drugset / Trial / NCT00848211

Clinical Study of TUTI-16 in Asymptomatic HIV-1 Infected Subjects

NCT00848211 ↗

Phase 1/2 Completed 24 enrolled Thymon, LLC
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

EvaluationDrugModalityDoseRoute
Subject TUTI-16 Vaccine 0.03 mg Subcutaneous
Subject TUTI-16 Vaccine 0.1 mg Subcutaneous
Subject TUTI-16 Vaccine 0.6 mg Subcutaneous