Half Yearly Report

22 September 2011

ValiRx Plc

("ValiRx" or "the Company")

Half-yearly Report

Valirx Plc (AIM: VAL), a life science company with a focus on cancer diagnostics and therapeutics for personalised medicine, announces its half-yearly report for the six months ended 30 June 2011.

'ValiRx establishes solid platform from which to drive the business forward'

Highlights

·; Revenue for the six months to 30 June 2011 rose to £418,263 (Six months to 30 June 2010: £64,474; year to 31 December 2010: £177,297)

·; Completion of sale of ValiBio SA

·; Launch of Chlamydia self-test kits

·; Completion of placing of new shares raising £3.3 million (before fees and expenses)

·; Advances with method of production of GeneICE (Val 101) and Val 201

·; Sale of Licence to Volition Singapore

·; Successful second year extension of Eurostar grant for GeneICE (Val 101)

Post period

·; Important therapeutic role for Val 201 established in collaboration with Oxford University

·; Acquisition of ValiRx Finland OY

·; Distribution agreement signed for Finland and Sweden for SELFCheck kits

·; Collaboration with Physiomics Plc to maximise Val 201's clinical prospects.

Dr Satu Vainikka, Chief Executive, commented that:

"I am delighted with the progress that we have made during the past six months. A significant capital injection via a placing, increased revenue, together with the sale of ValiBIO in the period, have strengthened our balance sheet, enabling us to concentrate on building incremental value in our cancer therapeutics and companion diagnostics, through product development. As we have seen, advances in GeneICE development and manufacturing are anticipated to save production costs and have enhanced the prospects for GeneICE products.

With additional pre-clinical studies of our lead drug candidates having been conducted this year and demonstrating their potential for filling unmet needs in a number of tumours, I am very pleased that we have been able to establish important collaborations, to further accelerate our preclinical programmes and to enhance their clinical outcomes. With your Company's lead therapeutic products being on the cusp of clinical trials, we have a solid platform from which to drive ValiRx forward and firmly position ourselves at the forefront of personalised medicine."

Enquiries:  

Chairman's statement

Strategic overview

The past half year has been a busy period for ValiRx and I am pleased to report that in the six months to 30 June 2011, ValiRx has made good progress on a number of fronts.

Revenues are up to £418,263, compared with £177,297 for the whole of 2010 and to £64,474 for the six months of 2010.

In January 2011, ValiRx successfully completed and announced the sale of Valibio SA, its wholly owned Belgian subsidiary, to a Singaporean-registered company, Singapore Volition Pte. Limited ("Volition"), for a total consideration of $1.1 million (approximately £670,000), of which $400,000 was in staged cash payments with the balance in ordinary shares in Volition. In June 2011 the Company announced the sale of a licence that was related to Volition's activities but was no longer core to ValiRx's activity; however the rights to the IP were retained by ValiRx for use in its therapeutic programmes and products.

This disposal was timely and it has enabled management to refocus on more immediate value-creating areas.

In February 2011, ValiRx announced an expansion to its SELFCheck home diagnostics kits through the launch of its Chlamydia SELFCheck "Over-The-Counter" health screening product across the UK. The retail and distribution of the self-diagnostic tests will be conducted by ValiMedix, the Company's sales and distribution division, and will be targeted at existing and new channels. The Company's HPV Real time PCR test continues it clinical evaluation and currently statistically significant data is being generated to show that it is capable of distinguishing high risk medium risk and low risk HPV subtypes robustly in routine clinical use.

The Company's £3.3 million placing that was announced on 16 February 2011 has enabled ValiRx to accelerate the development and commercialisation of its lead drug candidates Val 101 and 201 and the Board anticipates that one or possibly both of these compounds should be ready to enter Phase 1 trials during the next calendar year.

The Company has seen excellent progress with its therapeutic compound Val 201 during the period and we were pleased to report in July 2011 that a further late preclinical study into the development of the compound, carried out in collaboration with Oxford University, has firmly established a potentially important role for Val 201 in treating hormone induced refractory prostate cancer and other conditions of hormone induced uncontrolled cell growth including breast and ovarian cancer, among others. These conditions currently have high medical needs. This progress followed on from ValiRx's agreement with Oxford University, announced 14 April 2011, to accelerate the development of Val 201 and to study its therapeutic potential for additional indications.

ValiRx was also pleased to report in June 2011 that it has made an important advance in the production method of GeneICE ("Gene inactivation by chromatin engineering") drug candidates; Val101 being the most advanced of these currently. The new technique simplifies the manufacture of GeneICE molecules and by extension makes them cheaper to produce. We believe that the extra cost-saving that comes with the simplification of chemistry and a cleaner biological profile adds further value to GeneICE and its attraction to potential licensees and partners. Also announced was an extension of the Eurostar grant.

Since the end of the reporting period, on 18 August 2011, the Company announced that it had acquired, for a nominal amount, the outstanding equity of a Finnish non-trading company - ValiRx Finland OY ("ValiFinn") that it had jointly established with local partners in 2008. As a result of the acquisition, ValiFinn has become a wholly owned subsidiary of the Company.

The Board believes that the Company will benefit from the favourable environment for regulated medical and clinical studies in the Nordic region and we were pleased that ValiFinn was awarded a Finnish government grant of up to €55,000, which will be used for ValiRx's developmental therapeutic projects. Furthermore, there is the potential for continued further support. ValiFinn will conduct the management of certain aspects of Val 201's late preclinical work and it will assist on the regulatory work pertaining to the clinical trials alongside managing certain aspects of the non-clinical work regarding hormone induced refractory cancer.

ValiRx also announced after the period end that it had signed an agreement with Medcase OY MCO ("Medcase"), a Finnish distributor operating across the Nordic region, for the distribution and sale of Valimedix SELFCheck "Over-The-Counter" health screening products in Finland and Sweden.

The agreement, which includes a minimum upfront order for 300 kits for the purposes of marketing and assessment, will see Medcase use its distribution channels in Finland and Sweden to assist Valimedix in early stage and future sales and marketing of the Company's SELFCheck kits.

On 13 September 2011, the Company announced a new collaboration with Physiomics plc using their systems biology expertise and Virtual Tumour to aid Val 201's progress through the final phases of its pre-clinical programme and into clinical trials with respect to prostate cancer. Physiomics will not receive a fee for the work it carries out, but will instead be handed a percentage of any licensing income from the compound, regarding prostate cancer.

Furthermore, the Company is pleased to announce that it has contracted Pharmatest Services Limited (Turku Finland) to undertake various tests that are required on Val 201 prior to its use in clinical trials. Pharmatest has also been contracted to undertake independent confirmatory work on the positive results of the tests carried out by Oxford University in respect of Val 201 referred to above. In addition, the Company has also contracted Nexus Oncology (Edinburgh) to "audit" all the data generated about Val 201 to date and to assist in the design of the first clinical study and for some regulatory support.

We are now in an excellent position from which to drive the business forward.

N Thorniley

Chairman 

22 September 2011

Consolidated statement of comprehensive income

For the six months ended 30 June 2011

Consolidated statement of changes in equity

For the six months ended 30 June 2011

Consolidated statement of financial position

As at 30 June 2011

Consolidated cash flow statement

For the six months ended 30 June 2011

Notes to the interim financial statements

1 General information

Valirx Plc is a company incorporated in the United Kingdom, which is listed on the Alternative Investment Market of the London Stock Exchange Plc. The address of its registered office is 24 Greville Street, London EC1N 8SS.

2 Financial information

The interim consolidated financial information for the six months ended 30 June 2011 has not been audited or reviewed and does not constitute statutory accounts within the meaning of Section 434 of the Companies Act 2006. The Group's statutory accounts for the year ended 31 December 2010 have been delivered to the Registrar of Companies. The report of the independent auditors on those financial statements was unqualified and did not contain a statement under Sections 498 (2) or (3) of the Companies Act 2006.

The interim financial statements have been prepared in accordance with International Financial Reporting Standards ('IFRS') as adopted by the European Union, IFRIC interpretations and the Companies Act 2006 applicable to companies reporting under IFRS and under the historical cost convention. The accounting policies applied in preparing the interim financial information are consistent with those set out in the statutory accounts of the Company for the year ended 31 December 2010.

The interim consolidated financial statements are presented in pounds sterling because that is the currency of the primary economic environment in which the group operates.

3 Taxation

4 (Loss)/earnings per ordinary shares

The (loss)/earnings and number of shares used in the calculation of (loss)/earnings per share are as follows:

There was no dilutive effect from the share options outstanding during the period.

5 Dividends

The directors do not propose to declare a dividend in respect of the period.

6 Share capital

On 27 January 2011, the company issued 3,763,265 ordinary shares of 0.1p at 0.245p per share to satisfy a liability of £9,220.

On 16 February 2011, the company placed 549,500,000 ordinary shares of 0.1p each at 0.6p per share, raising £3.297m, before expenses.

The deferred shares effectively have no rights or value.

7 Copies of interim results

Copies of the interim results can be obtained from the website www.valirx.com. From this site you may access our financial reports and presentations, recent press releases and details about the company and its operations.

Notes to Editors

ValiRx plc is a biopharmaceutical company developing novel technologies and products in oncology therapeutics and diagnostics. It is headquartered in London and admitted to AIM in October 2006. The Group has a portfolio of innovative epigenetic technologies and products with worldwide exclusive rights and patents.

ValiRx operates through two divisions, ValiPharma, a UK-based epigenetic drug discovery and development business, and ValiMedix, a UK based trading business.