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Santhera and ReveraGen Complete NDA Submission to FDA for Vamorolone in Duchenne Muscular Dystrophy - CureDuchenne
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Humanigen starts rolling submission for Covid-19 drug in the UK
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NewLink Genetics Announces Merck Has Begun Rolling Submission of Licensure Application for Ebola vaccine V920 (rVSV∆G-ZEBOV-GP) to U.S. Food and Drug Administration | ISU Research Park
Call for Posts: Truth and Youth journal (Register by 15 Jan)
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Santhera and ReveraGen Start Rolling NDA Submission to the FDA for Vamorolone for the Treatment of Duchenne - Parent Project Muscular Dystrophy
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Sage Therapeutics and Biogen Initiate Rolling Submission of New Drug Application (NDA) to U.S. Food and Drug Administration for Zuranolone for the Potential Treatment of Major Depressive Disorder (MDD) | Sage Therapeutics,
Eisai Starting FDA Submission for Alzheimer's Therapy Lecanemab
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Merck Canada Initiates Rolling Submission to Health Canada for Molnupiravir, an Investigational Oral Therapeutic Agent for the Treatment of COVID-19
Madrigal starts rolling submission for NASH drug application with US FDA | Reuters
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Merck Canada Initiates Rolling Submission to Health Canada for Molnupiravir, an Investigational Oral Therapeutic Agent for the Treatment of COVID-19
Pfizer Inc. on Twitter: "BREAKING: Today, with @BioNTech_Group, we initiated the submission of a BLA for @FDA approval of the Pfizer-BioNTech #COVID19 vaccine to prevent COVID-19 in individuals 16 years and older.
Reata Pharmaceuticals on Twitter: "We're excited to announce that we have completed the rolling New Drug Application (NDA) for omaveloxolone." / Twitter
Sage Therapeutics and Biogen Initiate Rolling Submission of New Drug Application (NDA) to U.S. Food and Drug Administration for Zuranolone for the Potential Treatment of Major Depressive Disorder (MDD) | Business Wire