drugset / Trial / NCT04177355
Evaluating the Safety and Immunogenicity of HIV-1 BG505 SOSIP.664 gp140 With TLR Agonist and/or Alum Adjuvants in Healthy, HIV-uninfected Adults
Phase 1
Completed
127 enrolled
National Institute of Allergy and Infectious Diseases (NIAID)
Access to Advanced Health Institute (AAHI) · collabDynavax Technologies Corporation · collabFred Hutchinson Cancer Center · collabHIV Vaccine Trials Network · collabInternational AIDS Vaccine Initiative · collab
RandomizedSequentialQuadruple-blindPrevention
Summary
The purpose of this study is to evaluate the safety and immunogenicity of HIV-1 BG505 SOSIP.664 gp140 with TLR agonist and/or alum adjuvants in healthy, HIV-uninfected adults.
Timeline
- Start
- 2020-01-13
- Primary completion
- 2024-11-04
- Completion
- 2024-11-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | 1018 ISS | Unknown | 300 ug | Intramuscular |
| Subject | 3M-052-AF | Small molecule | 1 ug | Intramuscular |
| Subject | 3M-052-AF | Small molecule | 3 ug | Intramuscular |
| Subject | 3M-052-AF | Small molecule | 5 ug | Intramuscular |
| Subject | Alum | Unknown | 500 ug | Intramuscular |
| Subject | BG505 SOSIP.664 gp140 | Vaccine | 100 ug | Intramuscular |
| Subject | GLA-LSQ | Other / unclassified | 2 ug | Intramuscular |
| Subject | GLA-LSQ | Other / unclassified | 5 ug | Intramuscular |
| Subject | Trimer 4571 | Vaccine | 100 ug | Intramuscular |