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Clinical Trial Summary

The main purpose of the study was to evaluate the effectiveness of XC221, tablets, at a dose of 200 mg/day compared to placebo in patients with uncomplicated influenza or other acute respiratory viral infections (ARIs). An additional purpose of the study was to evaluate the safety of XC221, tablets, at a dose of 200 mg/day compared to placebo in patients with uncomplicated influenza or other ARIs.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05544916
Study type Interventional
Source Valenta Pharm JSC
Contact
Status Completed
Phase Phase 3
Start date August 5, 2022
Completion date May 4, 2023

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