drugset / Trial / NCT02291809
REMUNE HIV/AIDS Vaccine Phase II Pediatric Safety & Efficacy Clinical Study
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Remune | Vaccine | 2.5 ug | Intramuscular |
| Subject | Remune | Vaccine | 10 ug | Intramuscular |