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NCT01540604 Clinical Trial

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

Duchenne Muscular Dystrophy 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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01540604
Other study ID # Cardoz-004
Secondary ID
Status Completed
Phase Phase 2
First received February 23, 2012
Last updated October 1, 2012

Study information
Verified date October 2012
Source RSPR Pharma AB
Contact n/a
Is FDA regulated No
Health authority Sweden: Medical Products Agency
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 2 Years to 11 Years
Eligibility Inclusion Criteria:

- Documented diagnosis of dystrophinopathy

Exclusion Criteria:

- Severe functional impairment

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Drug:
• CRD007

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
RSPR Pharma AB

Country where clinical trial is conducted

Sweden, 

See also
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