AzTrials
AzTrials

Participants With or Without Stable Co-morbidities Associated With Progression to Severe COVID-19Phase 3ENSEMBLE 2NCT04614948

A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-mediated COVID-19 in Adults

A Phase 3 study testing Ad26.COV2.S in people with Participants With or Without Stable Co-morbidities Associated With Progression to Severe COVID-19, run by Janssen Vaccines & Prevention B.V. at 126 sites in 10 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study will evaluate the efficacy of Ad26.COV2.S in the prevention of molecularly confirmed moderate to severe/critical coronavirus disease-2019 (COVID-19), as compared to placebo, in SARS-CoV-2 seronegative adults in the double-blind phase and to describe COVID-19 outcomes, safety, and immunogenicity in the… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Ad26.COV2.S
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
31,835 participants
Where
126 sitesin 10 countries
Study dates
12 Nov 2020to 18 Jun 2023
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Contraceptive (birth control) use should be consistent with local regulations regarding the acceptable methods of contraception for those participating in clinical studies
  • All participants of childbearing potential must: have a negative highly sensitive urine pregnancy test at screening; and have a negative highly sensitive urine pregnancy test immediately prior to each study vaccine administration
  • Participant agrees to not donate bone marrow, blood, and blood products from the first study vaccine administration until 3 months after receiving the last dose of study vaccine
  • Must be willing to provide verifiable identification, has means to be contacted and to contact the investigator during the study
  • Must be able to read, understand, and complete questionnaires in the electronic clinical outcome assessment (eCOA) (that is, the coronavirus disease-2019 [COVID 19] signs and symptoms surveillance question, the e-Diary, and the electronic patient-reported outcomes (ePROs)

Who cannot join

  • Participant has a clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature greater than or equal to (>=) 38.0 degree Celsius (100.4-degree Fahrenheit) within 24 hours prior to the planned first dose of study vaccine; randomization at a later date is permitted at the discretion of the investigator and after consultation with the sponsor
  • Participant has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to vaccines or their excipients
  • Participant received or plans to receive: (a) licensed live attenuated vaccines - within 28 days before or after planned administration of study vaccine; and (b) other licensed (not live) vaccines - within 14 days before or after planned administration of study vaccine
  • Participant previously received a coronavirus vaccine
  • Participant received an investigational drug within 30 days (including investigational drugs for prophylaxis of COVID-19) or used an invasive investigational medical device within 30 days or received investigational immunoglobulin (Ig) or investigational monoclonal antibodies within 3 months, or received convalescent serum for COVID-19 treatment within 4 months or received an investigational vaccine (including investigational Adenoviral-vectored vaccines) within 6 months before the planned administration of the first dose of study vaccine or is currently enrolled or plans to participate in another investigational study during the course of this study

Trial locations and contacts

126 sites in 10 countries.

126 sites in 10 countries

United States63 sites
  • Medpharmics, LLC

    Albuquerque, New Mexico, 87102

  • Atlanta Center for Medical Research

    Atlanta, Georgia, 30331

  • JEM Research LLC

    Atlantis, Florida, 33462

  • Hassman Research Institute, LLC.

    Berlin, New Jersey, 08009

  • Synexus Clinical Research US Inc

    Cerritos, California, 90703

  • Medical University of South Carolina

    Charleston, South Carolina, 29425

  • American Health Network, LLC

    Charlotte, North Carolina, 28207

  • The University Of Chicago Medicine

    Chicago, Illinois, 60637

  • Great Lakes Clinical Trials

    Chicago, Illinois, 60640

  • eStudySite

    Chula Vista, California, 91911

  • CTI Clinical Trial and Consulting Services

    Cincinnati, Ohio, 45212

  • Prestige Clinical Research Center, Inc.

    Coral Gables, Florida, 33134

  • Avail Clinical Research, LLC

    DeLand, Florida, 32720

  • Henry Ford Health Systems

    Detroit, Michigan, 48202

  • Accel Research Sites

    Eatonton, Georgia, 31204

  • Centennial Medical Group

    Elkridge, Maryland, 21075

  • Meridian Clinical Research, LLC

    Endwell, New York, 13760

  • Regional Clinical Research, Inc.

    Endwell, New York, 13760

  • Cherry Street Services, Inc.

    Grand Rapids, Michigan, 49503

  • Velocity Clinical Research, Hallandale Beach

    Hallandale, Florida, 33009

  • Centex Studies, Inc.

    Houston, Texas, 77058

  • Centex Studies, Inc.

    Houston, Texas, 77073

  • Texas Center for Drug Development Inc

    Houston, Texas, 77081

  • Health Awareness inc.

    Jupiter, Florida, 33458

  • Centex Studies, Inc.

    Lake Charles, Louisiana, 70601

  • Altus Research, Inc

    Lake Worth, Florida, 33461

  • University of Kentucky

    Lexington, Kentucky, 40536

  • Woodland International Research Group

    Little Rock, Arkansas, 72211

  • Ark Clinical Research

    Long Beach, California, 90806

  • Anthony Mills Medical, Inc

    Los Angeles, California, 90069

  • Centex Studies, Inc.

    McAllen, Texas, 78504

  • Compass Research, Melbourne

    Melbourne, Florida, 32940

  • Suncoast Research Group

    Miami, Florida, 33135

  • Coastal Carolina Research Center

    Mt. Pleasant, South Carolina, 29464

  • Centennial Medical Center

    Nashville, Tennessee, 37203

  • Jersey Shore University Medical Center

    Neptune City, New Jersey, 07753

  • Ochsner Clinic Foundation

    New Orleans, Louisiana, 70121

  • Heartland Research Associates, LLC

    Newton, Kansas, 67114

  • Alliance for Multispeciality Research

    Norfolk, Virginia, 23502

  • Behavioral Clinical Research , Inc

    North Miami, Florida, 33161

  • Lynn Health Science Institute

    Oklahoma City, Oklahoma, 73112

  • Clinical NeuroScience Solutions Inc

    Orlando, Florida, 32806

  • Hope Research Institute

    Phoenix, Arizona, 85018

  • Central Phoenix Medical Clinic

    Phoenix, Arizona, 85020

  • Progressive Medical Research

    Port Orange, Florida, 32127

  • Allergy Asthma Immunology of Rochester, PC (AAIR) - Research Center

    Rochester, New York, 14618

  • Optimal Research

    Rockville, Maryland, 20850

  • Meridian Clinical Research, LLC

    Rockville, Maryland, 20854

  • Benchmark Research

    Sacramento, California, 95684

  • JBR Clinical Research

    Salt Lake City, Utah, 84107

  • Endeavor Clinical Trials, LLC

    San Antonio, Texas, 78229

  • Artemis Institute for Clinical Research

    San Diego, California, 92103

  • The South Bend Clinic Center for Research

    South Bend, Indiana, 46617-2808

  • Washington University School Of Medicine

    St Louis, Missouri, 63110-1035

  • Meridien Research

    St. Petersburg, Florida, 33709

  • Richmond Behavioral Associates

    Staten Island, New York, 10312

  • Quality of Life Medical & Research Center, LLC

    Tucson, Arizona, 85712

  • Synexus Clinical Research US Inc

    Tucson, Arizona, 85712

  • Achieve Clinical Research, LLC

    Vestavia Hills, Alabama, 35216

  • Tranquility Clinical Research

    Webster, Texas, 77598

  • Palm Beach Research Center

    West Palm Beach, Florida, 33409

  • Paradigm Clinical Research Centers, Inc.

    Wheat Ridge, Colorado, 80033

  • Wilmington Health Associates

    Wilmington, North Carolina, 28401

Other trials in United States

United Kingdom16 sites
  • Queen Elizabeth Hospital

    Birmingham, B15 2GW

  • Powys Teaching Local Health Board - Bronllys Hospital

    Brecon, LD3 0UL

  • Brighton & Sussex University Hospitals NHS Trust

    Brighton, BN2 5BE

  • University Hospitals Bristol NHS Trust

    Bristol, BS2 8HW

  • Cambridge University Hospitals NHS Foundation Trust

    Cambridge, CB2 0QQ

  • Ninewells Hospital

    Dundee, DD1 9SY

  • Royal Free Hospital

    Hampstead, NW3 2QG

  • Leicester Royal Infirmary

    Leicester

  • Guy's and St Thomas' Hospital

    London, SE1 9RT

  • Imperial College London and Imperial College Healthcare NHS Trust

    London, W2 1NY

  • Central Manchester University Hospitals NHS Foundation Trust

    Manchester, M13 9WL

  • Newcastle upon Tyne Hospitals NHS Foundation Trust

    Newcastle upon Tyne, NE1 4LP

  • University of Oxford

    Oxford, OX3 7JX

  • Derriford Hospital

    Plymouth, PL6 8DH

  • Sheffield Teaching Hospitals NHS Foundation Trust

    Sheffield, S10 2SB

  • Southampton General Hospital

    Southampton, SO16 6YD

Other trials in United Kingdom

Spain9 sites
  • Hosp. Univ. Germans Trias I Pujol

    Badalona, 08916

  • Hosp. Quiron Barcelona

    Barcelona, 08023

  • Hosp Clinic de Barcelona

    Barcelona, 08063

  • Hosp Univ Vall D Hebron

    Barcelona, 8035

  • Hosp. Univ. de La Princesa

    Madrid, 28006

  • Clinica Univ. de Navarra

    Madrid, 28027

  • Hosp. Univ. de La Paz

    Madrid, 28046

  • Hosp. Quiron Madrid Pozuelo

    Madrid, 28223

  • Clinica Univ. de Navarra

    Pamplona, 31008

Other trials in Spain

France8 sites
  • CHU de Montpellier Hopital Saint Eloi

    Montpellier, 34295 cedex 05

  • Hopital Cochin

    Paris, 75014

  • Hopital Saint-Antoine

    Paris, 75571

  • Groupe Hospitalier Sud Hôpital Haut-Leveque Service d'hematologie

    Pessac, 33604

  • CHU Saint Etienne Hopital Nord

    Saint-Etienne, 42055

  • Hopital Rangueil

    Toulouse, 31054

  • Hopital Purpan

    Toulouse, 31059

  • Hôpital de Brabois Adultes

    Vandœuvre-lès-Nancy, 54511

Other trials in France

South Africa8 sites
  • TREAD Research Tygerberg Hospital

    Cape Town, 7500

  • Centre of Tuberculosis Research Innovation

    Cape Town, 7700

  • Worthwhile Clinical trials

    Johannesburg, 1501

  • Peermed Clinical Trial Centre

    Kempton Park, 1619

  • Dr AA Mahomed Medical Centre

    Moloto South, 1022

  • VX Pharma

    Pretoria, 0002

  • Dr J.M. Engelbrecht Trial Site

    Somerset West, 7130

  • Be Part Yoluntu Centre

    Western Cape, 7626

Other trials in South Africa

Belgium6 sites
  • Anima

    Alken, 3570

  • Institute of Tropical Medicine Antwerp

    Antwerp, 2000

  • Center for Vaccinology (CEVAC)

    Ghent, 9000

  • UZ Leuven

    Leuven, 3000

  • Az Sint-Maarten

    Mechelen, 2800

  • Private Practice RESPISOM Namur

    Namur, 5101

Other trials in Belgium

Brazil5 sites
  • Hospital Nossa Senhora da Conceicao S A

    Porto Alegre, 91350 200

  • Ministerio da Saude - Hospital dos Servidores do Estado - RJ

    Rio de Janeiro, 20221-160

  • Instituto Nacional de Infectologia Evandro Chagas (INI) - FIOCRUZ

    Rio de Janeiro, 21040-900

  • Instituto de infectologia Emilio Ribas

    São Paulo, 01246-900

  • Centro de Referencia E Treinamento Dst/Aids

    São Paulo, 02141-000

Other trials in Brazil

Colombia5 sites
  • Fundacion Cardiomet CEQUIN

    Armenia

  • IPS Centro Cientifico Asisitencial Jose Luis Accini S.A.S.

    Barranquilla, 80020

  • Asistencia Cientifica de Alta Complejidad S.A.S

    Bogotá

  • Centro Medico Imbanaco de Cali S.A.

    Cali, 760042

  • T Y C Inversiones S A S Grupsalud

    Santa Marta, 470001

Other trials in Colombia

Philippines5 sites
  • Riverside Medical Center

    Bacolod, 6100

  • West Visayas State University Medical Center

    Iloilo City, 5000

  • Tropical Disease Foundation

    Makati, 1230

  • Makati Medical Center

    Manila, 1000

  • Medical Center Manila

    Manila, 1000

Other trials in Philippines

Germany1 site
  • Klinikum rechts der Isar der TU Munchen

    München, 81675

Other trials in Germany

About this study

Official title: A Randomized, Double-blind, Placebo-controlled Phase 3 Study to Assess the Efficacy and Safety of Ad26.COV2.S for the Prevention of SARS-CoV-2-mediated COVID-19 in Adults Aged 18 Years and Older

The study will evaluate the efficacy of Ad26.COV2.S in the prevention of molecularly confirmed moderate to severe/critical coronavirus disease-2019 (COVID-19), as compared to placebo, in SARS-CoV-2 seronegative adults in the double-blind phase and to describe COVID-19 outcomes, safety, and immunogenicity in the different study cohorts in open-label phase.

Read the detailed description

The aim of the COVID-19 vaccine clinical development program is to develop a safe and effective vaccine for the prevention of COVID-19. Ad26.COV2.S, a COVID-19 vaccine based on a human replication-incompetent Ad26 vector, constructed to encode the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) virus spike (S) protein, is being developed. The study will consist of: a screening phase (up to 28 days), study period (60-week), and a long-term follow-up period (1 additional year). The total study duration will be maximum 2 years and 3 months for the participants. Assessments for efficacy (COVID-19 signs and symptoms, etc.), immunogenicity (such as humoral immune responses), and safety (such as adverse events [AEs] monitoring) will be performed throughout the study.

Being tested
Ad26.COV2.S, Placebo

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Ad26.COV2.SBiological

    Also called JNJ-78436735, Ad26COVS1, VAC31518

    Ad26.COV2.S vaccine will be administered on Day 1 and Day 57 in the double-blind phase. At unblinding visit Ad26.COV2.S vaccine will be administered to participants at Day 57 who have not yet received second vaccination and in newly enrolled participants as either single dose on Day 1 or two doses on Day 1 and Day 57. Single dose of Ad26.COV2.S vaccine will also be administered to participants initially receiving placebo. Single booster dose of Ad26.COV2.S vaccine will be given to participants in the open label phase who have received only a single vaccination with Ad26.COV2.S.

  • PlaceboOther

    Placebo will be administered as IM injection on Day 1 and Day 57.

Study groups in NCT04614948
Study groupRoleWhat they receive
Ad26.COV2.SExperimentalParticipants will receive intramuscular (IM) injection of Ad26.COV2.S vaccine on Day 1 and Day 57 in the double-blind phase. At unblinding visit (open-label phase), participants who have not yet received second vaccination will receive second dose of Ad26.COV2.S vaccine on Day 57, if applicable and newly enrolled participants will either receive IM injection of one dose of Ad26.COV2.S vaccine on Day 1 or two doses of Ad26.COV2.S vaccine on Day 1 and Day 57. All ongoing participants who only received a single vaccination with Ad26.COV2.S in the study will be offered to receive single booster dose of Ad26.COV2.S in the open label phase preferably within 6 to 12 months after the participant's first Ad26.COV2.S vaccination.
Receives: Biological: Ad26.COV2.S
PlaceboPlacebo comparatorParticipants will receive IM injection of placebo on Day 1 and Day 57 in the double-blind phase. At unblinding visit (open-label phase), participants initially receiving placebo will be offered to receive IM injection of a single dose of Ad26.COV2.S vaccine. All ongoing participants who only received a single vaccination with Ad26.COV2.S in the study will be offered to receive single booster dose of Ad26.COV2.S in the open label phase preferably within 6 to 12 months after the participant's first Ad26.COV2.S vaccination.
Receives: Biological: Ad26.COV2.S; Other: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Double Blind Phase: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 in Seronegative Participants With Onset at Least 14 Days After the Second Vaccination

    Molecularly confirmed moderate to severe/critical COVID-19 was defined as a severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) positive reverse transcription/polymerase chain reaction (RT-PCR) or molecular test result from any available respiratory tract sample (example, nasal swab sample, sputum sample, throat swab sample, saliva sample) or other sample. Moderate included one sign or symptom such as respiratory rate >=20 breaths per minute (min) and symptoms such as shortness of breath or two signs or symptoms such as heart rate >=90 beats/min and symptoms such as cough from a list of signs and symptoms and severe/critical included one of the following signs and symptoms: respiratory rate >=30 breaths/min, heart rate >=125 beats/min, oxygen saturation (SpO2) <=93 percent (%) on room air at sea level respiratory failure, evidence of shock, significant acute renal, hepatic, or neurologic dysfunction, admission to Intensive Care Unit (ICU), death defined as per FDA guidance.

    Measured: From at least 14 days after second vaccination on Day 57 (Day 71) up to end of double blind phase (7.2 months)

Secondary outcomes (21)
  1. Double Blind Phase: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Serostatus With Onset At Least 1 Day After the First Day 1 Vaccination

    Molecularly confirmed moderate to severe/critical COVID-19 was defined as a SARS-CoV-2 positive RT-PCR or molecular test result from any available respiratory tract sample (example, nasal swab sample, sputum sample, throat swab sample, saliva sample) or other sample. Moderate included one sign or symptom such as respiratory rate greater than or equal to (>=) 20 breaths per minute and symptoms such as shortness of breath or two signs or symptoms such as heart rate >= 90 beats per min and symptoms such as cough from a list of signs and symptoms and severe/critical included one of the following signs and symptoms: respiratory rate >=30 breaths/minute, heart rate >=125 beats/minute, SpO2 less than or equal to (<=) 93% on room air at sea level respiratory failure, evidence of shock, significant acute renal, hepatic, or neurologic dysfunction, admission to the ICU, death defined as per US Food and Drug Administration (FDA) guidance.

    Measured: From at least 1 day after first vaccination on Day 1 (Day 2) up to end of double blind phase (7.2 months)

  2. Double Blind Phase: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Serostatus With Onset at Least 14 Days After the Second Vaccination

    Molecularly confirmed moderate to severe/critical COVID-19 was defined as a SARS-CoV-2 positive RT-PCR or molecular test result from any available respiratory tract sample (example, nasal swab sample, sputum sample, throat swab sample, saliva sample) or other sample. Moderate included one sign or symptom such as respiratory rate >= 20 breaths per minute and symptoms such as shortness of breath or two signs or symptoms such as heart rate >= 90 beats per min and symptoms such as cough from a list of signs and symptoms and severe/critical included one of the following signs and symptoms: respiratory rate >=30 breaths/minute, heart rate >=125 beats/minute, SpO2 <= 93% on room air at sea level respiratory failure, evidence of shock, significant acute renal, hepatic, or neurologic dysfunction, admission to the ICU, death defined as per FDA guidance.

    Measured: From at least 14 days after second vaccination on Day 57 (Day 71) up to end of double blind phase (7.2 months)

  3. Double Blind Phase: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 in Seronegative Participants With Onset at Least 1 Day After the First Day 1 Vaccination

    Molecularly confirmed moderate to severe/critical COVID-19 was defined as a SARS-CoV-2 positive RT-PCR or molecular test result from any available respiratory tract sample (example, nasal swab sample, sputum sample, throat swab sample, saliva sample) or other sample. Moderate included one sign or symptom such as respiratory rate >= 20 breaths per minute and symptoms such as shortness of breath or two signs or symptoms such as heart rate >= 90 beats per min and symptoms such as cough from a list of signs and symptoms and severe/critical included one of the following signs and symptoms: respiratory rate >=30 breaths/minute, heart rate >=125 beats/minute, SpO2 <= 93% on room air at sea level respiratory failure, evidence of shock, significant acute renal, hepatic, or neurologic dysfunction, admission to the ICU, death defined as per FDA guidance.

    Measured: From at least 1 day after first vaccination on Day 1 (Day 2) up to end of double blind phase (7.2 months)

  4. Double Blind Phase: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 With Onset at Least 14 Days After the First Day 1 Vaccination

    Molecularly confirmed moderate to severe/critical COVID-19 was defined as a SARS-CoV-2 positive RT-PCR or molecular test result from any available respiratory tract sample (example, nasal swab sample, sputum sample, throat swab sample, saliva sample) or other sample. Moderate included one sign or symptom such as respiratory rate >= 20 breaths per minute and symptoms such as shortness of breath or two signs or symptoms such as heart rate >= 90 beats per min and symptoms such as cough from a list of signs and symptoms and severe/critical included one of the following signs and symptoms: respiratory rate >=30 breaths/minute, heart rate >=125 beats/minute, SpO2 <= 93% on room air at sea level respiratory failure, evidence of shock, significant acute renal, hepatic, or neurologic dysfunction, admission to the ICU, death defined as per FDA guidance.

    Measured: From at least 14 days after first vaccination on Day 1 (Day 15) up to end of double blind phase (7.2 months)

  5. Double Blind Phase: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 With Onset at Least 28 Days After the First Day 1 Vaccination

    Molecularly confirmed moderate to severe/critical COVID-19 was defined as a SARS-CoV-2 positive RT-PCR or molecular test result from any available respiratory tract sample (example, nasal swab sample, sputum sample, throat swab sample, saliva sample) or other sample. Moderate included one sign or symptom such as respiratory rate >= 20 breaths per minute and symptoms such as shortness of breath or two signs or symptoms such as heart rate >= 90 beats per min and symptoms such as cough from a list of signs and symptoms and severe/critical included one of the following signs and symptoms: respiratory rate >=30 breaths/minute, heart rate >=125 beats/minute, SpO2 <= 93% on room air at sea level respiratory failure, evidence of shock, significant acute renal, hepatic, or neurologic dysfunction, admission to the ICU, death defined as per FDA guidance.

    Measured: From at least 28 days after the first vaccination on Day 1 (Day 29) up to end of double blind phase (7.2 months)

  6. Double Blind Phase: Number of Participants With First Occurrence of COVID-19 Requiring Medical Intervention With Onset at Least 14 Days After the Second Vaccination

    Number of participants with first occurrence of COVID-19 requiring medical intervention (such as a composite endpoint of hospitalization, ICU admission, mechanical ventilation, and extracorporeal membrane oxygenation [ECMO]), linked to objective measures such as decreased oxygenation, X-ray or computed tomography [CT] findings and linked to any molecularly confirmed, COVID-19 with onset at least 14 days post second vaccination were reported.

    Measured: From at least 14 days after second vaccination on Day 57 (Day 71) up to end of double blind phase (7.2 months)

  7. Double Blind Phase: Area Under the Curve (AUC) of SARS-CoV-2 Viral Load as Assessed by Quantitative RT-PCR in Participants With Molecularly Confirmed Symptomatic COVID-19 With Onset at Least 14 Days After Second Vaccination

    AUC of SARS-CoV-2 viral load was assessed in confirmed COVID-19 cases using RT-PCR. Nasal swabs were used to detect and/or quantify SARS-CoV-2. Due to change in the planned analysis, data was collected and analyzed for participants with molecularly confirmed symptomatic COVID-19 regardless of severity that is mild, moderate or severe and was not collected and analyzed separately for moderate to severe cases.

    Measured: From Day 71 up to end of the COVID-19 episode (up to 90 days)

  8. Double Blind Phase: Number of Participants With First Occurrence of Molecularly Confirmed Mild COVID-19 With Onset at Least 14 Days After the Second Vaccination

    Molecularly confirmed mild Covid-19 was defined as a SARS-CoV-2 positive RT-PCR or molecular test result from any available respiratory tract sample (example, nasal swab sample, sputum sample, throat swab sample, saliva sample) or other sample and one of the following signs and symptoms: fever (>=38 degree Celsius or >=100.4 degree Fahrenheit), sore throat, malaise (loss of appetite, generally unwell, fatigue, physical weakness), headache, muscle pain (myalgia), gastrointestinal symptoms, cough, chest congestion, runny nose, wheezing, skin rash, eye irritation or discharge, chills, new or changing olfactory or taste disorders, red or bruised looking feet or toes, or shaking chills or rigors.

    Measured: From at least 14 days after second vaccination on Day 57 (Day 71) up to end of double blind phase (7.2 months)

  9. Double Blind Phase: Number of Participants With First Occurrence of Molecularly Confirmed COVID-19 Defined by the US FDA Harmonized Case Definition With Onset at Least 14 Days After the Second Vaccination

    Molecularly confirmed COVID-19 was defined as SARS-CoV-2 positive RT-PCR or molecular test result from any available respiratory tract sample (example, nasal swab sample, sputum sample, throat swab sample, saliva sample) or other sample; and COVID-19 symptoms consistent with those defined by the US FDA harmonized case definition at the time of finalization of the study protocol: fever or chills, cough, shortness of breath or difficulty breathing, fatigue, muscle or body aches, headache, new loss of taste or smell, sore throat, congestion or runny nose, nausea or vomiting, and diarrhea.

    Measured: From at least 14 days after second vaccination on Day 57 (Day 71) up to end of double blind phase (7.2 months)

  10. Double Blind Phase: Number of Participants With Burden of Disease (BOD) Based on First Occurrence of Molecularly Confirmed Symptomatic COVID-19 With Onset at Least 14 Days After the Second Vaccination

    BOD is a weighted version of the mild, moderate, and severe/critical vaccine efficacies and was evaluated based on the first occurrence of molecularly confirmed COVID-19, including mild, moderate or severe/critical COVID-19 case.

    Measured: From at least 14 days after second vaccination on Day 57 (Day 71) up to end of double blind phase (7.2 months)

  11. Double Blind Phase: Number of Participants With Serologic Conversion Between Day 71 up to Unblinding Visit Using an Enzyme-linked Immunosorbent Assay (ELISA)

    Number of participants with serologic conversion between Day 71 up to unblinding visit using an ELISA were reported. Due to change in planned analysis, data was collected and analyzed between Day 71 up to unblinding visit instead of from baseline to unblinding visit.

    Measured: From Day 71 up to unblinding visit (7.2 months)

  12. Double Blind Phase: Number of Participants With Asymptomatic Infection Detected By Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR) With Onset at Least 14 Days After the Second Vaccination

    Number of participants with asymptomatic infection detected by RT-PCR with onset at least 14 days after the second vaccination (Day 71) were reported.

    Measured: From at least 14 days after second vaccination on Day 57 (Day 71) up to end of double blind phase (7.2 months)

  13. Double Blind Phase: Number of Participants With First Occurrence of SARS-CoV-2 Infection (Serologically and/or Molecularly Confirmed) With Onset at Least 14 Days After the Second Vaccination

    Number of participants with first occurrence of SARS-CoV-2 infection (serologically and/or molecularly confirmed) with onset at least 14 days after the second vaccination (Day 71) were reported.

    Measured: From at least 14 days after second vaccination on Day 57 (Day 71) up to end of double blind phase (7.2 months)

  14. Double Blind Phase: Number of Participants With Serious Adverse Events (SAEs)

    An AE was any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product that does not necessarily have a causal relationship with the vaccine. SAE was any untoward medical occurrence that at any dose may result in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, is a suspected transmission of any infectious agent via a medicinal product.

    Measured: From Day 1 up to end of double blind phase (7.2 months)

  15. Double Blind Phase: Number of Participants With Adverse Events of Special Interest (AESIs)

    Number of participants with AESIs were reported. AESIs were significant AEs that were judged to be of special interest because of clinical importance, known or suspected class effects, or based on nonclinical signals. Thrombosis with Thrombocytopenia Syndrome (TTS), a syndrome characterized by a combination of both a thrombotic event and thrombocytopenia, was considered to be an AESI in this study. A suspected TTS case was defined as: Thrombotic events: suspected deep vessel venous or arterial thrombotic events; Thrombocytopenia, defined as platelet count below 150,000/micro liter.

    Measured: From Day 1 up to end of double blind phase (7.2 months)

  16. Double Blind Phase: Number of Participants With Medically-Attended Adverse Events (MAAEs)

    An AE was any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product that does not necessarily have a causal relationship with the vaccine. MAAEs were defined as AEs with medically-attended visits including hospital, emergency room, urgent care clinic, or other visits to or from medical personnel for any reason.

    Measured: From Day 1 up to 7.2 months

  17. Double-Blind: Number of Participants With MAAEs Leading to Study Discontinuation

    An AE was any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product that does not necessarily have a causal relationship with the vaccine. MAAEs were defined as AEs with medically-attended visits including hospital, emergency room, urgent care clinic, or other visits to or from medical personnel for any reason.

    Measured: From Day 1 up to end of double blind phase (7.2 months)

  18. Double Blind Phase: Number of Participants With Solicited Local Adverse Events (AEs) During 7 Days Following Each Vaccination

    An AE was any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product that does not necessarily have a causal relationship with the vaccine. Participants who were enrolled in safety subset (SS) were asked to note in the e-Diary occurrences of injection site pain/tenderness, erythema, and swelling at the study vaccine injection site daily for 7 days post each vaccination (day of vaccination and the subsequent 7 days).

    Measured: 7 days after first vaccination on Day 1 (up to Day 8), 7 days after second vaccination on Day 57 (up to Day 64)

  19. Double Blind Phase: Number of Participants With Solicited Systemic AEs During 7 Days Following Each Vaccination

    An AE was any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product that does not necessarily have a causal relationship with the vaccine. Participants who were enrolled in safety subset were instructed on how to record daily temperature using a thermometer provided for home use. Participants recorded temperature in e-Diary in evening of the day of vaccination, and then daily for next 7 days approximately at same time each day. If more than 1 measurement was made on any given day, the highest temperature of that day was recorded in e-Diary. Fever was defined as endogenous elevation of body temperature >= 38.0 degree Celsius or >=100.4-degree Fahrenheit, as recorded in at least 1 measurement. Participants also noted the signs and symptoms in e-Diary on a daily basis for 7 days post each vaccination (day of vaccination and subsequent 7 days), for the following events: fatigue, headache, nausea, myalgia.

    Measured: 7 days after first vaccination on Day 1 (up to Day 8), 7 days after second vaccination on Day 57 (up to Day 64)

  20. Double Blind Phase: Number of Participants With Unsolicited Adverse Events (AEs) During 28 Days Post Each Vaccination

    An AE was any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product that does not necessarily have a causal relationship with the vaccine. Unsolicited AEs were all AEs for which the participant is not specifically questioned in the participant diary.

    Measured: 28 days after first vaccination on Day 1 (up to Day 29), 28 days after second vaccination on Day 57 (up to Day 85)

  21. Double Blind Phase: SARS-CoV-2 Binding Antibodies Assessed by ELISA

    Binding antibodies to SARS-CoV-2 S protein as assessed by ELISA to measure humoral immune response was reported. The lower limit of quantification (LLOQ) was 50.3 ELISA units per milliliter (EU/mL). A sample was considered positive if the value was strictly greater than the LLOQ (>LLOQ).

    Measured: At Baseline (Day 1), Days 29, 57 and 71

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Nov 2020
  2. Study start12 Nov 2020
  3. Primary completion18 Jun 2023
  4. Study completion18 Jun 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
31,835 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04614948
Sponsor's protocol ID
CR108916
Other IDs
2020-003643-29, VAC31518COV3009
Acronym
ENSEMBLE 2
Status last verified
Jan 2025
First submitted
3 Nov 2020
Last updated
4 Feb 2025
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: The data sharing policy of the Janssen Pharmaceutical Companies of Johnson \& Johnson is available at www.janssen.com/clinical-trials/transparency. As noted on this site, requests for access to the study data can be submitted through Yale Open Data Access (YODA) Project site at yoda.yale.edu
Expanded access
Available

Publications

  • Hardt K, Vandebosch A, Sadoff J, Le Gars M, Truyers C, Lowson D, Van Dromme I, Vingerhoets J, Kamphuis T, Scheper G, Ruiz-Guinazu J, Faust SN, Spinner CD, Schuitemaker H, Van Hoof J, Douoguih M, Struyf F; ENSEMBLE2 study group. Efficacy, safety, and immunogenicity of a booster regimen of Ad26.COV2.S vaccine against COVID-19 (ENSEMBLE2): results of a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Infect Dis. 2022 Dec;22(12):1703-1715. doi: 10.1016/S1473-3099(22)00506-0. Epub 2022 Sep 13.

    PubMed 36113538

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Ad26.COV2.S in people with Participants With or Without Stable Co-morbidities Associated With Progression to Severe COVID-19, run by Janssen Vaccines & Prevention B.V. at 126 sites in 10 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 126 sites in United States, United Kingdom, Spain, France, South Africa and 5 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 9 Oct 2024). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Double Blind Phase: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 in Seronegative Participants With Onset at Least 14 Days After the Second Vaccination (time frame: From at least 14 days after second vaccination on Day 57 (Day 71) up to end of double blind phase (7.2 months)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04614948, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Feb 2025.

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