drugset / Trial / NCT04368988

Evaluation of the Safety and Immunogenicity of a SARS-CoV-2 rS Nanoparticle Vaccine With/Without Matrix-M Adjuvant

NCT04368988

RandomizedParallel-groupQuadruple-blindPrevention

Summary

2019nCoV-101 is a 2-part, randomized, observer-blinded, placebo-controlled, Phase 1/2 trial. Part 1 (Phase 1) of the study is designed to evaluate the safety and immunogenicity of SARS-CoV-2 rS nanoparticle vaccine with or without Matrix-M adjuvant in 131 healthy participants ≥ 18 to 59 (inclusive) years of age at 2 sites in Australia. An interim analysis of Part 1 safety and immunogenicity will be performed prior to optional expansion to Part 2. Part 2 (Phase 2) of the study is designed to evaluate the immunogenicity, safety, and preliminary efficacy of a single construct of SARS-CoV-2 rS nanoparticle vaccine with Matrix-M adjuvant in up to 1,500 healthy participants ≥ 18 to 84 (inclusive) years of age at up to 40 sites across Australia and/or the United States.

Timeline

Start
2020-05-25
Primary completion
2022-06-01
Completion
2022-06-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject NVX-CoV2373 Vaccine 5 ug Intramuscular
Subject NVX-CoV2373 Vaccine 25 ug Intramuscular
Subject SARS-CoV-2 rS Vaccine 25 ug Intramuscular

Indications