drugset / Trial / NCT01230957

Study of Different Formulations of a Clostridium Difficile Toxoid Vaccine Given at Three Different Schedules in Adults

NCT01230957 ↗

Phase 2 Completed 650 enrolled Sanofi Pasteur, a Sanofi Company
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This study will further evaluate the ACAM-CDIFF™ vaccine in a population of middle-aged to elderly individuals at risk of exposure to Clostridium difficile because of impending hospitalization or residence in a care facility. Primary Objectives: * To describe the safety profile of subjects in each of the study groups. * To describe the immune responses elicited by toxoid A and toxoid B of subjects in each of the study groups. Observational Objective: * To describe the occurrence of first-time Clostridium difficile infection (CDI) episodes.

Timeline

Start
2010-10
Primary completion
2012-11
Completion
2013-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Clostridium difficile toxoids A and B Vaccine 50 ug Intramuscular
Subject Clostridium difficile toxoids A and B Vaccine 100 ug Intramuscular
Subject Clostridium difficile toxoids A and B Vaccine 0.5 ml Intramuscular