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The BRAVO Clinical Study Protocol: Oral Varespladib for Inhibition of Secretory Phospholipase A2 in the Treatment of Snakebite Envenoming.

Rebecca W CarterCharles J GerardoStephen P SamuelSurendra KumarSuneetha D KotehalPartha P MukherjeeFarshad M ShiraziPeter D AkpunonuChanaveerappa BammigattiAshish BhallaNeeraj ManikathTimothy F Platts-MillsMatthew R Lewinnull null
Published in: Toxins (2022)
This protocol was submitted to regulatory authorities in India and the US. A Clinical Trial No Objection Certificate from the India Central Drugs Standard Control Organisation, Drug Controller General-India, and a Notice to Proceed from the US Food and Drug Administration have been obtained. The study protocol was approved by properly constituted, valid institutional review boards or ethics committees at each study site. This study is being conducted in compliance with the April 1996 ICH Guidance for Industry GCP E6, the Integrated Addendum to ICH E6 (R2) of November 2016, and the applicable regulations of the country in which the study is conducted. The trial is registered on Clinical trials.gov, NCT#04996264 and Clinical Trials Registry-India, 2021/07/045079 000062.
Keyphrases
  • clinical trial
  • study protocol
  • randomized controlled trial
  • phase ii
  • phase iii
  • drug administration
  • emergency department
  • double blind
  • artificial intelligence
  • replacement therapy
  • human health
  • adverse drug