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Completed Phase 2 Interventional Accepts healthy volunteers Results available

A Study to Evaluate the Safety and Immunogenicity of IVX-A12 in Participants of 60 to 85 Years of Age

ClinicalTrials.gov ID: NCT05903183

Public ClinicalTrials.gov record NCT05903183. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 2:09 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2a Randomized, Observer-blind, Placebo-controlled, Dosage Optimization, Multi-center Clinical Trial to Evaluate the Safety and Immunogenicity of IVX-A12, a Respiratory Syncytial Virus and Human Metapneumovirus Bivalent Combination Virus-like Particle Protein Subunit Vaccine, in Adults 60 to 85 Years of Age

Study identification

NCT ID
NCT05903183
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Icosavax, Inc.
Industry
Enrollment
264 participants

Conditions and interventions

Conditions

Interventions

  • IVX-A12 Biological
  • Placebo Biological

Biological

Eligibility (public fields only)

Age range
60 Years to 85 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 14, 2023
Primary completion
Jun 4, 2023
Completion
Oct 24, 2024
Last update posted
Dec 4, 2025

2023 – 2024

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
AMR Phoenix Tempe Arizona 85281
Cenexel RCA Hollywood Florida 33024
Clinical Research Atlanta Stockbridge Georgia 30281
Velocity Clinical Research-Boise Meridian Idaho 83642
ASR, LLC Nampa Idaho 83587
Johnson City Clin-Trials (JCCT) Lenexa Kansas 66219
AMR Lexington Lexington Kentucky 40509
Velocity Clinical Research Omaha Nebraska 68134
Rochester Clinical Research, Inc Rochester New York 14609
PanAmerican Clinical Research Brownsville Texas 78520

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05903183, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 4, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05903183 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →