NCT04317092

Tocilizumab in COVID-19 Pneumonia (TOCIVID-19)

Multicenter Study on the Efficacy and Tolerability of Tocilizumab in the Treatment of Patients With COVID-19 Pneumonia

• Status: Unknown
• Phase: Phase 2
• Study type: Interventional
• Enrollment: 402 (actual)
• Sponsor: National Cancer Institute, Naples · Academic / Other
• Sex: All
• Age: —
• Healthy volunteers: Not accepted

Summary

This study project includes a single-arm phase 2 study and a parallel cohort study, enrolling patients with COVID-19 pneumonia.

Detailed description

Phase 2 study: this is a multicenter, single-arm, open-label, phase 2 study. All the patients enrolled are treated with tocilizumab. Two-week (14 days) and one-month (30 days) lethality rates are the co-primary endpoints. The parallel cohort includes patients who are treated with tocilizumab and cannot enter the phase 2 study because: 1. emergency conditions or infrastructural or operational limits prevented registration before the administration of the experimental drug or 2. they had been intubated more than 24 hours before registration or 3. the phase 2 study has been closed due to reached sample size. This means that, after closure of the phase 2 enrolment, patients who might be eligible for the phase 2 study will be included in the observational cohort study. The same information planned for the phase 2 cohort is required also for the parallel cohort study whose sample size is not defined a priori, and that will close at the end of the overall project. All the patients enrolled are treated with tocilizumab. In both study groups (phase 2 and parallel cohort), participants receive one dose of Tocilizumab 8 mg/kg (up to a maximum of 800mg per dose). A second administration (same dose) can be given after 12 hours if respiratory function has not recovered, at discretion of the Investigator.

Conditions

• COVID-19 Pneumonia

Interventions

Type	Name	Description
DRUG	Tocilizumab Injection	Tocilizumab 8 mg/kg (up to a maximum of 800mg per dose). A second administration (same dose) can be given after 12 hours if respiratory function has not recovered, at discretion of the Investigator.

Timeline

• Start date: 2020-03-19
• Primary completion: 2023-12-19
• Completion: 2023-12-19
• First posted: 2020-03-20
• Last updated: 2023-03-24

Locations

27 sites across 1 country: Italy