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Metabolite Bioanalysis in Drug Development: Recommendations from the IQ Consortium Metabolite Bioanalysis Working Group.

Wenkui LiFaye Vazvaei-SmithGordon DearJason BoerFilip CuyckensDaniela FraierYuexia LiangDing LuHeidi MangusPatricia MolinerMette Lund PedersenAndrea A RomeoDouglas K SpracklinDavid S WagnerSerge WinterXiaohui Sophia Xu
Published in: Clinical pharmacology and therapeutics (2023)
The intent of this perspective is to share the recommendations of the International Consortium for Innovation and Quality in Pharmaceutical Development (IQ Consortium) Metabolite Bioanalysis Working Group (WG) on the fit-for-purpose metabolite bioanalysis in support of drug development and registration. This report summarizes the considerations for the trigger, timing, and rigor of bioanalysis in the various assessments to address unique challenges due to metabolites, with respect to efficacy and safety, which may arise during drug development from IND enabling studies, and Phase I, Phase II, and Phase III clinical trials to regulatory submission. The recommended approaches ensure that important drug metabolites are identified in a timely manner and properly characterized for efficient drug development.
Keyphrases
  • phase ii
  • clinical trial
  • phase iii
  • open label
  • ms ms
  • double blind
  • placebo controlled
  • randomized controlled trial
  • emergency department