ValiRx Regulatory News (VAL)

For release at 07:00 on 19 August 2014

ValiRx Plc

("ValiRx" or "the Company")

Half Year Results

ValiRx Plc (AIM: VAL), a life science company with a focus on cancer diagnostics and therapeutics for personalised medicine, announces its interim results for the half year ended 30 June 2014.

HIGHLIGHTS

Operational Highlights

· Submission of clinical trial application ("CTA") and regulatory authorisation to progress VAL201 in human patient studies. This was accepted in August 2014; patient recruitment will commence on obtaining a favourable opinion on the authorised procedure from the Ethics Committee; 

· Expansion of product portfolio with ValiRx entering into a risk-sharing joint venture agreement with Tangent Reprofiling Limited ("Tangent Reprofiling") to progress the drug VAL401 through its remaining pre-clinical development and towards Phase II trials for the treatment of lung cancer and other oncology indications;

· Confirmation of safety of VAL401 from toxicological studies. We can now plan future detailed regulatory toxicology and pharmacokinetic studies with greater confidence in securing a positive outcome for clinical studies; and

· Securing of patent protection in the major markets. ValiRx now has granted patent protection for the NAV3 gene biomarker in Japan, Europe and Australia, and pending in the US and other territories, alongside granted and pending patents for its therapeutic technologies across Europe, the US, Canada and Australia.

Financial Highlights

· Sale of 510,811 shares in VolitionRx for US$601,578;

· Expenditure on Research and Development was down 43% to £0.56m as a result of forward ordering of the VAL201 compound in 2013 to build robust stability and sterility data ahead of filing the "CTA" application;

· Administration expenses were £0.64m (2013: £0.68m);

· Loss after taxation was £1.34m (2013: £1.49m) or 0.05p per ordinary share (2013: 0.09p); 

· Total comprehensive loss for the period of £1.75m (2013: £1.63m);

· Cash and cash equivalents as at 30 June 2014 of £0.76m (2013: £1.17m)

Oliver de Giorgio-Miller, Non-Exec Chairman of ValiRx, commented:

"We have made substantial progress during this period and are very pleased to see both VAL201 now making its way down the regulatory pathway and our portfolio of drug candidates enhanced and enlarged. With the Company's costs under control and with its lead therapeutics and other assets moving forward, as planned, the Company remains adequately funded to proceed with its current plans. I look forward to updating shareholders on further progress throughout the year."

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CHAIRMAN'S STATEMENT FOR THE HALF YEAR ENDED 30 AUGUST 2014

We are making strong progress this year in delivering our key priorities, which include taking our leading anti-cancer therapeutic VAL201 into clinical trials, expanding our product portfolio and progressing the biomarker side of the business.

This progress particularly applies to VAL201, for which the Company, with the support of its clinical trial project team, has successfully obtained Medicines and Healthcare Products Regulatory Agency ("MHRA") approval to enter the drug in a Phase l/II escalation study in patients with locally advanced or metastatic prostate cancer and other advanced solid tumours. We anticipate this study will commence before the end of this calendar year.

We have also expanded our portfolio of drug candidates through a joint venture arrangement with Tangent Reprofiling to further develop VAL401, a novel combination cancer drug with an already established safety profile. The joint venture has been formed to complete VAL401's remaining pre-clinical development and the Board believe this work will act as the springboard required to take VAL401 to Phase II trials for the treatment of lung cancer and other oncological indications.

We now have three therapeutics in our portfolio, VAL201, VAL101 and VAL401, each having multiple cancer indications. Alongside these, in the case of our GeneICE / VAL101 compounds, we have the potential to spawn a series of treatments for neurological and inflammatory diseases.  

The growth in both strength and depth of our business has been replicated at our subsidiary company, ValiFinn, which has developed and validated a range of companion diagnostics or genetic biomarkers to pair with the compounds VAL201 and VAL401.

In sum, we have made substantial progress during this period and are very pleased to see both VAL201 now making its way down the regulatory pathway and our portfolio of drug candidates enhanced and enlarged. With the Company's costs under control and with its lead therapeutics and other assets moving forward, as planned, the Company remains adequately funded to proceed with its current plans. I look forward to updating shareholders on further progress throughout the year.

Oliver de Giorgio-Miller

Non-Executive Chairman

19 August 2014

Consolidated statement of comprehensive income

Statement of changes in shareholders' equity

Consolidated statement of financial position

Cash flow statement

Notes to the interim financial statements

1 General information

ValiRx Plc is a company incorporated in the United Kingdom, which is listed on the AIM 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 2014 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 2013 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 2013.

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 per ordinary shares

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

5 Dividends

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

6 Share capital

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 for Editors

ValiRx Plc

ValiRx Plc is a biopharmaceutical company developing novel technologies and products in oncology therapeutics and diagnostics. The product focus is in the epigenomic analysis and treatment of cancer, but the technologies can be applied to other fields as well, such as neurology and inflammatory diseases.

The Company listed on AIM in October 2006 and is creating a portfolio of innovative products through investment in specific development projects. It actively manages projects within this portfolio as a trading company and is not an investment vehicle. The ValiRx business model spreads the risks of life science technology developments by minimising financial exposure and running a set of projects to defined commercial endpoints. This maximises returns to shareholders by adding value at the earlier stages where value increases per investment unit are the greatest.

The Company operates through the following divisional companies:

1. ValiFinn is the biomarkers and diagnostic development division

2. ValiPharma is the therapeutics division with two embedded technologies primarily directed at the treatment of cancers.