Browse 493 Dystrophy clinical trials enrolling across the United States and Canada. Search by city or state to find one near you.
Muscular dystrophy is not one disease but a group of more than 30 inherited conditions that weaken muscles over time, each caused by a different gene. Some, like Duchenne, begin in early childhood, while the most common adult form, myotonic dystrophy, may not appear until middle age. Most forms still have no treatment that slows them, and knowing the exact gene now opens the door to trials of gene therapies and medicines designed for one specific form.
Does Clinical Treatment of Mitochondrial Dysfunction Impact Autism Spectrum Disorder (ASD)?
for
Autism Spectrum Disorders, Mitochondrial Diseases
Location: Philadelphia PA
Sponsor: Drexel University
Sex: All
Age: 3 - 12
Code: NCT02348125
Phase 1, Recruiting
A Phase 2a, Single-dose, Open-label Study to Evaluate Diagnostic Performance and Safety of Pegsitacianine, an Intraoperative Fluorescence Imaging Agent for the Detection of Cancer, in Patients With Unknown Primary Head and Neck Cancer (ILLUMINATE STUDY)
for
Head and Neck Cancer, Unknown Primary Cancer,
Location: Dallas TX
Sponsor: University of Texas Southwestern Medical Center