drugset / Trial / NCT05249816

Phase 3 Boosting Study for the SARS-CoV-2 rS Vaccine

NCT05249816

Phase 3 Completed 1000 enrolled Cogna Technology Solutions LLC Novavax · collab
RandomizedParallel-groupTriple-blindPrevention

Summary

This is an observer-blinded Phase 3 study to evaluate the safety and immunogenicity of a single booster dose of the Novavax severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) recombinant (r) spike (S) protein nanoparticle vaccine adjuvanted with Matrix-MTM (NVX-CoV2373) in adults previously vaccinated with the BBIBP-CorV vaccine. The study will enroll approximately1,000 participants \>18 years of age. All participants will be randomized in a 1:1 ratio to receive a single booster dose of NVX-CoV2373 or the BBIBP-CorV vaccine. All participants will receive the booster dose on Day 0 and remain on study for immunogenicity and safety data collection through Day 180. An interim analysis will be performed of safety and immunogenicity data gathered through Day 28.

Timeline

Start
2022-03-18
Primary completion
2023-05-04
Completion
2023-05-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator BBIBP-CorV vaccine Vaccine Intramuscular
Subject NVX-CoV2373 Vaccine 5 ug Intramuscular
Subject NVX-CoV2373 Vaccine 50 ug Intramuscular

Indications