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Clinical Trial Summary

The efficacy and safety of K-237 0.3-0.4 mg/kg orally administered once daily for 3 days will be evaluated in patients with mild COVID-19 using a randomized, double-blind, parallel-group comparative method with placebo as a control. Efficacy will be assessed using a stratified log-rank test to determine the superiority of the drug over placebo in terms of time to improvement in clinical symptoms from the start of study drug administration to 168 hours.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05056883
Study type Interventional
Source Kowa Company, Ltd.
Contact Yuji Yoshikawa
Phone 81-3-3279-7454
Email [email protected]
Status Not yet recruiting
Phase Phase 3
Start date October 22, 2021
Completion date March 31, 2022

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