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Clinical Trial Summary

Clinical trial on safety and efficacy of KIN001 in non-hospitalized patients with COVID-19.


Clinical Trial Description

This is a prospective, double-blind, randomized and placebo-controlled phase II trial to evaluate the safety and efficacy of KIN001 in non-hospitalized patients suffering from COVID-19. Randomization to one of two treatment arms (KIN001 versus Placebo) is at a ratio of 1:1. Patients will receive treatment for 14 days and followed for another 14 days. The primary outcome is patient reported COVID-19 symptoms, using the FDA questionnaire developed for assessing COVID-19-related symptoms in outpatients. The trial will be conducted in Switzerland and Germany. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05659459
Study type Interventional
Source Kinarus AG
Contact
Status Suspended
Phase Phase 2
Start date August 25, 2022
Completion date October 31, 2025

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