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Arformoterol/Budesonide for COVID-19 — ABC  

Coronavirus Infection Clinical Trial

Official title:
A Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel, Phase 2 Study to Evaluate the Efficacy and Safety of UI030 in COVID-19 Patients

Clinical Trial Summary

This is a multi-center, randomized, double-blind, placebo-controlled, parallel, phase 2 study to evaluate the efficacy and safety of UI030 in COVID-19 patients

Clinical Trial Description

Patients with moderate and severe COVID-19 were randomly assigned (1:1) to receive either UI030 (Budesonide/Arformoterol dry powder inhaler, 2 inhalations b.i.d) or placebo for 2 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05055414
Study type Interventional
Source Korea United Pharm. Inc.
Contact
Status Not yet recruiting
Phase Phase 2
Start date November 1, 2021
Completion date November 1, 2022
View Details
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