Safety and Effectiveness Study of Tocilizumab in Patients With Severe COVID-19
NCT04924829 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300
Last updated 2021-06-14
Summary
Retrospective observational cohort study to evaluate the safety and effectiveness of tocilizumab in the treatment of severe COVID-19 pneumonia
Conditions
- Severe COVID 19 Pneumonia
- Tocilizumab
Interventions
- DRUG
-
Tocilizumab received as a single intravenous infusion over the period of 60 minutes. Dose of 8 mg/kg, maximum dose of 800 mg.
Sponsors & Collaborators
-
Hospital Italiano de Buenos Aires
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-06-01
- Primary Completion
- 2021-07-01
- Completion
- 2021-08-01
Countries
- Argentina
Study Locations
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