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Baricitinib plus Remdesivir for Hospitalized Adults with Covid-19.

Authors :
Kalil, Andre C
Kalil, Andre C
Patterson, Thomas F
Mehta, Aneesh K
Tomashek, Kay M
Wolfe, Cameron R
Ghazaryan, Varduhi
Marconi, Vincent C
Ruiz-Palacios, Guillermo M
Hsieh, Lanny
Kline, Susan
Tapson, Victor
Iovine, Nicole M
Jain, Mamta K
Sweeney, Daniel A
El Sahly, Hana M
Branche, Angela R
Regalado Pineda, Justino
Lye, David C
Sandkovsky, Uriel
Luetkemeyer, Anne F
Cohen, Stuart H
Finberg, Robert W
Jackson, Patrick EH
Taiwo, Babafemi
Paules, Catharine I
Arguinchona, Henry
Erdmann, Nathaniel
Ahuja, Neera
Frank, Maria
Oh, Myoung-Don
Kim, Eu-Suk
Tan, Seow Y
Mularski, Richard A
Nielsen, Henrik
Ponce, Philip O
Taylor, Barbara S
Larson, LuAnn
Rouphael, Nadine G
Saklawi, Youssef
Cantos, Valeria D
Ko, Emily R
Engemann, John J
Amin, Alpesh N
Watanabe, Miki
Billings, Joanne
Elie, Marie-Carmelle
Davey, Richard T
Burgess, Timothy H
Ferreira, Jennifer
Green, Michelle
Makowski, Mat
Cardoso, Anabela
de Bono, Stephanie
Bonnett, Tyler
Proschan, Michael
Deye, Gregory A
Dempsey, Walla
Nayak, Seema U
Dodd, Lori E
Beigel, John H
ACTT-2 Study Group Members
Kalil, Andre C
Kalil, Andre C
Patterson, Thomas F
Mehta, Aneesh K
Tomashek, Kay M
Wolfe, Cameron R
Ghazaryan, Varduhi
Marconi, Vincent C
Ruiz-Palacios, Guillermo M
Hsieh, Lanny
Kline, Susan
Tapson, Victor
Iovine, Nicole M
Jain, Mamta K
Sweeney, Daniel A
El Sahly, Hana M
Branche, Angela R
Regalado Pineda, Justino
Lye, David C
Sandkovsky, Uriel
Luetkemeyer, Anne F
Cohen, Stuart H
Finberg, Robert W
Jackson, Patrick EH
Taiwo, Babafemi
Paules, Catharine I
Arguinchona, Henry
Erdmann, Nathaniel
Ahuja, Neera
Frank, Maria
Oh, Myoung-Don
Kim, Eu-Suk
Tan, Seow Y
Mularski, Richard A
Nielsen, Henrik
Ponce, Philip O
Taylor, Barbara S
Larson, LuAnn
Rouphael, Nadine G
Saklawi, Youssef
Cantos, Valeria D
Ko, Emily R
Engemann, John J
Amin, Alpesh N
Watanabe, Miki
Billings, Joanne
Elie, Marie-Carmelle
Davey, Richard T
Burgess, Timothy H
Ferreira, Jennifer
Green, Michelle
Makowski, Mat
Cardoso, Anabela
de Bono, Stephanie
Bonnett, Tyler
Proschan, Michael
Deye, Gregory A
Dempsey, Walla
Nayak, Seema U
Dodd, Lori E
Beigel, John H
ACTT-2 Study Group Members
Source :
The New England journal of medicine; vol 384, iss 9, 795-807; 0028-4793
Publication Year :
2021

Abstract

BackgroundSevere coronavirus disease 2019 (Covid-19) is associated with dysregulated inflammation. The effects of combination treatment with baricitinib, a Janus kinase inhibitor, plus remdesivir are not known.MethodsWe conducted a double-blind, randomized, placebo-controlled trial evaluating baricitinib plus remdesivir in hospitalized adults with Covid-19. All the patients received remdesivir (≤10 days) and either baricitinib (≤14 days) or placebo (control). The primary outcome was the time to recovery. The key secondary outcome was clinical status at day 15.ResultsA total of 1033 patients underwent randomization (with 515 assigned to combination treatment and 518 to control). Patients receiving baricitinib had a median time to recovery of 7 days (95% confidence interval [CI], 6 to 8), as compared with 8 days (95% CI, 7 to 9) with control (rate ratio for recovery, 1.16; 95% CI, 1.01 to 1.32; P = 0.03), and a 30% higher odds of improvement in clinical status at day 15 (odds ratio, 1.3; 95% CI, 1.0 to 1.6). Patients receiving high-flow oxygen or noninvasive ventilation at enrollment had a time to recovery of 10 days with combination treatment and 18 days with control (rate ratio for recovery, 1.51; 95% CI, 1.10 to 2.08). The 28-day mortality was 5.1% in the combination group and 7.8% in the control group (hazard ratio for death, 0.65; 95% CI, 0.39 to 1.09). Serious adverse events were less frequent in the combination group than in the control group (16.0% vs. 21.0%; difference, -5.0 percentage points; 95% CI, -9.8 to -0.3; P = 0.03), as were new infections (5.9% vs. 11.2%; difference, -5.3 percentage points; 95% CI, -8.7 to -1.9; P = 0.003).ConclusionsBaricitinib plus remdesivir was superior to remdesivir alone in reducing recovery time and accelerating improvement in clinical status among patients with Covid-19, notably among those receiving high-flow oxygen or noninvasive ventilation. The combination was associated with fewer serious adverse events. (Funded by the

Details

Database :
OAIster
Journal :
The New England journal of medicine; vol 384, iss 9, 795-807; 0028-4793
Notes :
application/pdf, The New England journal of medicine vol 384, iss 9, 795-807 0028-4793
Publication Type :
Electronic Resource
Accession number :
edsoai.on1341878355
Document Type :
Electronic Resource