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Application of Bayesian methods to accelerate rare disease drug development: scopes and hurdles.

Kelley M KidwellSatrajit RoychoudhuryBarbara WendelbergerJohn ScottTara MorozShaoming YinMadhurima MajumderJohn ZhongRaymond A HumlVeronica Miller
Published in: Orphanet journal of rare diseases (2022)
The use of innovative trial designs such as master protocols and complex adaptive designs in conjunction with a Bayesian approach may help to reduce sample size, select the correct treatment and population, and accurately and reliably assess the treatment effect in the rare disease setting.
Keyphrases
  • clinical trial
  • randomized controlled trial
  • study protocol
  • phase iii
  • double blind
  • cell fate