CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 54 enrolled
Drug / intervention
Nintedanib (Ofev®)drug
Likely dose
Nintedanib (Ofev®) 150 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05285982
NCT05285982Phase 3Completed

An Open-label Trial of the Long-term Safety and Tolerability of Nintedanib Per os, on Top of Standard of Care, Over at Least 3 Years, in Children and Adolescents With Clinically Significant Fibrosing Interstitial Lung Disease (InPedILD®-ON)

Boehringer Ingelheim·interventional·Posted Mar 18, 2022·Updated Mar 4, 2026

In Brief

A Phase 3 clinical trial evaluating Nintedanib (Ofev®) for Lung Diseases, Interstitial. Completed, enrolled 54 participants across 28 sites in 17 countries.

Detailed Summary

This study is open to children and adolescents with interstitial lung disease (ILD) that causes lung fibrosis. This is a study for people who took part in a previous study called InPedILD (study 1199-0337) and for people who are between 6 and 17 years old (in France, between 12 and 17 years old) and have fibrosing ILD. This study tests a medicine called nintedanib. Nintedanib is already used to treat different types of lung fibrosis in adults. The purpose of the study is to find out how well long-term treatment with nintedanib is tolerated in children and adolescents. All participants take nintedanib capsules twice a day. Participants coming from the previous study are in this study for at least 3 years or until nintedanib or other treatment options become available outside of this study. New participants are in the study until the overall end of study meaning for at least 1.5 years. Participants visit the study site about 15 times for a study participation of 3 years. Afterwards, they visit the study site every 3 months. The doctors collect information on any health problems of the participants.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Belgium, Brazil, Canada, Czechia, Finland, France, Germany, Greece, Italy, Mexico, Norway, Poland, Portugal, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
2023202420252026
First PostedMar 18, 2022
Enrollment StartApr 6, 2022
Primary CompletionAug 13, 2025
TodayJul 2, 2026
Enrollment to primary: 3.4 yearsPosted 4.3 years ago

Interventions

Nintedanib (Ofev®)drug

Nintedanib soft capsules administered orally with doses ranged from 50 to 150 mg bid depending on body weight