drugset / Trial / NCT03220724

Evaluating the Safety and Immunogenicity of EnvSeq-1 and CH505 M5 gp120 Envs Adjuvanted With GLA-SE in Healthy, HIV-Uninfected Adults

NCT03220724

RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to evaluate the safety, tolerability, and immunogenicity of EnvSeq-1 and CH505 M5 gp120 Envs adjuvanted with GLA-SE in healthy, HIV-uninfected adults.

Timeline

Start
2017-08-22
Primary completion
2023-03-21
Completion
2023-03-21

Drugs

EvaluationDrugModalityDoseRoute
Subject CH505 M5 Unknown Intramuscular
Subject CH505TF gp120 Protein / enzyme biologic 20 ug Intramuscular
Subject CH505TF gp120 Protein / enzyme biologic 100 ug Intramuscular
Subject CH505TF gp120 Protein / enzyme biologic 400 ug Intramuscular
Subject CH505w53 Vaccine 400 ug Intramuscular
Subject CH505w78 Vaccine 400 ug Intramuscular
Background GLA-SE Other / unclassified Intramuscular