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    You are at:Home»News»GSK phase III study of drisapersen to treat patients with Duchenne Muscular Dystrophy fails to meet primary endpoint

    GSK phase III study of drisapersen to treat patients with Duchenne Muscular Dystrophy fails to meet primary endpoint

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    By Rajeev Singla on September 24, 2013 News

    GlaxoSmithKline (GSK), one of the world’s leading research-based pharmaceutical and healthcare companies, and Prosensa, a Dutch biotechnology company, have reported that GSK’s phase III clinical study of drisapersen, an investigational anti-sense oligonucleotide, for the treatment of Duchenne Muscular Dystrophy (DMD) patients with an amenable mutation, did not meet the primary endpoint of a statistically significant improvement in the 6 Minute Walking Distance (6MWD) test compared to placebo.

     

    To read full news, visit:

    http://pharmabiz.com/NewsDetails.aspx?aid=77785&sid=2

    References:

    http://pharmabiz.com/

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