drugset / Trial / NCT01441193

A Phase I Safety and Immunogenicity Preventive Vaccine Trial Based on the HIV-1 Tat and V2-deleted Env Proteins (ISS P-002)

NCT01441193 ↗

Phase 1 Terminated 11 enrolled Barbara Ensoli, MD Novartis Vaccines · collab
RandomizedParallel-groupOpen-labelPrevention

Summary

This Phase I study was directed at evaluating the safety profile and the immunogenicity of the vaccination with recombinant HIV-1 Tat and V2-deleted Env (delta-V2 Env) proteins administered in association in healthy, immunologically competent adults, compared to delta-V2 Env or Tat alone.

Timeline

Start
2011-09
Primary completion
2014-02
Completion
2014-02

Outcome

Outcome not reported

Stopped (Enrollment): “Enrollments were suspended due to delta-V2 Env unavailability, following the EMA/CHMP/BWP/534898/2008 guideline, not allowing the use of a retest date”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject HIV-1 Tat Vaccine 7.5 ug Intrathecal
Subject HIV-1 Tat Vaccine 30 ug Intrathecal
Subject HIV-1 delta-V2 Env Vaccine 100 ug Intrathecal