DISCLOSURE UNDER RULES 8.1(a), 8.1(b)(i) and 8.3 OF THE CITY CODE ON TAKEOVERS AND MERGERS

Date of dealing – 09/04/03

Dealing in RENEURON HOLDINGS

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In connection with the Offer, being made by KPMG Corporate Finance on behalf of St. James’s MGP Limited (“St. James’s”), the board of St James’s announces that the Offer Document and related Form of Acceptance are being posted today to ReNeuron Shareholders and, for information only, to participants in the ReNeuron Share Option Schemes.

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RECOMMENDED CASH OFFER
at 10 pence per share
by
KPMG Corporate Finance
on behalf of
St. James’s MGP Limited (“St. James’s”)
for
ReNeuron Holdings plc (“ReNeuron”)

Summary

The board of St. James’s and the Independent Directors of ReNeuron are pleased to announce that they have reached agreement on the terms of a recommended cash offer, to be made by KPMG Corporate Finance on behalf of St. James’s, to acquire the entire issued share capital of ReNeuron not already owned or contracted to be acquired by St. James’s. St. James’s is a newly incorporated company formed in order to implement the Offer and is owned and controlled by the Merlin Consortium.

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Lodge with Company Announcements Office and the Panel. Use a separate form for each class of securities in which dealings have been made.

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The Board of ReNeuron has noted the recent press speculation concerning the possibility of a sale of the Company. The Board confirms that it has received an approach and is in discussions which may or may not lead to an offer for the Company.

A further announcement will be made when appropriate.

Further information

Anna Rainbow
Smithfield Financial
020 7360 4900 or 07850 138260

Guildford, UK, 14 May 2009: ReNeuron Group plc (LSE: RENE.L) today provides a regulatory update regarding its ReN001 stem cell therapy for stroke. In January of this year, the UK Medicines and Healthcare Products Regulatory Agency (MHRA) granted regulatory approval for a Phase I clinical trial with ReN001 in disabled stroke patients, to be undertaken in Scotland at Glasgow Southern General Hospital. The decision was ratified by the Commission on Human Medicines, with the support of its Clinical Trials Expert Advisory Group which was also involved in reviewing the application.

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