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Clinical Trial to Evaluate the Safety and Efficacy of ATR-002 in Adult Hospitalized Patients With COVID-19 — RESPIRE  

COVID-19 Clinical Trial

Official title:
RESPIRE - A Randomized, Double-Blind, Placebo-Controlled, Multi-Centre Clinical Trial to Evaluate the Safety and Efficacy of ATR-002 in Adult Hospitalized Patients With COVID-19

Clinical Trial Summary

The purpose of the study is to assess the safety and efficacy of ATR-002 (in addition to standard-of-care) for the treatment of COVID-19

Clinical Trial Description

After being informed about the study and potential risks, all patients giving written informed consent will be undergoing a 1-day screening to determine eligibility for study entry. At day 1, patients who meet the eligibility requirements will be randomized in a double-blind manner (participant and investigator) in a 1:1 ratio to ATR-002 (900mg day 1, 600mg days 2 - 6) or placebo (once daily) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04776044
Study type Interventional
Source Atriva Therapeutics GmbH
Contact
Status Terminated
Phase Phase 2
Start date April 12, 2021
Completion date August 9, 2022
View Details
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