FDA Rejects Duchenne Muscular Dystrophy Drug Golodirsen, Pfizer Recalls Acute Migraine Treatment Relpax, Alzheimer Disease Update
Neurology News Network for the week ending August 24, 2019.
This week, Neurology News Network covered the complete response letter to Sarepta Therapeutics for its NDA for golodirsen to treat Duchenne muscular dystrophy, Pfizer's recall of its acute migraine treatment Relpax, and the second episode of the Mind Moments podcast on the amyloid hypothesis and future of Alzheimer disease (transcript below).
Jenna:
Welcome to Neurology News Network. I’m Jenna Payesko. Let’s get into the news from this week.
The FDA has issued a
Doug Ingram, president and CEO of Sarepta, said in a statement that Sarepta was “very surprised to have received the complete response letter.” Sarepta is immediately requesting a meeting with the FDA to determine next steps.
Those with an existing inventory of the lots that are being recalled should stop use and distribution and quarantine immediately. Any adverse reactions or problems with Relpax should be reported to the FDA’s MedWatch Adverse Event Reporting program.
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