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CRD007 for the Treatment of Duchenne Muscular Dystrophy, Becker Muscular Dystrophy and Symptomatic Carriers

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ClinicalTrials.gov Identifier: NCT01540604
Recruitment Status : Completed
First Posted : February 29, 2012
Last Update Posted : October 2, 2012
Information provided by (Responsible Party):
RSPR Pharma AB

Brief Summary:
This is an investigation of the efficacy and safety of CRD007 in Duchenne Muscular Dystrophy (DMD), Becker Muscular Dystrophy (BMD) and symptomatic carriers.

Condition or disease Intervention/treatment Phase
Duchenne Muscular Dystrophy Becker Muscular Dystrophy Drug: CRD007 Phase 2

Study Type : Interventional  (Clinical Trial)
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

Arm Intervention/treatment
Experimental: CRD007 10 mg tablet Drug: CRD007

Information from the National Library of Medicine

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Ages Eligible for Study:   2 Years to 11 Years   (Child)
Sexes Eligible for Study:   All

Inclusion Criteria:

  • Documented diagnosis of dystrophinopathy

Exclusion Criteria:

  • Severe functional impairment

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01540604

Stockholm, Sweden
Sponsors and Collaborators
RSPR Pharma AB
Principal Investigator: T Sejersen, MD PhD Karolinska University Hospital

Responsible Party: RSPR Pharma AB
ClinicalTrials.gov Identifier: NCT01540604     History of Changes
Other Study ID Numbers: Cardoz-004
First Posted: February 29, 2012    Key Record Dates
Last Update Posted: October 2, 2012
Last Verified: October 2012

Keywords provided by RSPR Pharma AB:
symptomatic carriers

Additional relevant MeSH terms:
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Muscular Disorders, Atrophic
Muscular Diseases
Musculoskeletal Diseases
Neuromuscular Diseases
Nervous System Diseases
Genetic Diseases, Inborn
Genetic Diseases, X-Linked