The FDA's Richard Pazdur will ultimately decide how to deal with the dangling accelerated approvals given to Sarepta Therapeutics for its Duchenne drugs.
Risk of “acute, serious, and life-threatening” heart inflammation is now on the label of Sarepta's gene therapy for Duchenne muscular dystrophy. What happens next?
This week on "The Readout LOUD" podcast: What does Rick Pazdur's new role mean for the FDA? And how much credit can the president take for lowering GLP-1 drug prices?
Intellia Therapeutics will find it challenging to survive now that its CRISPR gene-editing treatment has been tied to severe, potentially fatal, liver toxicity.