Safety and Immunogenicity First-in-human Dose-ranging Study of Self-Amplifying RNA Seasonal Influenza Vaccine in Adults

PHASE1CompletedINTERVENTIONAL
Enrollment

139

Participants

Timeline

Start Date

January 22, 2024

Primary Completion Date

August 10, 2024

Study Completion Date

January 7, 2025

Conditions
Influenza, Human
Interventions
BIOLOGICAL

ARCT-2138

Each participant will receive one 0.5 mL intramuscular (IM) dose into the deltoid muscle.

BIOLOGICAL

Licensed Quadrivalent Vaccine for younger adults

Each participant will receive one 0.5 mL intramuscular (IM) dose into the deltoid muscle.

BIOLOGICAL

Licensed Quadrivalent Vaccine for older adults

Each participant will receive one 0.5 mL intramuscular (IM) dose into the deltoid muscle.

Trial Locations (2)

3124

Emeritus Research Camberwell, Melbourne

Unknown

Nucleus Network Brisbane Clinic, Brisbane

Sponsors
All Listed Sponsors
collaborator

Seqirus

INDUSTRY

collaborator

Novotech (Australia) Pty Limited

INDUSTRY

lead

Arcturus Therapeutics, Inc.

INDUSTRY

NCT06125691 - Safety and Immunogenicity First-in-human Dose-ranging Study of Self-Amplifying RNA Seasonal Influenza Vaccine in Adults | Biotech Hunter | Biotech Hunter