drugset / Trial / NCT05172544
Trial of an Inactivated Yellow Fever Virus Vaccine
Phase 1
Completed
26 enrolled
Najit Technologies, Inc.
National Institute of Allergy and Infectious Diseases (NIAID) · collab
RandomizedParallel-groupDouble-blindPrevention
Summary
This trial will be a randomized, placebo controlled, double-blind (within dosing group), dose escalation Phase 1 trial, evaluating dosages of 1 mcg and 5 mcg of HydroVax-002 YFV vaccine given intramuscularly on Day 1 and Day 29 in up to 25 healthy adults healthy adults ≥ 18 and \< 50 years of age. The primary objective is to assess the safety, reactogenicity, and tolerability of the HydroVax-002 YFV vaccine administered intramuscularly in a two-dose series on Days 1 and 29 at a dose of 1 mcg or a dose of 5 mcg.
Timeline
- Start
- 2022-01-13
- Primary completion
- 2023-04-24
- Completion
- 2023-04-24
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HydroVax-002 YFV | Vaccine | 1 ug | Intramuscular |
| Subject | HydroVax-002 YFV | Vaccine | 5 ug | Intramuscular |