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Sarepta Shares Plunge After ESSENCE Phase 3 Miss in Duchenne Trial

The company will seek FDA guidance on converting its exon-skipping drugs from accelerated to full approval.

FDA Setback Puts uniQure’s Huntington’s Gene Therapy Filing in Doubt

First Human Trial Finds Enteral Ventilation Procedure Tolerable in Healthy Volunteers

Samsung Invests $110 Million in Grail to Bring Galleri Cancer Test to Asia