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Completed Phase 2 Interventional Accepts healthy volunteers Results available

A Study to Evaluate a Range of Dose Levels of an Adenovirus Serotype 26 (Ad26.RSV.preF)-Based Vaccine in Older Adults

ClinicalTrials.gov ID: NCT04453202

Public ClinicalTrials.gov record NCT04453202. 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 Sep 5, 2026, 6:37 AM 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 Randomized, Double-blind, Placebo-controlled Phase 2a Study to Evaluate a Range of Dose Levels of an Ad26.RSV.preF-based Vaccine in Adults Aged 60 Years and Older

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to explore the dose-response relationship of immune responses induced by different dose levels of an Ad26.RSV.preF based vaccine (Cohort 1) and to assess the safety and reactogenicity of different dose levels of the Ad26.RSV.preF-based vaccine (Cohorts 2 and 3).

Study identification

NCT ID
NCT04453202
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
459 participants

Conditions and interventions

Conditions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
60 Years and older
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
Jul 15, 2020
Primary completion
Sep 23, 2020
Completion
Apr 8, 2021
Last update posted
May 24, 2025

2020 – 2021

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Optimal Research San Diego California 92108
Clinical Research of South Florida, an AMR Company Coral Gables Florida 33134
Heartland Research Associates, an AMR Company El Dorado Kansas 67042
Optimal Research Rockville Maryland 20850
The Center for Pharmaceutical Research (CPR) Kansas City Missouri 64114
Meridian Clinical Research, LLC Norfolk Nebraska 68701
Meridian Clinical Research - Omaha Omaha Nebraska 68134
Tekton Research Inc. Yukon Oklahoma 73099
AMR New Orleans, Formerly New Orleans Center for Clinical Research - New Orleans, an AMR company Knoxville Tennessee 37920

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 NCT04453202, 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 May 24, 2025 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04453202 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →