Safety and Immunogenicity of the Sing2016 M2SR H3N2 Monovalent Influenza Vaccine in Adults Ages 50 to 85 Years Old

PHASE1CompletedINTERVENTIONAL
Enrollment

122

Participants

Timeline

Start Date

June 30, 2021

Primary Completion Date

November 30, 2021

Study Completion Date

November 30, 2021

Conditions
Influenza Vaccine
Interventions
BIOLOGICAL

Sing2016 M2SR H3N2 influenza vaccine

This group will receive a dose of the Sing2016 M2SR H3N2 monovalent influenza vaccine administered intranasally on Day 1 followed by IIV at least 28 days later.

OTHER

Placebo

This group will receive saline placebo administered intranasally on Day 1 followed by IIV at least 28 days later.

Trial Locations (3)

32127

Accel Clinical, DeLand

66219

Johnson County Clin Trials, Lenexa

92801

Anaheim Clinical Trials, Anaheim

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

lead

FluGen Inc

INDUSTRY

NCT04785794 - Safety and Immunogenicity of the Sing2016 M2SR H3N2 Monovalent Influenza Vaccine in Adults Ages 50 to 85 Years Old | Biotech Hunter | Biotech Hunter