To provide ruxolitinib through an expanded access program for the treatment of cytokine storm due to COVID-19 in the United States to patients who are eligible but not able to be hospitalized or who are hospitalized with a clinical diagnosis and/or positive test for SARD-CoV-2 infection.
Study Type
EXPANDED_ACCESS
Ruxolitinib starting dose level 5 mg orally, twice daily (BID).
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