drugset / Trial / NCT05222425

Treatment of Non-severe Covid-19 Outpatients With Xagrotin, Phase 3

NCT05222425 ↗

Phase 3 Unknown 3000 enrolled Biomad AS
RandomizedParallel-groupOpen-labelTreatment

Summary

This is an interventional, multi-center, randomized study. Adults with confirmed covid-19 disease not more than 10 days before enrollment date will be recruited (n=1000). Patients in same condition who get treated with standard of care will be randomly assigned to the control group (n=1000), and patients in same condition who get treated with standard of care will be randomly assigned to the placebo group (n=1000). The investigators analyze the effect of Xagrotin, and also investigate impact of different characteristics for instance gender, age, duration of disease, smoking habits and concomitant diseases on the outcome.

Timeline

Start
2022-06-01
Primary completion
2022-10-15
Completion
2022-12-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Xagrotin Traditional medicine (herbal / TCM) 2 g —

Indications