drugset / Trial / NCT00623259

Phase I Safety Study of a Recombinant MVA HIV Multiantigen Vaccine in HIV-infected Subjects

NCT00623259 ↗

Phase 1 Completed 15 enrolled Bavarian Nordic
Diagnostic

Summary

Monocentric study to assess the safety and immunogenicity of the recombinant MVA-HIV multiantigen vaccine MVA-mBN120B in HIV-infected subjects. 15 subjects will receive immunizations at day 0, after 4 and 12 weeks at a dose of 2E8 TCID50 MVA-mBN120B. The vaccine will be administered subcutaneously.

Timeline

Start
2008-05
Primary completion
2009-02
Completion
2009-04

Drugs

EvaluationDrugModalityDoseRoute
Subject MVA-mBN120B Vaccine 2e+08 unknown Subcutaneous