Effect of High-Dose Quadrivalent Influenza Vaccine (Efluelda®) Versus Standard-Dose (QIV-SD), in Subjects 65 Years of Age and Older on Innate Immunity, Including Gene Expression

PHASE4CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

November 15, 2021

Primary Completion Date

July 21, 2022

Study Completion Date

July 21, 2022

Conditions
Vaccine Reaction
Interventions
BIOLOGICAL

Experimental arm : High-Dose Quadrivalent Influenza Vaccine (Efluelda)

Patient will received one dose of High Dose Quadrivalent Influenza Vaccine according to marketing authorization.

BIOLOGICAL

Active Comparator: Standard-Dose Quadrivalent Influenza Vaccine

Patient will received one dose of Standard Dose Quadrivalent Influenza Vaccine according to marketing authorization.

Trial Locations (2)

74370

Centre Hospitalier Annecy Genevois, Annecy

Unknown

Centre Hospitalier Métropole Savoie, Chambéry

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Sanofi Pasteur, a Sanofi Company

INDUSTRY

collaborator

Euraxi Pharma

INDUSTRY

collaborator

Hospices Civils de Lyon

OTHER

collaborator

Institut National de la Santé Et de la Recherche Médicale, France

OTHER_GOV

collaborator

Eurofins Optimed

INDUSTRY

lead

Centre Hospitalier Annecy Genevois

OTHER

NCT05154383 - Effect of High-Dose Quadrivalent Influenza Vaccine (Efluelda®) Versus Standard-Dose (QIV-SD), in Subjects 65 Years of Age and Older on Innate Immunity, Including Gene Expression | Biotech Hunter | Biotech Hunter