Trial record 1 of 3 for:
cardoz
CRD007 for the Treatment of Duchenne Muscular Dystrophy, Becker Muscular Dystrophy and Symptomatic Carriers
This study has been completed.
Sponsor:
Cardoz AB
Information provided by (Responsible Party):
Cardoz AB
ClinicalTrials.gov Identifier:
NCT01540604
First received: February 23, 2012
Last updated: October 1, 2012
Last verified: October 2012
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Purpose
This is an investigation of the efficacy and safety of CRD007 in Duchenne Muscular Dystrophy (DMD), Becker Muscular Dystrophy (BMD) and symptomatic carriers.
| Condition | Intervention | Phase |
|---|---|---|
|
Duchenne Muscular Dystrophy Becker Muscular Dystrophy |
Drug: CRD007 |
Phase 2 |
| Study Type: | Interventional |
| Official Title: | An Open-label, Un-controlled, Single-centre Trial Investigating the Efficacy and Safety of CRD007 in Children With Duchenne Muscular Dystrophy (DMD) or Becker Muscular Dystrophy (BMD) or Children Being Symptomatic Carriers for DMD or BMD |
Resource links provided by NLM:
Genetics Home Reference related topics:
Duchenne and Becker muscular dystrophy
MedlinePlus related topics:
Muscular Dystrophy
U.S. FDA Resources
Further study details as provided by Cardoz AB:
Eligibility| Ages Eligible for Study: | 2 Years to 11 Years |
| Genders Eligible for Study: | Both |
Criteria
Inclusion Criteria:
- Documented diagnosis of dystrophinopathy
Exclusion Criteria:
- Severe functional impairment
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Cardoz AB |
| ClinicalTrials.gov Identifier: | NCT01540604 History of Changes |
| Other Study ID Numbers: | Cardoz-004 |
| Study First Received: | February 23, 2012 |
| Last Updated: | October 1, 2012 |
| Health Authority: | Sweden: Medical Products Agency |
Keywords provided by Cardoz AB:
|
DMD BMD symptomatic carriers |
Additional relevant MeSH terms:
|
Muscular Dystrophy, Duchenne Muscular Dystrophies Muscular Disorders, Atrophic Muscular Diseases Musculoskeletal Diseases |
Neuromuscular Diseases Nervous System Diseases Genetic Diseases, X-Linked Genetic Diseases, Inborn |
ClinicalTrials.gov processed this record on May 21, 2013