drugset / Trial / NCT01144026

Clinical Study of TUTI-16 in HIV-1 Infected and Uninfected Subjects

NCT01144026 ↗

Phase 1/2 Completed 15 enrolled Thymon, LLC
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This protocol represents the second in human study of TUTI-16, and is being conducted to continue to gather safety and human immunogenicity (anti-HIV-1 Tat titers) data of subcutaneously administered TUTI-16.

Timeline

Start
2010-09
Primary completion
2011-04
Completion
2011-04

Drugs

EvaluationDrugModalityDoseRoute
Subject TUTI-16 Vaccine 0.2 mg Subcutaneous
Subject TUTI-16 Vaccine 1 mg Subcutaneous