Study of an Investigational Drug, RO7239361 (BMS-986089), in Ambulatory Boys With DMD

  • Muscular Dystrophy
  • Duchenne Muscular Dystrophy (DMD)
Trial Status:


This trial runs in
  • Atlanta
  • Baltimore
  • Calgary
  • Chicago
  • Cincinnati
  • Gainesville
  • Kansas City
  • Los Angeles
  • Orlando
  • Ottawa
  • St. Louis
  • Stanford
Trial Identifier:

NCT02515669 WN40226 CN001-006

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      The source of the below information is the publicly available website It has been summarised and edited into simpler language.

      The below information is taken directly from the publicly available website within a week of any updates, and has not been edited.

      Results Disclaimer

      Trial Summary

      The purpose of this study is to determine the safety and tolerability of RO7239361 in boys with Duchenne Muscular Dystrophy with any genetic mutation.

      Hoffmann-La Roche Sponsor
      Phase 1/Phase 2 Phase
      NCT02515669 , CN001-006 , WN40226 Trial Identifier
      RO7239361, Placebo Treatments
      Muscular Dystrophy (DMD) Condition
      Official Title

      A Multi-Site, Randomized, Placebo-Controlled, Double-Blind, Multiple Ascending Subcutaneous Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of RO7239361 (BMS-986089) in Ambulatory Boys With Duchenne Muscular Dystrophy

      Eligibility Criteria

      Male Gender
      ≥5 Years & ≤ 10 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • Diagnosed with DMD
      • Able to walk without assistance
      • Able to walk up 4 stairs in 8 seconds or less
      • Weigh at least 15 kg
      • Taking corticosteroids for DMD
      Exclusion Criteria
      • Ejection fraction < 55% on echocardiogram, based on central read
      • Any behavior or mental issue that will affect the ability to complete the required study procedures
      • Previously or currently taking medications like androgens or human growth hormone
      • Use of a ventilator during the day
      • Unable to have blood samples collected or receive an injection under the skin
      • Treatment with exon skipping therapies 6 months prior to study start
      • Treatment with ataluren or any investigational drug currently or within 5 half-lives prior to study start

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