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Clinical Trial Summary

This phase III trial aims to assess the efficacy, safety and immunogenicity of Rotavirus RV3 Vaccine (Bio Farma) in neonates, lot-to-lot consistency, and antigen interference with co-administered EPI vaccines


Clinical Trial Description

This study is a randomized, double-blind, placebo-controlled study to investigate the efficacy, safety and immunogenicity following three doses of rotavirus RV3 vaccine (Bio Farma) administered as a neonatal schedule ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04185545
Study type Interventional
Source PT Bio Farma
Contact
Status Completed
Phase Phase 3
Start date October 30, 2020
Completion date May 30, 2023

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