CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 4,891 enrolled
Drug / intervention
Remdesivir +1 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/NCT04292899
NCT04292899Phase 3Completed

A Phase 3 Randomized Study to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants With Severe COVID-19

Gilead Sciences·interventional·Posted Mar 3, 2020·Updated Dec 31, 2020

In Brief

A Phase 3 clinical trial evaluating Remdesivir and Standard of Care for COVID-19. Completed, enrolled 4,891 participants across 183 sites in 15 countries.

Detailed Summary

The primary objective of this study is to evaluate the efficacy of 2 remdesivir (RDV) regimens with respect to clinical status assessed by a 7-point ordinal scale on Day 14.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCOVID-19
CountriesChina, France, Germany, Hong Kong, Italy, Japan, Netherlands, Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
2020202120222023202420252026
First PostedMar 3, 2020
Enrollment StartMar 6, 2020
Primary CompletionApr 9, 2020
Study CompletionJun 30, 2020
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 6.3 years ago

Interventions

Remdesivirdrug

Administered as an intravenous infusion

Standard of Caredrug

Standard of Care Treatment for COVID-19 Infection