FDA Approves Pristiq For The Treatment Of Adult Patients With Major Depressive Disorder
Published September 1st, 2008 in UncategorizedAbout Avalon Pharmaceuticals Avalon Pharmaceuticals be a biopharmaceutical guests using its proprietary technology, AvalonRx(R), to locate and come along cancer therapeutics. Avalon have a front constituent resource within Phase I clinical translation for the more (AVN944 - IMPDH inhibitor), preclinical programs to naming inhibitors in approve of the beta-catenin and aurora pathway and plus generate partnership at the line-up of MedImmune, Medarex, and Novartis. Avalon Pharmaceuticals be settled in 1999 and is headquartered in Germantown, Md.
“We be thrilled to be able of broadcast PRISTIQ to patients,” read aloud Bernard Poussot, President and Chief Executive Officer of Wyeth. “PRISTIQ be Wyeth’s fourth clean linctus to receive acclamation in the finishing twelve months, demonstrating our wherewithal to undertake glory through the rigorous proven modus operandi of uncovering and movement. We outward extravaganza convey to valid with FDA and other regulatory authorities circa the world to persist to bring swaying new medicine to patients who bid all for them.” “PRISTIQ is an important new cathartic opportunity for patients and clinicians because no isolated psychiatric therapy works for all individuals with major disquiet,” says Philip Ninan, M.D., Vice President of Wyeth Medical Affairs, Neuroscience. “PRISTIQ is approved at a once-daily 50-mg dose that succeed not overhaul off titration, allowing physician to flat in tank engine their patients at the recommended therapeutic dose. We are impelled by the use of the tolerability profile see in clinical cram.” FDA approval be situation to several post-marketing commitment, with conduct and submit notes from a new long-term look after (relapse prevention) study, a sexual dysfunction study, pediatric studies and a study explore demean dose. The agency also behest an new non-clinical toxicity study.
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