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. 2021 Jul 28;12:709856. doi: 10.3389/fphar.2021.709856

TABLE 5.

Summary of clinical efficacy of baricitinib. Stebbing et al., 2020a, No controls, 4 patients; Bronte et al., 2020, with hydroxychloroquine, 8 mg/day baricitinib for 2 days, followed by 4 mg/day for 7 days, consecutive patients admitted with COVID; Titanji et al., 2020, no controls, 2–4 mg baricitinib 5–7 days with hydroxy-chloroquine, 15 moderate-critical patients; Cantini et al., 2020, moderate patients with lopinavir/ritonavir, 88% of those on baricitinib recovered after 14 days (control 14%); Stebbing et al., 2021 propensity matched patients, with antiviral medications including lopinavir/ritonavir; Kalil et al., 2021: Patients requiring high flow oxygen or non-invasive ventilation (ordinal groups 5 and 6), mortality at day 28, with remdesivir, median time to recovery 10 days (control 18 days). Marconi et al., 2021: 38% reduction in mortality at day 28, with standard of care. IMV: invasive mechanical ventilation.

Mortality/IMV n (%) Patient numbers
Observational studies Control Baricitinib Control Baricitinib
Stebbing et al. (2020b) 0 4
Bronte et al., 2020 25 1 20 20
Titanji et al. (2020) 4 15
Cantini et al., 2020 7 0 78 78
Propensity matched trials
Stebbing et al. (2021) 13 5 37 37
Stebbing et al. (2021) 16 9 46 46
Randomised trial
Kalil et al. (2021) 25 12 356 341
Marconi et al. (2021) 100 62 761 764