drugset / Trial / NCT03182907
Bezlotoxumab (MK-6072) Versus Placebo in Children With Clostridium Difficile Infection (CDI) (MK-6072-001)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bezlotoxumab | Monoclonal antibody | 10 mg/kg | Intravenous |
| Background | Fidaxomicin | Other / unclassified | — | Oral |
| Background | Metronidazole | Small molecule | — | Oral |
| Background | Vancomycin | Other / unclassified | — | Oral |