Loading clinical trials...
Loading clinical trials...
Duchenne muscular dystrophy (DMD) is a X-linked recessive disorder due to a mutation of the dystrophin gene (Xp21). Dystrophin is a sarcolemmal protein of skeletal and cardiac muscle, and its absence ...
Keep your clinical trial research organized — questions to ask, what to expect, and key details.
Lead Sponsor
Istituto Auxologico Italiano
NCT07665424 · Osteoporosis, Osteoporotic Vertebral Compression Fractures
NCT07423026 · Duchenne Muscular Dystrophy (DMD)
NCT07160634 · Duchenne Muscular Dystrophy
NCT07027306 · Osteoporotic Fractures, Osteoporosis
NCT06817382 · Duchenne Muscular Dystrophy
Use Clareo to keep notes, questions, trial details, and next steps organized before and after appointments.
Start free trial →Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions