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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01540604
First Posted: February 29, 2012
Last Update Posted: October 2, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
RSPR Pharma AB
  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:


Further study details as provided by RSPR Pharma AB:

Arms Assigned Interventions
Experimental: CRD007 10 mg tablet Drug: CRD007

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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

Inclusion Criteria:

  • Documented diagnosis of dystrophinopathy

Exclusion Criteria:

  • Severe functional impairment
  Contacts and Locations
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


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

Responsible Party: RSPR Pharma AB
ClinicalTrials.gov Identifier: NCT01540604     History of Changes
Other Study ID Numbers: Cardoz-004
First Submitted: February 23, 2012
First Posted: February 29, 2012
Last Update Posted: October 2, 2012
Last Verified: October 2012

Keywords provided by RSPR Pharma AB:
DMD
BMD
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


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