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1 day agoA comparative Phase IV study of Merck & Co. and Schering-Plough’s Zetia (ezetimibe) and Abbott’s Niaspan (niacin) was stopped early last
1 day agoBy Anne Marie Murphy – FDA’s final rule requiring IRBs that review FDA-regulated clinical investigations to register through a system maintained
2 days agoNanyang Technological University (NTU)'s Associate Professor Zhong Guofu has made a significant contribution to the field of organic chemistry,
3 days agoJapanese regulators granted Astellas expanded approval to sell Prograf (tacrolimus) as a treatment for moderate-to-severe refractory ulcerative
3 days agoA final analysis of Phase III study data published Tuesday in The Lancet suggests that GlaxoSmithKline’s vaccine Cervarix protects against
3 days agoAmgen shares rose as much as 14 percent after markets closed Tuesday following the company’s announcement that denosumab met the primary and
5 days agoKing and Acura announced the receipt of a complete response letter regarding Acurox (oxycodone/niacin), in which the FDA “raises issues
5 days agoThe European Commission approved Novo Nordisk’s Victoza (liraglutide) for the treatment of type 2 diabetes in adults. The company hopes to
5 days agoSanofi-aventis announced that the FDA approved Multaq (dronedarone) to reduce the risk of cardiovascular hospitalisation in patients with
5 days agoFinding alternative indications is about finding potential problems as well! The therapeutic pathways gives warnings and opportunities!
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