drugset / Trial / NCT00848211
Clinical Study of TUTI-16 in Asymptomatic HIV-1 Infected Subjects
RandomizedSingle-groupQuadruple-blindTreatment
Summary
This protocol represents the first in human study of TUTI-16, and is being conducted to establish the safety and human immunogenicity (anti-HIV-1 Tat titers) of subcutaneously administered TUTI-16. Activity of TUTI-16 will also be determined in minimizing HIV-1 viral loads and sustaining CD4+ T-cell levels.
Timeline
- Start
- 2009-02
- Primary completion
- 2010-05
- Completion
- 2010-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TUTI-16 | Vaccine | 0.03 mg | Subcutaneous |
| Subject | TUTI-16 | Vaccine | 0.1 mg | Subcutaneous |
| Subject | TUTI-16 | Vaccine | 0.6 mg | Subcutaneous |