drugset / Trial / NCT02413645
Phase I, Open Label Dose Escalation Study to Evaluate Safety of iHIVARNA-01 in Chronically HIV-infected Patients
Non-randomizedSequentialOpen-labelTreatment
Summary
The main purpose of the study is to evaluate the safety and to establish the recommended dose of iHIVARNA-01 as a new therapeutic vaccine against HIV
Timeline
- Start
- 2015-06
- Primary completion
- 2016-06
- Completion
- 2016-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HTI | Unknown | 300 ug | Other |
| Subject | HTI | Unknown | 600 ug | Other |
| Subject | HTI | Unknown | 900 ug | Other |
| Subject | TriMix | Messenger RNA (mRNA) | 100 ug | Other |
| Subject | TriMix | Messenger RNA (mRNA) | 300 ug | Other |