CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 649 enrolled
Drug / intervention
Remdesivir +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04409262
NCT04409262Phase 3Completed

A Phase III, Randomized, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Remdesivir Plus Tocilizumab Compared With Remdesivir Plus Placebo in Hospitalized Patients With Severe COVID-19 Pneumonia

Hoffmann-La Roche·interventional·Posted Jun 1, 2020·Updated Feb 14, 2022

In Brief

A Phase 3 clinical trial evaluating Remdesivir, Tocilizumab, and 1 other intervention for COVID-19 Pneumonia. Completed, enrolled 649 participants across 54 sites in 4 countries.

Detailed Summary

This study will evaluate the efficacy and safety of combination therapy with remdesivir plus tocilizumab compared with remdesivir plus placebo in hospitalized patients with COVID-19 pneumonia.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBrazil, Russia, Spain, United States
CollaboratorsGilead Sciences

Timeline

Phase 3CompletedFinished
202120222023202420252026
First PostedJun 1, 2020
Enrollment StartJun 16, 2020
Primary CompletionFeb 1, 2021
Study CompletionMar 8, 2021
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 6.1 years ago

Interventions

Remdesivirdrug

Participants will receive intravenous (IV) RDV

Tocilizumabdrug

Participants will receive IV TCZ

Placebodrug

Participants will receive IV placebo matched to TCZ