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Parent Project Muscular Dystrophy and Sarepta Therapeutics Partner to Launch Duchenne Outcomes Research Interchange, a Patient-Data Warehouse Serving the Entire Duchenne Community

Parent Project Muscular Dystrophy (PPMD), a nonprofit organization leading the fight to end Duchenne muscular dystrophy (Duchenne), announced plans today to launch a patient- and physician-reported outcomes data warehouse – the Duchenne Outcomes Research Interchange (the Interchange) – which will combine data from The Duchenne Registry with clinician entered data provided by its inaugural partner, Sarepta Therapeutics, Inc., a commercial-stage biopharmaceutical company focused on the discovery and development of precision genetic medicines to treat rare neuromuscular diseases. The Duchenne Outcomes Research Interchange, scheduled to launch in 2019, will aggregate patient and clinician entered data obtained through various means, providing critical information to clinicians, sponsors, payers, regulators, and the patients/families who participate in PPMD’s Duchenne Registry.

Parent Project Muscular Dystrophy And Sarepta Therapeutics Partner To Launch Duchenne Outcomes Research Interchange, A Patient-Data Warehouse Serving The Entire Duchenne Community