drugset / Trial / NCT05279391

Combination of Inhaled DNase, Baricitinib and Tocilizumab in Severe COVID-19

NCT05279391

Unknown 150 enrolled Democritus University of Thrace
Non-randomizedSequentialOpen-labelTreatment

Summary

In patients with COVID-19, severe hypoxemic respiratory failure (SRF) leading to invasive mechanical ventilation (IMV), raises the mortality rate substantially. Thus, the management of patients with SRF to avoid intubation and intensive care admission is a challenging and crucial issue. This study describes, as rescue/compassionate treatment, a therapeutic protocol based on the multi-mechanistic nature of severe COVID-19, using the combination of inhaled DNase, Baricitinib and Tocilizumab on top of standard of care (SOC) consisting of heparin and dexamethasone. COVID-19 patients with SRF who were treated with SOC, SOC plus Anakinra (ANA), and SOC plus Tocilizumab (TOCI) will be studied as comparators. Primary endpoint will be the reduction of the in-hospital mortality rate, whereas secondary endpoints concern intubation rate, days of hospitalization and overall survival as derived from the last follow-up visit, either in-office or remote. This is a non-randomized, open-label, study, conducted in the First Department of Internal Medicine, University Hospital of Alexandroupolis, Greece.

Timeline

Start
2020-10-25
Primary completion
2021-11-30
Completion
2023-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Anakinra Protein / enzyme biologic 100 mg Intravenous
Comparator Baricitinib Small molecule 2 mg Oral
Comparator Baricitinib Small molecule 4 mg Oral
Comparator Tocilizumab Monoclonal antibody 8 mg/kg Intravenous
Comparator dornase alfa Protein / enzyme biologic 2500 iu Inhaled
Comparator Dexamethasone Small molecule 6 mg
Comparator Dexamethasone Small molecule 8 mg
Comparator Tinzaparin Other / unclassified 175 iu/kg

Indications