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Terminated Phase 2 Interventional Accepts healthy volunteers Results available

A Study of an Ad26.RSV.preF-based Regimen in the Prevention of Reverse Transcriptase Polymerase Chain Reaction (RT-PCR)-Confirmed Respiratory Syncytial Virus (RSV)-Mediated Lower Respiratory Tract Disease in Adults Aged 65 Years and Older

ClinicalTrials.gov ID: NCT03982199

Public ClinicalTrials.gov record NCT03982199. 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 Nov 5, 2026, 4:21 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled Phase 2b Study to Assess the Efficacy, Immunogenicity and Safety of an Ad26.RSV.preF-based Regimen in the Prevention of RT PCR-confirmed RSV-mediated Lower Respiratory Tract Disease in Adults Aged 65 Years and Older

Brief summary

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

The purpose of this study is to demonstrate the efficacy of active study vaccine in the prevention of reverse transcriptase polymerase chain reaction (RT-PCR) confirmed respiratory syncytial virus (RSV)-mediated lower respiratory tract disease (LRTD), when compared to placebo.

Study identification

NCT ID
NCT03982199
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
5,815 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
65 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
Aug 1, 2019 (Actual)
Primary completion
Jun 6, 2022 (Actual)
Completion
May 26, 2023 (Actual)
Last update posted
May 25, 2025

2019 – 2023

United States locations

U.S. sites
40
U.S. states
21
U.S. cities
38
Facility City State ZIP Site status
Optimal Research Huntsville Alabama 35802 —
Synexus Clinical Research US Inc Chandler Arizona 85224 —
Synexus Clinical Research US Inc Phoenix Arizona 85018 —
Central Phoenix Medical Clinic Phoenix Arizona 85020 —
Anaheim Clinical Trials, LLC Anaheim California 92801 —
Paradigm Clinical Research Centers, Inc. Redding California 96001 —
Benchmark Research Sacramento California 95684 —
Optimal Research San Diego California 92108 —
Synexus Clinical Research US Inc Aurora Colorado 80014 —
Lynn Institute Colorado Springs Colorado 80920 —
Optimal Research Melbourne Florida 32934 —
Advanced Clinical Research Boise Idaho 83642 —
Optimal Research Peoria Illinois 61614 —
Synexus Clinical Research US Inc Evansville Indiana 47714 —
The Iowa Clinic West Des Moines Iowa 50266 —
Hutchinson Clinic Hutchinson Kansas 67502 —
Johnson County Clin-Trials Lenexa Kansas 66219 —
Heartland Research Associates, LLC Newton Kansas 67114 —
Heartland Research Associates, LLC Wichita Kansas 67205 —
Optimal Research Rockville Maryland 20850 —
Synexus Clinical Research US Inc Richfield Minnesota 55432 —
The Center For Pharmaceutical Research Kansas City Missouri 64114 —
Sundance Clinical Research St Louis Missouri 63141 —
Synexus Clinical Research US Inc St Louis Missouri 63141 —
Synexus Clinical Research US Inc Elkhorn Nebraska 68022 —
Synexus Clinical Research US Inc Omaha Nebraska 68144 —
United Medical Associates Binghamton New York 13901 —
Regional Clinical Research, Inc. Endwell New York 13760 —
University of Rochester / Rochester General Hospital Rochester New York 14621 —
Synexus Clinical Research US Inc Akron Ohio 44311 —
Synexus Clinical Research US Inc Cincinnati Ohio 45236 —
Rapid Medical Research Cleveland Ohio 44122 —
Lynn Health Science Institute Oklahoma City Oklahoma 73112 —
Omega Medical Research Warwick Rhode Island 02886 —
Coastal Carolina Research Center Mt. Pleasant South Carolina 29464 —
Optimal Research Austin Texas 78705 —
Ventavia Research Group, LLC Fort Worth Texas 76104 —
Synexus Clinical Research US Inc Murray Utah 84123 —
Advanced Clinical Research Salt Lake City Utah 84123 —
Advanced Clinical Research West Jordan Utah 84088 —

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 NCT03982199, 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 25, 2025 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03982199 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →