drugset / Trial / NCT04377620

Assessment of Efficacy and Safety of Ruxolitinib in Participants With COVID-19-Associated ARDS Who Require Mechanical Ventilation (RUXCOVID-DEVENT)

NCT04377620

Phase 3 Terminated 211 enrolled Incyte Corporation
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of ruxolitinib in the treatment of participants with COVID-19-associated Acute Respiratory Distress Syndrome (ARDS) who require mechanical ventilation.

Timeline

Start
2020-05-24
Primary completion
2021-02-26
Completion
2021-02-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 5 mg Oral
Subject Ruxolitinib Small molecule 15 mg Oral

Indications