CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 733 enrolled
Drug / intervention
Proxalutamide (GT0918) +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/NCT04870606
NCT04870606Phase 3Completed

A Randomized, Double-blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Proxalutamide (GT0918) in Outpatients With Mild to Moderate COVID-19 Illness

Suzhou Kintor Pharmaceutical Inc,·interventional·Posted May 3, 2021·Updated Jan 2, 2024

In Brief

A Phase 3 clinical trial evaluating Proxalutamide (GT0918) and Placebo for Efficacy and Safety. Completed, enrolled 733 participants across 8 sites.

Detailed Summary

The purpose of this study is to assess the efficacy and safety of Proxalutamide (GT0918) as a treatment for outpatients COVID-19 subjects.

Study Details

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

Timeline

Phase 3CompletedFinished
20222023202420252026
First PostedMay 3, 2021
Enrollment StartMar 5, 2021
Primary CompletionJan 24, 2022
Study CompletionApr 6, 2022
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 5.2 years ago

Interventions

Proxalutamide (GT0918)drug

Proxalutamide (GT0918)+Standard of care determined by PI and local regulatory

Placebodrug

Placebo+Standard of care determined by PI and local regulatory