drugset / Trial / NCT04607928

Pirfenidone Compared to Placebo in Post-COVID19 Pulmonary Fibrosis COVID-19

NCT04607928

Phase 2 Unknown 148 enrolled Bellvitge Biomedical Research Institute
RandomizedParallel-groupTriple-blindPrevention

Summary

Study population: Patients with fibrotic lung sequelae after recovery from acute phase of severe COVID19 pneumonia Objectives: To evaluate the effect of pirfenidone administered for 24 weeks in patients who have pulmonary fibrotic changes after suffering severe COVID19 pneumonia, analysed by * % change in forced vital capacity (FVC) * % fibrosis in high resolution computed tomography (HRCT) of the lung

Timeline

Start
2020-08-01
Primary completion
2022-01-30
Completion
2022-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Pirfenidone Small molecule 2403 mg