Status:

COMPLETED

Rotavirus Efficacy and Safety Trial (REST)(V260-006)

Lead Sponsor:

Merck Sharp & Dohme LLC

Conditions:

Rotavirus Infections

Eligibility:

All Genders

6-12 years

Phase:

PHASE3

Brief Summary

This study was designed to evaluate the safety of the investigational rotavirus vaccine and the efficacy to prevent rotavirus gastroenteritis.

Eligibility Criteria

Inclusion

  • Healthy infants

Exclusion

  • None Specified

Key Trial Info

Start Date :

January 1 2001

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2004

Estimated Enrollment :

69274 Patients enrolled

Trial Details

Trial ID

NCT00090233

Start Date

January 1 2001

End Date

October 1 2004

Last Update

October 5 2015

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Rotavirus Efficacy and Safety Trial (REST)(V260-006) | DecenTrialz