The Food and Drug Administration approved the first gene therapy to treat the most common form of muscular dystrophy. Sarah Silbiger/Getty Images…
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Enlarge this image In a close vote, advisers to the Food and Drug Administration recommended approval of a gene therapy for muscular…
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Enlarge this image Susan and Chris Finazzo have enrolled their sons Dylan and Chase in a study of gene therapy for Duchenne…
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HealthDay Reporter WEDNESDAY, May 30, 2018 (HealthDay News) — President Donald Trump on Wednesday put his signature on a bill allowing terminally…
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HealthDay Reporter TUESDAY, Jan. 9, 2018 (HealthDay News) — In a potential advance for medical research, scientists say they’ve created the first…
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Feb. 14, 2017 — The U.S. launch of a drug for a rare disorder called Duchenne muscular dystrophy will be paused due…
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Feb. 10, 2017 — A new drug to treat Duchenne muscular dystrophy has been approved by the U.S. Food and Drug Administration.…
