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Study of an Investigational Pneumococcal Vaccine in Healthy Adult Volunteers

Pneumococcal Infections Clinical Trial

Clinical Trial Summary

This study was designed to evaluate the safety, tolerability, and immunogenicity of three doses of an investigational pneumococcal vaccine in healthy adult volunteers.

Primary Objective:

- To evaluate the safety and tolerability of an investigational Pneumococcal vaccine.

Clinical Trial Description

Each volunteer participant will receive two injections with one of three vaccine doses, administered on Day 0 and Day 30, in a dose-ascending manner, pending safety review at each dose level. All participants will be monitored for safety for 30 days after each injection. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01444001
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 1
Start date February 2007
Completion date August 2007
View Details
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