Safety of REPEVAX® Given One Month After REVAXIS®

Status Completed

Clinical Trial Summary

Primary objective:

- To describe the safety profile of a Tetanus, Diphtheria, Poliomyelitis and Pertussis vaccine (REPEVAX®) when administered as a pertussis booster 1 month after a Tetanus, Diphtheria, Poliomyelitis vaccine (REVAXIS®) as compared to the safety profile of REPEVAX® administered one month after Placebo.

Secondary objectives:

- To describe the safety of Td-IPV vaccine (REVAXIS®) or Placebo administered to healthy adults.

- To describe the safety of TdaP-IPV vaccine (REPEVAX®) administered one month after Td-IPV vaccine (REVAXIS®) or one month after Placebo.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Healthy Adult

Clinical Trial Details

NCT number	NCT00400309
Study type	Interventional
Source	Sanofi
Contact
Status	Completed
Phase	Phase 3
Start date	June 2006
Completion date	February 2007

View Details

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