drugset / Trial / NCT01446926

Study of Investigational Pneumococcal Vaccine in Healthy Adults, Toddlers and Infants

NCT01446926 ↗

Phase 1 Completed 280 enrolled Sanofi Pasteur, a Sanofi Company
RandomizedParallel-groupTriple-blindPrevention

Summary

This study is designed to explore the safety and tolerability of an investigational pneumococcal vaccine through a step-down enrollment. Primary Objective: * To evaluate the safety and tolerability of an investigational pneumococcal vaccine. Secondary Objective: * To evaluate the immunogenicity of an investigational pneumococcal vaccine.

Timeline

Start
2011-09
Primary completion
2013-03
Completion
2013-06

Drugs

EvaluationDrugModalityDoseRoute
Subject PPrV Vaccine 10 ug Intramuscular
Subject PPrV Vaccine 25 ug Intramuscular
Subject PPrV Vaccine 50 ug Intramuscular