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Towards comprehensive clinical trials for new tuberculosis drug regimens: policy recommendations from a stakeholder analysis.

Simone VillaPierpaolo de ColombaniLucia Dall'OlioGiuliano GargioniMario C Raviglione
Published in: BMJ global health (2024)
Researchers and research consortia embarking on phase 2 and 3 clinical trials should consider a broad set of elements when planning and designing trials' protocols, all aiming at lowering the price and improving access to emerging TB innovations, besides meeting regulatory criteria. This can only be achieved by consulting and engaging relevant stakeholders in the discussion.
Keyphrases
  • clinical trial
  • mycobacterium tuberculosis
  • public health
  • healthcare
  • phase ii
  • transcription factor
  • adverse drug
  • mental health
  • double blind
  • study protocol
  • randomized controlled trial
  • placebo controlled