A Study of IVX-A12 in Adults Participants
NCT06481579 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 143
Last updated 2025-08-26
Summary
The primary purpose of this study is to assess the immunogenicity and safety of IVX-A12 in adults 60 years of age and older.
Conditions
- Healthy Participants
Interventions
- BIOLOGICAL
-
IVX-A12
IVX-A12 IM injection.
- BIOLOGICAL
-
Licensed RSV Vaccine
Licensed RSV Vaccine (AREXVY) IM injection.
Sponsors & Collaborators
-
Icosavax, Inc.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-06-10
- Primary Completion
- 2024-07-17
- Completion
- 2024-12-19
- FDA Drug
- Yes
Countries
- United States
Study Locations
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