drugset / Trial / NCT05032391

Reactogenicity, Safety and Immunological Efficacy of the Live, Pentavalent Rotavirus Vaccine in Childhood Immunization

NCT05032391 ↗

Phase 3 Completed 100 enrolled Limited Liability Company Pharm Aid
RandomizedParallel-groupDouble-blindPrevention

Summary

The first multicenter prospective, randomized, double-blind, placebo-controlled clinical trial of the pentavalent live vaccine for RVI prevention was conducted in Russia among healthy infants aged 2 months at the time of the first vaccination.

Timeline

Start
2019-02-22
Primary completion
2019-09-22
Completion
2019-10-25

Drugs

EvaluationDrugModalityDoseRoute
Subject The pentavalent rotavirus vaccine Vaccine 2.5 ml Oral

Indications