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Nationwide Children's Hospital' Infant Corticosteroid Clinical Trial for Duchenne muscular dystrophy

Actively RecruitingPhase 4Reducing Inflammation

Study Overview

Age
0–3 years
Phase
Phase 4
Sponsor
Nationwide Children's Hospital
Therapeutic Approach
Reducing Inflammation
Variant Requirement
Established clinical diagnosis of DMD and documented dystrophin gene mutation predictive of DMD phenotype.
Eligible Sex
Male
Ambulation
Ambulatory
Study Start (Actual)
2021-04-30
Primary Completion (Estimated)
2026-08
Study Completion (Estimated)
2026-12
Enrollment (Estimated)
26
Countries
United States

Study Requirements and Criteria

Inclusion Criteria

  • Subjects ages 1 month through 30 months
  • Weakness consistent with Duchenne on exam, creatine kinase ≥ 20 times the upper limit of normal, and genetic mutation known to be causative for DMD.

Exclusion Criteria

Prior treatment with Glucocorticosteroids

Contact Information

This section provides contact details for people who can answer questions about joining this study

Clinical Trial Registry

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This information is provided for educational purposes only. Always consult the study investigators before making medical decisions.