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Efficacy and Safety of Longidaza® for the Treatment of Patients With Residual Changes in the Lungs After COVID-19

Fibrosis Clinical Trial

Official title:
Multicenter, Randomized, Double-blind, Placebo-controlled Parallel-group Study to Evaluate the Efficacy and Safety of Longidaza® for the Treatment of Patients With Residual Changes in the Lungs After COVID-19

Clinical Trial Summary

The goal of this clinical study is to evaluate the efficacy and safety of Longidaza®, lyophilizate for preparation of solution for injection, at a dose of 3000 IU compared to placebo in the treatment of adult patients with residual changes in the lungs after COVID-19 infection

Clinical Trial Description

The main objective of the clinical study was to prove the superiority of the efficacy of the drug Longidaza® over placebo when used in adult patients with residual changes in the lungs after COVID-19 infection based on the dynamics of respiratory function ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06383819
Study type Interventional
Source NPO Petrovax
Contact
Status Completed
Phase Phase 3
Start date April 8, 2022
Completion date December 31, 2023
View Details
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