Bioventix
plc
("Bioventix" or "the Company")
Results for the year ended
30 June 2024
Bioventix plc (BVXP), a UK company
specialising in the development and commercial supply of
high-affinity monoclonal antibodies for applications in clinical
diagnostics, announces its audited results for the year ended 30
June 2024.
Highlights:
·
Revenue up 6% to £13.6 million (2023: £12.82
million)
·
Profit before tax up 5% to £10.6 million (2023:
£10.13 million)
·
Cash at year end of £6.0 million (30 June 2023:
£5.7 million)
·
Second interim dividend of 87p per share (2023:
90p)
·
Total dividends 155p per share (2023:
152p)
Introduction and
Technology
Bioventix creates, manufactures
and supplies high affinity sheep monoclonal antibodies (SMAs) for
use in diagnostic applications.
Bioventix antibodies are preferred for use when they confer an
improved test performance compared to other available
antibodies.
Most of our antibodies are used on
blood-testing machines installed in hospitals and other
laboratories around the world. Bioventix makes antibodies
using our SMA technology for supply to diagnostic companies for
subsequent manufacture into reagent packs used on blood-testing
machines. These blood-testing machines are supplied by large
multinational in vitro diagnostics (IVD) companies such as Roche
Diagnostics, Siemens Healthineers, Abbott Diagnostics & Beckman
Coulter. Antibody-based blood tests are used to help diagnose
many different conditions including, amongst others, heart disease,
thyroid function, fertility, infectious disease and
cancer.
Testosterone is an example of a
blood test where a Bioventix SMA has facilitated an improved
test. In 2003, it became clear that testosterone tests
performed on automated IVD platforms were deficient. Whilst
the higher levels of testosterone in healthy adult males were
accurately reported, the lower levels of testosterone in
pre-pubescent boys and women were inaccurately reported. In
2005, Bioventix created an antibody called testo3.6A3 which was
evaluated by customers during 2006. Evaluations were
successful and following the necessary regulatory approvals, the
first testosterone assays based on testo3.6A3 were launched in
2009. A number of IVD companies still use this antibody for
revised tests that more accurately measure lower levels of
testosterone.
Over the past 20 years, we have
created and supplied approximately 25 different SMAs that are used
by IVD companies around the world. We currently sell a total
of 15-20 grams of purified physical antibody per year which
accounts for 25-30% of our annual revenue. In addition to
revenues from these physical antibody supplies, the sale by our
customers of diagnostic products (based on our antibodies) to their
downstream end-users attracts a modest percentage royalty payable
to Bioventix. These downstream royalties currently account
for the remaining 70-75% of our annual revenue.
Bioventix adopts one of two
commercial approaches when creating new antibodies. The first
is own-risk antibody creation projects which gives Bioventix the
complete freedom to commercialise the antibodies produced.
The second is contract antibody creation projects in partnership
with customers who supply materials, know-how and funding and to
create antibodies that can only be commercialised with the partner
company. In both cases, after initiation of a new project, it
takes around a year for our scientists to create a panel of
purified antibodies for evaluation by our customers. The
evaluation process at customers' laboratories generally requires
the fabrication of prototype tests which can be compared to other
tests, for example the customer's existing commercial test or
perhaps another "gold standard" method, on the assay machine
platform being considered. The process of subsequent
development thereafter by our customers can take many years before
registration or approval from the relevant authority, for example
the US Food and Drug Administration (FDA), the Medicines and Healthcare products Regulatory Agency
(MHRA), or EU authorities, is obtained and products can be
sold to the benefit of the customers, and of course Bioventix,
through the agreed sales royalty. This does mean that there
is a lead time of 4-10 years between our own research work and the
receipt by Bioventix of royalty revenue from product sales.
However, because of the resource required to gain such approvals,
after having achieved approval for an accurate diagnostic test
using a Bioventix antibody, there is a natural incentive for
continued antibody use. This results in a barrier to entry
for potential replacement antibodies which would require at least
partial repetition of the approval process arising on a change from
one antibody to another. This barrier to antibody replacement
arises from a combination of factors driven by the clinical
criticality of the test and the potential consequences of making
such a change which include the time and cost to register any
changes required to validate the performance of the replacement
antibody.
Another consequence of the lengthy
approval process is that the revenue for the current accounting
period is derived largely from antibodies created many years
ago.
2023/2024 Financial
Results
We are pleased to report our
results for the financial year ended 30 June 2024. Revenues
for the year increased by 6% to £13.6 million (2022/23: £12.8
million). Profits before tax for the year increased by 5% to
£10.6 million (2022/23: £10.1million). Cash balances at the
year-end were £6.0 million (30 June 2023 £5.7
million).
Our most significant revenue
stream continues to come from the vitamin D antibody called
vitD3.5H10. This antibody is used by a significant number of
diagnostic companies around the world for use in vitamin D
deficiency testing. Sales of vitD3.5H10 increased by 1% to
£5.9 million which reflects analysts' expectation for a relatively
mature global IVD market.
Sales of our other core historic
antibodies are featured below with the respective percentage
increase/decrease (+/-) in sales compared to the previous year
2022/23:
-
T3 (tri-iodothyronine): £.1.38 million (+21%)
-
biotins and biotin blockers: £1.14 million (+35%)
-
progesterone: £0.63 million (-15%)
-
estradiol:
£0.52 million (-7%)
-
testosterone: £0.33 million (-29%)
-
drug-testing
antibodies: £0.32 million (-21%)
During the year the Company became
aware that, due to a customer error in the incorrect application of
an historic royalty percentage, they had overreported and overpaid
troponin royalty revenues since July 2021. Royalty revenues
for the financial years 2021/22 and 2022/23 were overstated by
£132k and £195k respectively. These amounts are immaterial in
respect of each of the affected periods and therefore the Company
is not required to restate the audited financial statements for
those years, however the cumulative effect of a reduction of £327k
in respect of such royalty revenue has been included in the
financial statements for the current year to 30 June
2024.
After correctly allocating the
revenue to each of the years 2023/24 and 2022/23 our total troponin
antibody royalty revenue from Siemens Healthineers and another
separate technology sub-license increased by 3% during the year
from £1.41 million to £1.45 million. The level of these
royalties and their growth are below our previous expectations
based on downstream assumptions.
In contrast to the disappointment
of troponin sales in the current application of acute chest pain
(ie suspected heart attack in A&E centres), we are pleased to
note that Siemens have received FDA approval for a revised label
claim for their troponin assay that covers a new prognostic
application. This enables troponin levels to be measured in
"at risk" patients and/or patients who have already been diagnosed
with a cardiac condition, whose troponin levels may now be measured
to assess their impending risk of a future adverse cardiac
event. This risk information can then be used to help
clinicians consider additional diagnostic procedures or to review
therapeutic alternatives. We expect that this new application
will stimulate additional troponin assay use and our associated
royalties, thus increasing the market opportunity. As
previously disclosed, Siemens troponin revenues will terminate for
contractual reasons in June 2032.
Our shipments of physical antibody
to China continued to increase. Some sales are made directly
and some are made through five appointed distributors. More
regulatory approvals for domestic Chinese customers using our
antibodies have been registered leading to more significant flows
of royalty payments flowing from these customers.
Chinese customers declare and pay
royalties in arrears on a calendar year basis and we therefore have
to accrue for such revenue, in both full year and interim results,
basing our revenue expectation on previous experience. As a
result of internal and external audit processes it was only in May
2024 that we received payment from a Chinese customer for the
royalties earned in 2023 and therefore our revenue for 2023/24 has
benefited by £239k from our prudent assessment of accrued royalty
revenue in respect of previous periods.
The prospects for further short
term growth in China are good. Longer term, price pressures
and continued antibody technology development in China constitute
an anticipated threat. In addition to this, the current
global geopolitical climate has stimulated the desire for
"on-shoring" supply chains and our Chinese customers are likely to
be influenced by this trend.
Our research into Tau antibodies
and Alzheimer's diagnostics continues to progress and we are
delighted that our early work has now translated into a modest
revenue stream from antibodies now entering commercial
manufacture. Our commercial policy is to supply initial
evaluation samples of antibodies free of charge. If
antibodies perform well on prototype assay systems at our IVD
customers and additional supplies are ordered, these are charged at
regular prices and such repeat sales have generated revenues during
the year. These revenues are not only additive but also
indicate that our antibodies could feature in future commercial
assays. In addition to our conventional IVD customers, we
have also supplied antibodies to specialist platform customers, for
example Quanterix Corporation who specialise in assays for the
research market. The research market is established earlier
than more regulated tests for routine clinical use
and it is pleasing that royalty
revenues from such activities have already been established.
Total Tau revenues for the year were above our expectation at
£155k.
We estimate that 50-60% of our
total sales are directly linked to US Dollars via physical product
pricing in US Dollars or indirectly linked to US Dollars via
royalties based on downstream US Dollar sales. The remainder
of the currency split is dominated by Euros and important Asian
currencies. Our view continues to be that hedging mechanisms
would not, in the longer term, add value and may have the potential
to add risk to our business. Consequently, future movements
in exchange rates may therefore affect our Sterling
revenues.
Cash Flows and
Dividends
As reported above, the performance
of the business during the year generated cash balances at the
year-end of £6.0 million and royalties received during quarter 3 of
2024 have added to this balance.
Increases in the rate of
Corporation Tax from 19% to 25%, effective from 1 April 2023, have
had a full year impact on profit after tax, EPS, cashflow and
dividends for the year to 30 June 2024.
In consideration of our
established dividend policy and the available cashflows, the Board
is pleased to announce a second interim dividend of 87 pence per
share which, when added to the first interim dividend of 68 pence
per share makes a total of 155 pence per share for the current
year.
Accordingly, a dividend of 87
pence per share will be paid in November 2024. The shares
will be marked ex-dividend on 7 November 2024 and the dividend will
be paid on 21 November 2024 to shareholders on the register at
close of business on 8 November 2024.
Research and Future
Developments
Over the last few years, a
considerable amount of our laboratory resource has been allocated
to the Tau project and Alzheimer's disease (AD) diagnostics.
AD is a complex disease that manifests itself differently across
the patient population. At a cellular level, nerve cells
(neurons) become associated with amyloid (A) plaques that build up
outside the neurons. This is followed by the build-up of Tau
(T) tangles inside the neurons. These pathological processes
then result in neuronal cell death and the symptoms of
neurodegeneration (N) that accompany this. This "ATN"
framework is used by neurologists to define the AD pathway that
progresses many years before patient symptoms become more
obvious.
Recently, the approval of first
generation AD therapeutics (Lecanemab™ jointly developed by EISAI
and Biogen and Donanemab™ from Eli Lilly) have changed the
perception of AD therapy, and it is likely that second generation
therapeutics, or combination therapies will further help to slow
the disease process. Patients presenting early in the ATN
pathway appear to benefit most from therapy. Therefore, ATN
assessments can be used not only to screen for patients suitable
for therapy but also for monitoring patients whilst on
therapy.
The ATN status of patients can be
defined with the use of PET scans using appropriate amyloid and/or
Tau contrast agents together with other assays for biomarkers in
cerebral spinal fluid. It would be highly desirable if such
diagnostic procedures could be replaced or augmented with cheaper
and more convenient blood tests.
Bioventix has been working with
the University of Gothenburg since early 2020 to create new
antibodies to Tau and to develop prototype assays for use in
AD. The view of many neurological opinion leaders - and
shared by our IVD customers - is that blood-testing machines will
soon offer a panel of new neurological tests that will reveal
information about patient brain health which will be useful for
screening and therapy monitoring purposes.
We have supplied a number of major
IVD companies with antibodies from our growing Tau antibody
portfolio. It is encouraging that a small number of these
companies have requested additional quantities of the antibodies
supplied. Not only does this add modestly to our overall
revenues but it also offers some encouragement that our antibodies
will play some part in the future neurological panel offerings of
our customers.
Whilst our major IVD customers'
primary interest is in developing regulated tests for routine
clinical use, expert neurology centres are already adopting
"research use only" tests in advance of the availability of other
tests through hospital-orientated IVD companies. Some of
these R&D tests are run on Quanterix Corporation (Billerica,
MA) machines and our partnership with Quanterix has resulted in one
commercial R&D test for neurodegeneration (N) that uses an SMA
and which has generated on-going royalty revenues.
Pre-Diagnostics (in Oslo) and
their clinical collaborators have two amyloid beta assays based on
Bioventix antibodies available for research use. A current
focus for Pre-Diagnostics is ARIA (amyloid related imaging
abnormality) which is an important side-effect of new anti-amyloid
drugs for Alzheimer's. Pre-Diagnostics' assays relate to
amyloid metabolism and could help screen for ARIA vulnerable
patients, before or during treatment.
Our partners at CardiNor (also in
Oslo) have continued with their work to try and identify the
possible utility of secretoneurin in heart failure patients.
This has not progressed successfully and CardiNor are currently
restructuring both their operations and their financial
position. We have accordingly taken the decision to write off
the entire cost of our investment in CardiNor of £183k made
between July 2016 and June 2020.
Our pyrene lateral flow system for
industrial pollution biomonitoring is proceeding steadily as
planned. We have now completed a second manufacturing batch
of lateral flow cassettes and intend to conduct a field trial with
firefighters during 2025. The follow-on project for benzene
exposure has also progressed and lateral flow assay development has
recently commenced. Benzene exposure is known to be
carcinogenic and is of relevance to the petroleum industry.
An additional industrial pollution biomonitoring project featuring
isocyanates (hazardous chemicals used in the manufacture of
polyurethane paints and plastics) has also progressed well and
lateral flow assay development is due to start early in
2025.
We have recently embarked on a new
project focussing on sewage contamination of rivers and
lakes. Drugs contained in sewage such as paracetamol and
caffeine have each previously been used in research labs as a
convenient surrogate marker of sewage in waterways. The
project concept is to harness our experience with sandwich
antibodies, lateral flow systems, together with phone app
technology, to facilitate rapid riverside tests, the results of
which can be uploaded, pooled and shared. This will allow for
much greater intensity and geographical coverage of analysis that
will be available to all the many interested parties.
Antibodies have already been made for this application and lateral
flow assay development is due to commence soon.
The industrial biomonitoring and
water pollution projects have required significant external
expenditure during the year of approximately £200k. As we
develop the projects, we expect this expenditure to continue and
grow modestly into the future. Using our cash resources to
support the steady internal organic growth of our business has been
a consistent feature of our strategy.
Future
Strategy
We have previously identified
diagnostic biomarkers that we believe suit our antibody technology
and have found academic collaborators who have seen merit in
working with Bioventix. The Tau project and our collaboration
with the University of Gothenburg is an excellent example of this
strategy and we will seek additional such opportunities in the
future.
We will continue to rely on our
core SMA antibody creation technology which consistently helps us
to create superior antibodies for our research projects. We
are also incorporating additional newer technologies where such
technologies are helpful to us. We have successfully created
novel "sandwich" assay formats for small molecules using a
combination of primary SMA technology and a secondary synthetic
"anti-complex" antibody created using the "antibody library"
technology of a third party. We have recently created new
sandwich systems for benzene and isocyanates (to be more precise,
the urine metabolites of these chemicals) in addition to caffeine
and paracetamol to add to previous successes with pyrene and
THC/cannabis.
The Bioventix Team and
Facility
The composition of the Bioventix
team of 12 full-time equivalents (14 staff in total) has remained
stable over the year facilitating excellent performance and
know-how retention. This level of stability has formed an
excellent base upon which we have been able to build our new
products moving into the exciting new areas described above.
We are very fortunate to have such a dedicated and loyal team and
we are grateful to them for their continued enthusiastic input and
support.
Nick McCooke has recently informed
the Board that he wishes to step down as a Director of Bioventix
plc and accordingly Nick will not be seeking re-appointment
as a Director at the Company's forthcoming Annual General
Meeting. The Board would like to
acknowledge Nick's exceptional contribution to Bioventix plc since
his appointment to the Board in January 2014. Nick's acumen,
experience, independence of thought and wisdom are all highly
valued by his fellow Directors and the business and have played a
full part in the Company's progress and success over the last 10
years. We are very grateful to him and wish him a very happy
retirement. As is described in the Nomination Committee
report the Board will seek to appoint a further independent
non-Executive Director in due course.
Conclusion and
Outlook
We are pleased with our financial
results for the year which we believe reflect steady growth in the
use of our established products in more mature diagnostic
markets. We remain very encouraged by the very early signs of
success for our Tau/Alzheimer's antibodies and we look forward to
more progress into the future.
For further information please contact:
Bioventix plc
Peter Harrison
|
Chief Executive Officer
|
Tel: 01252 728 001
|
|
|
|
Cavendish (NOMAD and broker)
Geoff Nash/Abigail
Kelly
|
Corporate Finance
|
Tel: 020 7220 0500
|
Nigel Birks/Harriet Ward
|
ECM
|
|
This announcement contains inside information for the
purposes of Article 7 of the Market Abuse Regulation (EU) 596/2014
as it forms part of UK domestic law by virtue of the European Union
(Withdrawal) Act 2018 ("MAR"), and is disclosed in accordance with
the company's obligations under Article 17 of
MAR.
STATEMENT OF COMPREHENSIVE INCOME
FOR THE YEAR ENDED 30 JUNE 2024
|
Note
|
2024
£
|
2023
£
|
Turnover
|
4
|
13,606,584
|
12,816,225
|
Cost of sales
|
|
(925,527)
|
(828,410)
|
Gross profit
|
|
12,681,057
|
11,987,815
|
Administrative expenses
|
|
(1,994,691)
|
(1,768,950)
|
Difference on foreign
exchange
|
|
(42,180)
|
(36,679)
|
Research and development tax
credit
|
|
29,230
|
25,243
|
Share option charge
|
|
(89,223)
|
(174,080)
|
Operating profit
|
5
|
10,584,193
|
10,033,349
|
Impairment charge on value of
investments
|
|
(183,306)
|
-
|
Interest receivable and similar
income
|
8
|
201,962
|
101,094
|
Profit before tax
|
|
10,602,849
|
10,134,443
|
Tax on profit
|
9
|
(2,506,131)
|
(1,762,202)
|
Profit for the financial year
|
|
8,096,718
|
8,372,241
|
|
|
|
|
Total comprehensive income
for the year
|
|
8,096,718
|
8,372,241
|
|
|
|
|
Earnings per share:
|
|
|
|
|
|
2024
|
2023
|
Basic (pence per share)
|
|
155.12
|
160.63
|
Diluted (pence per
share)
|
|
152.86
|
158.28
|
The notes on pages 08 to 24 form
part of these financial statements.
STATEMENT OF FINANCIAL POSITION
FOR THE YEAR ENDED 30 JUNE 2024
|
Note
|
|
2024
£
|
|
|
2023
£
|
Fixed assets
|
|
|
|
|
|
|
Tangible assets
|
11
|
|
477,997
|
|
|
575,726
|
Investments
|
12
|
|
426,733
|
|
|
610,039
|
|
|
|
904,730
|
|
|
1,185,765
|
Current assets
|
|
|
|
|
|
|
Stocks
|
13
|
615,345
|
|
|
565,366
|
|
Debtors: amounts falling due
within
one year
|
14
|
6,211,919
|
|
|
5,814,761
|
|
Cash at bank and in
hand
|
15
|
5,998,953
|
|
|
5,715,819
|
|
|
|
12,826,217
|
|
|
12,095,946
|
|
Creditors: amounts falling due
within
one year
|
16
|
(1,728,289)
|
|
|
(1,199,714)
|
|
Net current assets
|
|
|
11,097,928
|
|
|
10,896,232
|
Total assets less current liabilities
|
|
|
12,002,658
|
|
|
12,081,997
|
Provisions for liabilities
|
|
|
|
|
|
|
Deferred tax
|
17
|
-
|
(18,224)
|
|
|
|
|
17
|
|
-
|
|
|
(18,224)
|
Deferred tax
|
Net assets
|
|
|
12,002,658
|
|
|
12,063,773
|
Capital and reserves
|
|
|
|
|
|
|
Called up share capital
|
18
|
|
260,983
|
|
|
260,983
|
Share premium account
|
19
|
|
1,471,315
|
|
|
1,471,315
|
Capital redemption
reserve
|
19
|
|
1,231
|
|
|
1,231
|
Profit and loss account
|
19
|
|
10,269,129
|
|
|
10,330,244
|
|
|
|
12,002,658
|
|
|
12,063,773
|
The financial statements were approved and authorised for issue by
the board and were signed on its behalf on:
Peter Harrison
Director
The notes on pages 08 to 24 form
part of these financial statements.
STATEMENT OF CHANGES IN EQUITY FOR THE YEAR ENDED 30 JUNE
2024
|
Called up
share
capital
|
Share premium
account
|
Capital redemption
reserve
|
Profit and
loss
account
|
Total
equity
|
|
£
|
£
|
£
|
£
|
£
|
At 1 July 2023
|
260,983
|
1,471,315
|
1,231
|
10,330,244
|
12,063,773
|
Comprehensive income for the year
|
|
|
|
|
|
Profit for the year
|
-
|
-
|
-
|
8,096,718
|
8,096,718
|
Other comprehensive income
for the year
|
-
|
-
|
-
|
-
|
-
|
Total comprehensive
income for the year
|
-
|
-
|
-
|
8,096,718
|
8,096,718
|
Contributions by and distributions to
owners
|
|
|
|
|
|
Dividends: Equity
capital
|
-
|
-
|
-
|
(8,247,056)
|
(8,247,056)
|
Share option charge
|
-
|
-
|
-
|
89,223
|
89,223
|
Total transactions with owners
|
-
|
-
|
-
|
(8,157,833)
|
(8,157,833)
|
At 30 June 2024
|
260,983
|
1,471,315
|
1,231
|
10,269,129
|
12,002,658
|
|
Called up
share
capital
|
Share premium
account
|
Capital
redemption reserve
|
Profit
and loss account
|
Total
equity
|
|
£
|
£
|
£
|
£
|
£
|
At 1 July 2022
|
260,467
|
1,332,471
|
1,231
|
10,226,981
|
11,821,150
|
Comprehensive income for the year
|
|
|
|
|
|
|
|
|
|
|
|
Profit for the year
|
-
|
-
|
-
|
8,372,241
|
8,372,241
|
|
|
|
|
|
|
Other comprehensive income
for the year
|
-
|
-
|
-
|
-
|
-
|
|
|
|
|
|
|
Total comprehensive income for the year
|
-
|
-
|
-
|
8,372,241
|
8,372,241
|
|
|
|
|
|
|
Contributions by and distributions to
owners
|
-
|
-
|
-
|
-
|
-
|
|
|
|
|
|
|
Dividends: Equity capital
|
-
|
-
|
-
|
(8,443,058)
|
(8,443,058)
|
|
|
|
|
|
|
Shares issued during the
year
|
516
|
138,844
|
-
|
-
|
139,360
|
|
|
|
|
|
|
Share option charge
|
-
|
-
|
-
|
174,080
|
174,080
|
|
|
|
|
|
|
Total transactions with owners
|
516
|
138,844
|
-
|
(8,268,978
|
(8,129,618)
|
|
|
|
|
|
|
At
30 June 2023
|
260,983
|
1,471,315
|
1,231
|
10,330,244
|
12,063,773
|
The notes on pages 08 to 24 form
part of these financial statements.
STATEMENT OF CASH FLOWS
FOR THE YEAR ENDED 30 JUNE 2024
|
2024
£
|
2023
£
|
Cash flows from operating activities
|
|
|
Profit for the financial
year
Adjustments for:
|
8,096,718
|
8,372,241
|
Depreciation of tangible
assets
|
113,636
|
129,227
|
Interest received
|
(201,962)
|
(101,094)
|
Taxation charge
|
2,506,131
|
1,762,202
|
(Increase) in stocks
|
(49,979)
|
(103,551)
|
(Increase) in debtors
|
(394,670)
|
(626,550)
|
Increase/(decrease) in
creditors
|
83,019
|
(52,612)
|
Corporation tax (paid)
|
(2,081,287)
|
(1,751,587)
|
Share option charge
|
89,223
|
174,080
|
Impairment of
investment
|
183,306
|
-
|
Net cash generated from operating
activities
|
8,344,135
|
7,802,356
|
Cash flows from investing activities
|
|
|
Purchase of tangible fixed
assets
|
(15,907)
|
(10,583)
|
Interest received
|
201,962
|
101,094
|
Net cash from investing activities
|
186,055
|
90,511
|
Cash flows from financing activities
|
|
|
Issue of ordinary
shares
|
-
|
139,360
|
Dividends paid
|
(8,247,056)
|
(8,443,058)
|
Net cash used in financing activities
|
(8,247,056)
|
(8,303,698)
|
Net increase/(decrease) in cash and cash
equivalents
|
283,134
|
(410,831)
|
Cash and cash equivalents at
beginning of year
|
5,715,819
|
6,126,650
|
Cash and cash equivalents at the end of
year
|
5,998,953
|
5,715,819
|
Cash and cash equivalents at the end of year
comprise:
|
|
|
Cash at bank and in
hand
|
5,998,953
|
5,715,819
|
|
5,998,953
|
5,715,819
|
The notes on pages 08 to 24 form
part of these financial statements.
|
|
|
NOTES TO THE
FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
1. General
information
Bioventix Plc (04923945) is a
public limited company registered in England and Wales. The
Registered Office is 27-28 Eastcastle Street, London, W1W
8DH.
1.1 Valuation of investments
Investments in unlisted Company
shares, whose market value can be reliably determined, are
remeasured to market value at each reporting date. Gains and losses
on remeasurement are recognised in the Statement of comprehensive
income for the period. Where market value cannot
be reliably determined, such investments are stated at historic
cost less impairment.
2. Accounting
policies
2.1 Basis of preparation of financial
statements
The financial statements have been
prepared under the historical cost convention unless otherwise
specified within these accounting policies and in accordance with
Financial Reporting Standard 102, the Financial Reporting Standard
applicable in the UK and the Republic of Ireland and the Companies
Act 2006.
The preparation of financial
statements in compliance with FRS 102 requires the use of certain
critical accounting estimates. It also requires management to
exercise judgment in applying the Company's accounting policies
(see note 3).
The following principal accounting
policies have been applied:
2.2 Revenue
Turnover is recognised for product
supplied or services rendered to the extent that it is probable
that the economic benefits will flow to the Company and the
turnover can be reliably measured. Turnover is measured as the fair
value of the consideration received or receivable, excluding
discounts, rebates, value added tax and other sales taxes. The
following criteria determine when turnover will be
recognised:
Direct sales
Direct sales are generally
recognised at the date of dispatch unless contractual terms with
customers state that risk and title pass on delivery of goods, in
which case revenue is recognised on delivery.
R&D income
Subcontracted R&D income is
recognised based upon the stage of completion at the
year-end.
Licence revenue and
royalties
Annual licence revenue is
recognised, in full, based upon the date of invoice. Royalties are
accrued over period to which they relate and revenue is recognised
based upon returns and notifications received from customers. In
the event that subsequent adjustments to royalties are identified
they are recognised in the period in which they are
identified.
NOTES TO THE
FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
2. Accounting policies
(continued)
2.3 Foreign currency translation
Functional and presentation currency
The Company's functional and
presentational currency is GBP.
Transactions and balances
Foreign currency transactions are
translated into the functional currency using the spot exchange
rates at the dates of the transactions.
At each period end foreign
currency monetary items are translated using the closing rate. Non-
monetary items measured at historical cost are translated using the
exchange rate at the date of the transaction and non-monetary items
measured at fair value are measured using the exchange rate when
fair value was determined.
2.4 Interest income
Interest income is recognised in
profit or loss using the effective interest method.
2.5 Pensions
Defined contribution pension plan
The Company operates a defined
contribution plan for its employees. A defined contribution plan is
a pension plan under which the Company pays fixed contributions
into a separate entity. Once the contributions have been paid the
Company has no further payment obligations.
The contributions are recognised
as an expense in profit or loss when they fall due. Amounts not
paid are shown in accruals as a liability in the Statement of
financial position. The assets of the plan are held separately from
the Company in independently administered funds.
2.6 Current and deferred
taxation
Current and deferred tax are
recognised as an expense or income in the Statement of
Comprehensive Income, except when they relate to items credited or
debited directly to equity, in which case the tax is also
recognised directly in equity. The current income tax charge is
calculated on the basis of tax rates and laws that have been
enacted or substantively enacted by the reporting date in the
countries where the Company operates and generates
income.
Deferred tax balances are
recognised in respect of all timing differences that have
originated but not reversed by the reporting date, except
that:
§ The
recognition of deferred tax assets is limited to the extent that it
is probable that they will be recovered against the reversal of
deferred tax liabilities or other future taxable profits;
and
§ Any
deferred tax balances are reversed if and when all conditions for
retaining associated tax allowances have been met.
NOTES TO THE
FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
2. Accounting policies
(continued)
Deferred tax balances are not
recognised in respect of permanent differences except in respect of
business combinations, when deferred tax is recognised on the
differences between the fair values of assets acquired and the
future tax deductions available for them and the differences
between the fair values of liabilities acquired and the amount that
will be assessed for tax. Deferred tax is determined using tax
rates and laws that have been enacted or substantively enacted by
the reporting date.
2.7 Research and development
Research and development
expenditure is written off in the year in which it is
incurred.
2.8 Tangible fixed assets
Tangible fixed assets under the
cost model are stated at historical cost less accumulated
depreciation and any accumulated impairment losses. Historical cost
includes expenditure that is directly attributable to bringing the
asset to the location and condition necessary for it to be capable
of operating in the manner intended by management.
Land is not depreciated.
Depreciation on other assets is charged so as to allocate the cost
of assets less their residual value over their estimated useful
live
Freehold property
|
-
|
2% straight line
|
Plant and equipment
|
-
|
15% straight line
|
Motor Vehicles
|
-
|
25% straight line
|
Fixtures & Fittings
|
-
|
15% straight line
|
Equipment
|
-
|
25% straight line
|
2.9 Stocks
Stocks are stated at the lower of
cost and net realisable value, being the estimated selling price
less costs to complete and sell. Cost includes all direct costs and
an appropriate proportion of fixed and variable
overheads.
At each balance sheet date, stocks
are assessed for impairment. If stock is impaired, the carrying
amount is reduced to its selling price less costs to complete and
sell. The impairment loss is recognised immediately in profit or
loss.
2.10 Debtors
Short-term debtors are measured at
transaction price, less any impairment. Loans receivable are
measured initially at fair value, net of transaction costs, and are
measured subsequently at amortised cost using the effective
interest method, less any impairment.
2.11 Cash and cash equivalents
Cash is represented by cash in
hand and deposits with financial institutions repayable without
penalty on notice of not more than 24 hours. Cash equivalents are
highly liquid investments that mature in no more than twelve months
from the date of acquisition and that are readily convertible to
known amounts of cash with insignificant risk of change in
value.
In the Statement of cash flows,
cash and cash equivalents are shown net of bank overdrafts that are
repayable on demand and form an integral part of the Company's cash
management.
NOTES TO THE
FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
2. Accounting policies
(continued)
2.12 Stocks
Stocks are stated at the lower of
cost and net realisable value, being the estimated selling price
less costs to complete and sell. Cost includes all direct costs and
an appropriate proportion of fixed and variable
overheads.
At each balance sheet date, stocks
are assessed for impairment. If stock is impaired, the carrying
amount is reduced to its selling price less costs to complete and
sell. The impairment loss is recognised immediately in profit or
loss.
2.13 Debtors
Short-term debtors are measured at
transaction price, less any impairment. Loans receivable are
measured initially at fair value, net of transaction costs, and are
measured subsequently at amortised cost using the effective
interest method, less any impairment.
2.14 Cash and cash equivalents
Cash is represented by cash in
hand and deposits with financial institutions repayable without
penalty on notice of not more than 24 hours. Cash equivalents are
highly liquid investments that mature in no more than twelve months
from the date of acquisition and that are readily convertible to
known amounts of cash with insignificant risk of change in
value.
In the Statement of cash flows,
cash and cash equivalents are shown net of bank overdrafts that are
repayable on demand and form an integral part of the Company's cash
management.
2.15 Creditors
Short-term creditors are measured
at the transaction price. Other financial liabilities, including
bank loans, are measured initially at fair value, net of
transaction costs, and are measured subsequently at amortised cost
using the effective interest method.
2.16 Provisions for liabilities
Provisions are recognised when an
event has taken place that gives rise to a legal or constructive
obligation, a transfer of economic benefits is probable and a
reliable estimate can be made. Provisions are measured as the best
estimate of the amount required to settle the obligation, taking
into account the related risks and uncertainties. Increases in
provisions are generally charged as an expense to profit or
loss.
2.17 Financial instruments
The Company has elected to apply
the provisions of Section 11 "Basic Financial Instruments" of FRS
102 to all of its financial instruments.
Basic financial assets
Basic financial assets, which
include trade and other receivables, cash and bank balances, are
initially measured at their transaction price including transaction
costs and are subsequently carried at their amortised cost using
the effective interest method, less any provision for impairment,
unless the arrangement constitutes a financing transaction, where
the transaction is measured at the
NOTES TO THE
FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
2. Accounting policies
(continued)
2.17 Financial instruments (continued)
present value of the future
receipts discounted at a market rate of interest.
Discounting is omitted where the
effect of discounting is immaterial. The Company's cash and cash
equivalents, trade and most other receivables due with the
operating cycle fall into this category of financial
instruments.
Financial liabilities
Financial liabilities and equity
instruments are classified according to the substance of the
contractual arrangements entered into. An equity instruments any
contract that evidences a residual interest in the assets of the
Company after the deduction of all its liabilities.
Basic financial liabilities, which
include trade and other payables, bank loans and other loans are
initially measured at their transaction price after transaction
costs. When this constitutes a financing transaction, whereby the
debt instrument is measured at the present value of the future
payments discounted at a market rate of interest. Discounting is
omitted where the effect of discounting is immaterial.
Debt instruments are subsequently
carried at their amortised cost using the effective interest rate
method.
Trade payables are obligations to
pay for goods and services that have been acquired in the ordinary
course of business from suppliers. Trade payables are classified as
current liabilities if the payment is due within one year. If not,
they represent non-current liabilities. Trade payables are
initially recognised at their transaction price and subsequently
are measured at amortised cost using the effective interest method.
Discounting is omitted where the effect of discounting is
immaterial.
2.18 Dividends
Equity dividends are recognised
when they become legally payable. Interim equity dividends are
recognised when paid. Final equity dividends are recognised when
approved by the shareholders at an annual general
meeting.
2.19 Employee benefits-share-based compensation
The company operates an
equity-settled, share-based compensation plan. The fair value of
the employee services received in exchange for the grant of the
options is recognised as an expense over the vesting period. The
total amount to be expensed over the vesting period is determined
by reference to the fair value of the options granted. At each
balance sheet date, the company will revise its estimates of the
number of options are expected to be exercisable. It will recognise
the impact of the revision of original estimates, if any, in the
profit and loss account, with a corresponding adjustment to equity.
The proceeds received net of any directly attributable transaction
costs are credited to share capital (nominal value) and share
premium when the options are exercised.
NOTES TO THE FINANCIAL
STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
3. Judgments in applying accounting policies and key sources of
estimation uncertainty
In the application of the company's
accounting policies (as described in note 2), management is
required to make judgments, estimates and assumptions. These
estimates and underlying assumptions are reviewed on an ongoing
basis.
Carrying value of Unlisted investments
The Company holds two unlisted
investments in companies carrying out research in identifying
biomarkers for diagnosing health conditions. The directors have
reviewed the progress of this research over the last year. In
common with much scientific research there is uncertainty, both in
relation to the science and to the commercial outcome, and no
information to be able to reliably calculate a fair value for these
investments.
An impairment provision against the
value of the investment in shares of CardiNor AS has been
made in the year ended 30 June 2024 following notification of that
company's intention to file for bankruptcy received on 11th July
2024. Subsequently CardiNor AS has raised further equity thereby
substantially diluting existing shareholdings and has also stated
its intention to further dilute shareholdings by the conversion of
debt into equity. The Impairment charge is shown in the Statement
of comprehensive income and the carrying value of investments in
Note 12 to the accounts.
The carrying value of the remaining
investment will continue to be historic cost.
Royalty Revenue Accrual
The Company is notified and
receives royalty revenue from one customer on a calendar year basis
annually in arrears it is therefore necessary to estimate this
revenue for the first 6 months of the calendar year and process an
accrual in respect of it.
Valuation of Share based payments
The Company operates two share
option schemes: an Approved EMI Share Option Scheme and an
Unapproved Share Option Scheme. In calculating the charge to profit
or loss in respect of options granted to employees under these
schemes the Company has applied the requirements of FRS 102 which
includes making estimates for both the expected volatility of the
Company's shares and the risk free interest rate the details of
which are shown in Note 21 to the accounts.
4.
|
Turnover
An analysis of turnover by class
of business is as follows:
|
|
|
|
2024
£
|
|
2023
£
|
|
Product revenue and R&D
income
|
4,459,290
|
|
4,232,829
|
|
Royalty and licence fee
income
|
9,147,294
|
|
8,583,396
|
|
|
13,606,584
|
|
12,816,225
|
|
|
2024
£
|
|
2023
£
|
|
United Kingdom
|
405,455
|
|
961,904
|
|
Other EU
|
1,507,551
|
|
1,604,187
|
|
Rest of the world
|
11,693,578
|
|
10,250,134
|
|
|
13,606,584
|
|
12,816,225
|
NOTES TO THE FINANCIAL
STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
5.
|
Operating profit
|
|
|
|
|
The operating profit is stated
after charging:
|
|
|
|
|
|
2024
£
|
|
2023
£
|
|
Depreciation of tangible fixed
assets
|
113,636
|
|
129,227
|
|
Fees payable to the Company's
auditor and its associates for the audit of the Company's annual
financial statements
|
32,500
|
|
25,000
|
|
Exchange differences
|
42,180
|
|
36,679
|
|
Research and development
costs
|
999,418
|
|
1,201,398
|
6.
|
Employees
Staff costs, including directors'
remuneration, were as follows:
|
|
|
|
|
|
2024
£
|
|
2023
£
|
|
Wages and salaries
|
1,153,004
|
|
1,001,959
|
|
Social security costs
|
138,056
|
|
119,075
|
|
Share option charge
|
89,223
|
|
174,080
|
|
Cost of defined contribution
scheme
|
91,692
|
|
71,513
|
|
|
1,471,975
|
|
1,366,627
|
The average monthly number of
employees, including the directors, during the year was as
follows:
|
|
2024
|
|
2023
|
|
|
No.
|
|
No.
|
|
Management and
administration
|
6
|
|
5
|
|
Scientific
|
11
|
|
11
|
|
|
|
|
|
|
|
17
|
|
16
|
NOTES TO THE FINANCIAL
STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
7.
|
Directors' remuneration
|
|
|
|
|
|
|
|
|
|
|
2024
|
|
2023
|
|
|
£
|
|
£
|
|
Directors' emoluments
|
537,847
|
|
412,059
|
|
Company contributions to defined
contribution pension schemes
|
50,815
|
|
36,890
|
|
|
588,662
|
|
448,949
|
During the year
retirement benefits were accruing to
1 director (2023 - 1) in
respect of defined contribution pension
schemes.
8.
|
Interest receivable
|
|
|
|
|
|
|
|
|
|
|
2024
|
|
2023
|
|
|
£
|
|
£
|
|
|
|
|
|
|
Other interest receivable
|
201,962
|
|
101,094
|
NOTES TO THE
FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
9.
|
Taxation
|
|
|
|
|
|
|
|
|
|
|
2024
|
|
2023
|
|
|
£
|
|
£
|
|
Corporation tax
|
|
|
|
|
|
|
|
|
|
Current tax on profits for the
year
|
2,526,844
|
|
1,788,254
|
|
|
|
|
|
|
Deferred tax
|
|
|
|
|
|
|
|
|
|
Origination and reversal of timing
differences
|
(20,713)
|
|
(26,052)
|
|
|
|
|
|
|
Taxation on profit on ordinary activities
|
2,506,131
|
|
1,762,202
|
|
|
|
|
|
Factors affecting tax charge for the year
The tax assessed for the year is
lower than (2023 - lower
than) the standard rate of corporation tax in the UK
of 25% (2023 -
25%). The differences are explained below:
|
2024
£
|
2023
£
|
Profit on ordinary activities
before tax
|
10,602,849
|
10,134,444
|
Profit on ordinary activities
multiplied by standard rate of corporation
tax in the UK of 25% (2023 - 25%)
|
2,650,712
|
2,533,611
|
Effects of:
|
|
|
Expenses not deductible for tax
purposes, other than goodwill amortisation and
impairment
|
381
|
341
|
Capital allowances for year in
excess of depreciation
|
22,493
|
27,289
|
Amounts written off
investments
|
45,827
|
-
|
Research and development tax
credit
|
(214,875)
|
(356,784)
|
Share based payments
|
22,306
|
(23,222)
|
Deferred tax movement
|
(20,713)
|
(26,052)
|
Change in tax rate during the
year
|
-
|
(392,981)
|
Total tax charge for the year
|
2,506,131
|
1,762,202
|
Factors that may affect future tax charges
There were no factors that may
affect future tax charges.
NOTES TO THE
FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
10.
|
Dividends
|
|
|
|
|
|
|
|
|
|
|
2024
|
|
2023
|
|
|
£
|
|
£
|
|
|
|
|
|
|
Dividends paid 158 pence per share
(2023:162 pence per share)
|
8,247,056
|
|
8,443,058
|
|
|
|
|
|
|
|
|
|
|
|
|
8,247,056
|
|
8,443,058
|
11. Tangible fixed
assets
|
Freehold
|
|
Plant &
|
|
Motor
|
|
Fixtures &
|
|
Office
|
|
property
£
|
|
Machinery
£
|
|
Vehicles
£
|
|
Fittings
£
|
|
Equipment
£
|
Cost or valuation
|
|
|
|
|
|
|
|
|
|
At 1 July 2023
|
475,000
|
|
479,527
|
|
13,090
|
|
407,115
|
|
39,525
|
Additions
|
-
|
|
10,586
|
|
-
|
|
5,321
|
|
-
|
At 30 June 2024
|
475,000
|
|
490,113
|
|
13,090
|
|
412,436
|
|
39,525
|
Depreciation
|
|
|
|
|
|
|
|
|
|
At 1 July 2023
|
156,750
|
|
382,026
|
|
8,182
|
|
263,594
|
|
27,979
|
Charge for the year on owned
assets
|
7,125
|
|
41,490
|
|
3,273
|
|
56,754
|
|
4,994
|
At 30 June 2024
|
163,875
|
|
423,516
|
|
11,455
|
|
320,348
|
|
32,973
|
Net book value
|
|
|
|
|
|
|
|
|
|
At 30 June 2024
|
311,125
|
|
66,597
|
|
1,635
|
|
92,088
|
|
6,552
|
At 30 June 2023
|
318,250
|
|
97,501
|
|
4,908
|
|
143,521
|
|
11,546
|
NOTES TO THE FINANCIAL
STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
11.
|
Tangible fixed assets
|
Freehold
|
|
Plant &
|
|
Motor
|
|
Fixtures &
|
|
Office
|
|
|
property
£
|
|
Machinery
£
|
|
Vehicles
£
|
|
Fittings
£
|
|
Equipment
£
|
|
Cost or valuation
|
|
|
|
|
|
|
|
|
|
|
At 1 July 2023
|
475,000
|
|
479,527
|
|
13,090
|
|
407,115
|
|
39,525
|
|
Additions
|
-
|
|
10,586
|
|
-
|
|
5,321
|
|
-
|
|
At 30 June 2024
|
475,000
|
|
490,113
|
|
13,090
|
|
412,436
|
|
39,525
|
|
Depreciation
|
|
|
|
|
|
|
|
|
|
|
At 1 July 2023
|
156,750
|
|
382,026
|
|
8,182
|
|
263,594
|
|
27,979
|
|
Charge for the year on owned
assets
|
7,125
|
|
41,490
|
|
3,273
|
|
56,754
|
|
4,994
|
|
At 30 June 2024
|
163,875
|
|
423,516
|
|
11,455
|
|
320,348
|
|
32,973
|
|
Net book value
|
|
|
|
|
|
|
|
|
|
|
At 30 June 2024
|
311,125
|
|
66,597
|
|
1,635
|
|
92,088
|
|
6,552
|
|
At 30 June 2023
|
318,250
|
|
97,501
|
|
4,908
|
|
143,521
|
|
11,546
|
NOTES TO THE FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE
2024
11.
|
Tangible fixed assets (continued)
|
Total
|
|
|
£
|
|
Cost or valuation
|
|
|
At 1 July 2023
|
1,414,257
|
|
Additions
|
15,907
|
|
At 30 June 2024
|
1,430,164
|
|
Depreciation
|
|
|
At 1 July 2023
|
838,531
|
|
Charge for the year on owned
assets
|
113,636
|
|
At 30 June 2024
|
952,167
|
|
Net book value
|
|
|
At 30 June 2024
|
477,997
|
|
At 30 June 2023
|
575,726
|
Included within land and buildings is freehold land at cost of
£118,750 which is not depreciated.
(2023 - £118,750).
NOTES TO THE FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE
2024
12.
|
Fixed asset investments
|
|
|
|
|
|
|
Unlisted
Investments
|
|
|
£
|
|
|
|
|
Cost or valuation
|
|
|
At 1 July 2023
|
610,039
|
|
Impairment
|
(183,306)
|
|
|
|
|
|
|
|
At 30 June 2024
|
426,733
|
|
|
|
The value of the investment in
shares of CardiNor AS was written down to nil off following
notification of that company's intention to file for bankruptcy
which was received on 11th July 2024.Subsequently CardiNor AS has
raised further equity thereby substantially diluting existing
shareholdings and has also stated its intention to further dilute
shareholdings by the conversion of debt into equity.
13.
|
Stocks
|
|
|
|
|
|
|
|
|
|
|
2024
|
|
2023
|
|
|
£
|
|
£
|
|
Finished goods and goods for
resale
|
615,345
|
|
565,366
|
14.
|
Debtors
|
2024
|
|
2023
|
|
|
£
|
|
£
|
|
Trade debtors
|
1,521,963
|
|
1,170,512
|
|
Other debtors
|
26,375
|
|
501
|
|
Prepayments and accrued
income
|
4,661,092
|
|
4,643,748
|
|
Deferred taxation
|
2,489
|
|
-
|
|
|
6,211,919
|
|
5,814,761
|
15.
|
Cash and cash equivalents
|
|
|
|
|
|
|
|
|
|
|
2024
|
|
2023
|
|
|
£
|
|
£
|
|
Cash at bank and in
hand
|
5,998,953
|
|
5,715,819
|
NOTES TO THE FINANCIAL
STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
16.
|
Creditors: Amounts falling due within one
year
|
2024
|
|
2023
|
|
|
£
|
|
£
|
|
Trade creditors
|
169,982
|
|
77,725
|
|
Corporation tax
|
1,154,816
|
|
709,259
|
|
Other taxation and social
security
|
28,428
|
|
76,298
|
|
Accruals and deferred
income
|
375,063
|
|
336,432
|
|
|
1,728,289
|
|
1,199,714
|
17.
|
Deferred taxation
|
2024
|
|
2023
|
|
|
£
|
|
£
|
|
At beginning of year
|
(18,224)
|
|
(44,276)
|
|
Charged to profit or
loss
|
20,713
|
|
26,052
|
|
At end of year
|
2,489
|
|
(18,224)
|
|
The deferred taxation balance is
made up as follows:
|
|
|
|
|
|
2024
£
|
|
2023
£
|
|
Accelerated capital
allowances
|
2,489
|
|
(18,224)
|
|
|
2,489
|
|
(18,224)
|
18.
|
Share capital
|
|
|
|
|
Allotted, called up and fully paid
|
2024
£
|
|
2023
£
|
|
5,219,656 (2023 - 5,219,656) Ordinary shares of
£0.05 each
|
260,983
|
|
260,983
|
The holders of ordinary shares are
entitled to receive dividends as declared and are entitled to one
vote per share at meetings of the Company. All ordinary shares rank
equally with regard to the Company's residual assets.
NOTES TO THE FINANCIAL
STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
19. Reserves
Share premium account
The share premium reserve contains
the premium arising on issues of equity shares, net of issue
expenses.
Capital redemption reserve
The capital redemption arose on
the buy-back of shares by the company.
Profit & loss account
The profit and loss reserve
represents cumulative profits or losses, net of dividends paid and
other adjustments.
20. Share-based
payments
During the year the company
operated 2 share option schemes; an Approved EMI
Share Option Scheme and an Unapproved Share Option Scheme to
incentivise employees.
The company has applied the
requirements of FRS 102 Section 26 Share-based Payment to all the
options granted under both schemes. The terms for granting share
options under both schemes are the same and provide for an option
price equal to the market value of the Company's shares on the date
of the grant and for the Approved EMI Share Option Scheme this
price is subsequently agreed with HMRC Shares and Assets Valuation
Division.
The contractual life of an option
under both schemes is 10 years from the date of grant. Options
granted become exercisable on the third anniversary of the date of
grant. Exercise of an option is normally subject to continued
employment, but there are also considerations for good leavers. All
share based remuneration is settled in equity shares.
|
Weighted average
exercise
price
(pence)
2024
|
Number
2024
|
Weighted
average
exercise
price
(pence)
2023
|
Number
2023
|
Outstanding at the beginning of
the year
|
3544
|
77,281
|
2896
|
51,997
|
Granted during the year
|
-
|
-
|
3855
|
39,708
|
Forfeited during the
year
|
-
|
-
|
3855
|
(4,101)
|
Exercised during the
year
|
-
|
-
|
1350
|
(10,323)
|
Outstanding at the end of the
year
|
3544
|
77,281
|
3544
|
77,281
|
NOTES TO THE
FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
|
2024
|
2023
|
Option pricing model
used
|
Black
Scholes
|
Black
Scholes
|
Issue price
|
£13.50-£38.50
|
£13.50-£38.50
|
Exercise price (pence)
|
£13.50-£38.50
|
£13.50-£38.50
|
Option life
|
10 years
|
10
years
|
Expected volatility
|
7.459%
|
7.459%
|
Fair value at measurement
date
|
£4.66 -
£26.91
|
£4.66 -
£26.91
|
Risk-free interest rate
|
1.5%
|
1.5%
|
20. Share-based payments
(continued)
The expected volatility for the
options issued in the year to 30 June 2023 was based upon the
volatility over that 12 month period.
For previous years it was based
upon the historical volatility over the period since the Company's
shares were listed on AIM.
The expense recognised for
share-based payments during the year ended 30 June 2024 was £89,223
(2023 : £174,080).
The number of staff and officers
holding share options at 30 June 2024 was 16 (2023: 16). The share
options have been issued to underpin staff service
conditions.
21. Earnings per share
The weighted average number of
shares in issue for the basic earnings per share calculation is
5,219,656 (2023: 5,212,220) and for the diluted earnings per share,
assuming the exercise of all share options is 5,296,937 (2023:
5,289,501).
The calculation of the basic
earnings per shares is based on the profit for the period of
£10,585,108 (2023: £8,372,241) divided by the weighted average
number of shares in issue of 5,219,656 (2023: 5,212,220), the basic
earnings per share is 155.12p (2023: 160.63p). The diluted earnings
per share, assuming the exercise of all of the share options is
based on 5,296,937 (2023: 5,289,501) shares and is 152.86p (2023:
158.28p).
NOTES TO THE
FINANCIAL STATEMENTS FOR THE YEAR ENDED 30 JUNE 2024
22. Pension commitments
The company operates a defined
contributions pension scheme. The assets of the scheme are held
separately from those of the company in an independently
administered fund. The pension charge represents contributions
payable by the company to the fund and amounted to £91,692 (2023:
£71,512). No contributions were owing at the year end (2023:
£nil).
23. Related party
transactions
During the year a dividend of
£525,199 (2023: £775,764) was paid to a director and his
wife.
24. Controlling party
During the year there has not been
an individual controlling party.