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. Issue 12 (December 2022)
- Record Type:
- Journal Article
- Title:
- 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. Issue 12 (December 2022)
- Main Title:
- 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
- Authors:
- Hardt, Karin
Vandebosch, An
Sadoff, Jerald
Le Gars, Mathieu
Truyers, Carla
Lowson, David
Van Dromme, Ilse
Vingerhoets, Johan
Kamphuis, Tobias
Scheper, Gert
Ruiz-Guiñazú, Javier
Faust, Saul N
Spinner, Christoph D
Schuitemaker, Hanneke
Van Hoof, Johan
Douoguih, Macaya
Struyf, Frank
Garibaldi, Brian T.
Albertson, Timothy E.
Sandrock, Christian
Lee, Janet S.
Looney, Mark R.
Tapson, Victor F.
Wiysonge, Charles Shey
Velarde, Luis Humberto Anaya
Backenroth, Daniel
Bhushanan, Jisha
Brandenburg, Börries
Cárdenas, Vicky
Chen, Bohang
Chen, Fei
Chetty, Polan
Chu, Pei-Ling
Cooper, Kimberly
Custers, Jerome
Delanghe, Hilde
Duca, Anna
Henrick, Tracy
Juraszek, Jarek
Nalpas, Catherine
Peeters, Monika
Pinheiro, Jose
Roels, Sanne
Ryser, Martin F.
Salas, Jose
Santoro Matias, Samantha
Scheys, Ilse
Shetty, Pallavi
Shukarev, Georgi
Stoddard, Jeffrey
Talloen, Willem
Tran, NamPhuong
Vaissiere, Nathalie
van Son-Palmen, Elisabeth
Xu, Jiajun
Goecker, Erin A.
Greninger, Alexander L.
Jerome, Keith R.
Roychoudhury, Pavitra
Takuva, Simbarashe G.
Accini Mendoza, Jose Luis
Achtyes, Eric
Ahsan, Habibul
Alhatemi, Azhar
Allen, Nancy
Arribas, Jose R.
Bahrami, Ghazaleh
Bailon, Lucia
Bajwa, Ali
Baker, Jonathan
Baron, Mira
Benet, Susana
Berdaï, Driss
Berger, Patrick
Bertoch, Todd
Bethune, Claire
Bevilacqua, Sybille
Biagioni Santos, Maria Silvia
Binnian, Ian
Bisnauthsing, Karen
Boivin, Jean-Marc
Bollen, Hilde
Bonnet, Sandrine
Borobia, Alberto M.
Botelho-Nevers, Elisabeth
Bright, Phil
Britten, Vianne
Brown, Claire
Buadi, Amanda
Buntinx, Erik
Burgess, Lesley
Bush, Larry
Capeding, Maria Rosario
Carr, Quito Osuna
Carrasco Mas, Amparo
Catala, Hélène
Cathie, Katrina
Caudill, T. Shawn
Cereto Castro, Fernando
Chau, Kénora
Chavoustie, Steven
Chowdhury, Marie
Chronos, Nicolas
Cicconi, Paola
Cifuentes, Liliana
Cobo, Sara Maria
Collins, Helen
Colton, Hayley
Cuaño, Carlos Rolando G.
D'Onofrio, Valentino
Dargan, Paul
Darton, Thomas
Deane, Peter
Del Pozo, Jose Luis
Derdelinckx, Inge
Desai, Amisha
Dever, Michael
Díaz-Pollán, Beatriz
DiBuono, Mark
Doust, Matthew
Duncan, Christopher
Echave-Sustaeta, Jose Maria
Eder, Frank
Ellis, Kimberly
Elzi, Stanton
Emmett, Stevan
Engelbrecht, Johannes
Evans, Mim
Farah, Theo
Felton, Timothy
Ferreira, João Pedro
Floutier, Catherine
Flume, Patrick
Ford, Stacy
Fragoso, Veronica
Freedman, Andrew
Frentiu, Emilia
Galloway, Christopher
Galtier, Florence
Garcia Diaz, Julia
García García, Irene
Garcia, Alcaide
Gardener, Zoe
Gauteul, Pascale
Geller, Steven
Gibson, Andrew
Gillet, Claudia
Girerd, Nicolas
Girodet, Pierre-Olivier
Gler, Maria Tarcela
Glover, Richard
Go, Herschel Don D.
Gokani, Karishma
Gonthier, Damien
Green, Christopher
Greenberg, Richard
Griffin, Carl
Grobbelaar, Coert
Guancia, Adonis
Hakkarainen, Gloria
Harris, James
Hassman, Michael
Heimer, Deirdre
Hellstrom-Louw, Elizabeth
Herades, Yoan
Holroyd, Christopher
Hussen, Nazreen
Isidro, Marie Grace Dawn
Jackson, Yvonne
Jain, Manish
João Filho, Esaú Custódio
Johnson, Daniel
Jones, Ben
Joseph, Natasha
Jumeras, Analyn
Junquera, Patricia
Kellett-Wright, Johanna
Kennedy, Patrick
Kilgore, Paul E.
Kim, Kenneth
Kimmel, Murray
Konis, George
Kutner, Mark
Lacombe, Karine
Launay, Odile
Lazarus, Rajeka
Lederman, Samuel
Lefebvre, Gigi
Lennon Collins, Katrina
Leroux-Roels, Isabel
Lim, Kenneth Wilson O.
Lins, Muriel
Liu, Edward
Llewelyn, Martin
Mahomed, Akbar
Maia, Bernardo Porto
Marín-Candon, Alícia
Martínez-Gómez, Xavier
Martinot, Jean Benoit
Mazzella, Andrea
McCaughan, Frank
McCormack, Louise
McGettigan, John
Mehra, Purvi
Mejeur, Rhonda
Miller, Vicki
Mills, Anthony
Molto Marhuenda, Jose
Moodley, Prebashan
Mora-Rillo, Marta
Mothe, Beatriz
Mullan, Daniel
Munro, Alasdair
Myers, Paul
Nell, Jeremy
Newman Lobato Souza, Tamara
O'Halloran, Jane A.
Ochoa Mazarro, Maria Dolores
Oliver, Abigail
Onate Gutierrez, Jose Millan
Ortega, Jessica
Oshita, Masaru
Otero Romero, Susana
Overcash, Jeffrey Scott
Owens, Daniel
Packham, Alice
Pacurar, Mihaela
Paiva de Sousa, Leonardo
Palfreeman, Adrian
Pallares, Christian José
Patel, Rahul
Patel, Suchet
Pelkey, Leslie
Peluso, Denise
Penciu, Florentina
Pinto, S. Jerry
Pounds, Kevin
Pouzar, Joe
Pragalos, Antoinette
Presti, Rachel
Price, David
Qureshi, Ehsaan
Ramalho Madruga, José Valdez
Ramesh, Mayur
Rankin, Bruce
Razat, Béatrice
Riegel Santos, Breno
Riesenberg, Robert
Riffer, Ernie
Roche, Siobhan
Rose, Katie
Rosellini, Pietro
Rossignol, Patrick
Safirstein, Beth
Salazar, Hernan
Sanchez Vallejo, Gregorio
Santhosh, Smrithi
Seco-Meseguer, Enrique
Seep, Michael
Sherry, Emma
Short, Philip
Soentjens, Patrick
Solis, Joel
Soriano Viladomiu, Alejandro
Sorli, Caroline
Spangenthal, Selwyn
Spence, Niamh
Stephenson, Elaine
Strout, Cynthia
Surowitz, Ronald
Taladua, Kristy Michelle
Tellalian, David
Thalamas, Claire
Thiriphoo, Nang
Thomas, Judith
Thomas, Nicholas
Trout, Guillermo
Urroz, Mikel
Veekmans, Bernard
Veekmans, Laurent
Villalobos, Ralph Elvi M.
Warren, Sarah
Webster, Brian
White, Alexander
Williams, Gail
Williams, Hayes
Wilson, Barbara
Winston, Alan
Wiselka, Martin
Zervos, Marcus
… (more) - Abstract:
- Summary: Background: Despite the availability of effective vaccines against COVID-19, booster vaccinations are needed to maintain vaccine-induced protection against variant strains and breakthrough infections. This study aimed to investigate the efficacy, safety, and immunogenicity of the Ad26.COV2.S vaccine (Janssen) as primary vaccination plus a booster dose. Methods: ENSEMBLE2 is a randomised, double-blind, placebo-controlled, phase 3 trial including crossover vaccination after emergency authorisation of COVID-19 vaccines. Adults aged at least 18 years without previous COVID-19 vaccination at public and private medical practices and hospitals in Belgium, Brazil, Colombia, France, Germany, the Philippines, South Africa, Spain, the UK, and the USA were randomly assigned 1:1 via a computer algorithm to receive intramuscularly administered Ad26.COV2.S as a primary dose plus a booster dose at 2 months or two placebo injections 2 months apart. The primary endpoint was vaccine efficacy against the first occurrence of molecularly confirmed moderate to severe–critical COVID-19 with onset at least 14 days after booster vaccination, which was assessed in participants who received two doses of vaccine or placebo, were negative for SARS-CoV-2 by PCR at baseline and on serology at baseline and day 71, had no major protocol deviations, and were at risk of COVID-19 (ie, had no PCR-positive result or discontinued the study before day 71). Safety was assessed in all participants;Summary: Background: Despite the availability of effective vaccines against COVID-19, booster vaccinations are needed to maintain vaccine-induced protection against variant strains and breakthrough infections. This study aimed to investigate the efficacy, safety, and immunogenicity of the Ad26.COV2.S vaccine (Janssen) as primary vaccination plus a booster dose. Methods: ENSEMBLE2 is a randomised, double-blind, placebo-controlled, phase 3 trial including crossover vaccination after emergency authorisation of COVID-19 vaccines. Adults aged at least 18 years without previous COVID-19 vaccination at public and private medical practices and hospitals in Belgium, Brazil, Colombia, France, Germany, the Philippines, South Africa, Spain, the UK, and the USA were randomly assigned 1:1 via a computer algorithm to receive intramuscularly administered Ad26.COV2.S as a primary dose plus a booster dose at 2 months or two placebo injections 2 months apart. The primary endpoint was vaccine efficacy against the first occurrence of molecularly confirmed moderate to severe–critical COVID-19 with onset at least 14 days after booster vaccination, which was assessed in participants who received two doses of vaccine or placebo, were negative for SARS-CoV-2 by PCR at baseline and on serology at baseline and day 71, had no major protocol deviations, and were at risk of COVID-19 (ie, had no PCR-positive result or discontinued the study before day 71). Safety was assessed in all participants; reactogenicity, in terms of solicited local and systemic adverse events, was assessed as a secondary endpoint in a safety subset (approximately 6000 randomly selected participants). The trial is registered with ClinicalTrials.gov, NCT04614948, and is ongoing. Findings: Enrolment began on Nov 16, 2020, and the primary analysis data cutoff was June 25, 2021. From 34 571 participants screened, the double-blind phase enrolled 31 300 participants, 14 492 of whom received two doses (7484 in the Ad26.COV2.S group and 7008 in the placebo group) and 11 639 of whom were eligible for inclusion in the assessment of the primary endpoint (6024 in the Ad26.COV2.S group and 5615 in the placebo group). The median (IQR) follow-up post-booster vaccination was 36·0 (15·0–62·0) days. Vaccine efficacy was 75·2% (adjusted 95% CI 54·6–87·3) against moderate to severe–critical COVID-19 (14 cases in the Ad26.COV2.S group and 52 cases in the placebo group). Most cases were due to the variants alpha (B.1.1.7) and mu (B.1.621); endpoints for the primary analysis accrued from Nov 16, 2020, to June 25, 2021, before the global dominance of delta (B.1.617.2) or omicron (B.1.1.529). The booster vaccine exhibited an acceptable safety profile. The overall frequencies of solicited local and systemic adverse events (evaluated in the safety subset, n=6067) were higher among vaccine recipients than placebo recipients after the primary and booster doses. The frequency of solicited adverse events in the Ad26.COV2.S group were similar following the primary and booster vaccinations (local adverse events, 1676 [55·6%] of 3015 vs 896 [57·5%] of 1559, respectively; systemic adverse events, 1764 [58·5%] of 3015 vs 821 [52·7%] of 1559, respectively). Solicited adverse events were transient and mostly grade 1–2 in severity. Interpretation: A homologous Ad26.COV2.S booster administered 2 months after primary single-dose vaccination in adults had an acceptable safety profile and was efficacious against moderate to severe–critical COVID-19. Studies assessing efficacy against newer variants and with longer follow-up are needed. Funding: Janssen Research & Development. … (more)
- Is Part Of:
- Lancet infectious diseases. Volume 22:Issue 12(2022)
- Journal:
- Lancet infectious diseases
- Issue:
- Volume 22:Issue 12(2022)
- Issue Display:
- Volume 22, Issue 12 (2022)
- Year:
- 2022
- Volume:
- 22
- Issue:
- 12
- Issue Sort Value:
- 2022-0022-0012-0000
- Page Start:
- 1703
- Page End:
- 1715
- Publication Date:
- 2022-12
- Subjects:
- Communicable diseases -- Periodicals
Infection -- Periodicals
Communicable Diseases -- Periodicals
Infection -- Periodicals
Maladies infectieuses -- Périodiques
Infection -- Périodiques
Communicable diseases
Infection
Periodicals
616.905 - Journal URLs:
- http://www.mdconsult.com/public/search?search_type=journal&j_sort=pub_date&j_issn=1473-3099 ↗
http://www.sciencedirect.com/science/journal/14733099 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/S1473-3099(22)00506-0 ↗
- Languages:
- English
- ISSNs:
- 1473-3099
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