drugset / Trial / NCT03204617

Safety and Immunogenicity Study of DNA.HTI, MVA.HTI and ChAdOx1.HTI in HIV-1-positive Patients (AELIX-002)

NCT03204617

Phase 1 Completed 45 enrolled Aelix Therapeutics
RandomizedParallel-groupQuadruple-blindBasic science

Summary

The AELIX-002 study aims to evaluate the safety and the immunogenicity of an heterologous prime-boost regimen with DNA.HTI, MVA.HTI and ChAdOx1.HTI in early diagnosed and treated HIV-1 positive individuals, males and females,18-60 years of age.

Timeline

Start
2017-07-07
Primary completion
2020-07-01
Completion
2021-03-10

Drugs

EvaluationDrugModalityDoseRoute
Subject ChAdOx1.HTI Vaccine 0.5 ml
Subject DNA.HTI Vaccine 0.5 ml
Subject MVA.HTI Vaccine 0.5 ml