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Sarepta Therapeutics Soars on Expanded Approval for Its Muscular Dystrophy Drug

Pavlo Gonchar / SOPA Images / LightRocket via Getty Images

Key TakeawaysSarepta Therapeutics shares jumped in premarket trading Friday, a day after the biotech firm received Food and Drug Administration approval for wider use of its drug to treat a rare muscle disease.The company's Elevidys received traditional approval for those at least 4 years old with Duchenne muscular dystrophy who can walk, and accelerated approval to treat patients who cannot walk.Sarepta said it is currently holding a Phase 3 trial to gain more FDA clearance for Elevidys' use.
Sarepta Therapeutics (SRPT) shares soared in premarket trading Friday, a day after the Food and Drug Administration (FDA) allowed expanded use of the biotech’s treatment for a rare muscle disease in children, which especially affects boys.The company said its drug, Elevidys, was given traditional approval for patients who are at least 4 years old and suffer from Duchenne muscular dystrophy (DMD) with a confirmed mutation in the DMD gene and can walk.Phase 3 Trial for Non-Ambulatory Individuals With DMD Currently UnderwaySarepta said regulators granted accelerated approval for use in those who cannot walk, and continued approval “may be contingent upon verification of clinical benefit in a confirmatory trial.” The company added that a Phase 3 study to make that confirmation is currently underway.The FDA gave accelerated approval for the gene-therapy medicine in 4- and 5-year-olds last year, despite some questions about its efficacy. Dr. Jerry Mendell, co-inventor of Elevidys and a senior adviser at Sarepta, said that the initial approval was a significant milestone, “and the expanded indication means clinicians now have a treatment option for the great majority of boys and young men living with Duchenne.”Sarepta shares soared 35% to $167.00 an hour before the opening bell Friday after closing Thursday up 5.1% to $123.50.

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