drugset / Trial / NCT02291809

REMUNE HIV/AIDS Vaccine Phase II Pediatric Safety & Efficacy Clinical Study

NCT02291809

Phase 2 Unknown 26 enrolled Immune Response BioPharma, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective is to compare \& evaluate between the treatment groups the changes in decline/reduction of HIV viral load \& increase changes in WBC white blood cell counts in the adult Remune dose vs the low dose Remune placebo groups. Additional objectives include changes in CD4+ \& CD8+ T cell counts along with increased HIV immunity.

Timeline

Start
2017-11
Primary completion
2019-11
Completion
2019-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Remune Vaccine 2.5 ug Intramuscular
Subject Remune Vaccine 10 ug Intramuscular

Indications