MAP Pharmaceuticals Announces FDA Will Not Require A Second Pivotal Efficacy Study For LEVADEX(TM) NDA Submission
January 12th, 2010 by adminMAP Pharmaceuticals, Inc. (Nasdaq: MAPP) announced that the U.S. Food and Drug Administration (FDA) has informed the Company that a second pivotal efficacy study is not required for the Company’s LEVADEX(TM) new drug application (NDA) submission for the acute treatment of migraine…
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