drugset / Trial / NCT03182907

Bezlotoxumab (MK-6072) Versus Placebo in Children With Clostridium Difficile Infection (CDI) (MK-6072-001)

NCT03182907

Phase 3 Completed 148 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupTriple-blindPrevention

Summary

The primary objectives of this study are to evaluate the pharmacokinetics (PK), safety, and tolerability of bezlotoxumab (MK-6072) in children aged 1 to \<18 years of age with a confirmed diagnosis of Clostridium difficile infection (CDI) who are receiving antibacterial drug treatment. The primary hypothesis is that the area under the concentration-time curve from 0 to infinity (AUC0-inf) of bezlotoxumab after treatment of pediatric participants with bezlotoxumab is similar when compared to the AUC0-inf of bezlotoxumab after treatment of adults with bezlotoxumab.

Timeline

Start
2018-03-27
Primary completion
2022-05-12
Completion
2022-05-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Bezlotoxumab Monoclonal antibody 10 mg/kg Intravenous
Background Fidaxomicin Other / unclassified Oral
Background Metronidazole Small molecule Oral
Background Vancomycin Other / unclassified Oral