drugset / Trial / NCT04393051

Baricitinib Compared to Standard Therapy in Patients With COVID-19

NCT04393051

Phase 2 Unknown 126 enrolled Azienda Ospedaliero, Universitaria Pisana
RandomizedParallel-groupOpen-labelTreatment

Summary

There is urgent need of an effective therapy for Covid-19. To date, the best treatment of SARS-CoV-2 infection is unknown. Baricitinib has been identified as potential treatment for 2019-nCoV acute respiratory disease, because of its immunomodulating and hypothesized antiviral activity. This is a multicenter randomized clinical trial that aims to evaluate the efficacy and safety of baricitinib in patients with SARS-CoV2 pneumonia. Patients will be randomized to receive or not baricitinib as adjunctive therapy. All patients will continue to receive the ongoing standard therapy: chloroquine/idrossichloroquine and low-molecular weight heparin (LMWH) eventually associated with ritonavir/lopinavir or darunavir/ritonavir will be allowed for all included patients. The primary endpoint measure is the efficacy of baricitinib in reducing the number of patients requiring invasive ventilation after 7 and 14 days of treatment. Secondary endpoints will be mortality rates and toxicity of baricitinib.

Timeline

Start
2020-05-20
Primary completion
2020-06-30
Completion
2020-07-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Baricitinib Small molecule 2 mg
Subject Baricitinib Small molecule 4 mg