CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 156 enrolled
Drug / intervention
Remdesivir (RDV) +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/NCT04539262
NCT04539262Phase 2Completed

A Phase 1b/2a Study in Participants With Early Stage COVID-19 to Evaluate the Safety, Efficacy, and Pharmacokinetics of Remdesivir Administered by Inhalation

Gilead Sciences·interventional·Posted Sep 4, 2020·Updated Mar 3, 2022

In Brief

A Phase 2 clinical trial evaluating Remdesivir (RDV) and Placebo for COVID-19. Completed, enrolled 156 participants across 28 sites.

Detailed Summary

The primary objective of this study is to characterize the impact of inhaled remdesivir (RDV) on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral load in participants with early stage coronavirus disease 2019 (COVID-19).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCOVID-19
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
202120222023202420252026
First PostedSep 4, 2020
Enrollment StartSep 14, 2020
Primary CompletionFeb 26, 2021
Study CompletionMar 22, 2021
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 5.8 years ago

Interventions

Remdesivir (RDV)drug

Administered as an aerosolized solution

Placebodrug

Administered as an aerosolized solution