A double blind, randomised, placebo-controlled trial to evaluate the doseexposure 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. (Boehringer Interstitial Lung Disease (ILD) 1199-0337).
The main objective of the study is to evaluate dose-exposure and
safety of nintedanib in children and adolescents with fibrosing ILD.
Study details
Study-ID: NCT04093024, 2018-004530-14
Study-ID: NCT04093024, 2018-004530-14
DZL Disease Area: DPLD
DZL Disease Area: DPLD
Study Type: Interventional
Study Type: Interventional
DZL Role: DZL recruiting center
DZL Role: DZL recruiting center
Funding: Externally - industry
Funding: Externally - industry
DZL Participating Sites: BIH / Charité - Associated Partner
DZL Participating Sites: BIH / Charité - Associated Partner
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