Wednesday, July 9, 2008

Pharmacopeia Initiates Second Phase 2 Hypertension Study With PS433540 (DARA) Part 2




PS433540 be a dual-acting angiotensin (AII) and endothelin (ET1) receptor antagonist that is to say anyone mechanized in lines of a forthcoming usage in support of hypertension and diabetic nephropathy. PS433540, the exit and merely DARA combination in change for the in good levitra professional, possesses two clinically validate gears of accomplishment in a spinster compound. There is palpable preclinical and opening clinical notes suggesting that associate to any agent alone, at once blocking the appointments of both AII and ET1 may horses importantly superior treatment option for several cardiovascular disease.



ABOUT PHARMACOPEIA Pharmacopeia is a clinical development time biopharmaceutical solidarity staunch to discover and sprouting innovative baby molecule therapeutics to address having an important effect medical desires. The company have a significant portfolio of clinical and preclinical candidate underneath development internally or via partner with seven clinical compound in Phase 2 or Phase 1 development address multiple manifestation including hypertension, diabetic nephropathy, muscle wasting, inflammation and respiratory bug. The company is leveraging its fully integrated pills uncovering stand for to sustain the dissemination out of its development pipeline. Pharmacopeia has settled strategic agreements implicit utmost important pharmaceutical and biotechnology company, including Bristol-Myers Squibb, Celgene, Cephalon, GlaxoSmithKline, Organon, Schering-Plough, and Wyeth Pharmaceuticals. For more gen clear happy send for sphere-shaped the company's website at This wring rescue, and oral statement made with honour to information contained here press release, constitute forward-looking statements within the story of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements embrace those which voice line of attack, anticipation, set, aspiration, contingency or approaching development and/or otherwise be not statements of historical realness. These statements are groundwork upon management's contemporary expectations and are speciality to chance and uncertainties, known and unknown, which could require actual grades and development to show a discrepancy materially from those expressed or implied in such statements. These forward- construct your eye by the side of statements include, but are not enclosed to, statements in the region of the winning finishing of Pharmacopeia's strategic policy, Pharmacopeia's plans coming up and about along PS433540, a service buoyant from its DARA program, Pharmacopeia's Phase 2 and Phase 1 clinical study with respect to PS433540, including time and looked-for outcome of such studies, Pharmacopeia's plans to develop PS178990, a product candidate from its SARM program, Pharmacopeia's Phase 1 clinical studies with respect to PS178990, including timing and expected outcomes of such studies, Pharmacopeia's plans to develop PS031291, a product candidate from its chemokine receptor CCR1 program, Pharmacopeia's estimate of the marketplace opportunity for its product candidates, including PS433540, PS178990 and PS031291, Pharmacopeia's skilfulness to jubilantly complete under its help with Bristol-Myers Squibb, Cephalon, GlaxoSmithKline, Schering-Plough and Wyeth, Pharmacopeia's ability to piece its pipeline of novel drug candidates through its personal internally-funded drug discovery programs, third get-together collaborations and in-licensing, Pharmacopeia's ability to elevate spare wherewithal, Pharmacopeia's expectations on the topic of the development priority of its collaborator, their ability to successfully develop compounds and its acceptance of milestone and royalty from the collaborations, Pharmacopeia's anticipated operating results, wholesale and industry disorder, liquidity and capital possessions, Pharmacopeia's expectations concerning the permissible protection afford by U.S. and mixed elite rights canon, Pharmacopeia's ability to persecute the development of scalding compounds and other commercial matter squat infringing the patent rights of others, additional gala, and change in financial stipulations.



Further information about these and other useful risks and uncertainties may be found in Pharmacopeia's Reports on Form 8-K, 10-Q and 10-K file with the U.S. Securities and Exchange Commission. Pharmacopeia urge you to guardedly analysis and muse the disclosure found in its filings which are unclaimed in the SEC EDGAR database at and from Pharmacopeia at All forward-looking statements in this press release and oral statements made with respect to information contained in this press release are qualified entirely by the threatening statements integrated in this press release and such filings. These risks and uncertainties could cause actual results to differ materially from results expressed or implied by such forward-looking statements. These forward-looking statements cry only since the date of this press release. Pharmacopeia undertake no must to (and expressly disclaim any such obligation to) publicly update or modify the statements made herein or the risk factor that may report thereto whether by this way of new information, future measures, or otherwise.



Pharmacopeia



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