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RNS Number : 0409O
Hemogenyx Pharmaceuticals PLC
30 September 2019
 

Hemogenyx Pharmaceuticals plc

("Hemogenyx" or "the Company")

 

Half-year Report

Interim Results for the period ended 30 June 2019

 

Hemogenyx Pharmaceuticals plc (LSE: HEMO), the Standard Listed biopharmaceutical group developing therapies designed to transform blood disease treatment, announces unaudited interim results for the six months ended 30 June 2019.

 

All financial amounts are stated in GBP British pounds unless otherwise indicated.

 

Key highlights

 

CDX bi-specific antibodies

·     First data results show CDX antibodies can attack and eliminate Acute Myelogenous Leukaemia ("AML") both in vitro and in vivo

·     Continued progress towards the goal of submitting an Investigational New Drug ("IND") application to the US Food and Drug Administration ("FDA") for CDX antibodies

·   Preliminary discussions regarding a potential licensing deal are continuing with the global biopharmaceutical company following a Development Agreement announced in May 2018

 

Humanised mice

·    Hemogenyx's wholly owned subsidiary Immugenyx, LLC ("Immugenyx") has developed an Advanced peripheral blood Hematopoietic Chimera ("ApbHC"), a novel type of humanised mouse that presents several advantages over other mouse models

·    Collaboration agreement with Janssen Research & Development, LLC ("Janssen"), one of the Janssen Pharmaceutical Companies of Johnson & Johnson, on the development of a model of systemic lupus erythematosus (SLE) is progressing

·     Immugenyx is in discussions with potential industry partners to further develop and commercialise the humanised mice platform

Human Postnatal Hemogenic Endothelial Cell ("Hu-PHEC") cell therapy

·     Hemogenyx established a wholly owned subsidiary, Hemogenyx-Cell SPRL ("Hemogenyx-Cell") which was incorporated in Belgium on 9 April 2019

·     Hemogenyx-Cell is focused on developing Hu-PHEC, a cell replacement product candidate that aims to generate cancer-free, patient-matched blood stem cells after transplantation into the patient

·     Hemogenyx-Cell continues to consider non-dilutive funding opportunities in relation to the Hu-PHEC suite of products

 

Fuller details on these developments are contained in the Interim Management Report below.

 

Commenting on the Outlook for Hemogenyx, Sir Marc Feldmann, Executive Chairman, said:

"The Board is very pleased with the progress being made with the unlocking of additional opportunities for the CDX antibodies, as well as the potential value that can be created through the Company's updated humanised mouse model. The Company is confident that these novel humanised mice will continue to attract the interest of large biopharmaceutical companies and are proving to be the basis of significant collaborations. The Board believes that the Company is well advanced on the planned development steps for its CDX antibodies that were announced at Admission, and we hope to provide further updates to shareholders as we progress. The Company looks forward to the future with confidence."

 

Interim Management Report

 

Hemogenyx Pharmaceuticals plc is the holding company for Hemogenyx LLC ("Hemogenyx"), a US based biotechnology company developing therapies to transform bone marrow and blood stem cell transplant procedures. The Company is developing products for the multi-billion dollar bone marrow/haematopoietic stem cell transplant market which could replace chemotherapy and radiation as a means of pre-transplant conditioning and treat several types of leukaemia, as well as addressing the problem of stem cell donor availability and issues around relapse or cell rejection after transplantation.

 

These products are:

 

Conditioning product ("CDX antibodies") - CDX bi-specific antibodies which redirect a patient's own immune cells to eliminate unwanted blood stem cells preparing a patient for bone marrow transplantation;

 

Cell therapy product ("Hu-PHEC") - a cell replacement product using Human Postnatal Hemogenic Endothelial Cells to generate cancer-free, patient-matched blood stem cells after transplant into the patient.

 

The Company has also developed a platform technology for disease modelling and drug discovery:

 

Advanced Hematopoietic Chimeras ("AHC") - Hemogenyx has developed a new type of humanised mice to advance the development of its CDX antibodies. The unique properties of the AHC give them a functional human immune system that converts them into a platform technology that is opening up exciting opportunities for the Company. These include disease modelling (blood cancers and severe autoimmune diseases) and pre-clinical testing of novel drugs and treatments. AHC are a source of revenue for the Company via paid collaborations with biopharmaceutical companies and research institutions. In addition, Hemogenyx's wholly owned subsidiary Immugenyx, LLC has developed ApbHC, a novel type of humanised mouse that presents several advantages over other mouse models, as described in further detail in the progress update below. Immugenyx was established by the Company to develop and commercialise the Company's AHC or humanised mice, and the new ApbHC represents a significant further development in that direction.

 

To date, Hemogenyx has made impressive progress on its products whilst efficiently using the Company's limited financial resources. The main focus is to progress the CDX antibodies to readiness for clinical trials, as well as to continue to develop the Hu-PHEC cell therapy product.

 

H1 progress update

 

During the first half of the year, Hemogenyx continued to make progress towards the completion of a development agreement with a global biopharmaceutical company and the goal of submitting an IND (Investigational New Drug) application to the FDA for CDX antibodies.

 

The Company was able to demonstrate that CDX bi-specific antibodies were capable of attacking and eliminating the blood cancer Acute Myelogenous Leukaemia (AML) in vivo, demonstrating that the lead candidate is effective in the treatment of AML. The Company has demonstrated that CDX is capable of conditioning bone marrow transplants in AHC (humanised mice) in vivo. The Company hopes to be able to show that CDX bi-specific antibodies are capable of redirecting a patient's own immune cells to eliminate both AML and blood stem cells, preparing a patient with relapsed/refractory AML for bone marrow transplantation. If successful, this product would be able to complement, or possibly replace, traditional methods of chemotherapy and radiation currently used both in AML treatment and conditioning. The Company has also demonstrated that CDX is capable of eliminating a subset of acute lymphoblastic leukaemia (ALL) cells in vitro.

 

The ApbHC was initially developed as a research and development tool for the investigation of mature blood cell populations such as human T-cells, B-cells and antibody-producing plasma cells. The major advantage of the ApbHC compared to other humanised mouse models known to the Directors is the absence of Graft versus Host Disease (GvHD), a disease that complicates and often renders impossible the efficient use of peripheral blood mononuclear cells in transplanted mice. Hemogenyx has demonstrated that the ApbHC can potentially be used for testing multi-specific antibodies, including its own bi-specific CDX antibody for the elimination of acute myeloid leukaemia (AML) and the conditioning of patients for bone marrow transplantation. ApbHC may also be used for the development and testing of new cell therapies involving immune cell reprogramming, such as CAR-T. Immugenyx has further demonstrated that the ApbHC can potentially be used for the modeling of autoimmune diseases, such as Systemic Lupus Erythematosus (aka Lupus), with a goal of developing fundamentally new treatments for those diseases. The Directors also believe that the ApbHC could potentially be used as a tool for the rapid development and/or isolation of human antibodies against unknown human-specific pathogens (biodefence applications).

 

As with AHC, the Company believes that the ApbHC will be of considerable interest to other drug developers and the initial interest shown is promising.

 

Hemogenyx has primarily focused attention on the CDX antibody product candidate and humanised mouse model but has also taken clear steps to bring forward its Human Postnatal Hemogenic Endothelial Cell ("Hu-PHEC") based suite of product candidates, including the incorporation of Hemogenyx-Cell in April 2019. Hemogenyx-Cell continues to consider non-dilutive funding opportunities for the development of this promising therapy.

 

Financial Results

 

During the six months ended 30 June 2019 the Company recorded a loss of £706,670  (H1 2018: £647,423 loss). The increase in loss from the comparable period in 2018 reflects a continued increase in operational development, and in particular diversification of activities, made possible by the reverse acquisition and fundraising completed in October 2017.

 

The Company recorded consultancy income of £82,763 during the period ended 30 June 2019 (H1 2018: £91,358) which relates to funds received from a third party under a research collaboration programme associated with humanised mice.

 

Outlook

 

Overall the Board is very pleased with the progress being made, in particular the unlocking of opportunities for CDX antibodies, as well as the potential value that can be created through the Company's new type of humanised mice. Hemogenyx is confident that its ApbHC will be of further interest to large biopharmaceutical companies and has the potential to form the basis of significant future collaborations. The Company hopes to update shareholders on progress in this area.

 

The Board believes that the Company is well-advanced on the planned development steps that were described in the 2018 annual report and it hopes to provide further updates to shareholders as the Company progresses. The Company looks forward to the future with confidence.

 

Responsibility Statement

 

We confirm that to the best of our knowledge:

 

§ the Half Year Report has been prepared in accordance with International Accounting Standards 34, Interim Financial Reporting, as adopted by the EU; and

 

§ gives a true and fair view of the assets, liabilities, financial position and loss of the Group; and

 

§ the Half Year Report includes a fair review of the information required by DTR 4.2.7R of the Disclosure and Transparency Rules, being an indication of important events that have occurred during the first six months of the financial year and their impact on the set of interim financial statements; and a description of the principal risks and uncertainties for the remaining six months of the year; and

 

§ the Half Year Report includes a fair review of the information required by DTR 4.2.8R of the Disclosure and Transparency Rules, being the information required on related party transactions.

 

 

The Half Year Report was approved by the Board of Directors and the above responsibility statement was signed on its behalf by:

 

 

Dr Vladislav Sandler

CEO

 

27 SEPTEMBER 2019

 

 

Market Abuse Regulation (MAR) Disclosure

 

Certain information contained in this announcement would have been deemed inside information for the purposes of Article 7 of Regulation (EU) No 596/2014 until the release of this announcement.

 

 

Contacts

 

Hemogenyx Pharmaceuticals plc 

www.hemogenyx.com 

Dr Vladislav Sandler, Chief Executive Officer & Co-Founder 

[email protected] 

 

Sir Marc Feldmann, Chairman 

 

 

 

SP Angel Corporate Finance LLP 

Tel: +44 (0)20 3470 0470 

Matthew Johnson, Vadim Alexandre, Soltan Tagiev 

 

 

 

Peterhouse Corporate Finance Limited 

Tel: +44 (0)20 7469 0930 

Lucy Williams, Duncan Vasey 

 

 

 

US Media enquiries 

Tel: +1 (323) 646-3249 

Lowell Goodman 

[email protected]  

 

Condensed Consolidated Interim Statement of Comprehensive Loss

For the six months ended 30 June 2019

 

Continuing Operations

Note

 

6 months to 30 June 2019

Unaudited

6 months to 30 June 2018

Unaudited

 

 

 

£

£

Revenue

 

 

                -  

                -  

 

 

 

 

 

Administrative Expenses

 

 

        759,598

        715,474

Depreciation Expense

 

 

         27,554

         24,747

 

 

 

 

 

Operating Loss

 

 

   (787,152)

   (740,221)

 

 

 

 

 

Other Income

5

 

        82,763

        91,358

 

 

 

 

 

Interest income

 

 

9,220

1,440

Finance Costs

 

 

       (11,501)

        -

 

 

 

 

 

Loss before Taxation

 

 

    (706,670)

    (647,423)

 

 

 

 

 

Tax credit

 

 

-  

-  

 

 

 

 

 

Loss for the period attributable to equity owners

 

 

    (706,670)

    (647,423)

 

 

 

 

 

Items that will be reclassified subsequently to profit or loss:

 

 

 

 

   Translation of foreign operations

 

 

        (3,137)

        20,783

Other Comprehensive income for the year

 

 

        (709,807)

        (626,639)

 

 

 

 

 

Total comprehensive income to the year attributable to the equity owners

 

 

    (709,807)

    (626,639)

 

 

 

 

 

Basic and diluted earnings (per share)

6

 

            (0.00)

            (0.00)

 

 

Condensed Consolidated Interim Statement of Financial Position

As at 30 June 2019

 

Note

 

30 June 2019

Unaudited

Year Ended

31 December 2018

Audited

 

 

 

£

£

Assets

 

 

 

Non-current assets

 

 

 

 

Property, plant and equipment

7

 

      153,712

173,943

Intangible asset

 

 

       273,759

    272,753

Total non-current assets

 

 

        427,471

    446,696

 

 

 

 

 

Current assets

 

 

 

 

Trade and other receivables

 

 

       30,844

     90,475

Cash and cash equivalents

 

 

    1,092,702

   1,762,428

Total current assets

 

 

     1,123,546

     1,852,903

Total assets

 

 

     2,299,599

 

 

 

 

 

Equity and Liabilities

 

 

 

 

Equity attributable to shareholders

 

 

 

 

Paid-in Capital

 

 

 

 

Called up share capital

8

 

    3,601,762

     3,601,762

Share premium

 

 

    7,377,925

     7,340,267

Other reserves

 

 

    616,197

    620,059

Reverse asset acquisition reserve

 

 

(6,157,894)

  (6,157,894)

Foreign currency translation reserve

 

 

        33,910

    37,047

Retained Earnings

 

 

 (5,188,745)

 (4,482,075)

 

Total Equity

 

 

     283,155

     959,166

 

 

 

 

 

Liabilities

 

 

 

 

Non-current liabilities

 

 

 

 

Borrowings

 

 

1,176,973  

    1,172,826  

Total non-current liabilities

 

 

         1,176,973  

             1,172,826  

 

 

 

 

 

Current liabilities

 

 

 

 

Trade and other payables

 

 

       90,889

        167,607

Total Current Liabilities

 

 

        90,889

        167,607

Total Liabilities

 

 

        1,267,862

        1,340,433

Total equity and liabilities

 

 

     1,551,017

     2,299,599

 

The 2018 comparatives are the audited consolidated group for the year ended 31 December, 2018 as published on 29 April 2019.

 

Condensed Consolidated Interim Statement of Changes in Equity

For the six months ended 30 June 2019

 

 

Called up Share Capital

Share Premium

 

Other reserves

 

Reverse acquisition reserve

Foreign currency translation reserve

Retained losses

Total Equity

 

£

£

£

£

£

£

£

As at 1 January 2018

             3,600,514

              7,341,056

 

369,147

 

(6,157,894)

 

(13,984)

            (3,006,982)

              2,131,857

 Loss in period

-

-

-

-

 

 (647,423)

 (647,423)

 Other Comprehensive Income

-

-

 

-

 

-

 

20,783

                         -  

                         20,783  

 Total comprehensive income for the period

    -  

-  

 

 

-

 

 

-

 

 

20,783

(647,423)

(626,640)

 Issue of share capital

                 1,248

                 3,745

 

-

-

-

-

                 4,993

Issue of options (Note 8)

-

-

77,507

-

-

-

77,507

Market value of warrants

-

(4,170)

 

4,170

 

-

 

-

-

-

 

As at 30 June 2018 (unaudited)

3,601,762

7,340,631

 

450,824

 

(6,157,894)

 

6,799

(3,654,405)

1,587,717

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

As at 1 January 2019

       3,601,762

       7,340,267

 

620,059

 

(6,157,894)

 

37,047

      (4,482,075)

       959,166

 Loss in period

-

-

-

-

 

 (706,670)

 (706,670)

 Other Comprehensive Income

-

-

 

-

 

-

 

(3,137)

                         -  

                         (3,137)  

 Total comprehensive income for the period

    -  

-  

 

 

-

 

 

-

 

 

(3,137)

(706,670)

(709,807)

Embedded derivative - Convertible loans

-

-

6,280

-

-

-

6,280

Issue of options (Note 8)

-

-

27,516

-

-

-

27,516

Market value of warrants

-

37,658

 

(37,658)

 

-

 

-

-

-

 

As at 30 June 2019 (unaudited)

3,601,762

7,377,925

 

616,197

 

(6,157,894)

 

33,910

(5,188,745)

283,155

 

 

 

 

 

 

 

 

Condensed Consolidated Interim Statement of Cash Flows

For the six months ended 30 June 2019

   

Group

Note

 

6 months to 30 June 2019

Unaudited

6 months to 30 June 2018

Unaudited

 

 

 

£

£

Cash flows generated from operating activities

 

 

 

 

Loss for the period

 

 

 (706,670)

 (647,423)

Depreciation

       

 

27,554

24,747

 Other non-cash items interest/professional fees (shares issued)

 

 

        -

        -

Foreign exchange gain

 

 

(6,920)

-

Interest income 

 

 

        (9,220)

        (1,440)

Interest expense

 

 

    11,501

    -

Share based payments

   9          

 

         27,516

         77,507

(Decrease)/increase in trade and other payables

 

 

     (75,039)

     32,276

Decrease/(increase) in trade and other receivables

 

 

58,477

(113,430)

Net cash outflow used in operating activities

 

 

(672,801)

(627,763)

 

 

 

 

 

Cash flows generated from financing activities

 

 

 

 

Proceeds from issuance of equity securities

 

 

    -

    4,993

Net cash flow generated from financing activities

 

 

    -

    4,993

 

 

 

 

 

Cash flows generated from investing activities

 

 

 

 

Interest income

 

 

           9,220

           1,440

Purchase of property, plant & equipment

 

 

  (7,098)

  (24,351)

Net cash flow generated from investing activities

 

 

   2,122

   (22,911)

 

 

 

 

 

Net decrease in cash and cash equivalent

 

 

     (670,679)

     (645,681)

 

 

 

 

 

Effect of exchange rates on cash

 

 

     953

     11,952

 

 

 

 

 

Cash and cash equivalents at the beginning of the period

 

 

     1,762,428

     1,876,655

Cash and cash equivalents at the end of the period

 

 

      1,092,702

      1,242,926

 

Major non-cash transactions

There were no major non-cash transactions during the period.

 

Notes to the Condensed Consolidated Interim Financial Statements

 

1.            General Information

 

The Group's business is preclinical-stage biotechnology focused on the discovery, development and commercialisation of innovative treatments relating to bone marrow/hematopoietic (blood-forming) stem cell (BM/HSC) transplants for blood diseases, including leukaemia, lymphoma and bone marrow failure. The products under development are designed to address a range of problems that occur with current standard of care treatments.

 

The Company's registered office is located at 5 Fleet Place, London EC4M 7RD, and it is listed on the London Stock Exchange.

 

2.            Interim financial information

 

The condensed consolidated interim financial statements are for the six months period ended 30 June 2019. The condensed consolidated interim financial statements do not include all the information required for full annual financial statements and should be read in conjunction with the consolidated financial statements of the Group for the year ended 31 December 2018, which were prepared under International Financial Reporting Standards (IFRS) as adopted by the European Union (EU).

 

The condensed consolidated interim financial statements have not been audited nor have they been reviewed by the Group's auditors under ISRE 2410 of the Auditing Practices Board. These condensed consolidated interim financial statements do not constitute statutory accounts as defined in Section 434 of the Companies Act 2006. The Group's statutory financial statements for the year ended 31 December 2018 prepared under IFRS have been filed with the Registrar of Companies. The auditor's report on those financial statements was unqualified and did not contain a statement under Section 498(2) of the Companies Act 2006.

 

3.            Basis of preparation and changes to the Group's Accounting Policies

 

The principal accounting policies applied in the preparation of these consolidated interim condensed financial statements are set out below. These policies have been consistently applied to all the periods presented, unless otherwise stated.

 

Basis of Preparation

 

The condensed consolidated interim financial statements have been prepared in accordance with IAS 34 'Interim Financial Reporting'. The accounting policies adopted in this report are consistent with those of the annual financial statements for the year to 31 December 2018 as described in those financial statements. A number of new or amended standards became applicable for the current reporting period, but they did not have any impact on the group's accounting policies and did not require retrospective adjustments.

 

Going Concern

 

The preparation of financial statements requires an assessment on the validity of the going concern assumption.

 

The Consolidated Financial Statements have been prepared on a going concern basis. As a pharmaceutical development company, Hemogenyx has a continuing need for funds to take forward its product candidates and to explore any additional projects that may be identified. The Company has a number of discussions in hand which may bring in revenues or non-dilutive funding. However, the Company may in due course need to raise additional capital.

 

Segmental Reporting

 

The Group's operations are located in New York, USA and Liège, Belgium, with the head office located in the United Kingdom.

 

The Group currently has one reportable segment: a biotechnology business focused on the discovery, development and commercialisation of innovative treatments relating to bone marrow/hematopoietic (blood-forming) stem cell (BM/HSC) transplants for blood disease.

 

Accounting Policies

 

The accounting policies applied by the Group in these half-yearly results are the same as those applied by the Group in its consolidated financial information in its 2018 Annual Report and Accounts, with the exception of the new standards the Group adopted as of 1 January 2019, included below.

 

The same accounting policies, presentation and methods of computation have been followed in these condensed interim financial statements as were applied in the preparation of the Group's annual financial statements for the year ended 31 December 2018 except for the impact of the adoption of the Standards and interpretations described below.

 

Changes in accounting policy and disclosures

 

(a) Accounting developments during 2019

 

The International Accounting Standards Board (IASB) issued various amendments and revisions to International Financial Reporting Standards and IFRIC interpretations. The amendments and revisions were applicable for the period ended 30 June 2019 but did not results in any material changes to the financial statements of the Group.

 

The following standards were adopted by the Group during the year:

 

·     IFRS 16 - Leases (effective 1 January 2019)

·     IFRS 9 (Amendments) - Prepayment features with negative compensation (effective 1 January 2019)

·     Annual Improvements 2015-2017 Cycle

·     IAS 19 - Plan amendment, curtailment or settlements (effective 1 January 2019)

·     IAS 28 - Long term interests in associates and joint ventures (effective 1 January 2019)

·     IFRIC 23 - Uncertainty over income tax treatments (effective 1 January 2019)

 

IFRS 16 became effective for the Group as of 1 January 2019 and was adopted from this date. IFRS 16, which replaces IAS 17, leases, requires the Group to recognise lease liabilities in relation to leases which had previously been classified as 'operating leases' under the principles of the old standards.

 

Management has assessed all arrangements which could be considered to contain a lease and assessed the impact of transition to the new standard on the financial statements. There has been no material effect of transition to the Group as there are no material lease arrangements in the Group.

 

(b) New standards, amendments and interpretations in issue but not yet effective or not yet endorsed and not early adopted

 

Standard

 

Effective date

 

 

 

IFRS 3 (Amendments)

Business Combinations

1 January 2020

IAS 1 (Amendments)

Presentation of Financial Statements

1 January 2020

IAS 8 (Amendments)

Accounting policies, Changes in Accounting Estimates

1 January 2020

IFRS 17

Insurance

1 January 2021

 

* Subject to EU endorsement

 

The Directors are actively considering the effects upon the financial statements and at the time of approval do not consider that the financial statements will be subject to material changes.

 

4.            Significant accounting judgments, estimates and assumptions

 

The preparation of the financial statements in conformity with International Financial Reporting Standards requires the use of certain critical accounting estimates. It also requires management to exercise its judgement in the process of applying the Company's accounting policies. Actual results may differ from these estimates.

 

In preparing these condensed interim financial statements, the significant judgements made by management in applying the Group's accounting policies and the key sources of estimation uncertainty were the same as those applied to the consolidated financial statements for the year ended 31 December 2018.

 

5.            Other income

 

Other income of £82,763 during the period ended 30 June 2019 (H1 2018: £91,358) relates to funds received from a third party under a research collaboration programme relating to humanised mice.

 

6.            Earnings per share

 

The calculation of the Basic and fully diluted earnings per share is calculated by dividing the loss for the six months from continuing operations of £706,670 (six months to 30 June 2018: £647,423) for the Group by the weighted average number of ordinary shares in issue during those periods of 360,176,186 and 360,072,739 respectively.

 

Dilutive loss per Ordinary Share equals basic loss per Ordinary Share as, due to the losses incurred in the six months to 30 June 2019 and six months to 30 June 2018, there is no dilutive effect from the subsisting share options.

 

7.            Property, Plant and Equipment

 

During the six months ended 30 June 2019, the Group acquired assets with a cost of £7,098 (the six months ended 30 June 2018: £24,351).

 

8.            Called up Share Capital

 

Group

 

 

Ordinary shares

Number

£

As at 1 January 2018

 

 

360,051,358

3,600,514

Issue of shares for exercise of warrants 29 May 2018

 

 

124,826

1,248

As at 30 June 2018

 

 

360,176,184

3,601,762

As at 1 January 2019

 

 

360,176,184

3,601,762

As at 30 June 2019

 

 

360,176,184

3,601,762

 

9.            Share-based payments

 

Options

 

During the six months to 30 June 2019 no options were issued to directors or employees and no options were cancelled.

 

A schedule of options granted is below:

 

 

Number options

Employees, including directors

26,725,616

Members of the Scientific Advisory Board

9,346,125

Total

36,071,741

 

The weighted average fair value of the options granted during the six months ended 30 June 2019 was £Nil (30 June 2018: £0.0086).

 

There were no options issued for the six months ended 30 June 2019. The following table lists the inputs to the models used for the plan for the six months ended 30 June 2018:

 

 

January 2018

(EMP)

April 2018

(EMP)

 

 

 

Expected volatility %

50.09

45.32

Risk-free interest rate %

0.577

0.918

Expected life of options (years)

2

3

Weighted average exercise price  - pence

3.5

3.5

Weighted average share price

2.4

3.2

Expected dividend yield

-

-

Model used

Black Scholes

Black Scholes

 

For the six months ended 30 June 2019, the Group has recognised £27,516 of share-based payment expense in the statement of profit or loss (30 June 2018: £77,507).

 

Warrants

 

The share placement that completed on 4 October 2017 with the issue of 57,142,857 shares at £0.035 carried 1 for 2 warrants for qualifying shareholders over 62,021,429 new ordinary shares at £0.04 per share. In order to qualify for these warrants the shareholder must have retained the shares for a period of 60 days after admission.

 

A total of 49,361,678 warrants had been issued to eligible IPO participants who had been identified, and of this amount 124,826 warrants had been exercised. The period of time allowed for eligible IPO participants to claim warrants has expired and the 12,659,751 unidentified warrants can no longer be claimed. No value for these unclaimed warrants has been brought to account in the Condensed Consolidated Interim Statement of Financial Position.

 

10.          Events after the reporting period

 

There have been no significant events post period end.

 

 


This information is provided by RNS, the news service of the London Stock Exchange. RNS is approved by the Financial Conduct Authority to act as a Primary Information Provider in the United Kingdom. Terms and conditions relating to the use and distribution of this information may apply. For further information, please contact [email protected] or visit www.rns.com.
 
END
 
 
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