Safety and Immunogenicity of High-Dose Quadrivalent Influenza Vaccine in Patients ≥65 Years

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

175

Participants

Timeline

Start Date

September 15, 2017

Primary Completion Date

November 28, 2017

Study Completion Date

November 28, 2017

Conditions
Influenza
Interventions
BIOLOGICAL

QIV-HD by IM

IM, injected into the upper arm (deltoid area)

BIOLOGICAL

QIV-SD by SC

SC, injected into the upper arm (posterior region)

BIOLOGICAL

QIV-HD by SC

SC, injection into the upper arm (posterior region)

Trial Locations (2)

Unknown

Sanofi Pasteur Investigational Site, Ōsaka

Sanofi Pasteur Investigational Site, Tokyo

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Sanofi

INDUSTRY

lead

Sanofi Pasteur, a Sanofi Company

INDUSTRY

NCT03233217 - Safety and Immunogenicity of High-Dose Quadrivalent Influenza Vaccine in Patients ≥65 Years | Biotech Hunter | Biotech Hunter