A Study to Examine Respiratory Combination Vaccines Against Respiratory Syncytial Virus (RSV) and Flu in Older Adults

PHASE1CompletedINTERVENTIONAL
Enrollment

508

Participants

Timeline

Start Date

March 9, 2023

Primary Completion Date

September 27, 2023

Study Completion Date

September 27, 2023

Conditions
Healthy
Interventions
BIOLOGICAL

RSVpreF+qIRV

RSVpreF containing 2 stabilized RSV prefusion F antigens, in equal amounts from virus subgroups A and B combined with Quadrivalent influenza modRNA vaccine (qIRV) encoding HA of 4 strains as recommended for the influenza season (2 A strains, 2 B strains)

BIOLOGICAL

qIRV

Quadrivalent influenza modRNA vaccine (qIRV) encoding HA of 4 strains as recommended for the influenza season (2 A strains, 2 B strains)

BIOLOGICAL

RSVpreF

RSVpreF containing 2 stabilized RSV prefusion F antigens, in equal amounts from virus subgroups A and B

DRUG

Placebo

0.9% saline for injection

BIOLOGICAL

RSVpreF + qIRV 1.0 mL formulation

RSVpreF containing 2 Stabilized RSV prefusion F antigens, in equal amounts from virus subgroups A and B plus qIRV Encoding HA of 4 strains as recommended for the influenza season (2 A strains and 2 B strains) plus sterile water as diluent for injection

BIOLOGICAL

RSVpreF + qIRV 0.5 mL formulation

RSVpreF containing 2 Stabilized RSV prefusion F antigens, in equal amounts from virus subgroups A and B plus qIRV Encoding HA of 4 strains as recommended for the influenza season (2 A strains and 2 B strains)

Trial Locations (1)

1426

Hospital Militar Central Cirujano Mayor Dr. Cosme Argerich, Buenos Aires

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY