drugset / Trial / NCT03474055

Study on Liquid Bovine Rotavirus Pentavalent Vaccine (LBRV-PV) to Evaluate Lot-to-Lot Consistency and to Compare Non-Inferiority With ROTASIIL (Lyophilized BRV-PV) in Healthy Infants in India

NCT03474055 ↗

Phase 2/3 Completed 1500 enrolled Serum Institute of India Pvt. Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

This study has been designed to compare the liquid formulation of BRV-PV (LBRV-PV) with the lyophilized formulation (ROTASIIL) by testing the vaccine in infants (three doses administered 4 weeks apart, starting at 6-8 weeks of age) in order to demonstrate the non-inferiority in the induction of specific anti-rotavirus IgA antibodies by these vaccines. The study will also evaluate lot-to-lot consistency in the manufacture of LBRV-PV by demonstrating equivalence in the induction of specific anti-rotavirus IgA antibodies across three production lots.

Timeline

Start
2017-10-30
Primary completion
2018-06-25
Completion
2018-06-25

Outcome

Met primary endpoint

paper The immunological non-inferiority of LBRV-PV against Rotasiil® as well as lot-to-lot consistency of LBRV-PV was demonstrated. PMID 30955982 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject LBRV-PV Unknown — —

Indications