Efficacy and Safety of Sarilumab in Hospitalized Patients With Coronavirus Disease 2019: A Randomized Clinical Trial.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
24 08 2022
Historique:
received: 12 11 2021
pubmed: 27 2 2022
medline: 30 8 2022
entrez: 26 2 2022
Statut: ppublish

Résumé

Open-label platform trials and a prospective meta-analysis suggest efficacy of anti-interleukin (IL)-6R therapies in hospitalized patients with coronavirus disease 2019 (COVID-19) receiving corticosteroids. This study evaluated the efficacy and safety of sarilumab, an anti-IL-6R monoclonal antibody, in the treatment of hospitalized patients with COVID-19. In this adaptive, phase 2/3, randomized, double-blind, placebo-controlled trial, adults hospitalized with COVID-19 received intravenous sarilumab 400 mg or placebo. The phase 3 primary analysis population included patients with critical COVID-19 receiving mechanical ventilation (MV). The primary outcome was proportion of patients with ≥1-point improvement in clinical status from baseline to day 22. There were 457 and 1365 patients randomized and treated in phases 2 and 3, respectively. In phase 3, patients with critical COVID-19 receiving MV (n = 298; 28.2% on corticosteroids), the proportion with ≥1-point improvement in clinical status (alive, not receiving MV) at day 22 was 43.2% for sarilumab and 35.5% for placebo (risk difference, +7.5%; 95% confidence interval [CI], -7.4 to 21.3; P =.3261), a relative risk improvement of 21.7%. In post hoc analyses pooling phase 2 and 3 critical patients receiving MV, the hazard ratio for death for sarilumab vs placebo was 0.76 (95% CI, .51 to 1.13) overall and 0.49 (95% CI, .25 to .94) in patients receiving corticosteroids at baseline. This study did not establish the efficacy of sarilumab in hospitalized patients with severe/critical COVID-19. Post hoc analyses were consistent with other studies that found a benefit of sarilumab in patients receiving corticosteroids. NCT04315298.

Sections du résumé

BACKGROUND
Open-label platform trials and a prospective meta-analysis suggest efficacy of anti-interleukin (IL)-6R therapies in hospitalized patients with coronavirus disease 2019 (COVID-19) receiving corticosteroids. This study evaluated the efficacy and safety of sarilumab, an anti-IL-6R monoclonal antibody, in the treatment of hospitalized patients with COVID-19.
METHODS
In this adaptive, phase 2/3, randomized, double-blind, placebo-controlled trial, adults hospitalized with COVID-19 received intravenous sarilumab 400 mg or placebo. The phase 3 primary analysis population included patients with critical COVID-19 receiving mechanical ventilation (MV). The primary outcome was proportion of patients with ≥1-point improvement in clinical status from baseline to day 22.
RESULTS
There were 457 and 1365 patients randomized and treated in phases 2 and 3, respectively. In phase 3, patients with critical COVID-19 receiving MV (n = 298; 28.2% on corticosteroids), the proportion with ≥1-point improvement in clinical status (alive, not receiving MV) at day 22 was 43.2% for sarilumab and 35.5% for placebo (risk difference, +7.5%; 95% confidence interval [CI], -7.4 to 21.3; P =.3261), a relative risk improvement of 21.7%. In post hoc analyses pooling phase 2 and 3 critical patients receiving MV, the hazard ratio for death for sarilumab vs placebo was 0.76 (95% CI, .51 to 1.13) overall and 0.49 (95% CI, .25 to .94) in patients receiving corticosteroids at baseline.
CONCLUSIONS
This study did not establish the efficacy of sarilumab in hospitalized patients with severe/critical COVID-19. Post hoc analyses were consistent with other studies that found a benefit of sarilumab in patients receiving corticosteroids.
CLINICAL TRIALS REGISTRATION
NCT04315298.

Identifiants

pubmed: 35219277
pii: 6537638
doi: 10.1093/cid/ciac153
pmc: PMC8903479
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
sarilumab NU90V55F8I

Banques de données

ClinicalTrials.gov
['NCT04315298']

Types de publication

Journal Article Randomized Controlled Trial Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e380-e388

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002556
Pays : United States

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America.

Références

J Immunother Cancer. 2020 Aug;8(2):
pubmed: 32784217
JAMA. 2020 Mar 17;323(11):1061-1069
pubmed: 32031570
J Med Virol. 2020 Jul;92(7):814-818
pubmed: 32253759
Clin Trials. 2017 Jun;14(3):264-276
pubmed: 28397569
Proc Natl Acad Sci U S A. 2020 May 19;117(20):10970-10975
pubmed: 32350134
Lancet. 2020 Mar 28;395(10229):1033-1034
pubmed: 32192578
JAMA. 2021 Aug 10;326(6):499-518
pubmed: 34228774
Rheumatology (Oxford). 2020 Feb 1;59(2):292-302
pubmed: 31312844
N Engl J Med. 2021 Apr 22;384(16):1491-1502
pubmed: 33631065
N Engl J Med. 2021 Feb 25;384(8):693-704
pubmed: 32678530
N Engl J Med. 2021 Feb 11;384(6):497-511
pubmed: 33264556
Lancet. 2021 May 01;397(10285):1637-1645
pubmed: 33933206
Eur J Intern Med. 2020 Jun;76:36-42
pubmed: 32448770
JAMA Intern Med. 2020 Jul 1;180(7):934-943
pubmed: 32167524
J Med Virol. 2020 Nov;92(11):2368-2370
pubmed: 32472703
Chest. 2020 Oct;158(4):1397-1408
pubmed: 32553536
Nat Med. 2020 Oct;26(10):1636-1643
pubmed: 32839624
Clin Immunol. 2020 May;214:108393
pubmed: 32222466

Auteurs

Sumathi Sivapalasingam (S)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

David J Lederer (DJ)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Rafia Bhore (R)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Negin Hajizadeh (N)

Institute for Clinical Outcomes Research, Feinstein Institutes for Medical Research, Northwell Health, Manhasset, New York, New York, and Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Northwell Health, Hempstead, New York, New York, USA.

Gerard Criner (G)

Department of Thoracic Medicine and Surgery, Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania, USA.

Romana Hosain (R)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Adnan Mahmood (A)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Angeliki Giannelou (A)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Selin Somersan-Karakaya (S)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Meagan P O'Brien (MP)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Anita Boyapati (A)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Janie Parrino (J)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Bret J Musser (BJ)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Emily Labriola-Tompkins (E)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Divya Ramesh (D)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Lisa A Purcell (LA)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Daya Gulabani (D)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Wendy Kampman (W)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Alpana Waldron (A)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Michelle Ng Gong (M)

Department of Medicine, Montefiore-Moses, Bronx, New York, USA.

Suraj Saggar (S)

Department of Infectious Disease, Holy Name Medical Center, Teaneck, New Jersey, USA.

Steven J Sperber (SJ)

Department of Infectious Disease, Hackensack Meridian School of Medicine and Hackensack University Medical Center, Hackensack, New Jersey, USA.

Vidya Menon (V)

Department of Medicine, NYC Health + Hospitals/Lincoln, Bronx, New York, USA.

David K Stein (DK)

Department of Medicine, Jacobi Medical Center, Bronx, New York, USA.

Magdalena E Sobieszczyk (ME)

Department of Medicine, Columbia University, New York, New York, USA.

William Park (W)

Pulmonary and Sleep Disorder Clinic, Valley Medical Center, Renton, Washington, USA.

Judith A Aberg (JA)

Division of Infectious Diseases, Icahn School of Medicine at Mount Sinai, New York, New York, USAand.

Samuel M Brown (SM)

Department of Internal Medicine, Intermountain Medical Center and University of Utah, Salt Lake City, Utah, USA.

Jack A Kosmicki (JA)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Julie E Horowitz (JE)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Manuel A Ferreira (MA)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Aris Baras (A)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Bari Kowal (B)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

A Thomas DiCioccio (A)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Bolanle Akinlade (B)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Michael C Nivens (MC)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Ned Braunstein (N)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

Gary A Herman (GA)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

George D Yancopoulos (GD)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

David M Weinreich (DM)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York, USA.

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