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NicOx Updates On Naproxcinod FDA Approval

The FDA Arthritis Drugs Advisory Committee and Drug Safety and Risk Management Committee based their recommendation on a review of data from the Naproxcinod clinical development program, which

Aventis Releases New Delhi SITE Study Results

Aventis Pharma said that SITE is the first cross-sectional study to assess the prevalence of diagnosed and undiagnosed cases of diabetes and hypertension amongst nearly 20,000 patients visiting

Aeterna Zentaris Q1 Revenues Increase

Aeterna Zentaris has posted a net loss of $5.9m for the first quarter of 2010, or $0.09 per diluted share, compared to $12.4m, or $0.23 per diluted share,

Shire Sues Actavis Elizabeth, Actavis

Shire said that the lawsuit results from an abbreviated new drug application (ANDA) filed by Actavis for generic versions of 1mg, 2mg, 3mg and 4mg guanfacine hydrochloride extended