June 23, 2017
RARECast: Summit Pursues A Different Approach to Treating Duchenne
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January 19, 2017
Why Health Insurers Won't Cover this $300,000-a-year Rare Disease Drug
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November 2, 2016
cTAP Announces Two Research Publications Categorizing and Predicting Disease Progression in Duchenne Muscular Dystrophy
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September 30, 2016
RARECast: A Controversial Approval for a Duchenne Drug and What Lies Ahead
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September 17, 2015
Rare Disease Reports: FDA Accepts Sarepta’s Sarepta’s NDA for Eteplirsen. PDUFA Date Set
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August 13, 2014
FDA Boosts Sarepta With Prognosis for its Rare Disease Drug
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March 11, 2014
JPMorgan Dad Turns Biotech CEO in Quest to Save his Son
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May 1, 2013
Highlights from the World Orphan Drug Congress 2013
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October 3, 2012
Sarepta Therapeutics Clinical Trial Results with Eteplirsen Brings Kids with Duchenne Muscular Dystrophy Closer to Treatment
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