Immunogenicity and Safety of the Concomitant Administration of OVX836 Influenza Vaccine, Quadrivalent Inactivated Influenza Vaccines and Placebo in Healthy Subjects.

PHASE2CompletedINTERVENTIONAL
Enrollment

478

Participants

Timeline

Start Date

May 10, 2023

Primary Completion Date

August 10, 2023

Study Completion Date

January 15, 2024

Conditions
Influenza
Interventions
BIOLOGICAL

OVX836 480µg

One single administration intramuscularly at Day 1

BIOLOGICAL

Fluarix Tetra

One single administration intramuscularly at Day 1

BIOLOGICAL

Afluria Quad

One single administration intramuscularly at Day 1

BIOLOGICAL

Placebo

One single administration intramuscularly at Day 1

Trial Locations (9)

2019

Emeritus Research Sydney, Sydney

2148

Paratus Clinical Research Western Sydney, Sydney

2259

Paratus Clinical Research Central Coast, Kanwal

3124

Emeritus, Melbourne

4010

Paratus Clinical Research Brisbane, Brisbane

4101

Mater Misericordiae Limited, Brisbane

4506

UniSC Clinical Trials Moreton Bay, Morayfield

4556

University of Sunshine Coast, Sippy Downs

5000

CMAX Fusion Clinical Research, Adelaide

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Novotech (Australia) Pty Limited

INDUSTRY

collaborator

Mater Misericordiae Limited

UNKNOWN

lead

Osivax

INDUSTRY