drugset / Trial / NCT01032408

Immunogenicity, Safety, and Tolerability of MF59-Adjuvanted Versus Non-Adjuvanted Influenza Vaccines in Patients With HIV-1 Infection

NCT01032408

Phase 3 Completed 154 enrolled Chiltern Pesquisa Clinica Ltda
RandomizedParallel-groupOpen-labelPrevention

Summary

This is a phase III, randomized, controlled, open label study with two vaccine regimens. The study will assess the relative safety and immunogenicity of vaccine regimens comparing adjuvanted versus non-adjuvanted formulations of A(H1N1) inactivated influenza virus vaccine in subjects with Human Immunodeficiency Virus Type 1 (HIV-1) Infection and to compare safety and immunogenicity data with a contemporaneously enrolled control group of age-comparable, healthy subjects. Because certain individuals may be hypo-responsive to influenza vaccination, additional studies with high-risk groups are warranted in order to determine the optimal vaccine formulation and dosing schedule for prevention of novel H1N1 virus infection.

Timeline

Start
2010-04
Primary completion
2011-09
Completion
2012-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Begrivac® Vaccine 15 ug
Subject Focetria Vaccine 7.5 ug