 
    Sarepta Seeks Broader Approval for Gene Therapy Even After Drug Trial Fizzled
      Normally when a drug fails to show a clear effect in a final-stage trial, the company developing it
      2023-11-01 05:25
     
    Gene Therapy for Kids’ Deadly Muscle Disease Fails to Reach Trial Goal 
      Roche Holding AG shares dropped after a trial of its gene therapy for Duchenne muscular dystrophy did not
      2023-10-31 16:59
     
    Drug Companies Are Minting Billions on Unproven Treatments With FDA Shortcut
      When Exondys 51 was approved to treat Duchenne muscular dystrophy, a deadly disease that puts kids in wheelchairs
      2023-05-15 07:23
    