A Study of IVX-A12 in Adults Participants

NCT06481579 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 143

Last updated 2025-08-26

Study results available
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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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06481579 on ClinicalTrials.gov