Arecor Therapeutics
plc
("Arecor", the "Company" or the "Group")
INTERIM RESULTS FOR THE SIX
MONTHS ENDED 30 JUNE 2024
-
AT278 insulin candidate
demonstrates superiority to current best insulins in a Phase I
clinical trial in Type 2 diabetics with high BMI
-
Expansion of diabetes
and obesity pipeline, with oral GLP-1 receptor agonist development
initiated and partnership inked with Medtronic on implantable
insulin pumps
-
AT220
generating growing royalties under a worldwide
licensing agreement
-
Growing technology
partnerships portfolio offering significant future upside potential
from licensing
-
Dr.
Helen Parris appointed Senior Vice President, Commercial and
General Manager, Tetris Pharma
-
Successful placing, subscription and retail offer raises £6.4
million, including support from two international life science
healthcare investors, providing sound financial platform for
further investment in Group R&D and in Tetris Pharma to drive
Ogluo® product sales
Cambridge, UK, 26 September 2024: Arecor Therapeutics plc (AIM: AREC), the biopharmaceutical
group advancing today's therapies to enable healthier lives, today
announces its interim results for the six months ended 30 June
2024.
Sarah Howell, Chief Executive Officer of Arecor,
said: "During the period we have significantly
advanced and expanded our diabetes and obesity portfolio, reporting
very positive Phase I clinical results for AT278 demonstrating its
clear superiority and potential to improve outcomes and lower the
burden for people living with diabetes, and expanding our
technology platform in the development of the oral delivery of
peptides, initially GLP-1, a potential high value, high growth
proposition. With multiple opportunities for value creation, we
continue to build momentum across the business. With a strengthened
financial position following our fundraise we are confident in our
ability to deliver against our strategy and excited about what can
be achieved through 2024 and beyond."
Operational highlights (including post period
events)
•
Significant progress in development of AT278 insulin candidate,
demonstrating superiority to current best insulins in a Phase I
clinical trial in Type 2 diabetics with high BMI
• Expansion
of diabetes and obesity pipeline, with oral GLP-1 receptor agonist
development initiated
• Entered a
strategic research collaboration with Medtronic to develop a novel
formulation of insulin for implantable intraperitoneal insulin pump
delivery, fully funded by Medtronic
•
Arestat™-enabled product,
AT220, generating growing royalties under a
worldwide licensing agreement
• Growing
technology partnerships portfolio offering significant future
upside potential from licensing, including expansion of ongoing
collaboration with pharmaceuticals division of one of the world's
largest chemicals marketing and pharmaceuticals companies, in
addition to Medtronic partnership
• Pipeline
of future technology partnerships and licensing
opportunities
•
Dr. Helen Parris joins Group as Senior Vice
President, Commercial and General Manager of Tetris Pharma
Ltd
Financial highlights
• Revenue of
£2.0 million (first half 2023 unaudited: £1.67 million)
• Total
income of £2.03 million (first half 2023 unaudited: £2.33
million)
• Investment
in R&D of £2.09 million (first half 2023 unaudited: £2.86
million)
• Loss after
tax for the period of £4.64 million (first half 2023 unaudited:
£4.53 million)
• Cash, cash
equivalents and short-term investments of £2.53 million at 30 June
2024 (at 30 June 2023 unaudited: £6.61 million)
• Post
period fundraise of £6.4 million (before expenses), including
support from two international life science healthcare investors,
to be employed
towards delivering significant value inflection points including
investment in R&D to drive high-value partnerships and working
capital inventory investment for Ogluo®, and balance sheet
strength
Outlook (H2 2024 and beyond)
• Continued
strategic discussions around AT278 including evaluation of a
co-development opportunity
•
Non-clinical pharmacokinetic proof of concept
study in oral GLP-1 receptor agonist
collaboration anticipated in 1H 2025 following initial positive
results from the current formulation development phase
• Pipeline
of future technology partnerships and potential near term licensing
opportunities
•
Focus on accelerating growth of Tetris Pharma
initially in the UK and Germany though timing of sales potentially
impacted by recent supply chain issues
•
The Board continues to target achieving consensus
analyst revenue market expectations for 2024 though this remains
subject to inherent uncertainty, such as the quantum of royalties
on sales of AT220, the magnitude and timing of licensing
transactions which are under active negotiation and the pace of the
growth of Ogluo® product sales through the remainder of the
year
Analyst conference call today
Dr Sarah Howell, Chief Executive
Officer, will host a meeting and webcast for analysts and investors
at 9.30am UK time today. Join the webcast
here. A copy of the interim
results presentation will be released later this morning on the
Company website at www.arecor.com.
Please contact ICR Consilium for details on
arecor@consilium-comms.com
/ +44 203709 5700.
For
more information, please contact:
Arecor Therapeutics plc
|
www.arecor.com
|
Dr Sarah Howell, Chief Executive
Officer
|
Tel: +44 (0) 1223 426060
Email: info@arecor.com
|
|
|
Panmure Liberum Limited (NOMAD
and Joint Broker)
Freddy Crossley, Emma Earl
(Corporate Finance)
Rupert Dearden (Corporate
Broking)
|
Tel: +44 (0) 20 7886 2500
|
|
|
WG
Partners LLP (Joint Broker)
Nigel Barnes, Satheesh
Nadarajah,
David Wilson, Claes Spang
|
Tel: +44 (0)20 3705 9321
|
|
|
ICR
Consilium
Chris Gardner, David Daley, Lindsey
Neville
|
Tel: +44 (0) 20 3709 5700
Email: arecor@consilium-comms.com
|
Notes to Editors
About Arecor
Arecor Therapeutics plc is a
globally focused biopharmaceutical company transforming patient
care by bringing innovative medicines to market through the
enhancement of existing therapeutic products. By applying our
innovative proprietary technology platform, Arestat™, we are
developing an internal portfolio of proprietary products in
diabetes and other indications, as well as working with leading
pharmaceutical and biotechnology companies to deliver therapeutic
products. The Arestat™ platform is supported by an extensive patent
portfolio.
For further details please see our
website, www.arecor.com
Corporate overview
We continued to build strong
momentum across the business during the first half of 2024,
supporting the growth of Arecor's diverse portfolio of both
proprietary in-house products and partnered programmes.
We further delivered on our diabetes
strategy, generating additional clinical data that strengthen the
potential of our ultra-concentrated, ultra-rapid acting insulin
candidate, AT278, and established a development path forward that
provides the best opportunity to maximise value for shareholders. Within our broader product portfolio,
our oral glucagon-like peptide-1 (GLP-1)
receptor agonist programme presents opportunities within high value
global markets and offers the potential to further expand our
technology platform to the oral delivery of peptides, which is a
key target for global pharmaceutical companies.
Strong progress across Arecor's
partnered portfolio highlights the value of our Arestat™
technology in driving revenue growth in
2024 and beyond. These partnerships are
revenue-generating from inception and offer significant upside
potential from licensing, as illustrated by AT220, the first
launched product incorporating Arestat™ technology, which is
providing Arecor with a growing revenue stream from sales
royalties, under a worldwide license. Sanofi continues to progress
the registrational enabling study for SAR447537, formerly INBRX-101 (AT292), which incorporates an
Arestat™ novel formulation
under license from Arecor.
Tetris Pharma, the Group's specialty
pharmaceutical business, continues to focus on its key diabetes
product, Ogluo® (glucagon prefilled autoinjector pen) and, with
increased inventory enabled by the Group's fundraise in July 2024,
the team is focused on accelerating commercial growth, initially in
the UK and Germany. There has been a recent, third-party supply
chain issue with respect to Ogluo® packaging, which is anticipated
to lead to a near-term delay in our enhanced ability to increase
Ogluo® stock in the market. This is being actively managed and is
expected to be short term in nature.
The Group has been actively engaged
in a search for a new Chief Financial Officer (CFO) and
had identified and progressed a preferred candidate. Due to
circumstances beyond Arecor's control that candidate is no
longer available. The process remains underway and the
Group intends to appoint an interim CFO as soon as
possible.
Arecor has multiple opportunities
for revenue growth and value creation for shareholders and the £6.4
million gross raised in July 2024, including support from two
international life science healthcare investors, provides a sound
financial platform allowing Arecor to deliver significant valuation
inflexion points. The Group will continue to invest in Arecor
research and development, focused on areas
in which our Arestat™ technology can
deliver transformational opportunities, including the development
of enhanced injectables through our portfolio of technology
partnerships with leading pharmaceutical and biotech companies, and
innovation in the field of oral delivery of peptides.
We also continue to explore options, including
strategic co-development and non-dilutive funding, to progress a
three-day insulin pump study for AT278, which we believe is a major
value accretion point, increasing both the potential and value of
future dealmaking.
Operational review (including post period
events)
Proprietary product
portfolio
During the period we made
significant clinical progress within our diabetes portfolio,
announcing in May 2024 that the Group's ultra-concentrated,
ultra-rapid acting, insulin candidate, AT278, had met all primary and secondary endpoints, and had also
demonstrated superiority to NovoRapid® and Humulin® R U-500, in a
Phase I clinical trial in Type 2 diabetics with a high body mass
index (BMI).
Together with its superior profile
in the earlier Phase I clinical study in Type 1 diabetic patients,
AT278 has demonstrated its ability to maintain a fast and superior
onset of action and glucose lowering profile irrespective of
diabetes type and BMI. Not only does it have the potential to
significantly improve post-prandial glucose control whilst lowering
the burden for anybody with diabetes who has a high daily insulin
need, AT278 is set to be a powerful catalyst in the development of
next generation, truly miniaturised, longer-wear insulin pumps, a
key focus for patients, physicians and the industry.
Earlier this month, the results from
the latest study were presented at the 60th Annual Meeting of the
European Association for the Study of Diabetes (EASD) in Madrid.
The abstract, which was selected as a late-breaking presentation,
was well received at the international congress, with recognition
of AT278's unique characteristics in the competitive field of
insulin analogues and the opportunity it presents to improve the
future management of diabetes.
As previously communicated, we
believe the optimal value inflexion point for AT278 and potential
value for shareholders is likely to be best achieved through
conducting an insulin pump study, to provide sufficient data for
potential licensing partners. Arecor continues to explore funding
options, including but not limited to co-development partnerships,
to conduct the clinical pump study.
The Group's proprietary product
portfolio provides significant opportunities to further expand its
proprietary pipeline of different therapeutic injectables for
partnering and is a continued focus of research and
development.
In March 2024, Arecor established a
research collaboration with TRx Biosciences, a drug development
company applying novel lipid technology to the oral delivery of
challenging molecules, for the formulation development of an oral
GLP-1 receptor agonist product. The collaboration is progressing at
pace, with initial positive results from the current formulation
development phase, and we anticipate commencing non-clinical
pharmacokinetic (PK) studies in 1H 2025.
With current treatment options
mostly limited to injectable therapies, many patients in need are
unable to benefit from these highly effective treatments, providing
a significant market opportunity within the GLP-1 market, which is
forecast to exceed $100 billion by 2030. The collaboration with TRx
Biosciences provides scope for expansion to develop further oral
peptide products and combination approaches which may be key in the
treatment of obesity-related health conditions, as well as for
other peptide products targeting multiple therapeutic areas. If
technically successful, Arecor anticipates its oral GLP-1 receptor
agonist product to be highly commercially attractive to partners
but, potentially of more significance, this would allow expansion
more broadly into oral delivery of peptides.
Partnership
products
A robust portfolio of
revenue-generating partnered programmes underscores the strength of
Arecor's Arestat™ technology and its value to our
partners in the development of enhanced formulations of their
proprietary products which would otherwise be
unachievable.
Commercialisation by Arecor's
partner of the first product incorporating Arestat™ technology,
AT220, commenced in November 2023 and the reach of that product continues to grow within multiple major
global markets. This is providing Arecor with a revenue stream from
royalties on AT220 sales under a worldwide license, which is
growing in line with the Group's expectations.
In May 2024, Sanofi announced the
completion of its acquisition of Inhibrx's assets and liabilities
associated with SAR447537, formerly INBRX-101
(AT292), an
Arestat™ formulated optimised recombinant human AAT-Fc fusion
protein, for treatment of patients with emphysema due to alpha-1
antitrypsin deficiency, which is under license to Sanofi. A
registration-enabling clinical trial of
SAR447537 commenced in 2023. Sanofi's acquisition of Inhibrx
further endorses our Arestat™ platform and highlights the value of
this novel therapy for patients and its future commercial
potential.
In May 2024 Arecor added to its
portfolio of technology partnerships with leading pharmaceutical
and medtech companies by establishing a research collaboration with
Medtronic, the global leader in healthcare technology. Through the
partnership, Medtronic is funding Arecor's development of an
Arestat™ enabled novel, high concentration, thermostable insulin,
for use by Medtronic's Diabetes business in intraperitoneal therapy
via an implantable insulin pump system. This new insulin has the
potential to bring significant advancements in the current insulin
treatment options for an extremely vulnerable patient group who
have limited options for controlling their diabetes with
traditional therapy.
An ongoing collaboration, which
Arecor established in 2023, with the pharmaceutical division of one
of the world's largest chemicals marketing and pharmaceuticals
companies to develop a differentiated, RTU liquid formulation of
the company's product, AT351, was expanded in January
2024.
The Group anticipates further
expansion of its technology partnerships portfolio, alongside the
conversion of new licenses from existing partnerships, to continue
driving revenue growth in 2024 and beyond.
Tetris
Pharma
Tetris Pharma, the Group's specialty
pharmaceutical business, continues to focus on its key diabetes
product, Ogluo® (glucagon prefilled autoinjector pen). Dr. Helen
Parris, who was appointed Senior Vice President, Commercial and
General Manager of Tetris Pharma in January 2024, is focused on
ensuring sufficient stock of Ogluo® to meet demand and implementing
targeted awareness campaigns to drive further demand and revenue
growth.
While first half of 2024 sales were
significantly tempered by the availability of Ogluo® stock, the
Group's fundraise in July 2024 has enabled increased investment in
this business to continue commercial expansion. Through the remainder of 2024 and in 2025, Tetris Pharma is
focused on implementing targeted awareness campaigns in two key
territories, the UK and Germany, where the RTU glucagon market is
estimated to be worth approximately £18 million and £9.5 million
respectively.
In recent weeks, Tetris Pharma has
been informed of an issue related to the sealed foil pouches that
protect the product from light and moisture, in the latest
consignments of Ogluo® intended for Tetris Pharma. This is not
related to the quality of the autoinjector pen itself, however, it
is likely that there will be a short-term impact on supply in
Germany and, potentially, in the UK. The issue was identified at
the packaging stage and does not impact any product released to the
market. Tetris is working closely with its manufacturing partner to
resolve the issue and to prevent any recurrence. While there is
expected to be some impact on Ogluo® product sales, any impact on
cash will be minimised by adjusting the timing of future inventory
investment accordingly, and cash will be proactively
managed.
Intellectual property
portfolio
Arecor's broad and robust global
patent portfolio has >90 granted patents across key territories
protecting both the Arestat™ technology platform as well as the
enhanced versions of therapeutic medicines that we develop
leveraging Arestat™. That portfolio was bolstered in January 2024
by a patent from the European Patent Office protecting novel
formulations of the Group's proprietary insulin products, AT278 and
AT247, alongside patents of similar scope that were granted
in Australia, India and Mexico.
Finance
The consolidated financial results
for the period ended 30 June 2024 reflect the performance of Arecor
Therapeutics plc and its trading subsidiaries; Arecor Limited and
Tetris Pharma Ltd.
Total income for the six months to
30 June 2024 of £2.03 million (Restated H1 2023: £2.33 million).
Other operating income for the
period was £39,000 (Restated H1 2023: £656,000). This decrease was
due to the completion of a UK Government research grant in the
prior year and therefore not repeating in the current
period.
Investment in R&D of £2.09
million (H1 2023: £2.86 million) reflecting
a reduced R&D spend on clinical development in our proprietary
diabetes portfolio. Future R&D expenditure will increasingly
focus on areas in which the Group's Arestat™ technology can deliver transformational
opportunities, including within diabetes and the field of oral
delivery of peptides.
Sales, General and Administrative
costs were £4.78 million (H1 2023: £4.38 million).
The total loss after tax for the
six-month period was £4.64 million (H1 2023: £4.53
million).
The Group ended H1 2024 with cash,
cash equivalents and short-term investments of £2.53 million (H1
2023: £6.61 million).
Post the period end, the Company
raised £6.4 million (before expenses) from
new and existing shareholders. These funds will be made available
to the subsidiaries within the group to enable continuation of
R&D activities and growth of sales.
The Company continues to examine
cost mitigation and manage cash as efficiently as possible. A
targeted reduction in headcount will deliver annualised
savings.
Summary and outlook
The Company remains confident in its
strategy and opportunities for significant valuation creation.
Following the positive AT278 clinical readout, we are continuing
positive co-development discussions with potential partners to
maintain progress in our diabetes portfolio. With a strengthened
cash position, and multiple opportunities for valuation creation
across the Group, including the potentially transformational impact
from enhanced delivery of oral peptides, we look forward to
building momentum through the rest of the year and
beyond.
Reflecting the Company's near-term
pipeline of technology partnership licensing opportunities and
anticipated growth in both AT220 royalties and sales of Ogluo®, we
anticipate revenue growth over the full year. The Board continues
to target achieving consensus analyst revenue market expectations
for 2024 though this remains subject to inherent uncertainty, such
as the quantum of royalties on sales of AT220, the magnitude and timing of licensing transactions which are
under active negotiation, and the pace of the growth of Ogluo®
product sales through the remainder of the year.
Sarah Howell
Chief Executive Officer
Arecor Therapeutics plc
INTERIM RESULTS FOR THE SIX MONTHS ENDED 30 JUNE
2024
Consolidated Statement of Comprehensive
Income
|
Notes
|
Period ended 30 June
2024
|
Period ended 30 June 2023 (Re-stated)
|
Year
ended 31 December 2023
|
|
|
Unaudited
|
Unaudited
|
Audited
|
|
|
£000
|
£000
|
£000
|
|
|
|
|
|
Revenue
|
4
|
1,995
|
1,669
|
4,573
|
|
|
|
|
|
Other operating income
|
|
39
|
656
|
1,142
|
Total Income
|
|
2,034
|
2,325
|
5,715
|
|
|
|
|
|
Research and Development
|
|
(2,087)
|
(2,858)
|
(5,977)
|
Sales, General and
Administrative
|
5
|
(4,781)
|
(4,375)
|
(8,913)
|
|
|
|
|
|
Operating loss
|
|
(4,834)
|
(4,908)
|
(9,175)
|
|
|
|
|
|
Other income
|
|
-
|
-
|
5
|
Finance income
|
|
55
|
164
|
284
|
Finance expense
|
7
|
(12)
|
(10)
|
(15)
|
|
|
|
|
|
Loss
before tax
|
|
(4,791)
|
(4,754)
|
(8,901)
|
|
|
|
|
|
Taxation
|
8
|
151
|
226
|
347
|
|
|
|
|
|
Loss
for the period
|
|
(4,640)
|
(4,528)
|
(8,554)
|
|
|
|
|
|
|
|
|
|
|
Basic and diluted loss per share
(£)
|
9
|
(0.15)
|
(0.15)
|
(0.28)
|
|
|
|
|
|
There were no other items of
comprehensive income during the periods under review.
Arecor Therapeutics plc
INTERIM RESULTS FOR THE SIX MONTHS ENDED 30 JUNE
2024
Consolidated Statement of Financial Position
|
Notes
|
30 June
2024
|
30 June
2023
|
31
December 2023
|
|
|
Unaudited
|
Unaudited
|
Audited
|
|
|
£000
|
£000
|
£000
|
Assets
Non-current assets
|
|
|
|
|
Intangible Assets
|
|
1,743
|
1,815
|
1,812
|
Goodwill
|
|
1,484
|
1,484
|
1,484
|
Property, Plant and
Equipment
|
|
694
|
720
|
834
|
Other receivables
|
|
69
|
48
|
77
|
|
|
3,990
|
4,067
|
4,207
|
|
|
|
|
|
Current assets
|
|
|
|
|
Trade and other
receivables
|
10
|
2,753
|
4,671
|
3,189
|
Inventory
|
|
446
|
1,564
|
771
|
Current tax receivable
|
|
632
|
1,598
|
458
|
Cash and cash equivalents
|
11
|
2,529
|
6,610
|
5,093
|
Short term investments
|
11
|
16
|
1,619
|
1,659
|
|
|
6,376
|
16,062
|
11,170
|
|
|
|
|
|
Current liabilities
|
|
|
|
|
Trade and other payables
|
12
|
(4,551)
|
(6,254)
|
(4,903)
|
Lease liabilities
|
|
(111)
|
(116)
|
(118)
|
Provisions
|
|
(1)
|
-
|
(129)
|
|
|
(4,663)
|
(6,370)
|
(5,150)
|
|
|
|
|
|
Non-current liabilities
|
|
|
|
|
Lease liabilities
|
|
(169)
|
(51)
|
(220)
|
Provisions
|
|
(19)
|
|
(28)
|
Deferred tax
|
|
(437)
|
(496)
|
(452)
|
|
|
(625)
|
(547)
|
(700)
|
|
|
|
|
|
|
|
|
|
|
Net
Assets
|
|
5,078
|
13,212
|
9,527
|
|
|
|
|
|
Equity
Share capital
|
13
|
306
|
306
|
306
|
Share premium account
|
|
28,976
|
28,976
|
28,976
|
Share-based payment
reserve
|
|
1,638
|
1,143
|
1,518
|
Other reserves
|
|
11,455
|
11,455
|
11,455
|
Merger relief reserve
|
|
2,014
|
2014
|
2,014
|
Foreign exchange reserve
|
|
51
|
14
|
(20)
|
Retained earnings
|
|
(39,362)
|
(30,696)
|
(34,722)
|
|
|
|
|
|
Shareholder's funds
|
|
5,078
|
13,212
|
9,527
|
Arecor Therapeutics plc
INTERIM RESULTS FOR THE SIX MONTHS ENDED 30 JUNE
2024
Consolidated Statement of Cash Flows
|
Period ended 30 June
2024
|
Period ended 30 June 2023 (Re-stated)
|
Year
ended 31 December 2023
|
|
Unaudited
|
Unaudited
|
Audited
|
|
£000
|
£000
|
£000
|
Cash flow from operating activities
|
|
|
|
Loss before tax
|
(4,791)
|
(4,754)
|
(8,901)
|
Finance income
|
(55)
|
(164)
|
(284)
|
Finance costs
|
12
|
10
|
15
|
Share-based compensation
|
120
|
263
|
638
|
Depreciation
|
157
|
198
|
390
|
Amortisation
|
69
|
103
|
106
|
Foreign exchange
movements
|
73
|
132
|
135
|
RDEC receivable
|
(39)
|
(47)
|
(116)
|
|
(4,454)
|
(4,259)
|
(8,017)
|
|
|
|
|
Changes in working capital
|
|
|
|
(Increase)/ decrease in
inventory
|
325
|
(433)
|
360
|
(Increase)/ decrease in trade and
other receivables
|
444
|
(2,456)
|
(1,003)
|
Increase/(decrease) in trade and
other payables
|
(352)
|
2,728
|
1,377
|
Decrease/(increase) in
provisions
|
(126)
|
-
|
157
|
Tax received
|
-
|
-
|
1,285
|
|
291
|
(161)
|
2,176
|
|
|
|
|
Net
cash used in operating activities
|
(4,163)
|
(4,420)
|
(5,841)
|
|
|
|
|
Cash flow from investing activities
|
|
|
|
Purchase of property, plant &
equipment
|
(15)
|
(73)
|
(151)
|
Sale of property, plant &
equipment
|
-
|
-
|
5
|
Transfer of short term
investments
|
1,643
|
6,422
|
6,382
|
Interest received
|
55
|
164
|
284
|
|
|
|
|
Net
cash used in investing activities
|
1,683
|
6,513
|
6,520
|
|
|
|
|
Cash flow from financing activities
|
|
|
|
Repayment of loans by
Directors
|
10
|
-
|
38
|
Capital payments on lease
liabilities
|
(63)
|
(114)
|
(203)
|
Interest paid on lease
liabilities
|
(12)
|
(10)
|
(15)
|
|
|
|
|
Net
cash (used in) / generated by financing
activities
|
(65)
|
(124)
|
(180)
|
|
|
|
|
Net (decrease) / increase in cash
and cash equivalents
|
(2,545)
|
1,969
|
499
|
Exchange (losses) / gains on
cash and cash equivalents
|
(19)
|
(124)
|
(171)
|
Cash and cash equivalents at
beginning of period or financial year
|
5,093
|
4,765
|
4,765
|
|
|
|
|
Cash and cash equivalents at end of period or financial
year
|
2,529
|
6,610
|
5,093
|
Arecor Therapeutics plc
INTERIM RESULTS FOR THE SIX MONTHS ENDED 30 JUNE
2024
Notes to the financial information
COMPANY INFORMATION
Arecor Therapeutics plc ("Arecor" or
the "Company") is a public limited company registered in England
and Wales at Chesterford Research Park, Little Chesterford, Saffron
Walden, CB10 1XL with registered number 13331147.
The principal activity of the Company
is to act as a holding company. The Group has two wholly owned
trading subsidiaries; Arecor Limited and Tetris Pharma
Ltd.
Tetris Pharma Ltd and its wholly
owned subsidiary Tetris Pharma B.V were acquired on 4th August
2022.
1. CHANGE IN ACCOUNTING POLICY AS
RESTATEMENT OF PRIOR YEAR INTERIM COMPARATIVE
The accounting policy relating to
the treatment of Research and Development Expenditure Credits
(RDEC) has changed to align with recommended practice. The change
in accounting policy has been adopted during the year ended 31
December 2023, with the prior mid-year comparatives also
restated.
Previously, both RDEC and the Small
and Medium Entity (SME) R&D tax relief scheme were reported in
the Income Statement as Taxation. RDEC claims are now reported
gross of any tax due as other income. The corresponding corporation
tax payable on this income is also reflected within the taxation
line. This change has no impact on the statement of financial
position, therefore an additional statement of financial position
showing the impact of this change, as prescribed in IAS 1 paragraph
40A, is not required.
By enacting this change, a balance
of £0.47 million is reported as Other income for the period ended
30 June 2023. The restated prior year other income balance has
increased by £0.47 million with a corresponding reduction in the
taxation line. As the financial statements for the year ended 31
December 2023 were prepared on the revised basis, no restatement of
this comparative is required.
2. BASIS OF PREPARATION
The financial statements for the
period ended 30 June 2024 incorporate the results of Arecor
Therapeutics plc and its trading subsidiaries. The consolidated
interim financial statements for the period to 30 June 2024 are
unaudited and were approved by the board of directors on 25
September 2024.
The consolidated interim financial
statements have been prepared in accordance with the AIM rules for
Companies and should be read in conjunction with the Group's Annual
Report for the Year ended 31 December 2023. The financial
information has been prepared on the basis of IFRS that the
Directors expect to be applicable at 31 December 2024.
The financial information contained
in these interim financial statements does not constitute statutory
accounts as defined in section 434 of the Companies Act 2006. These
interim financial statements do not include all of the information
and disclosures required in the annual financial statements. The
financial information for the six months ended 30 June 2024 and 30
June 2023 is unaudited.
Financial statements for year ended
31 December 2023 have been filed with the Registrar of Companies
for Arecor Therapeutics plc (Company registration number 13331147).
The audit report for this period, previously filed, was
unmodified.
All intra-Group transactions,
balances, income and expenses have been eliminated in full on
consolidation.
The financial information is
presented in Sterling, which is the functional currency of the
Group and has been rounded to the nearest £000.
3. PRINCIPAL ACCOUNTING
POLICIES
The interim financial statements
have been prepared in accordance with the accounting policies set
out in the audited financial statements for the period ended 31
December 2023 and IFRS. There have been no changes to the
accounting policies or the application of the accounting standards
during the period of review.
a) Going Concern
The Directors have reviewed current
cash and short- term investments together with forecast receivables
to support forecast operating expenditure and planned investment in
R&D. Sensitivities included the impact of reduced receivables
and mitigating actions. The review indicated that in potential
downside scenarios, cash flow forecasts extended to a period beyond
12 months from the date of approval of the consolidated interim
results.
In reaching their decision to
prepare these unaudited interim financial statements on a going
concern basis, the Directors have a reasonable expectation that the
Group has adequate resources to continue in operational existence
for the foreseeable future.
Accordingly, they continue to adopt
the going concern basis in preparing these unaudited interim
financial statements.
4. REVENUE AND OPERATING
SEGMENTS
|
Period ended 30 June
2024
|
Period
ended 30 June 2023
|
Year ended
31 December 2023
|
|
£000
|
£000
|
£000
|
UK
|
1,267
|
1,190
|
2,893
|
The Netherlands
|
191
|
-
|
-
|
Germany
|
95
|
79
|
332
|
Switzerland
|
203
|
77
|
488
|
Italy
|
54
|
-
|
274
|
Rest of Europe
|
-
|
45
|
-
|
USA
|
185
|
248
|
556
|
India
|
-
|
30
|
30
|
Total revenue
|
1,995
|
1,669
|
4,573
|
Operating segments are reported in a
manner consistent with the internal reporting provided to the chief
operating decision makers. Information reported includes revenue by
project, expenditure by type and department, cashflows and EBITDA
for the Group.
The Board of Directors has been
identified as the chief operating decision makers, who are
responsible for allocating resources, assessing the performance of
the operating segment and making strategic decisions. Accordingly,
the Directors consider there to be a single operating
segment.
|
Period ended 30 June
2024
|
Period
ended 30 June 2023
|
Year ended
31 December 2023
|
|
£000
|
£000
|
£000
|
Formulation development
projects
|
383
|
342
|
923
|
Milestones from licence
agreements
|
-
|
108
|
683
|
Royalties
|
203
|
-
|
26
|
Total revenue recognised from contracts with
customers
|
586
|
450
|
1,632
|
Sale of pharmaceuticals
|
1,409
|
1,219
|
2,941
|
Total revenue
|
1,995
|
1,669
|
4,573
|
Revenue from formulation development
projects has been recognised as the performance obligations set out
in agreements are satisfied over time.
Revenue from Milestones defined in
license agreements has been recognised when a milestone is
achieved.
Sales of pharmaceuticals are product
sales which have been recognised as the rights and obligations
pertaining to those items are transferred to the buyer.
5. SALES, GENERAL AND ADMINISTRATIVE
COSTS
Operating expenditure which is not
considered as Research and Development is treated as Sales, General
and Administrative costs. This includes Finance, HR, Administrative
and sales and marketing and Business Development teams, building
facilities, sale of pharmaceutical products and costs relating to
the Board of Directors.
6. SHARE BASED
COMPENSATION
The Company operates an All-Employee
Share Option Plan (AESOP) and grants share options to eligible
employees. The options vest over time.
The Company's Long Term Incentive
Plan (LTIP) is principally used to grant options to Executive
directors and senior management. The LTIP options vest after three
years subject to meeting performance criteria as defined in the
option agreement. These can be a combination of both
operational objectives and share price performance compared to a
benchmark. These performance conditions are approved by the Board
on each occasion prior to the grant of the options. Ordinary shares
acquired on exercise of the LTIP options are subject to a holding
period of a minimum of one year from the date of
vesting.
The movement in share options in the
period was as follows:
|
Number of
Options
|
Balance at 1 January 2023
|
1,627,803
|
AESOP options granted
|
86,250
|
LTIP options granted
|
190,000
|
AESOP options exercised
|
(7,471)
|
Options lapsed
|
(235,167)
|
Balance at 30 June 2023
|
1,661,415
|
AESOP options granted
|
-
|
LTIP options granted
|
-
|
AESOP options exercised
|
(1,332)
|
Options lapsed
|
(1,750)
|
Balance at 31 December 2023
|
1,658,333
|
AESOP options granted
|
382,250
|
LTIP options granted
|
540,000
|
AESOP options exercised
|
-
|
Options lapsed
|
(695,333)
|
Balance at 30 June 2024
|
1,885,250
|
Shared Based Payment charges to the Statement of Comprehensive
Income
|
£000
|
Period to June 2024
|
118
|
Period to June 2023
|
263
|
Year to December 2023
|
638
|
7. FINANCE
EXPENSES
In the period ended 30 June 2024,
the finance expenses of £12,000 were interest costs on finance
leases (period ended 30 June 2023: £10,000).
8. TAXATION
|
Period ended 30 June
2024
|
Period
ended 30 June 2023
|
Year ended
31 December 2023
|
|
£000
|
£000
|
£000
|
R&D Tax credit
receivable
|
151
|
226
|
458
|
Total taxation
|
151
|
226
|
458
|
On 1 April 2023 the UK Government's
rates of tax relief for loss making SME R&D tax credits
decreased from 14.5% to 10%. On the same date, the tax relief for
the RDEC scheme increased from 13% to 20%. The Group utilises both
schemes and has calculated the balance receivable based on the
applicable rates for expenditure incurred before and after the date
of transition.
9. EARNINGS PER SHARE
Basic earnings per share is
calculated by dividing the loss attributable to ordinary
shareholders by the
weighted average number of ordinary
shares outstanding during the period.
Given the Company's reported loss
for the periods and financial year, share options were not taken
into account when determining the weighted average number of
ordinary shares in issue during the year as they would be
anti-dilutive, and therefore the basic and diluted loss per share
are the same.
Basic and diluted loss per
share
|
Period
ended
30 June
2024
|
Period
ended
30
June
2023
|
Year
ended
31
December 2023
|
|
|
|
|
Loss for the period
(£000)
|
(4,640)
|
(4,528)
|
(8,554)
|
Weighted average number of ordinary
shares (number)
|
30,626,986
|
30,619,091
|
30,622,622
|
Loss per share from continuing
operations (£ per share)
|
(0.15)
|
(0.15)
|
(0.28)
|
10. TRADE AND OTHER
RECEIVABLES
Current Assets
|
Period ended 30 June
2024
|
Period
ended 30 June 2023
|
Year ended
31 December 2023
|
|
£000
|
£000
|
£000
|
Trade receivables
|
1,625
|
3,688
|
2,268
|
Other receivables
|
91
|
175
|
102
|
Amounts receivable from
employees
|
-
|
-
|
129
|
Accrued income
|
136
|
-
|
87
|
Grant receivables
|
-
|
423
|
280
|
Prepayments
|
902
|
385
|
323
|
Total Trade and other receivables
|
2,753
|
4,671
|
3,189
|
Non-Current Assets
|
Period ended 30 June
2024
|
Period
ended 30 June 2023
|
Year ended
31 December 2023
|
|
£000
|
£000
|
£000
|
Other receivables
|
69
|
48
|
77
|
Total Trade and other receivables
|
69
|
48
|
77
|
Trade receivables for pharmaceutical
products are gross of rebates payable to wholesalers. Rebates are
reported in Trade payables and accruals.
11. CASH AND CASH EQUIVALENTS AND
SHORT TERM INVESTMENTS
|
Period ended 30 June
2024
|
Period
ended 30 June 2023
|
Year ended
31 December 2023
|
|
£000
|
£000
|
£000
|
Cash and cash equivalents
|
2,529
|
6,610
|
5,093
|
Short term investments
|
16
|
1,619
|
1,659
|
Total cash, cash equivalents and short term
investments
|
2,545
|
8,229
|
6,752
|
Short term investments relate to
balances held in either fixed term accounts with a six-month
maturity or notice accounts with a 95 day notice period.
All significant cash, cash
equivalents and short-term investments are deposited in the UK with
large international banks.
12. TRADE AND OTHER
PAYABLES
Current liabilities
|
Period ended 30 June
2024
|
Period
ended 30 June 2023
|
Year ended
31 December 2023
|
|
£000
|
£000
|
£000
|
Trade payables
|
2,268
|
2,779
|
2,246
|
Other tax and social
security
|
159
|
123
|
100
|
Other creditors
|
245
|
1,172
|
192
|
Contract liabilities
|
202
|
682
|
232
|
Accruals
|
1,677
|
1,498
|
2,133
|
Total Trade and other payables
|
4,551
|
6,254
|
4,903
|
The growth in Trade payables and
Accruals include rebate amounts due to wholesalers on the sales of
pharmaceutical products by Tetris Pharma Ltd.
Other creditors of £1.2 million
includes VAT payable and stock provisions which were nil in the
prior period ended 30 June 2022.
13. EQUITY
Share Capital
|
At 30 June
2024
|
At 30 June
2023
|
At 31 December
2023
|
|
Number
|
Number
|
Number
|
Allotted, called up and fully paid
|
|
|
|
Ordinary shares of £0.01
|
30,626,986
|
30,625,654
|
30,626,986
|
|
|
|
|
Total share capital
|
30,626,986
|
30,625,654
|
30,626,986
|
|
|
|
|
|
At 30 June
2024
|
At 30 June
2023
|
At 31 December
2023
|
|
£'000
|
£'000
|
£'000
|
Allotted, called up and fully paid
|
|
|
|
Ordinary shares of £0.01
|
306
|
306
|
306
|
|
|
|
|
Total share capital
|
306
|
306
|
306
|
14. EVENTS AFTER THE BALANCE SHEET
DATE
In accordance with a Sale and
Purchase Agreement dated 1st August 2022, the
acquisition of Tetris Pharma Ltd included contingent consideration
of three earn out payments, which may become payable on the first,
second and third anniversary following completion. The second
earn out payment was subject to Tetris Pharma Ltd achieving
low-double-digit million-pound net sales and a low single-digit
million-pound EBITDA profit in the period 13-24 months following
completion. Earn out accounts were prepared by an independent
accountant and have been provided to the previous shareholders of
Tetris Pharma Ltd. The earn out accounts determined that the
first earn out target was not achieved and therefore contingent
consideration of £1,500,000 for the second earn out period was not
payable.
On 8 August 2024, Arecor
Therapeutics successfully completed a fundraising round of £6.4
million (before expenses) from new and existing shareholders. These
funds will be made available to the subsidiaries within the group
to enable continuation of R&D activities and growth of
sales.
15. COPIES OF THE INTERIM REPORT
Copies of the consolidated interim
financial statements are available to the public free of charge
from the Company at Chesterford Research Park, Little Chesterford,
Saffron Walden, CB10 1 XL during normal business hours for 14 days
from today.
Copies are also available on the
Company's website at www.arecor.com.