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Clinical Trial Summary

The primary objective of this observational study is to investigate the correlation between changes from baseline at 52 weeks in forced vital capacity (FVC) and changes from baseline at 52 weeks in dyspnea score points or cough score points as measured with the pulmonary fibrosis questionnaire (L-PF) questionnaire over 52 weeks of nintedanib treatment in patients suffering from chronic fibrosing interstitial lung disease (ILD) with a progressive phenotype (excluding idiopathic pulmonary fibrosis (IPF)).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04702893
Study type Observational
Source Boehringer Ingelheim
Contact
Status Active, not recruiting
Phase
Start date May 28, 2021
Completion date March 31, 2024

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