drugset / Trial / NCT04347915

The Phase 2 Study to Evaluate the Safety and Efficacy of Clevudine in Patients With Moderate COVID-19

NCT04347915

Phase 2 Completed 64 enrolled Bukwang Pharmaceutical
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this clinical trial is to assess the safety and efficacy of Clevudine 120 mg versus placebo once daily administration with standard of care therapy for 14 days (maximum up to 21 days) in patients with moderate COVID-19.

Timeline

Start
2020-05-26
Primary completion
2021-02-24
Completion
2021-02-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Clevudine Small molecule 120 mg Oral

Indications