Clinical Trials Directory

Trials / Completed

CompletedNCT00092469

Study of an Investigational Vaccine in Healthy Infants in Taiwan (V441-001)(COMPLETED)

A Registration Study of the Safety, Tolerability, and Immunogenicity of V441 in Healthy Infants in Taiwan

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
151 (planned)
Sponsor
Merck Sharp & Dohme LLC · Industry
Sex
All
Age
6 Weeks – 8 Weeks
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate the safety, tolerability, and immune response of an investigational vaccine being evaluated to reduce the incidence of diphtheria, pertussis, tetanus, hepatitis B, poliomyelitis, and Haemophilus influenza type b.

Detailed description

The duration of treatment is 65 weeks.

Conditions

Interventions

TypeNameDescription
BIOLOGICALV441, diptheria, tetanus, acellular pertussis, inactivated poliomyelitis, hepatitis B (recombinant), & Haemophilus influenza type b conjugate vaccine

Timeline

Start date
2002-03-01
Primary completion
2003-08-01
Completion
2003-08-01
First posted
2004-09-27
Last updated
2015-10-07

Source: ClinicalTrials.gov record NCT00092469. Inclusion in this directory is not an endorsement.