The FDA has given Sarepta Therapeutics the green light for its phase 2 Duchenne muscular dystrophy clinical trial after slapping the biotech with a clinical hold in June. The hold came after a grade 3 adverse event was reported in the midstage trial. Now, only a few months later, the agency has lifted the hold, and we'll discuss why there was a quick turnaround on the hold and what to expect next. 
To learn more about topics in this episode: 

Sarepta picks up momentum as FDA lifts hold on phase 2 DMD trial 
As EU challenge intensifies, Illumina clocks a stateside win in FTC antitrust case over Grail buy 
EU blocks Illumina's yearslong quest for Grail 
Philips recalls 17M CPAP and BiPAP machine masks due to potential magnet interference 
GSK helps SpringWorks double payday from boosted combo deal as it also reels $225M in new funding 
BMS-backed Arsenal Bio pulls trigger on $220M series B, touting potential fleet of gene-edited cell therapies 
Amylyx's ALS drug faces tough FDA scrutiny ahead of 2nd advisory panel meeting

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