drugset / Trial / NCT06383819

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

NCT06383819

Phase 3 Completed 392 enrolled NPO Petrovax
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The goal of this clinical study is to evaluate the efficacy and safety of Longidaza®, lyophilisate 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

Timeline

Start
2022-04-08
Primary completion
2023-12-31
Completion
2023-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Bovhyaluronidase azoximer Unknown 3000 iu Intramuscular