19 September 2024
CRISM Therapeutics
Corporation
("CRISM",
"CRISM Therapeutics" or the "Company" or the "Group")
Half Year
Report
CRISM Therapeutics Corporation (AIM:
CRTX), the innovative UK drug delivery
company focused on the localised delivery of chemotherapy drugs,
today announces its Interim Results for the six
months ended 30 June 2024 (the "Period").
Highlights & Background
· Admitted to AIM on 31 May 2024, following
the Reverse Takeover of Amur Minerals Corporation by Extruded
Pharmaceuticals Limited (the "Reverse Takeover"), changing name to
CRISM Therapeutics Corporation
· Reverse Takeover providing funds of
approximately £1.95 million (after transaction costs), as of 30
June 2024 the Company held £1,862,000 in cash
· Funds will be utilised for the
preparation of a Phase 2 clinical trial, with clinical trial
authorisation ("CTA") submission on course for H2 2024 and trial
commencement in Q4 2025
· New Board appointed on Admission
comprising a combination of expertise in R&D, commercialisation
in healthcare and public markets
· CRISM has developed an innovative drug
delivery technology, ChemoSeed®
· ChemoSeed is an
implantable biodegradable drug delivery technology designed for the
sustained delivery of chemotherapy directly into cancer tissue
improving clinical performance
· Initial therapeutic focus is in high
grade glioma (brain tumour) owing to the very significant unmet
need and attractive market, valued at £1.7 billion
· ChemoSeed has an attractive risk profile
owing to using pre-approved chemotherapy drugs such as
irinotecan
· Assuming no need for further toxicology
studies, conditional marketing authorisation would be expedited and
reduce costs of development by £400,000
· Based on preclinical
data, the Tessa Jowell BRAIN MATRIX SAB has approved ChemoSeed in a
Phase 2 platform (open label) clinical trial, providing an
efficient and cost-effective clinical development
opportunity
· The Company intends to
demonstrate ChemoSeed's potential as a platform for other cancers
such as pancreatic, bladder and prostate.
Post
Period End Highlights
· CRISM's
drug formulation expertise was validated on 30 July 2024, by the
signing of a service agreement with UK biotech company imphatec
Limited ("imphatec") for approximately £230,000, providing the
Company with additional revenue
· In
September 2024, CRSIM was awarded an Innovation Passport from the
MHRA as part of the Innovative Licensing and Access Pathway
Programme ("ILAP"), which recognises ChemoSeed as an innovative
technology in an area of unmet medical need and will enable the
Company to benefit from expedited and increased access to medical,
regulatory and scientific stakeholders
· Received
£25,000 in Grant Funding from SPARK the Midlands (supported by
Innovate UK and the West Midlands Combined Authority), recognising
the unmet medical need that CRISM is addressing
· CRISM's
drug delivery approach to administer irinotecan locally into the
resection margin was validated on 3 September 2024 with the
publication of a peer reviewed research article in journal,
Cancers.
https://www.mdpi.com/2072-6694/16/17/3008
Commenting on the Interim Results, CRISM CEO Andrew Webb
said: "We were pleased to complete the Reverse
Takeover of Amur Minerals and since CRISM has become a listed
entity, the Company has made good progress across its strategic
goals. We remain on track with our principal short term
strategic goal which is to submit a clinical trial authorisation
for ChemoSeed in high grade glioma by the end of this
year.
"Since the period end, the Company was awarded an Innovation
Passport from the MHRA which we believe to be a significant
developmental milestone and validates ChemoSeed to potentially
enhance the lives of brain tumour patients as well as provide a
quicker route to market. In
addition, and as part of our stated strategy, the Company signed a
service agreement with imphatec which will provide welcome
near-term revenue. Generating near term revenues by utilising
our drug formulation expertise remains an important part of our
strategy and CRISM Therapeutics remains in discussion with other
biotech companies to utilise our formulation expertise.
"We are optimistic about CRISM's prospects, and believe our
proposition is attractive owing to our favourable risk profile by
using pre-approved drugs such as irinotecan as well our support
from organisations such as the MHRA and Tessa Jowell BRAIN MATRIX.
Finally, I would like to thank shareholders for their support, and
we look forward to keeping the market up to date with our
progress."
-Ends-
Enquiries:
Company
|
Nomad and
Broker
|
Financial
PR
|
CRISM Therapeutics
Corporation
|
S.P. Angel Corporate Finance
LLP
|
Burson
Buchanan
|
Andrew
Webb, CEO
Chris
McConville, CSO
|
Richard
Morrison
Adam
Cowl
|
Mark
Court / Jamie Hooper
CRISM@buchanancomms.co.uk
|
via
Burson Buchanan
|
+44 (0)
20 3470 0470
|
+44 (0)
20 7466 5000
|
About CRISM Therapeutics Corporation
CRISM Therapeutics Corporation has
developed an innovative drug delivery technology to improve the
clinical performance of cancer treatments for solid tumours through
the local delivery of chemotherapy drugs.
ChemoSeed, CRISM's lead product, can
be implanted directly into the tumour or the resection margin
following the removal of a tumour. This directs that therapeutic
concentrations of chemotherapy drugs reach the deep-seated tumour
tissue or cover the entire resection margin. In the case of
treating high-grade glioma, ChemoSeeds can be implanted during
surgery thereby bypassing the blood brain barrier, which prevents
other treatments from being able to reach the tumour and be
effective.
CRISM plans to submit a clinical
trial authorisation submission in H2 2024 for ChemoSeed® in
high-grade glioma.
Based on preclinical data, the Tessa Jowell BRAIN MATRIX Scientific
Advisory Board has approved ChemoSeed in a Phase 2 platform
clinical trial which is an efficient and cost-effective clinical
development opportunity.
For more information please
visit: https://www.crismtherapeutics.com/
CEO
REPORT
Introduction
It is a privilege to present my
first CEO Statement for CRISM Therapeutics for the six-month period
ended 30 June 2024.
CRISM began trading on AIM following
the Reverse Takeover of Amur Minerals Corporation by Extruded
Pharmaceuticals Limited on 31 May 2024 ("Readmission"). The
Company's name was changed to CRISM Therapeutics Corporation at
that time and the name of Extruded Pharmaceuticals Limited was
subsequently changed to CRISM Therapeutics Limited.
Consequently, these interim financial statements present results
for the Group for the period from Readmission to 30 June 2024,
combined with the results of CRISM Therapeutics Limited for the
period 1 January 2024 to 31 May 2024.
The Group comprises CRISM
Therapeutics Corporation, CRISM Therapeutics Limited and a dormant
Cypriot subsidiary, Irosta Trading Limited, historically set-up to
hold Amur Minerals Corporation's Russian mining assets, which were
disposed of in March 2023. The directors are in the process of
liquidating Irosta Trading Limited.
Background
CRISM is a UK-based pharmaceutical
company which has developed an innovative drug delivery technology,
ChemoSeed, to improve the clinical performance of cancer treatments
for solid tumours through the local delivery of chemotherapy.
ChemoSeed is a polymer the size of a grain of rice, administering
irinotecan, a generic drug approved to treat brain cancer and can
be implanted directly into a tumour or the resection margin
following the removal of a tumour. ChemoSeed will initially
be used to treat high grade glioma, a type of brain tumour with no
satisfactory treatment. To treat high grade glioma, ChemoSeeds will
be implanted during surgery to bypass the blood brain barrier,
which prevents other treatments from being able to reach the tumour
and be effective.
CRISM operates in a significant
market where brain tumours are the biggest cancer killer of
children and adults under the age of 40. In the UK,
approximately 16,000 new cases are diagnosed annually, with an
estimated 60,000 people living with the condition. Despite this,
just one per cent of cancer research funding has been allocated to
brain tumours since records began in 2002.
ChemoSeed addresses a significant,
unmet medical need in the treatment of high grade glioma. There are
no current cures and present treatments merely seek to extend life,
often by just a few months, with serious adverse side effects. Each
ChemoSeed consists of the pre-approved chemotherapy drug,
irinotecan, and the biodegradable polymer PLGA, both of which have
been previously administered to the brain with no toxicity issues.
The treatment's low side-effect profile, combined with the unmet
medical needs of the target market for ChemoSeed, means CRISM could
potentially receive conditional marketing authorisation in the UK
on the back of positive Phase 2 clinical trial data. This
authorisation could be received as early as 2028, therefore
reducing the time and cost to commercialisation of irinotecan
loaded ChemoSeeds for high-grade glioma and bringing a new
treatment to the market for a serious unmet medical
need.
Intellectual Property (IP) Development
CRISM recognises the importance of
obtaining and protecting the Company's intellectual property and
the necessary intellectual property for ChemoSeed has been assigned
to CRISM. As of 30 June 2024, the Company has a pending UK
application and international applications filed in the EU, USA,
China and Japan.
People and Organisation
The Directors of CRISM are cognisant
of the importance of minimising CRISM's overheads given its stage
of development and as such the Group's management team continues to
outsource a number of functions including contract development,
clinical research and certain administrative functions.
Consequently the only employees of the Company are its four
directors.
Financial Review
As a result of the Reverse Takeover
of Amur Minerals Corporation by Extruded Pharmaceuticals Limited,
the Company acquired cash balances of approximately £1.95
million. These funds are being used to progress a clinical
trial authorisation submission, cover regulatory and
submission costs and to provide working capital for the
Company.
The Reverse Takeover and Readmission
are important steps in the Company executing its research and
development strategy, giving it access to future funding which will
support the Company's journey towards clinical trials, and then to
drug commercialisation.
Results
As previously highlighted, these
interim financial statements present results for the Group for the
period from Readmission to 30 June 2024, combined with the results
of CRISM Therapeutics Limited for the period 1 January 2024 to 31
May 2024. The comparative results are that of CRISM Therapeutics
Limited.
The Group recognised a loss for the
Period of £13,000 (H1 2023: £135,000). In the first half of 2024,
administration expenses amounted to £300,000 (H1 2023: £118,000),
which includes research and development of £75,000, consulting fees
of £105,000, and professional fees of £77,000. The Company also
recognised a gain on the forgiveness of Director loans totalling
£298,000 (H1 2023: £nil). As of 30 June 2024, the Company
held £1,862,000 in cash (December 31, 2023: £1,000). The cash
balances are anticipated to provide the Company with sufficient
resources to fund the ongoing costs of its clinical trial
submission and working capital requirements.
Post Period-End Events
On 30 July 2024, CRISM signed an
agreement to provide formulation development services to imphatec
Limited, a private UK biotech company, with a value of
approximately £230,000. This agreement is in line with CRISM's
strategy to leverage its drug formulation expertise by winning
service contracts to generate near term revenues, and the Company
is seeking to sign further similar revenue generating service
contracts. In addition to the imphatec service contract, the
Company secured £25,000 in grant funding from SPARK which
recognises the unmet medical need CRISM is addressing.
The Company announced on 2 September
2024, the award of an Innovation Passport from the MHRA for
ChemoSeed in high grade glioma as part of the MHRA's Innovative
Licensing and Access Pathway programme.
The Company believes this to be a
significant milestone in the development of ChemoSeed as it aims to
accelerate the development of innovative technologies in an area of
unmet need. The Innovation Passport will enable CRISM
to benefit from expedited and increased access to key stakeholders
in the medical, scientific and regulatory communities.
ChemoSeed will benefit further from the ILAP programme, with the
next stage being the creation of a Target Development Profile which
sets out to establish the optimal approach for the clinical
development of ChemoSeed.
Outlook
CRISM has enjoyed a positive start
as an AIM quoted company, having achieved a few important
milestones, namely the award of the Innovation Passport from the
MHRA as well as the signing of a service contract with imphatec
Limited, as such the Board views CRISM's future prospects with
optimism.
The directors believe that CRISM has
developed a unique drug delivery system in ChemoSeed. Given the
large addressable market, in brain tumours, the Company is
optimistic that ChemoSeed has the potential to disrupt current drug
delivery systems and improve the standard of care for many brain
tumour patients across multiple geographical markets. A critical
objective in this phase of CRISM's development is the submission of
the CTA before the end of 2024 and commencement of clinical trials
in Q4 2025, which the Company remains on track to
do.
CRISM's focus is on achieving the
key milestones that are set out in the Admission Document. CRISM
continues to evaluate additional indications and other initiatives
that may enhance the Group's potential for commercial success and
shareholder value.
Andrew Webb
Chief Executive Officer
18 September 2024
CRISM THERAPEUTICS CORPORATION
(FORMERLY AMUR MINERALS CORPORATION)
NOTES TO THE INTERIM
REPORT
FOR THE six months ENDED 30 June
2024
(Amounts in thousands of GBP)
1.
Reporting Entity
CRISM Therapeutics Corporation
(formerly Amur Minerals Corporation) (the "Company") is a company
domiciled in the British Virgin Islands. The consolidated interim
financial information as at and for the six months ended 30 June
2024 comprise the results of the Company and its subsidiaries
(together referred to as the "Group").
The Group has a principal activity
being a biotechnology company, focused on the development of
innovative drug delivery technology to improve the clinical
performance of cancer treatments for solid tumours through the
local delivery of chemotherapy drugs.
2.
BASIS OF
PREPARATION
The financial information set out in
this report is based on the consolidated financial information of
CRISM Therapeutics Corporation and its subsidiary companies. The
financial information of the Group for the 6 months ended 30 June
2024 was approved and authorised for issue by the Board on 18
September 2024. The interim results have not been audited.
This financial information has been prepared in accordance with the
accounting policies that are expected to be applied in the Report
and Accounts of CRISM Therapeutics Corporation for the year ended
31 December 2024 and are consistent with the recognition and
measurement requirements of IFRS as issued by the International
Accounting Standards Board ("IASB") and interpretations issued by
the International Financial Reporting Interpretations Committee
("IFRIC").
The comparative amounts are CRISM
Therapeutics Limited (formerly known as Extruded Pharmaceuticals
Limited) for the year ended 31 December 2023 and for the 6-month
period ended 30 June 2023. See note 3 for explanation.
The Group financial information is
presented in GBP and values are rounded to the nearest thousand
Pound. The Group changed its functional and presentation currency
from US Dollars to Sterling during the period. Further information
has been included in note 5.
The same accounting policies,
presentation and methods of computation are followed in the interim
consolidated financial information as were applied in the Group's
latest annual financial statements except for those disclosed at
notes 3 to 5, which have been newly adopted.
New standards and interpretations
effective for the first time for periods beginning on (or after) 1
January 2024 have been determined by management to have no impact
on these interim financial statements,
3.
SHARE BASED
PAYMENTS - REVERSE ACQUISITION
On 29 May 2024, the Company acquired
CRISM Therapeutics Limited (formerly Extruded Pharmaceuticals
Limited) via a reverse takeover which resulted in the Company
becoming the ultimate holding company of the Group. The transaction
was accounted for as a reverse acquisition since it did not meet
the definition of a business combination under IFRS 3. In
accordance with IFRS 2, a share-based payment expense equal to the
deemed cost of the acquisition less the fair value of the net
assets of the Company at acquisition was recognised. The
comparatives within the consolidated statement of financial
position, the consolidated statement of comprehensive income,
consolidated statement of changes in equity and the consolidated
cashflow statement represent that of the legal subsidiary and
accounting acquirer, CRISM Therapeutics Limited for the
periods-ended 30 June 2023 and 31 December 2023. In the
consolidated statement of financial position, the share capital and
premium as at 30 June 2024 is that of CRISM Therapeutics
Corporation with the reverse acquisition reserve representing the
difference between the deemed cost of the acquisition and the net
assets of CRISM Therapeutics Corporation (formerly Amur Minerals
Corporation) as at 29 May 2024. The consolidated statement of
comprehensive income for the 12-month period to 30 June 2024
represents the results of both CRISM Therapeutics Corporation and
CRISM Therapeutics Limited. For more details on the key terms of
the reverse takeover ("RTO") and a breakdown of what the reverse
acquisition reserve as of 30 June 2024 comprises, see note
9.
4.
INTANGIBLE
ASSETS
IAS 38 Intangible Assets requires
management to differentiate between research and the development
phase of R&D activities and their related costs (including
patent costs). In accordance with IAS 38, an intangible asset
arising from development shall be recognised if, and only, if, an
entity can demonstrate certain criteria. The Board continually
monitors its activities against the prescribed criteria to
determine the point in which the Group would enter the development
phase of its activities. The entity is currently in the phases of
formulation, design and evaluation of its product and therefore
management is confident that the entity is in the research phase.
As a result, any expenditure arising regarding patent costs are
expensed in the Statement of Comprehensive Income.
5.
CHANGE IN
FUNCTIONAL AND PRESENTATIONAL CURRENCY
On 29 May 2024 the functional and
the presentation currency of the Group changed from US Dollars to
Sterling. The change in functional currency was aligned with that
of the Group's operating subsidiary, CRISM Therapeutics Ltd and was
deemed to better represent the core activities of the
Group.
Ordinarily, and in accordance with
IAS 21 "The Effects of Changes in Foreign Exchange Rates", a change
in the presentational currency of an entity should be applied
retrospectively and results in a restatement of the prior period
results presented into the new presentational currency. However,
after applying the requirements of IFRS 2 in respect of reverse
acquisition accounting principles, the prior period results of the
Company have not been presented. The only restatement required is
that of the Company's share capital and share premium which has
been restated per IFRS 2 & IAS 21 due to the aforementioned
reserve acquisition which occurred on the 29 May 2024, the opening
balances have further been restated for the change in accounting
currency from USD to GBP which is the functional currency of the
group post RTO and as such represents the ongoing functional
currency of the group.
A change in functional currency is
applied prospectively from the date of the change.
In accordance with the guidance
defined in IAS 21 "The Effects of Changes in Foreign Exchange
Rates", the results of CRISM Therapeutics Corporation have been
translated to Sterling as follows:
o Assets and liabilities were translated into Sterling at
closing rates of exchange.
o Trading results were translated into Sterling at average rates
of exchange for the period. Differences resulting from the
re-translation on the opening net assets and the results for the
year have been taken to the foreign currency translation reserve
(FCTR);
o Share capital, share premiums and other reserves were
translated at historic rates prevailing at the dates of
transactions; and
o All
exchange rates used were extracted from the Group's underlying
financial records.
The exchange rates used were as
follows:
Balance sheet (31 December
2023)
|
USD:GBP
|
1.27303
|
Profit and loss (2023
average)
|
USD:GBP
|
1.2436
|
6.
GOING
CONCERN
On 29 May 2024 the Company completed
the acquisition of CRISM Therapeutics Ltd for aggregate
consideration of £5.5 million, satisfied by the issue of 23,939,986
New Ordinary Shares. On the date of the Readmission, the Company
had cash on hand of £2.356m, of which a large portion has been
retained and will facilitate the Group's planned research and
development activity.
The Directors have reviewed the
Group's cash flow forecasts and believe the Group has sufficient
cash resources to cover planned and committed expenditures over the
period to 30 September 2025. Significant expenditure will be
required to fund the Group's activities to the stage of generating
commercial revenues. Consequently, the Group will require
further funding by way of equity issues to new and existing
investors and additional grant funding.
The Directors are confident that
throughout the going concern forecast period the Group will have
sufficient funds to meet obligations as they fall due, and thus,
the Directors continue to prepare the consolidated financial
statements on a going concern basis.
7.
LOSS PER
SHARE
Basic and diluted loss per share is
calculated and set out below. The effects of warrants and share
options outstanding at the period end are anti-dilutive as they
will serve to reduce the loss per share.
|
Unaudited
6 Months
ended
30 June
2024
|
|
Unaudited
6 Months
ended
30 June
2023
|
|
Unaudited
Year ended
31 December
2023
|
|
|
|
|
|
|
Net loss
for the year attributable to equity shareholders (expressed in
£'000)
|
(13)
|
|
(135)
|
|
(196)
|
|
|
|
|
|
|
Weighted
average number of shares for the period/year
|
6,075,521
|
|
16,000
|
|
16,000
|
|
|
|
|
|
|
Basic loss per
share
|
£ (0.002)
|
|
£ (8.438)
|
|
£ (12.250)
|
8. TRADE AND OTHER PAYABLES
|
Unaudited
6 Months
ended
30 June
2024
|
Unaudited
6 Months
ended
30 June
2023
|
Unaudited
Year ended
31 December
2023
|
Trade payables
|
151
|
-
|
-
|
Director's loans
|
-
|
286
|
304
|
Accruals
|
79
|
4
|
8
|
Other payables
|
121
|
17
|
23
|
Total trade and other payables
|
351
|
307
|
335
|
Other payables as at 30 June 2024
included £86,000 of unclaimed dividends.
Prior to the completion of the RTO,
the Directors of CRISM Therapeutics Ltd agreed to waive all amounts
owed to them, resulting in the forgiveness of Directors loans
amounting to £298,000.
9. Reverse
acquisition
On 29 May 2024, the Company acquired
the entire issued and to be issued share capital of CRISM
Therapeutics Ltd. Although the transaction resulted in CRISM
Therapeutics Ltd becoming a wholly owned subsidiary of the Company,
the transaction constituted a reverse acquisition, as the previous
shareholders of CRISM Therapeutics Ltd own a substantial majority
of the Ordinary Shares of the Company and the executive management
of CRISM Therapeutics Ltd became the executive management of the
Company.
In substance, the shareholders of
CRISM Therapeutics Ltd acquired a controlling interest in the
Company and the transaction will therefore be accounted for as a
reverse acquisition.
The acquisition cost of CRISM
Therapeutics Ltd was £5,500,000. The consideration for the
transaction was satisfied by the issue and allotment of a total of
23,939,986 Consideration Shares to the shareholders of CRISM
Therapeutics Limited (the "Sellers"), such shares having an implied
issue price of £0.23.
Because the legal subsidiary, CRISM
Therapeutics Limited (formerly Extruded Pharmaceuticals Limited),
was treated on consolidation as the accounting acquirer and the
legal Parent Company, CRISM Therapeutics Corporation (formerly Amur
Minerals Corporation), was treated as the accounting subsidiary,
the fair value of the shares deemed to have been issued by CRISM
Therapeutics Limited, was calculated at £1,004,889 using the number
of CRISM Therapeutics Corporation shares held by the current
shareholders at the date of acquisition (8,738,164 shares),
multiplied by the closing share price of CRISM Therapeutics
Corporation on the date of RTO (£0.115).
According to IFRS 2 the value of the
share-based payment is calculated as the difference between the
deemed cost and the fair value of the net assets as at acquisition.
The following reflects these figures as at 29 May 2024;
|
£
|
Deemed Cost
|
1,004,889
|
|
|
Current assets
|
2,755,808
|
Current liabilities
|
(529,755)
|
Fair value of assets
acquired
|
2,226,053
|
Deemed bargain purchase
|
1,221,164
|
The difference between the deemed
cost (£1,004,889) and the fair value of the net assets assumed per
above of £2,226,053 resulted in £1,221,164 being a deemed bargain
purchase in accordance with IFRS 2, Share-based Payments,
reflecting the economic gain to CRISM Therapeutics Limited
shareholders of acquiring a cash shell and of obtaining a listing.
This amount was taken to the merger reserve.
The reverse acquisition reserve
which arose from the reverse takeover is made up as
follows;
|
£
|
|
Pre-acquisition retained losses
(a)
|
(55,318,626)
|
CRISM Therapeutics Limited share
capital at acquisition (b)
|
496,726
|
Investment in CRISM Therapeutics
Limited (c)
|
(5,500,000)
|
Deemed bargain purchase
|
(1,221,164)
|
|
(61,543,064)
|
|
|
|
|
(a) Recognition of
pre-acquisition retained losses of CRISM as at 29 May
2024
(b) CRISM Therapeutics
Limited had issued share capital of £115 and share premium of
£496,661. As the financial statements present the capital structure
of the legal parent entity, the equity of CRISM Therapeutics
Limited is eliminated.
(c) The value of shares
issued by CRISM Therapeutics Corporation in exchange for the entire
share capital of CRISM Therapeutics Limited. The above entry is
required to eliminate the Statement of Financial Position impact of
this transaction.
10. BORROWINGS
In January 2022 CRISM Therapeutics Limited entered
into a convertible loan note ("CLN") agreement for up to £250,000,
of which £80,000 was drawn. The loan was unsecured, bore 6% simple
annual interest and was repayable two years after the advance. Upon
a conversion event, the investor can elect to convert the
outstanding advance into ordinary shares of the Company at a
discount of 25% to the price of the conversion round. In accordance
with the agreement the investors were also issued with a total of
57 warrants with an expiry date of ten years and a strike price of
200% above the price on conversion of the CLNs.
In accordance with IAS 32, it was
determined that the warrants attached to the 27 January 2022 CLNs
should be classified as a derivative liability, however it was
further assessed that the warrants were closely related to their
non-derivative host and should be accounted together with the host
contract.
In December 2022 the Company entered
into a convertible loan note ("CLN") agreement for up to £300,000,
of which £275,000 was drawn. The loan was unsecured, bore 10%
simple annual interest and was repayable two years after the
advance. Upon a conversion event, the investor can elect to convert
the outstanding advance into ordinary shares of the Company at a
discount of 25% to the price of the conversion round. There were no
warrants attached to the instrument.
The RTO constituted a conversion
event and on 23 April 2024, prior to the completion of the RTO, the
CLN holders converted all outstanding CLNs and outstanding interest
into new ordinary Shares of £0.01 each in the capital of CRISM
Therapeutics Limited. This resulted in 1,012 additional shares
being issued at the conversion price of £390 per share.
|
Unaudited
6 Months
ended
30 June
2024
|
|
Unaudited
6 Months
ended
30 June
2023
|
|
Unaudited
Year ended
31 December
2023
|
|
|
|
|
|
|
Current (Less than 1 year)
|
|
|
|
|
|
|
|
|
|
|
|
Unsecured
non-convertible loan notes
|
-
|
|
87
|
|
89
|
|
-
|
|
87
|
|
89
|
Non-current (More than 1
year)
|
|
|
|
|
|
|
|
|
|
|
|
Unsecured
non-convertible loan notes
|
-
|
|
291
|
|
304
|
|
-
|
|
291
|
|
304
|
Total
borrowings
|
-
|
|
378
|
|
393
|
The movement in convertible loan is
analysed as follows:
|
30 June
2024
|
|
£
|
Convertible loan note
|
|
Proceeds of issue of convertible loan
notes
|
355
|
|
|
Interest
|
|
Opening interest payable - 1 January
2023
|
6
|
Interest charged for the
period
|
32
|
Total interest payable to
date
|
38
|
|
|
Total at 31 December 2023
|
393
|
|
|
Conversion of loan notes - 29 May
2024 (Completion date)
|
(393)
|
|
|
Total at 30 June 2024
|
-
|
|
|
11.
share Capital and share premium
|
|
|
|
|
|
Number of
shares
|
Ordinary
shares
£
|
Share
premium
£
|
Total
£
|
At 1 January 2023
|
100
|
-
|
-
|
-
|
At 31 December 2023
|
100
|
-
|
-
|
-
|
At
1 January 2024
|
100
|
-
|
-
|
-
|
Issue of new shares - 9 February
2024
|
527
|
-
|
102
|
102
|
Conversion of convertible loan notes
- 23 April 2024
|
1,031
|
-
|
395
|
395
|
Reallocation to reverse acquisition
reserve
|
(1,658)
|
(-)
|
(497)
|
(497)
|
Recognition of Company equity
at acquisition of subsidiary - 31 May 2024
|
8,705,289
|
63,464
|
3,360
|
66,824
|
Issue of new shares - 31 May
2024
|
23,939,986
|
5,500
|
-
|
5,500
|
Issue of bonus shares - 31 May
2024
|
32,875
|
8
|
-
|
8
|
At
30 June 2024
|
32,678,150
|
68,972
|
3,360
|
72,332
|
12.
EVENTS AFTER THE REPORTING DATE
On 30 July 2024 CRISM signed an
agreement to provide formulation development services to imphatec
Limited, a private UK biotech company, with a value of
approximately £230,000. In addition to the imphatec service
contract, the Company secured £25,000 grant funding from SPARK
which recognises the unmet medical need CRISM is
addressing.
The Company announced on 2 September
2024, the award of an Innovation Passport from the MHRA for
ChemoSeed in high grade glioma as part of the MHRA's Innovative
Licensing and Access Pathway programme.