RT Journal Article SR Electronic T1 Study design of a randomised, placebo-controlled trial of nintedanib in children and adolescents with fibrosing interstitial lung disease JF ERJ Open Research JO erjor FD European Respiratory Society SP 00805-2020 DO 10.1183/23120541.00805-2020 VO 7 IS 2 A1 Robin Deterding A1 Matthias Griese A1 Gail Deutsch A1 David Warburton A1 Emily M. DeBoer A1 Steven Cunningham A1 Annick Clement A1 Nicolaus Schwerk A1 Kevin R. Flaherty A1 Kevin K. Brown A1 Florian Voss A1 Ulrike Schmid A1 Rozsa Schlenker-Herceg A1 Daniela Verri A1 Mihaela Dumistracel A1 Marilisa Schiwek A1 Susanne Stowasser A1 Kay Tetzlaff A1 Emmanuelle Clerisme-Beaty A1 Lisa R. Young YR 2021 UL http://openres.ersjournals.com/content/7/2/00805-2020.abstract AB Childhood interstitial lung disease (chILD) comprises >200 rare respiratory disorders, with no currently approved therapies and variable prognosis. Nintedanib reduces the rate of forced vital capacity (FVC) decline in adults with progressive fibrosing interstitial lung diseases (ILDs). We present the design of a multicentre, prospective, double-blind, randomised, placebo-controlled clinical trial of nintedanib in patients with fibrosing chILD (1199-0337 or InPedILD; ClinicalTrials.gov: NCT04093024).Male or female children and adolescents aged 6–17 years (≥30; including ≥20 adolescents aged 12–17 years) with clinically significant fibrosing ILD will be randomised 2:1 to receive oral nintedanib or placebo on top of standard of care for 24 weeks (double-blind), followed by variable-duration nintedanib (open-label). Nintedanib dosing will be based on body weight-dependent allometric scaling, with single-step dose reductions permitted to manage adverse events. Eligible patients will have evidence of fibrosis on high-resolution computed tomography (within 12 months of their first screening visit), FVC ≥25% predicted, and clinically significant disease (Fan score of ≥3 or evidence of clinical progression over time). Patients with underlying chronic liver disease, significant pulmonary arterial hypertension, cardiovascular disease, or increased bleeding risk are ineligible. The primary endpoints are pharmacokinetics and the proportion of patients with treatment-emergent adverse events at week 24. Secondary endpoints include change in FVC% predicted from baseline, Pediatric Quality of Life Questionnaire, oxygen saturation, and 6-min walk distance at weeks 24 and 52. Additional efficacy and safety endpoints will be collected to explore long-term effects.We describe the design of InPedILD™, a study of 24 weeks' nintedanib or placebo on top of standard of care, followed by variable duration open-label nintedanib in children with ILD (ClinicalTrials.gov: NCT04093024) #PedILD https://bit.ly/3j5GQsB https://bit.ly/3tC1a7P