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Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Study to Evaluate Dose Levels of Ad26.COV2.S Administered as a Two-dose Schedule in Healthy Adults

ClinicalTrials.gov ID: NCT04908722

Public ClinicalTrials.gov record NCT04908722. 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 Oct 30, 2026, 3:00 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 Randomized, Double-blind, Phase 3 Study to Evaluate 6 Dose Levels of Ad26.COV2.S Administered As a Two-Dose Schedule in Healthy Adults

Brief summary

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

The purpose of this study is to demonstrate non-inferiority (NI) in terms of humoral immune responses after 6 dose levels of Ad26.COV2.S.

Study identification

NCT ID
NCT04908722
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
1,609 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 55 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
Jun 18, 2021 (Actual)
Primary completion
Jul 10, 2023 (Actual)
Completion
Jul 10, 2023 (Actual)
Last update posted
Feb 4, 2025

2021 – 2023

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Baptist Health Center For Clinical Research Little Rock Arkansas 72205 —
Anaheim Clinical Trials, LLC Anaheim California 92801 —
Ark Clinical Research Long Beach California 90815 —
Paradigm Clinical Research Centers, Inc. Redding California 96001 —
Wr McCr Llc San Diego California 92120 —
Ark Clinical Research Tustin California 92780 —
Velocity Clinical Research, Hallandale Beach Hallandale Florida 33009 —
Floridian Research Institute Miami Florida 33179 —
Medpharmics, LLC Metairie Louisiana 70006 —
Clinical Research Center of Nevada Las Vegas Nevada 89106 —
Rochester Clinical Research, Inc Rochester New York 14609 —
Wake Research Associates Raleigh North Carolina 27612 —
Trial Management Associates, LLC Wilmington North Carolina 28403 —
Tekton Research Inc. Yukon Oklahoma 73099 —
Coastal Carolina Research Center North Charleston South Carolina 29405 —
Ventavia Research Group, LLC Keller Texas 76248 —
Research Your Health Plano Texas 75093 —
Clinical Research Partners, LLC Richmond Virginia 23226 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04908722, 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 Feb 4, 2025 · Synced Oct 30, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04908722 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →