Half-year Financial Report

Summary by AI BETAClose X

Genflow Biosciences Plc reported its half-year results for the period ending 30 June 2026, highlighting the successful completion of its lead canine healthspan and sarcopenia clinical trial, SLAB, validating its SIRT6 centenarian platform. The company transitioned its human health programs to mRNA-lipid nanoparticle delivery and expanded into ophthalmology with a glaucoma program in partnership with Iris Pharma and Acuitas, targeting a market valued at nearly USD 9 billion. Financially, Genflow ended the period with cash reserves of £632,553, an increase from £111,792 at the end of 2025, following an equity fundraising of £1,148,875. Administration expenses decreased to £454,311 from £982,725 in the prior year's comparable period, though director's fees saw an increase. The company remains debt-free.

Disclaimer*

Genflow Biosciences PLC
29 September 2026
 

THE INFORMATION CONTAINED WITHIN THIS ANNOUNCEMENT IS DEEMED BY THE COMPANY TO CONSTITUTE INSIDE INFORMATION AS STIPULATED UNDER THE MARKET ABUSE REGULATION (EU) NO. 596/2014 AS IT FORMS PART OF UK DOMESTIC LAW PURSUANT TO THE EUROPEAN UNION (WITHDRAWAL) ACT 2018, AS AMENDED. UPON THE PUBLICATION OF THIS ANNOUNCEMENT VIA A REGULATORY INFORMATION SERVICE, THIS INFORMATION IS CONSIDERED TO BE IN THE PUBLIC DOMAIN.

 

29 September 2026

Genflow Biosciences Plc

 

("Genflow" or "the Company")

 

HALF YEAR RESULTS

 

Genflow (LSE: GENF) (OTCQB:GENFF) is pleased to announce its half year results for the six-month period ended 30 June 2022.

 

Chairman's Statement

 

It is my pleasure to update shareholders of Genflow Biosciences Plc ("Genflow" or the "Company") on our performance during the first six months of 2026.

 

As of 30 June 2026, Genflow reached a landmark milestone with the successful completion of SLAB, our lead canine healthspan and sarcopenia clinical trial - a significant achievement that validates our SIRT6 centenarian platform in a real-world aging population and strengthens the Company's position at the forefront of longevity science. Alongside this milestone, Genflow continued to make strong progress across its programs in both human health and animal health, advancing our mission to extend healthspan through our proprietary SIRT6 centenarian-based gene therapies. These two dimensions of our pipeline are deeply complementary: our human programs target age-related diseases with high unmet need, while our veterinary initiatives allow us to generate translational data, demonstrate safety and feasibility, and explore commercial opportunities in the growing companion animal health sector.

 

Animal Health Pipeline


The most notable achievement of the period was the successful completion of SLAB, our comparative, randomized Healthspan and sarcopenia clinical trial in aged Beagle dogs, testing GF-1004, our naked DNA construct. This is a landmark achievement for Genflow, providing strong validation of our SIRT6 cent platform in a real-world aging population and reinforcing our pioneering position in applying SIRT6 cent science to veterinary medicine, complementing our human health programs.

 

The trial successfully confirmed the safety and tolerability of GF-1004 and generated valuable functional and healthspan data across its endpoints, an encouraging validation of our platform's real-world applicability. We look forward to presenting full results at the Animal Longevity Summit (ALOS) in Toronto on 2nd October 2026, alongside a scientific manuscript in preparation for peer-reviewed publication. At the same time, we have continued confidential discussions with several leading animal health companies under confidential disclosure agreements, underscoring strong industry interest in innovative approaches to age-related decline in companion animals.

 

Human Health Pipeline


In human health, our pipeline spans MASH ("Metabolic Dysfunction-Associated Steatohepatitis"), sarcopenia, Werner Syndrome, and exploratory programs in ophthalmology. Collectively, these programs highlight the versatility of SIRT6 centenarian in addressing fundamental mechanisms of aging across multiple systems. During H1 2026, the Company implemented a transition to mRNA-lipid nanoparticle (mRNA-LNP) delivery across its human health programs.

 

A particularly exciting development during the period was our expansion into ophthalmology, where SIRT6-based therapies hold promise in corneal pathologies and glaucoma. Current glaucoma treatments focus primarily on reducing intraocular pressure, yet do not prevent degeneration of the optic nerve. Preclinical findings suggest that SIRT6 cent overexpression can protect retinal ganglion cells and preserve optic nerve integrity, opening the door to a paradigm shift in treatment - from symptom management to true neuroprotection. During H1 2026, we initiated a dedicated glaucoma program in partnership with Iris Pharma and Acuitas, incorporating Acuitas' lipid nanoparticle (LNP) technology for ocular delivery - an important step forward for this program. With the global glaucoma market valued at nearly USD 9 billion and projected to reach USD 12-14 billion by the early 2030s, this represents a compelling long-term growth opportunity for Genflow.

 

In parallel, we continue to progress our MASH program. Recent approvals of two new therapies including GLP-1 agonists have provided effective therapies for patients in the earlier stages of disease (approximately two-thirds of the population), while a profound unmet need remains in advanced MASH with fibrosis, where Genflow has repositioned GF-1002 to target the high-need, antifibrotic-responsive population. During H1 2026, GF-1002 transitioned to mRNA-LNP delivery, and the Company is working to secure a prolongation of its Wallonia Region non-dilutive grant (Convention 8971) supporting the program's continued development.

 

In parallel, our Mitosir and Exofastrack programs continued to progress during the period, both advancing through mRNA-LNP formulation development supported by non-dilutive research grants.

 

Strategic Integration of Human and Animal Health


Our programs in human health and animal health are mutually reinforcing. The veterinary studies provide a real-world proof-of-concept environment to evaluate SIRT6 cent-based therapies in aging populations, while our human programs extend the platform into areas of high unmet need such as MASH, sarcopenia, Werner Syndrome, and ophthalmology. Together, they expand the reach of our SIRT6 platform and strengthen Genflow's leadership in healthspan science.

 

Financial Overview

 

As of 30 June 2026, the Group had cash reserves of £632,553 (31 December 2025: £111,792) which has been derived from equity fundraising of £1,148,875 (net of expenses) during H1 2026. The Company remains debt free.

 

Administration expenses for 30 June 2026 totalled £454,311 (30 June 2025: £982,725), which primarily consisted of research and development costs of £119,445 (30 June 2025: £665,862), legal and professional fees totalling £133,934 (30 June 2025: £156,094) and Directors' fees of £126,142 (30 June 2025: £55,272).

 

Other Comprehensive Income was charged with a translation loss of £11,831 (30 June 2025: £31,075) upon converting the Subsidiary's results for the period to GBP.

 

Future

 

Looking ahead to the second half of 2026 and into 2027, building on the successful completion of SLAB-VET-001, we look forward to presenting full trial results at the Animal Longevity Summit on 2nd October 2026 and advancing our discussions with leading animal health companies. In parallel, we will continue to progress our newly initiated glaucoma program with Iris Pharma and Acuitas, and advance GF-1002 and our other MASH-directed programs, Mitosir and Exofastrack, through mRNA-LNP formulation development. By integrating progress across both human and veterinary health, Genflow is building a comprehensive platform capable of delivering meaningful innovations in longevity and age-related disease.

 

The Company is also working hard to secure further non-dilutive funding, including a prolongation of the Wallonia Region grant supporting GF-1002's development. We look forward to updating shareholders further once this process has been finalised.

 

On behalf of the Board, I would like to thank our shareholders, partners, and dedicated team for their continued support as we work to translate the science of SIRT6 into therapies that improve lives.

 

 

Gad Berdugo

Chairman

 

 

Market Abuse Regulation (MAR) Disclosure

The information contained within this announcement is deemed to constitute inside information as stipulated under the Market Abuse Regulation ("MAR") (EU) No. 596/2014, as incorporated into UK law by the European Union (Withdrawal) Act 2018. Upon the publication of this announcement, this inside information is now considered to be in the public domain

 

 

Contacts

Genflow Biosciences

ON365 Partners Inc.

Dr Eric Leire, CEO

Eric Laub, Investor Relations

+32-477-495-881

+1 617-444-9509


www.on365ptrs.com

 

 

About Genflow Biosciences

 

Founded in 2020, Genflow Biosciences Plc. (LSE:GENF) (OTCQB:GENFF), a biotechnology company headquartered in the UK with R&D facilities in Belgium, is pioneering gene therapies for age-related diseases, with the goal of promoting longer and healthier lives while mitigating the financial, emotional, and social impacts of a fast-growing aging global population. Genflow's lead compound, GF-1002, works through the delivery of a centenarian variant of the SIRT6 gene which has yielded promising preclinical results. Genflow's proof-of-concept clinical trial evaluating its SIRT6-centenarian gene therapy in aged dogs began in March 2025. Other programs include a clinical trial that will explore the potential benefits of GF-1002 in treating MASH (Metabolic Dysfunction Associated Steatohepatitis), the most prevalent chronic liver disease for which there is a persistent unmet medical need. Genflow is also advancing an ophthalmology program, GF-1006, an mRNA-based SIRT6 therapy targeting corneal pathologies and glaucoma - a leading cause of irreversible blindness for which current treatments reduce intraocular pressure but do not prevent degeneration of the optic nerve. Please visit www.genflowbio.com and follow the Company on LinkedIn and X.

 

consolidated STATEMENT OF FINANCIAL POSITION
AS AT 30 June 2026

 

 

 

Note

 

Unaudited

30 June 2026


 

Audited

31 December 2025


 

Unaudited

30 June 2025 Restated








 

Non-current assets







Property, plant & equipment


1,421


1,066


1,528

Total non-current assets

 

1,421

 

1,066

 

1,528








Current assets







Trade and other receivables

6

115,017


339,528


187,408

Cash and cash equivalents


632,553


111,792


279,445

Total current assets


747,570

 

451,320


466,853

Total assets

 

748,991

 

452,386

 

468,381

 

 





 

Current liabilities

 





 

Trade and other payables

7

559,138


1,003,171


771,384

Total current liabilities

 

559,138

 

 1,003,171


771,384


 


 

 


 

Total liabilities

 

559,138

 

1,003,171


771,384

Net Assets/(Liabilities)

 

189,853

(550,785)


(303,003)

 

 





 

Equity

 





 

Share capital

8

169,922


148,064


136,064

Share premium

8

7,222,938


6,095,921


5,667,921

Other reserves

9

225,890


213,894


221,730

Retained earnings

 

(7,428,897)


(7,008,664)


(6,328,718)

Total equity

 

189,853

 

(550,785)


(303,003)

 

 

The financial statements were approved and authorised for issue by the Board of Directors on 28 September 2026 and were signed on its behalf by:

 

 

Eric Leire

Chief Executive Officer

 

 

 

CONSOLIDATED STATEMENT of COMPREHENSIVE INCOME
FOR THE six months ENDED 30 June 2026

 

 

 






 


Notes

Unaudited

6 Months ended

30 June

2026


Audited

12 Months

ended

31 December 2025


Unaudited

6 Months ended

30 June

2025

Other operating income

 

34,583

 

 

585,607

 

 

245,107

Administrative expenses

4

(454,311)


(2,003,171)


(982,725)

Operating loss

 

(419,728)

 

(1,417,564)


(737,618)








Finance costs


(505)


-


-








Loss before tax

 

(420,233)

 

(1,417,564)

 

(737,618)








Tax expense                                                           


-


-


-

Loss for the period / year attributable to owners of the parent

 

(420,233)

 

(1,417,564)

 

(737,618)

 

 


 

 

 

 

Other Comprehensive loss:

 


 

 

 

 

Items that could be reclassified to profit or loss

 


 

 

 

 

Exchange differences on translation of foreign operations

 

(11,831)


(38,911)


(31,075)

 

 


 


 

 

 

 


 


 

 

Total comprehensive loss for the period / year attributable to owners of the parent

 

(408,402)

 

(1,456,475)

 

(768,693)

 

 


 

 

 

 

Loss per share (pence) from continuing operations attributable to owners of the Parent - Basic & Diluted

 

5

(0.080)


(0.332)

 

(0.192)


CONSOLIDATED STATEMENT OF CASH FLOWS
FOR THE SIX MONTHS ENDED 30 JUNE 2026

 

 

 

 

Unaudited

6 Months ended

30 June 2026

 

Audited

12 Months ended

31 December 2025

 

Unaudited

6 Months ended

30 June 2025

 

 

Cash flows used in operating activities:

 






 

Loss after taxation

 

(420,233)


(1,417,564)


(737,618)

 

Adjustments for:

 






 

Depreciation & amortisation

 

285


1,093


597

 

Share based payments

 

165


-


-

 

(Increase)/decrease in trade and other receivables

 

221,354


(234,369)


(82,249)

 

Increase/(decrease) in trade and other payables

 

(435,514)


214,255


(17,532)

 

Net cash outflow from operating activities

 

(633,943)


(1,436,585)

 

(836,802)

 


 






 

Cash flow used in investing activities:

 






 

Purchase of property, plant & equipment

 

(651)


-


-

 

Net cash used in investing activities

 

(651)

 

-

 

-

 


 






 

Cash flow from financing activities:

 






 

Proceeds from issue of shares net of issue costs

 

1,148,875


1,308,698


868,698

 

Net cash generated from financing activities

 

1,148,875


1,308,698

 

868,698

 








 

Net increase/(decrease) in cash and cash equivalents


514,281

 

(127,887)

 

31,896

 

Cash and cash equivalents at beginning of period / year


111,792


278,682


278,682

 

FX on cash


6,480


(39,003)


(31,133)

 

Cash and cash equivalents at end of period

 

632,553

 

111,792

 

279,445

 




















 

 

 

 

CONSOLIDATED STATEMENT of CHANGES IN EQUITY
FOR THE six months ENDED 30 June 2026

 

 

Share capital

Share

premium

 

Other reserves

 

Retained earnings/loss

 

 

Total

Unaudited- 30 June 2026

 

 

 

 

 

At 1 January 2026

148,064

6,095,921

213,894

(7,008,664)

(550,785)

Loss of the period

-

-

-

(420,223)

(420,223)

Exchange differences on translation of foreign operations

-

-

11,831

-

11,831

Total comprehensive loss for the period

-

-

11,831

(420,223)

(408,402)

Transactions with owners






Issue of ordinary shares

21,858

1,137,517

-

-

1,159,375

Cost of capital - share issue costs

-

(10,500)

-

-

(10,500)

Total Transactions with owners

21,858

1,127,017

-

-

1,148,875

At 30 June 2026 (unaudited)

169,922

7,222,938

225,890

7,428,897

189,853

 

 

 

 

Unaudited- 30 June 2025

 

 

 

 

 

At 1 January 2025

104,912

4,830,375

252,805

(5,591,100)

(403,008)

Loss of the period

-

-

-

(737,618)

(737,618)

Exchange differences on translation of foreign operations

-

-

(31,075)

-

(31,075)

Total comprehensive loss for the period

-

-

(31,075)

(737,618)

(768,693)

Transactions with owners

 

 

 

 

 

Issue of ordinary shares

31,152

902,932

-

-

934,084

Cost of capital - share issue costs

-

(65,386)

-

-

(65,386)

Total Transactions with owners

31,152

837,546

-

-

868,698

At 30 June 2025 (unaudited)

136,064

5,667,921

221,730

(6,328,718)

(303,003)

 

 

 

 

 

 

 

 

 

 

 

 

Audited- 31 December 2025

 

 

 

 

 

At 1 January 2025

104,912

4,830,375

252,805

(5,591,100)

(403,008)

Loss for the year

-

-

-

(1,417,564)

(1,417,564)

Other comprehensive income

-

-

(38,911)

-

(38,911)

Total comprehensive income for the period

-

-

(38,911)

(1,417,564)

(1,456,475)

Transactions with owners

 

Issue of ordinary shares

1,330,932

-

-

1,374,084

Cost of capital - share issue costs

-

(65,386)

-

-

(65,386)

Total Transactions with owners

43,152

1,265,546

-

-

1,308,698

At 31 December 2025 (audited)

148,064

6,095,921

213,894

(7,008,664)

(550,785)

 

NOTES TO THE INTERIM REPORT
FOR THE six months ENDED 30 June 2026

 

1.         Reporting Entity 

 

Genflow Biosciences Plc (the "Company") is a company domiciled in the United Kingdom. The consolidated interim financial information as at, and for the six months ended, 30 June 2026 comprise the results of the Company and its subsidiaries (together referred to as the "Group").

 

The consolidated financial statements of the Group as at, and for the year ended, 31 December 2025 are available upon request from the Company's registered office at 6 Heddon Street, London, W1B 4BT or at genflowbio.com.

 

2.         BASIS OF PREPARATION

 

The financial information of the Group for the 6 months ended 30 June 2026 was approved and authorised for issue by the Board of the Company on 28 September 2026. 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 the Company for the year ended 31 December 2026 and are consistent with the recognition and measurement requirements of IFRS as adopted by the United Kingdom. The comparative information for the full year ended 31 December 2025 is not the Group's full annual accounts for that period but has been derived from the annual financial statements for that period. 

 

The consolidated financial information incorporates the results of the Group as at 30 June 2026. The corresponding amounts are for the year ended 31 December 2025 and for the 6-month period ended 30 June 2025.

 

The Group financial information is presented in Pound Sterling and values are rounded to the nearest pound. 

 

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 audited financial statements except for those that relate to new standards and interpretations effective for the first time for periods beginning on (or after) 1 January 2026 and will be adopted in the 2025 annual financial statements. 

 

A number of new standards and amendments became effective on 1 January 2025 and have been adopted by the Group. None of these standards have materially affected the Group.

 

3.         GOING CONCERN

 

The preparation of financial information requires an assessment on the validity of the going concern assumption. The Company successfully raised £1.16 million (before expenses) through the allotment and issue of new ordinary shares during the period. Further funding will be required by the Company in order to execute the Group's research and development strategy and to continue to meet its financial commitments. The Company has various funding options currently available to it and is assessing their terms in order to select the option which is most favourable to the Company and its shareholders. At 30 June 2026, the Group is in a net asset position totalling £189,853.

 

The Directors are of the opinion that the Company has adequate working capital to execute its operations for the present time and expected to cover working capital for a period which will allow for further fundraising. It is confident in its ability to access additional financing over the next 12 months. The Directors, therefore, have made an informed judgement, at the time of approving these financial statements, that there is a reasonable expectation that the Company has adequate resources to continue in operational existence for the foreseeable future. As a result, the Directors have continued to adopt the going concern basis of accounting in preparing the annual financial statements, however, notes that, due to the timing of securing additional funding, a material uncertainty related to going concern exists. This is not uncommon with companies in the biotech sector in a similar stage of its development to the Company.

 

 

 

4.         EXPENSES BY NATURE


Unaudited

6 Months ended

30 June 2026

£

Audited

Year ended

31 December 2025

£

Unaudited

6 Months ended

30 June 2025

£





Directors' fees

126,547

363,995

55,272

Directors' pensions

-

-

-

Directors' social security contributions

9,328

29,967

27,059

Employee salaries

19,629

-

-

Fees payable to the Company's auditors for the audit of the Parent Company and group financial statements

-

55,000

-

Professional, legal and consulting fees

132,953

315,133

170,807

PR and marketing

33,494

92,891

40,779

Insurance

11,039

21,713

10,829

Office and administrative expenses

7,541

7,172

5,027

IT and software services

2,802

8,447

2,385

Travel and entertainment

9,387

6,336

2,038

Research and development costs

119,445

1,110,486

665,862

Share based payments

165

-

-

Depreciation

287

1,093

597

Other expenses

(18,306)

(9,062)

2,019

Total administrative expenses

454,311

2,003,171

982,725

 

 

5.         LOSS PER SHARE

 

 


Unaudited

6 Months ended

30 June

2026

£

Audited

Year ended

31 December 2025

£

Unaudited

6 Months ended

30 June

2025

£

 




Net loss for the year from continued operations attributable to equity shareholders

420,233

1,417,564

737,618





Weighted average number of shares for the period/year

524,541,550

426,711,928

384,282,436





Basic loss per share for continued operations (expressed in pence)

(0.080)

(0.332)

(0.192)

 

 

6.            TRADE AND OTHER RECEIVABLES

 


Unaudited

6 Months ended

30 June

2026

£

Audited

Year ended

31 December 2025

£

Unaudited

6 Months ended

30 June

2025

£

VAT receivable

24,475

28,107

65,606

Prepayments

33,637

44,096

38,708

Other receivables  

56,905

267,325

83,094

 

115,017

339,528

187,408

 

Trade and other receivables are all due within one year. The fair value of all receivables is the same as their carrying values stated above. These assets, excluding prepayments, are the only form of financial asset within the Group, together with cash and cash equivalents. There are no trade receivables therefore an aging analysis has not been provided. 

 

 

7.            TRADE AND OTHER PAYABLES


Unaudited

6 Months ended

30 June

2026

£

Audited

Year ended

31 December 2025

£

Unaudited

6 Months ended

30 June

2025

£

Trade payables

354,314

646,660

573,297

Accruals

76,955

323,167

12,646

Other payables

127,869

33,344

185,441

 

559,138

1,003,171

771,384

All trade and other payables are due for payment within twelve months. Trade payables are settled within normal commercial terms, usually between 30-60 days.

8.         Share capital AND SHARE PREMIUM

 

 

Company

Number of shares

Ordinary shares

£

Share premium

£

Total

£

Issued and fully paid





At 1 January 2025

349,706,618

104,912

4,830,375

4,935,287

Issue of new shares

103,841,324

31,152

902,932

934,084

Cost of Capital

-

-

(65,386)

(65,386)

At 30 June 2025

453,547,942

136,064

5,667,921

5,803,985

At 1 January 2026

493,547,942

148,064

6,095,921

6,243,985

Issue of new shares

72,861,840

21,858

1,137,517

1,159,375

Cost of Capital

-

-

(10,500)

(10,500)

At 30 June 2026

566,409,782

169,922

7,222,938

7,392,860

 

On 11 March 2026, the Company issued and allotted 42,105,263 new Ordinary Shares at a price of 0.019 pence per share for gross proceeds of £800,000 (excluding expenses).

 

On 13 May 2026, the Company issued and allotted 2,631,578 new Ordinary Shares at a price of 0.019 pence per share for gross proceeds of £50,000 (excluding expenses).

 

On 13 May 2026, the Company issued and allotted 28,124,999 new Ordinary Shares at a price of 0.011 pence per share for gross proceeds of £309,375 (excluding expenses).

 

9.         Share WARRANT reserve

 

The balance held in the share options reserve relates to the fair value of the share warrants that have been charged to the profit or loss since adoption of IFRS 2 'Share-based payment'.

 

Warrants:

 

 

2026


2025

 

Number

Weighted average exercise price (£)

 

Number

Weighted average exercise price (£)

Outstanding at beginning of period

130,360,000

0.015

 

27,860,000

0.02

Granted

42,105,263

0.019


102,500,000

0.013

Adjustments

22,727,272

0.015




Exercised

(30,756,577)

0.015




Outstanding as at period end

164,435,958

0.014

 

130,360,000

0.015

Exercisable at period end

164,435,958

0.014

 

130,360,000

0.015

 

62,500,000 warrants were subject to adjustment in certain circumstances including a reset of the exercise price if the Company completes a share issuance during the exercise period at a price lower than the exercise price. As such, the exercise price was adjusted to 1.1p and the number of warrants granted was increased proportionately, such that the aggregate exercise value remained unchanged.

 

£Nil was charge to loss for the year in respect of outstanding warrants (2025: £Nil).

 

 

10.        Share OPTION reserve

 

30,316,563 options were granted to the Director's during the period (the "Options"). The Options will vest in 12 equal monthly amounts and will be fully vested 29 June 2028. The Options were issued at an exercise price of 2.2 pence and will expire 29 June 2036, being 10 years from grant date.

 

The fair value of the Options was determined using the Black Scholes valuation model and at 30 June 2026 £165 has been recognised within the profit and loss.

 

11.        COMMITMENTS

 

The commitments stated in the Group's Annual Financial Statements for the year ended 31 December 2025 remain in place.

 

 

12.        EVENTS AFTER THE REPORTING DATE

 

There were no events after the reporting date.

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