The randomized, double-blind, multi-center studies were randomly assigned to treatment with either PA32540 or 325mg enteric-coated aspirin once daily. The primary endpoint, a significant reduction in the cumulative
The company can begin with the Phase III clinical trials, which include the efficacy study, since Phases I and II are not required for the product. Human fibrinogen
Quidel received FDA clearance in December 2011 to run its Quidel Molecular Influenza A+B and hMPV assays on Life Technologies’ Applied Biosystems 7500 Fast DX thermocycler. The product
In a multi-center double-blind randomized non-inferiority Phase III trial known as Study OPT-80-004, 509 adults with Clostridium difficile infection (CDI) received 400mg/day oral Dificlir or 500mg/day oral vancomycin
According to Indo Asian News Service, in the province, the distribution of Viagra to males with erectile dysfunction will be free and under obligatory medical prescription. Argentine health
The solution is the generic morphine oral solution to be approved by the FDA and is available in 100 milligrams per 5mL (20 milligrams per 1mL). Morphine sulfate
Fit Artery offers ethyl eicosapentaenoic acid, docosahexaenoic acid, gamma linoleic acid, noni and Omega-3 fatty acids, while Fit Bone provides calcium, vitamin D, vitamin K2 and magnesium. The
The new product is based on the latest research conducted by the National Institute of Health, which discovered the key ingredients that help prevent the onset of macular
The approval was based on a double-blind trial, in which BYETTA 10 micrograms or placebo was added to existing insulin glargine therapy, which was titrated to achieve target
Financial terms of the agreement have not been disclosed. FBMFarma will be responsible for obtaining regulatory approval, marketing and distribution in Brazil. Ampio CEO Michael Macaluso said that
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