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Share Name | Share Symbol | Market | Type | Share ISIN | Share Description |
---|---|---|---|---|---|
Argent Biopharma Limited | LSE:RGT | London | Ordinary Share | AU0000326647 | ORD NPV (DI) |
Price Change | % Change | Share Price | Bid Price | Offer Price | High Price | Low Price | Open Price | Shares Traded | Last Trade | |
---|---|---|---|---|---|---|---|---|---|---|
0.00 | 0.00% | 6.50 | 5.00 | 8.00 | 6.50 | 6.50 | 6.50 | 1,662 | 00:00:00 |
Industry Sector | Turnover | Profit | EPS - Basic | PE Ratio | Market Cap |
---|---|---|---|---|---|
0 | 0 | N/A | 0 |
RNS Number:0938T ReGen Therapeutics PLC 10 December 2003 ReGen Therapeutics Plc 10th December 2003 Research & Development Update Percy Lomax, chairman of ReGen Therapeutics Plc, ("ReGen" or "the Company") which is developing ColostrininTM, as a treatment for Alzheimer's disease, is today chairing a briefing to investors and analysts, when he will be updating them on research and development progress made over the last 12 months. A clinical trial of ColostrininTM on 106 patients demonstrated statistically significant efficacy as measured by ADAS cog (a measure of cognitive/memory function) in treated patients, with no safety concerns. Following completion of this trial ReGen has, over the last 18 months, been undertaking an extensive scientific development programme, much of it in collaboration with the University of Texas Medical Branch (UTMB). Key areas of activity have focused on developing a greater understanding of the mode of action of ColostrininTM, which in turn has enabled development of bio-assays and the identification of animal (in-vivo) models. These are crucial elements in developing an effective manufacturing process and fully evaluating the therapeutic potential of ColostrininTM in Alzheimer's and other diseases. Progress made to date encourages the Company to believe that continuation of this work will place ReGen in a position to begin the next stage of clinical development around the end of 2004. The Company anticipates that such clinical trials will be undertaken in collaboration with a co-development/commercialisation partner. In this context ReGen states that it is working with a licensing company to assist with finding such a partner. ReGen has also made considerable progress in planning the development opportunities for ColostrininTM as a nutraceutical, in particular in the United States. With regard to the manufacturing of ColostrininTM, it has been confirmed that the more readily available bovine colostrum (as opposed to ovine), can be used as the source material, and a contract has recently been agreed and is awaiting signature with a major US bovine colostrum processor, which will enable cost-effective access to a manufacturing facility without any major capital expenditure. Finally, although preliminary data only is available at the moment a proteomics screen with ColostrininTM has shown that it has the ability to selectively modulate the expression of proteins by nerve cells in culture. This confirms that active principles within ColostrininTM are able to activate cells and direct the synthesis of proteins. The nature of these proteins is now being investigated. This work offers the prospect of shedding even more light on the way ColostrininTM works and identifying new potential disease targets and uses. Further information: Andrew Marshall Marshall Robinson Roe Tel No: 020 7960 6007 This information is provided by RNS The company news service from the London Stock Exchange END RESFFIFESSDSEDE
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