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Baricitinib plus Remdesivir for Hospitalized Adults with Covid-19
- 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
- et al.
Published Web Location
https://doi.org/10.1056/nejmoa2031994Abstract
Background
Severe 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.Methods
We 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.Results
A 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).Conclusions
Baricitinib 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 National Institute of Allergy and Infectious Diseases; ClinicalTrials.gov number, NCT04401579.).Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
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