drugset / Trial / NCT02585700
A Study of a Seasonal Trivalent Split, Inactivated Influenza Vaccine
Phase 1
Completed
60 enrolled
Institute of Virology, Vaccines and Sera, Torlak
Comac Medical · collabDepartment of Health and Human Services · collabPATH · collabWorld Health Organization · collab
RandomizedParallel-groupQuadruple-blindPrevention
Summary
This is a phase I, double-blind, randomized, placebo-controlled trial with two groups of participants to receive seasonal trivalent split, inactivated influenza vaccine (A/H1N1; A/H3N2 and B) or placebo (phosphate buffered saline). A total of 60 healthy male and female adults 18 through 45 years of age will be randomized to receive vaccine (30) or placebo (30).
Timeline
- Start
- 2015-11
- Primary completion
- 2016-03
- Completion
- 2016-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Influenza vaccine, split inactivated | Vaccine | 15 ug | Other |
| Subject | Influenza vaccine, split inactivated | Vaccine | 0.5 ml | Other |