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A Double Blind, Randomised, Placebo-controlled Trial to Evaluate the Dose-exposure and Safety of Nintedanib Per os on Top of Standard of Care for 24 Weeks, Followed by Open Label Treatment With Nintedanib of Variable Duration, in Children and Adolescents (6 to 17 Year-old) With Clinically Significant Fibrosing Interstitial Lung Disease
Conditions
Interventions
Nintedanib
Placebo
Locations
43
United States
Children's Hospital Los Angeles
Los Angeles, California, United States
Children's Hospital Colorado
Aurora, Colorado, United States
Riley Hospital for Children at Indiana University Health
Indianapolis, Indiana, United States
Children's Mercy Hospitals and Clinics
Kansas City, Missouri, United States
Weill Cornell Medicine
New York, New York, United States
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
Start Date
December 3, 2019
Primary Completion Date
May 24, 2022
Completion Date
May 24, 2022
Last Updated
July 9, 2024
NCT04707781
NCT06122233
NCT05722340
NCT04325217
NCT05285982
NCT06385301
Lead Sponsor
Boehringer Ingelheim
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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