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Dose Confirmation Efficacy Study (V260-007)

Rotavirus Infections Clinical Trial

Official title:
Study of the Efficacy, Safety, and Immunogenicity of V260 at Expiry

Clinical Trial Summary

This study was designed to evaluate the safety of the investigational Rotavirus Vaccine and the efficacy to prevent Rotavirus Gastroenteritis.

Clinical Trial Description

The duration of treatment is 10 months. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00092443
Study type Interventional
Source Merck Sharp & Dohme Corp.
Contact
Status Completed
Phase Phase 3
Start date September 2002
Completion date June 2004
View Details
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