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PPMD Applauds FDA for Landmark Approval of First-Ever Gene Therapy Treatment for Duchenne for Patients Ages 4-5 Years Old

PPMD Applauds FDA for Landmark Approval of First-Ever Gene Therapy Treatment for Duchenne for Patients Ages 4-5 Years Old
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United statesJerry mendellDuchenne outcomes research interchange theGene therapy initiativeElectronic health recordDrug administrationOrganization will continueSupport patient accessDrive policiesProjects that support developmentProject muscular dystrophyAccelerated approvalSarepta therapeuticsNationwide childrenHospital abigail wexner research instituteTherapy town hall

PPMD Applauds FDA for Landmark Approval of First-Ever Gene Therapy Treatment for Duchenne for Patients Ages 4-5 Years Old

/PRNewswire/ Parent Project Muscular Dystrophy (PPMD), a nonprofit organization leading the fight to end Duchenne muscular dystrophy (Duchenne), heralded.

United statesJerry mendellGene therapy initiativeElectronic health recordDuchenne outcomes research interchange theDrug administrationOrganization will continueSupport patient accessDrive policiesProjects that support developmentProject muscular dystrophyAccelerated approvalSarepta therapeuticsNationwide childrenAbigail wexner research instituteGene therapy town hall