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Clinical Trial Summary

To evaluate the antiviral effect of TG-1000 compared with placebo in adult patients with acute uncomplicated influenza virus infection.


Clinical Trial Description

This study is a multicenter, randomized, double-blind, dose-ranging study to evaluate the efficacy and safety of different doses of TG-1000 compared with placebo in adult patients with acute uncomplicated influenza virus infection. Approximately 200 patients will be randomly assigned to 1 of 4 treatments groups in a ratio of 1:1:1:1 to receive study treatment orally: "40 mg TG-1000", "80 mg TG-1000", "40mg+40mg TG-1000" or "placebo". ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04706468
Study type Interventional
Source TaiGen Biotechnology Co., Ltd.
Contact
Status Completed
Phase Phase 2
Start date December 15, 2020
Completion date February 15, 2022

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