A Follow-up Study Investigating Long Term Treatment With Nintedanib in Patients With Progressive Fibrosing Interstitial Lung Disease (PF-ILD)
Lung Diseases, Interstitial
About this trial
This is an interventional treatment trial for Lung Diseases, Interstitial
Eligibility Criteria
Inclusion Criteria:
- Male or female patients who completed the INBUILD® trial as planned and who did not prematurely discontinue blinded treatment.
- Signed and dated written informed consent in accordance with ICH-GCP and local legislation prior to admission to the trial.
- Women of childbearing potential (WOCBP)1 must continue to use highly effective methods of birth control per ICH M3 (R2) that result in a low failure rate of less than 1% per year when used consistently and correctly, as well as one barrier method, for 28 days prior to and 3 months after nintedanib administration. A list of contraception methods meeting these criteria is provided in the patient information
Exclusion Criteria:
- Any disease that may put the patient at risk when participating in this trial. Reconsider carefully all exclusion criteria of the INBUILD® trial. However, patients may qualify for participation even though exclusion criteria may have been met during the course of participation in INBUILD®, if the investigator's benefit-risk assessment remains favourable.
- Patients who must or wish to continue the intake of restricted medications or any drug considered likely to interfere with the safe conduct of the trial
- Patient not compliant in parent trial (INBUILD®), with trial medication or trial visits, according to investigator's judgement.
- Previous enrolment in this trial. Further exclusion criteria apply.
Sites / Locations
- University of Alabama at Birmingham
- University of California Los Angeles
- University of California Davis
- National Jewish Health
- Yale University School of Medicine
- Pulmonary and Sleep of Tampa Bay
- University of Florida College of Medicine
- Emory University
- University of Chicago
- Loyola University Medical Center
- University of Kansas Medical Center
- Johns Hopkins Hospital
- Pulmonary and Critical Care Associates of Baltimore
- Brigham and Women's Hospital
- Beth Israel Deaconess Medical Center
- Henry Ford Health System
- Mayo Clinic, Rochester
- The Lung Research Center, LLC
- Creighton University
- Dartmouth-Hitchcock Medical Center
- Icahn School of Medicine at Mount Sinai
- Columbia University Medical Center-New York Presbyterian Hospital
- NewYork-Presbyterian/Weill Cornell Medical Center
- Duke University Medical Center
- The Oregon Clinic
- Penn State Milton S. Hershey Medical Center
- University of Pennsylvania
- Baylor University Medical Center
- University of Texas Southwestern Medical Center
- Diagnostics Research Group
- Medical Arts and Research Center (MARC)
- University of Utah Health Sciences Center
- Inova Fairfax Medical Campus
- Centro Dr. Lazaro Langer S.R.L
- Centro de Investigaciones Metabólicas (CINME)
- CEMER-Centro Medico De Enfermedades Respiratorias
- INSARES
- Instituto Médico de la Fundación Estudios Clínicos
- ULB Hopital Erasme
- UZ Leuven
- Centre Hospitalier Universitaire de Liège
- Yvoir - UNIV UCL de Mont-Godinne
- Winnipeg Clinic
- St. Joseph's Healthcare Hamilton
- Toronto General Hospital
- CHUS Fleurimont
- Hospital Clínico Reg. de Concepción "Dr. G. Grant Benavente"
- Instituto Nacional del Tórax
- Centro de Investigación del Maule
- Peking Union Medical College Hospital
- Nanjing Drum Tower Hospital
- The First Hospital of China Medical University
- HOP Avicenne
- HOP Louis Pradel
- HOP Côte de Nacre
- CHRU Lille
- HOP Nord
- HOP Arnaud de Villeneuve
- HOP Pasteur
- HOP Bichat
- HOP Maison Blanche
- HOP Pontchaillou
- HOP Civil
- HOP Bretonneau
- Universitätsklinikum Bonn AöR
- Fachkrankenhaus Coswig GmbH
- Klinik Donaustauf
- Ruhrlandklinik, Westdeutsches Lungenzentrum am Universitätsklinikum Essen gGmbH
- Medizinische Hochschule Hannover
- Thoraxklinik-Heidelberg gGmbH am Universitätsklinikum Heidelberg
- Petrus-Krankenhaus
- A.O.U. Policlinico Vittorio Emanuele
- Ospedale "G.B. Morgagni - L. Pierantoni" ausl forli
- Azienda Ospedaliera Policlinico di Modena
- A.O. San Gerardo di Monza
- Poli Univ A. Gemelli
- A.O.U. Senese Policlinico Santa Maria alle Scotte
- Tosei General Hospital
- Kurume University Hospital
- Sapporo Medical University Hospital
- National Hospital Organization Himeji Medical Center
- Kobe City Medical Center General Hospital
- Ibarakihigashi National Hospial
- Kanagawa Cardiovascular and Respiratory Center
- Saiseikai Kumamoto Hospital
- Tohoku University Hospital
- National Hospital Organization Kinki-Chuo Chest Medical Center
- Osaka Medical College Hospital
- Hamamatsu University Hospital
- Tokushima University Hospital
- Tokyo Medical and Dental University Hospital
- Toranomon Hospital
- JR Tokyo General Hospital
- Center Hospital of the National Center for Global Health and Medicine
- The Catholic University of Korea, Bucheon St.Mary's Hospital
- Seoul National University Bundang Hospital
- Asan Medical Center
- University Clinical Center, Gdansk
- Leszek Giec Upper-Silesian Med.Cent.Silesian Med.Univ.
- Norbert Barlicki University Clinical Hospital No.1, Lodz
- Nat.Instit.of Tuberculosis&LungDiseases,Outpat.Clin,warszawa
- Clinical Hospital No. 1, n.a. Prof. Szyszko from Silesian MA
- Res.Inst.-Compl.Iss.Cardi.Dis.
- Central Scientific Research Insitute of Tuberculosis
- Moscow 1st State Med.Univ.n.a.I.M.Sechenov
- 1stPavlov St.Med.Univ.St.-Petersburg Res.Inst.
- Emergency Clinical Hospital n. a. N. V. Solovyev, Yaroslavl
- Hospital Santa Creu i Sant Pau
- Hospital de Galdakao
- Hospital de Bellvitge
- Hospital La Princesa
- Hospital Central de Asturias
- Hospital Son Espases
- Hospital de Canarias
- Hospital Virgen del Rocío
- Royal Infirmary of Edinburgh
- St James's University Hospital
- Royal Brompton Hospital
- Wythenshawe Hospital
- University Hospital Llandough
- Royal Stoke University Hospital
Arms of the Study
Arm 1
Experimental
Nintedanib
Patients taking 150 milligram (mg) bid blinded trial medication (active drug or placebo) at the end of INBUILD® started treatment with nintedanib 150 mg bid in this extension trial. Patients taking 100 mg bid blinded trial medication (active drug or placebo) at the end of INBUILD® started treatment with nintedanib in this extension trial either at 100 mg bid or at an increased dose of 150 mg bid at the discretion of the investigator orally as soft gelatine capsule, twice daily (bid), together with a glass of water (~250 mL), in a dose interval of 12 hours. With an optional dose reduction to 100 mg bid temporarily or permanently to manage adverse events (AEs). The treatment had a duration of 96 weeks or until nintedanib was made available to the patients outside of the clinical trial. Treatment was stopped if any reason for withdrawal was met.