CRD007 for the Treatment of Duchenne Muscular Dystrophy, Becker Muscular Dystrophy and Symptomatic Carriers
NCT01540604 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2012-10-02
Summary
This is an investigation of the efficacy and safety of CRD007 in Duchenne Muscular Dystrophy (DMD), Becker Muscular Dystrophy (BMD) and symptomatic carriers.
Conditions
- Duchenne Muscular Dystrophy
- Becker Muscular Dystrophy
Interventions
- DRUG
-
CRD007
Sponsors & Collaborators
-
RSPR Pharma AB
lead INDUSTRY
Principal Investigators
-
T Sejersen, MD PhD · Karolinska University Hospital
Eligibility
- Min Age
- 2 Years
- Max Age
- 11 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
Countries
- Sweden
Study Locations
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