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Characteristics of Clinical Trial Participants with Duchenne Muscular Dystrophy: Data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet).

Katherine D MathewsKristin M ConwayAmber M GedlinskeNicholas JohnsonNatalie StreetRussell J ButterfieldMan HungEmma CiafaloniPaul A Romitti
Published in: Children (Basel, Switzerland) (2021)
Clinical trial participation was identified among 17.9% (MD STARnet site: 3.7-27.3%) of 358 individuals with DMD. Corticosteroids, tadalafil, and ataluren (PTC124) were the most common trial medications recorded. Fewer non-Hispanic blacks or Hispanics than non-Hispanic whites participated in clinical trials. Trial participants tended to reside in counties with lower percentages of non-Hispanic blacks. Conclusion: Understanding characteristics associated with clinical trial participation is critical for identifying participation barriers and generalizability of trial results. MD STARnet is uniquely able to track clinical trial participation through surveillance and describe patterns of participation.
Keyphrases
  • clinical trial
  • duchenne muscular dystrophy
  • phase ii
  • phase iii
  • muscular dystrophy
  • physical activity
  • study protocol
  • open label
  • double blind
  • molecular dynamics
  • public health
  • african american
  • artificial intelligence