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Wyeths SERM Bazedoxifene receives approvable letter from the FDA

Posted on May 23, 2008 by crimsoncanary

Wyeth have received an approvable letter from the FDA for their SERM bazedoxifene, in development for the treatment of postmenopausal osteoporosis.  The FDA requires further analyses concerning the incidence of stroke and venous thrombotic events.

Filed under: Nuclear Receptor | Tagged: Bazedoxifene, estrogen receptor, ser, viviant, wyeth

« US and WO patent update for the week ending 05/23 Repros Therapeutics Progesterone receptor antagonist Proellex safe in uterine fibroids »

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