drugset / Trial / NCT05284799
Immunogenicity and Safety of the Concomitant Administration of OVX836 and Quadrivalent Influenza Vaccine in Healthy Volunteers.
Phase 2
Completed
180 enrolled
Osivax
Harmony Clinical Research BVBA · collabNorthern Beaches Clinical Research · collabNovotech (Australia) Pty Limited · collab
RandomizedParallel-groupDouble-blindPrevention
Summary
The present study will evaluate the concomitant administration of a Quadrivalent Inactivated Influenza Vaccine with the highest dose level of OVX836 (480µg) tested in the clinic to date, for which the likelihood for interference with Quadrivalent Inactivated Influenza Vaccine is considered the highest.
Timeline
- Start
- 2022-05-09
- Primary completion
- 2022-07-19
- Completion
- 2022-12-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Fluarix Tetra | Vaccine | — | Intramuscular |
| Subject | OVX836 | Vaccine | 480 ug | Intramuscular |