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The study also comfortably met the main secondary endpoint, demonstrating that naproxcinod 750mg bid was statistically non-inferior to naproxen 500mg bid on the Womac pain and function subscales

The complete response addresses the FDA approvable letter received in March 2008 related to the ceftobiprole new drug application (NDA) for the treatment of complicated skin and skin

Coartem, a fixed-dose combination of two antimalarials, is said to be a highly effective three-day malaria treatment that according to studies achieves cure rates of over 96% even

In the two Phase III clinical trials, patients were randomly assigned to treatment with Botox or placebo injections every 12 weeks. The primary analysis was performed at week

The MDS study is designed as a protocol amendment expanding the ongoing Phase II trial of sapacitabine in elderly patients with acute myeloid leukemia (AML) to include a

The study is a randomized, double-blind, placebo-controlled, dose-ranging study to evaluate the safety, tolerability and efficacy of daily TT-223 treatments for 12 weeks with a six-month follow-up. Approximately

In total, the agreement grants rights to Menarini for Ranexa in 68 countries, including the 27 countries of the EU, the Commonwealth of Independent States, and select countries

Valeant has received approximately $425 million in cash from Meda at closing, which is subject to certain closing adjustments. Goldman, Sachs & Co served as financial advisor to

According to the company, the implantable monitor enables physicians to evaluate heart rhythm signals over a longer period of time than allowed by standard monitoring tests, and is