KER-065 granted FDA Orphan Drug designation for DMD
KER-065, an experimental Duchenne muscular dystrophy (DMD) drug, has been granted Orphan Drug designation by the FDA.
KER-065, an experimental Duchenne muscular dystrophy (DMD) drug, has been granted Orphan Drug designation by the FDA.
DYNE-251, developed by Dyne Therapeutics and aimed at treating DMD, has received a Breakthrough Therapy Designation.
A recent case report examines the rare case of a teenage girl with DMD that was complicated by acute respiratory distress syndrome.
Sarepta Therapeutics has announced that it will voluntarily stop all shipments of the DMD therapeutic agent Elevidys.
Beta-blocker therapy appears to be beneficial in the context of Duchenne muscular dystrophy (DMD) complicated by cardiac dysfunction.
Accommodating the functional impairments associated with DMD appears to involve substantial costs for households.
Cholesterol and triglyceride levels appear to be inversely correlated with bone density in patients with Duchenne muscular dystrophy (DMD).
Boys with DMD, their parents and health professionals have a mix of perspectives on the use of bisphosphonates to prevent osteoporosis.
Muscle contractures contribute significantly to walking (gait) abnormalities in patients with Duchenne muscular dystrophy (DMD).
Initiation of home mechanical ventilation around the age of 20 appears to slow respiratory deterioration in patients with DMD.