drugset / Trial / NCT04363853

Tocilizumab Treatment in Patients With COVID-19

NCT04363853

Phase 2 Active not recruiting 200 enrolled National Cancer Institute of Mexico Roche Pharma AG · collab
NaSingle-groupOpen-labelTreatment

Summary

A phase II clinical trial will be carried out with the objective of studying the impact of the administration of Tocilizumab on the evolution of the acute respiratory distress syndrome (ARDS) in patients with severe or critical SARS-CoV-2 infection. Due to the high mortality of severe forms of SARS-CoV-2 and for ethical reasons, a control arm will not be included. Patients will be recruited by signing an informed consent and the baseline variables of interest will be recorded. Tocilizumab will be administered in one or two doses, depending on the case, and will be followed up for 30 days. The response to treatment, survival and evolution will be studied. Factors associated with improvement of ARDS and survival will be identified through multivariate analyzes. The results will be compared with those reported internationally.

Timeline

Start
2020-06-01
Primary completion
2026-12-01
Completion
2027-12-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tocilizumab Monoclonal antibody 8 mg/kg Intravenous

Indications