programme and has
been accounted for using the equity method. Sareum's interest in
the associate partnership is 27.5%. As at 30 June 2024 the
partnership had net assets of £34,000 (2023: £83,000) and had
incurred cumulative losses of £0.8 million (2023: £0.7
million).
10. TRADE
AND OTHER RECEIVABLES
|
|
2024
£'000
|
2023
£'000
|
Amounts falling due within one year:
|
|
|
|
Corporation tax
|
|
1,180
|
823
|
Other taxation receivable
|
|
41
|
75
|
Prepayments and accrued
income
|
|
78
|
81
|
|
|
|
|
|
|
1,299
|
979
|
|
|
|
|
11. CASH AND CASH
EQUIVALENTS
|
|
2024
£'000
|
2023
£'000
|
Bank deposit accounts
|
|
1,459
|
994
|
|
|
|
|
12. TRADE AND OTHER
PAYABLES
|
|
2024
£'000
|
2023
£'000
|
Amounts falling due within one year:
|
|
|
|
Trade creditors
|
|
542
|
694
|
Social security and other
taxes
|
|
19
|
22
|
Other creditors
|
|
35
|
5
|
Accrued expenses
|
|
57
|
146
|
|
|
|
|
|
|
653
|
867
|
|
|
|
|
Trade payables and accruals principally
comprise amounts outstanding for trade purchases and ongoing costs.
The average credit term agreed with suppliers is 30 days and
payment is generally made within the agreed terms.
13. LEASING
AGREEMENTS
The Group has not applied IFRS 16 as
the lease on the only office occupied by the Group is of low value,
expiring in December 2026 and the rent payments in the year are
also not material to the financial statements.
14. FINANCIAL
INSTRUMENTS
The Group's principal financial instruments are
trade and other receivables, trade and other payables and cash. The
main purpose of these financial instruments is to finance the
Group's ongoing operational requirements. The Group does not trade
in derivative financial instruments.
The major financial risks faced by the Group,
which remained unchanged throughout the year, are interest rate
risk, foreign exchange risk and liquidity risk. Policies for the
management of these risks are shown below and have been
consistently applied.
MARKET
RISKS
Interest rate
risk
The Group is exposed to interest rate risk as
cash balances in excess of immediate needs are placed on short term
deposit. The Group seeks to optimise the interest rates received by
continuously monitoring those available. The value of the Group's
financial instruments is not considered to be materially sensitive
to these risks and therefore no sensitivity analysis has been
provided.
Foreign
exchange risk
The Group's activities expose it to
fluctuations in the exchange rate for the Euro and the US dollar.
Funds are maintained in sterling and foreign currency is acquired
on the basis of committed expenditure. The value of the Group's
financial instruments is not considered to be materially sensitive
to these risks and therefore no sensitivity analysis has been
provided.
NON-MARKET
RISKS
Liquidity
risk
The Board has responsibility for reducing
exposure to liquidity risk and ensures that adequate funds are
available to meet anticipated requirements from existing operations
by a process of continual monitoring. The value of the Group's
financial instruments is not considered to be materially sensitive
to these risks and therefore no sensitivity analysis has been
provided.
15. SHARE
CAPITAL
Called up, allotted and fully paid
|
|
2024
£'000
|
2023
£'000
|
|
|
|
|
107,945,783 (2022: 68,069,416)
Ordinary Shares of 1.25p each
|
|
1,349
|
851
|
|
|
|
|
The Ordinary Shares carry equal rights in
respect of voting at a general meeting of shareholders, payment of
dividends and return of assets in the event of a winding
up.
During the year the following share issues took
place
(i) On 8 August 2023,
1,953,543 Ordinary Shares were issued at 9.98 pence per Ordinary
Share in respect of a financing arrangement with Riverfort. A
further 48,839 Ordinary Shares were issued at £1.02 per Ordinary
Share to Riverfort at the same time. Together these raised £2
million before expenses.
(ii) On 30 October 2023, 190,080
Ordinary Shares were issued at 30 pence per Ordinary Share in
respect of the exercise of share options by certain Directors that
raised, in aggregate, £57,024 before expenses.
(iii) 12,660,488 Ordinary Shares were
issued to Riverfort on various dates between 12 March 2024 and 26
April 2024 which in aggregate raised £300,000.
(iv) On 5 April 2024 23,339,733 Ordinary Shares
were issued at 10 pence per Ordinary Share to individual investors
as part of a placing and WRAP exercise, which in aggregate raised
£2,333,973 before expenses.
(v) On 5 April 2024 576,698 Ordinary
Shares were issued at 10 pence per Ordinary Share to certain
Directors in lieu of salary payments owed to them, which in
aggregate raised £57,670 before expenses.
(vi) On 13 May 2024, 1,106,986 Ordinary Shares
were issued at 10 pence per Ordinary Share to Riverfort in respect
of their exercise of certain warrants, which in aggregate raised
£110,699.
16. PENSION
COMMITMENTS
The Group makes contributions to its employees'
own personal pension schemes. The contributions for the period of
£28,000 (2023: £29,000) were charged to the profit and loss
account. At the balance sheet date contributions of £4,000 (2023:
£5,000) were owed and are included in creditors.
17.
RESERVES
Reserve
|
Description and purpose
|
Share capital
|
Amount of the contributions made by
shareholders in return for the issue of shares.
|
Share premium
|
Amount subscribed for share capital
in excess of nominal value.
|
Retained earnings
|
Cumulative net gains and losses
recognised in the consolidated and the Company Balance
Sheet.
|
Foreign exchange reserve
|
Arising on consolidation of the
overseas subsidiary
|
Share-based compensation reserve
|
Cumulative fair value of share
options granted and recognised as an expense in the Income
Statement.
|
Details of movements in each reserve are set
out in the Consolidated Statement of Changes in Equity.
18. CONTINGENT
LIABILITIES
There are no contingent liabilities (2023:
£nil).
19.
RECONCILIATION OF LOSS BEFORE INCOME TAX TO CASH GENERATED FROM
OPERATIONS
|
|
2024
£'000
|
2023
£'000
|
|
|
|
|
Operating loss from continuing operations
|
|
(4,602)
|
(4,024)
|
Adjustments for:
|
|
|
|
Depreciation
|
|
1
|
1
|
Share of loss of
associate
|
|
60
|
18
|
Foreign exchange
differences
|
|
5
|
24
|
Finance
income
|
|
(32)
|
(41)
|
|
|
|
|
Operating cash flows before movements in working
capital
|
|
(4,568)
|
(4,022)
|
Decrease/(increase) in
receivables
|
|
42
|
(65)
|
Increase in payables
|
|
(213)
|
411
|
|
|
|
|
Cash used in operations
|
|
(4,739)
|
(3,676)
|
|
|
=======
|
=======
|
20. POST BALANCE SHEET
EVENTS
With effect from 10 July 2024 Tim Mitchell,
co-founder and Chief Executive Officer (CEO), transitioned to the
part-time role of Chief Operating Officer (COO) and Stephen Parker,
previously Non-Executive Chairman, assumed the
position of Executive Chairman. Additionally at that time, Clive
Birch was appointed as Senior Independent Director.
In October 2024, the Company
completed fundraises as follows:
(i)
£2.4 million (before expenses), from certain high net worth
individuals, corporates and an institution, via a subscription for
a total of 11,820,000 new Ordinary Shares at a price of 20 pence
per new Ordinary Share; and
(ii)
£1.0 million (before expenses), from certain investors including
the institution that participated in the above fundraise, via a
subscription for a total of 4,444,444 new Ordinary Shares at a
price of 22.5 pence per new Ordinary Share.