Safety and Immunogenicity of IVX-A12 in Healthy Older Adults

PHASE1CompletedINTERVENTIONAL
Enrollment

140

Participants

Timeline

Start Date

September 21, 2022

Primary Completion Date

January 24, 2024

Study Completion Date

January 24, 2024

Conditions
Healthy
Interventions
BIOLOGICAL

IVX-121

75 mcg of IVX-121 without MF59®

BIOLOGICAL

IVX-241

75 mcg of IVX-241 without MF59®

BIOLOGICAL

Placebo

Diluent

BIOLOGICAL

IVX-121

75 mcg of IVX-121, without MF59®

BIOLOGICAL

IVX-241

150 mcg IVX-241, without MF59®

BIOLOGICAL

IVX-241

225 mcg of IVX-241, without MF59®

BIOLOGICAL

IVX-121

75 mcg of IVX-121, with MF59®

BIOLOGICAL

IVX-241

75 mcg of IVX-241, with MF59®

BIOLOGICAL

IVX-241

150 mcg IVX-241, with MF59®

OTHER

MF59®

MF59® as an adjuvant

Trial Locations (4)

30331

CenExcel ACMR, Atlanta

33024

CenExcel RCA, Hollywood

68134

Meridien Clinical Research, Omaha

78520

PanAmerican Clinical Research, Brownsville

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Icosavax, Inc.

INDUSTRY

NCT05664334 - Safety and Immunogenicity of IVX-A12 in Healthy Older Adults | Biotech Hunter | Biotech Hunter