drugset / Trial / NCT01706367

Evaluation of a 3-dose Vaccination Regimen With One of Three Ascending Dose Levels of Clostridium Difficile Vaccine With or Without Adjuvant in Healthy Adults Aged 50 to 85 Years

NCT01706367

Phase 1 Completed 192 enrolled Pfizer
RandomizedParallel-groupSingle-blindBasic science

Summary

This is a first-in-human study (phase 1) of a 3-dose vaccination regimen with one of three dose levels of C difficile vaccine with or without adjuvant in healthy adults aged 50 to 85 years. The main goal of the study is to determine how safe and well-tolerated the vaccine is. In addition, the study aims to assess the immune response to the C difficile vaccine.

Timeline

Start
2012-09
Primary completion
2014-01
Completion
2014-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Aluminum hydroxide Unknown Intramuscular
Subject C difficile vaccine Vaccine 50 ug Intramuscular
Subject C difficile vaccine Vaccine 100 ug Intramuscular
Subject C difficile vaccine Vaccine 200 ug Intramuscular