Study Phase 3

A Double-Blind, Randomized, Multi-Center, Parallel-Group, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Dose of a 500-mg Chewable Tablet of Mebendazole in the Treatment of Soil-Transmitted Helminth Infections (Ascaris Lumbricoides and Trichuris Trichiura) in Pediatric Subjects

Trial Information

Generic NameMebendazoleProduct NameVERMOXTherapeutic AreaAntiparasitic Products, Insecticides, and RepellentsProduct ClassAnthelminticsPharmacological SubgroupAntinematodal AgentsChemical SubgroupBenzimidazole DerivativesCondition StudiedHelminth Infections
Sponsor Protocol NumberMEBENDAZOLGAI3003Enrollment295Data PartnerJohnson & Johnson% Female51.5%Mean/Median Age (Years)7.8% WhiteN/A

Supporting Documentation

  • Collected Datasets Available
  • Data Definition Specification Available
  • Protocol with Amendments Available
  • Clinical Study Report Available

Approved Data Requests Associated with this Trial

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