Jan 09, 2008 - VIVUS, Inc (NASDAQ: VVUS) a pharmaceutical company dedicated to the development and commercialization of novel therapeutic products, announced it has initiated a six-month extension study for patients currently enrolled in the OB-202 diabetes study. The OB-202 study is a 28 week, randomized, double blind, placebo controlled, efficacy and safety study of Qnexa(TM) in the glycemic management of obese Type 2 diabetics. The newly initiated study, DM-230, will allow subjects to continue, in a blinded fashion as randomized, in the study for an additional 28 weeks... VIVUS ' Press Release -
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- Medtronic, FDA Approval of CGMS iPro Continuous G...
- Arena Pharmaceuticals, APD668, Glucose-Dependent I...
- Daiichi Sankyo's Welchol, FDA Approval to Reduce B...
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- Incyte, HM74a agonist program for type 2 diabetes
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- DexCom, Joint Development Agreement with Animas Co...
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- VIVUS , Extension Study with Qnexa for Diabetes
- DiObex, Patent for the Prevention of Insulin-Induc...
- DIAMYD, PHASE III TRIAL WITH DIABETES VACCINE
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