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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |