- Trials with a EudraCT protocol (317)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
317 result(s) found for: Interstitial.
Displaying page 1 of 16.
EudraCT Number: 2017-000992-10 | Sponsor Protocol Number: FHM-1-2017 | Start Date*: 2017-06-28 | |||||||||||||||||||||
Sponsor Name:Universitets klinik for nyresygdomme og Hypertension | |||||||||||||||||||||||
Full Title: Prednisolone treatment in acute interstitial nephritis | |||||||||||||||||||||||
Medical condition: Acute interstitial nephritis | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004555-39 | Sponsor Protocol Number: 3652-CL-0018 | Start Date*: 2012-05-07 | ||||||||||||||||||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | ||||||||||||||||||||||||||||
Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel group, Adaptive, combined Proof of Concept and Dose-Finding study to investigate Efficacy, Safety, Pharmacodynamics and Pharmacokin... | ||||||||||||||||||||||||||||
Medical condition: Bladder Pain Syndrome / Interstitial Cystitis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) NL (Completed) CZ (Completed) DE (Completed) LV (Completed) PT (Completed) ES (Completed) PL (Completed) DK (Completed) LT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006559-27 | Sponsor Protocol Number: OMALI2008 | Start Date*: 2009-01-27 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Exploratory study on Omalizumab in patients affected by Painful Bladder Syndrome | |||||||||||||
Medical condition: Painful bladder syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004495-30 | Sponsor Protocol Number: CYCLOIC-1 | Start Date*: 2015-12-14 | ||||||||||||||||
Sponsor Name:Oulu University Hospital | ||||||||||||||||||
Full Title: Safety of intravesical bladder instillations among patients with severe interstitial cystitis | ||||||||||||||||||
Medical condition: Interstitial cystitis and bladder pain syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002324-15 | Sponsor Protocol Number: P01092 | Start Date*: 2007-09-04 | |||||||||||
Sponsor Name:University of East Anglia | |||||||||||||
Full Title: The efficacy and safety of co-trimoxazole therapy in patients with idiopathic interstitial pneumonia | |||||||||||||
Medical condition: Idiopathic Interstitial Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005103-39 | Sponsor Protocol Number: AP01-005 | Start Date*: 2021-04-16 | |||||||||||
Sponsor Name:Avalyn Pharma, Inc. | |||||||||||||
Full Title: Access to Pirfenidone Solution for Inhalation (AP01) for Treatment of Progressive, Fibrosing Interstitial Lung Diseases, including Idiopathic Pulmonary Fibrosis | |||||||||||||
Medical condition: Interstitial Lung Diseases (ILD), including but not limited to idiopathic pulmonary fibrosis (IPF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) NL (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000861-32 | Sponsor Protocol Number: KKS-206 | Start Date*: 2015-12-01 | ||||||||||||||||||||||||||
Sponsor Name:Justus Liebig Universität Giessen | ||||||||||||||||||||||||||||
Full Title: Exploring Efficacy and Safety of oral Pirfenidone for progressive, non-IPF Lung Fibrosis (RELIEF) A randomized, double-blind, placebo-controlled, parallel group, multi-center, phase II trial | ||||||||||||||||||||||||||||
Medical condition: 1.Fibrotic NSIP., 2.Chronic Hypersensitivity Pneumonitis 3. Lung fibrosis associated with collagen / vascular diseases, 4.Asbestos-induced lung fibrosis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-003584-18 | Sponsor Protocol Number: KKS-307 | Start Date*: 2023-06-26 | ||||||||||||||||
Sponsor Name:Philipps University Marburg | ||||||||||||||||||
Full Title: Tezepelumab (Anti-TSLP-mab) in progressive pulmonary fibrosis interstitial lung disease with evidence of eosinophilia | ||||||||||||||||||
Medical condition: Progressive pulmonary fibrosis interstitial lung disease with evidence of eosinophilia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003367-23 | Sponsor Protocol Number: 672-CL-035 | Start Date*: 2006-02-13 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of YM672 in the Treatment of Painful Bladder Syndrome/Interstitial Cystitis | |||||||||||||
Medical condition: Interstitial Cystitis / Painful Bladder Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002421-37 | Sponsor Protocol Number: A4291043 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Pfizer Ltd., Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK | |||||||||||||
Full Title: A PHASE 2, 12 WEEK, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO- CONTROLLED, PARALLEL GROUP, PROOF OF CONCEPT STUDY EVALUATING THE EFFICACY AND SAFETY OF PD 0299685 FOR THE TREATMENT OF SYMPTOMS... | |||||||||||||
Medical condition: INTERSTITIAL CYSTITIS/PAINFUL BLADDER SYNDROME. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) FR (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002491-24 | Sponsor Protocol Number: BMS-IM101-563 | Start Date*: 2016-05-11 | ||||||||||||||||
Sponsor Name:Universitätsklinikum Freiburg, vertreten durch den Leitenden Ärztlichen Direktor | ||||||||||||||||||
Full Title: Safety of Abatacept in patients with interstitial lung disease and common variable immunodeficiency (CVID) and related disease | ||||||||||||||||||
Medical condition: CVID patients confirmed according to ESID/PAGID criteria or related disorders which fulfill the diagnostic criteria for CVID and interstitial lung disease or granuloma diagnosed by chest CT positiv... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004355-20 | Sponsor Protocol Number: 2013OE005B | Start Date*: 2014-03-20 | |||||||||||
Sponsor Name:Royal Brompton and Harefield NHS Foundation Trust | |||||||||||||
Full Title: Randomised, controlled crossover trial to evaluate the Effects of Ambulatory Oxygen on health status in patients with Fibrotic Lung Disease (FLD) | |||||||||||||
Medical condition: Fibrotic Lung Diseases (FLDs) are chronic and progressive conditions resulting in substantial morbidity and mortality. The cardinal symptom of all fibrotic Interstitial Lung Diseases (ILDs) is shor... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007168-40 | Sponsor Protocol Number: 68Ga-DOTA-NOC/ILD01/2008 | Start Date*: 2009-01-20 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Use of 68Ga-DOTA-NOC for the evaluation of patients with Idiopathic pulmonary fibrosis STUDY CODE: 68Ga-DOTA-NOC/ILD 01/2008 | |||||||||||||
Medical condition: patients with Idiopathic pulmonary fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002744-17 | Sponsor Protocol Number: MA39189 | Start Date*: 2017-03-29 | |||||||||||
Sponsor Name:Roche Farma S.A, que representa en España a F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: MULTICENTER, INTERNATIONAL, DOUBLEBLIND, TWO-ARM, RANDOMIZED, PLACEBO CONTROLLED PHASE II TRIAL OF PIRFENIDONE IN PATIENTS WITH UNCLASSIFIABLE PROGRESSIVE FIBROSING ILD | |||||||||||||
Medical condition: Fibrosing interstitial lung disease (ILD) of unknown origin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DK (Completed) CZ (Completed) DE (Completed) PL (Completed) PT (Completed) GR (Completed) BE (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002766-21 | Sponsor Protocol Number: 1199.33 | Start Date*: 2012-05-02 | |||||||||||
Sponsor Name:Boehringer Ingelheim Hellas | |||||||||||||
Full Title: An open-label extension trial of the long term safety of oral BIBF 1120 in patients with Idiopathic Pulmonary Fibrosis (IPF) | |||||||||||||
Medical condition: Idiopathic Pulmonary Fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) PT (Completed) BE (Completed) ES (Completed) DE (Completed) FI (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) IT (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020223-44 | Sponsor Protocol Number: FinalVersion | Start Date*: 2010-08-03 |
Sponsor Name:Medizinische Universität Wien, Univ.Klinik f.Radiodiagnostik | ||
Full Title: (18)F-FDG PET/CT in patients with idiopathic interstitial pneumonias: correlation of tracer uptake and histological findings, and texture-based recognition of usual interstitial pneumonia | ||
Medical condition: Interstitial lung disease of unknown etiology | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003633-42 | Sponsor Protocol Number: RBHIPF004 | Start Date*: 2013-10-18 | |||||||||||||||||||||||||||||||
Sponsor Name:Royal Brompton and Harefield NHS Foundation Trust | |||||||||||||||||||||||||||||||||
Full Title: A randomized, double blind controlled trial comparing rituximab against intravenous cyclophosphamide in connective tissue disease associated interstitial lung disease | |||||||||||||||||||||||||||||||||
Medical condition: A diagnosis of connective tissue disease associated interstitial lung disease, based on internationally accepted criteria, in one of the following categories: o Systemic sclerosis o Idiopathic inte... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014597-17 | Sponsor Protocol Number: A4091035 | Start Date*: 2010-05-03 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 2B, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, DOSE RANGING STUDY EVALUATING THE EFFICACY AND SAFETY OF TANEZUMAB FOR THE TREATMENT OF MODERATE TO SEVERE PAIN ASSOCIATED WITH INTERSTITIA... | |||||||||||||
Medical condition: Chronic pain including the pain of interstitial cystitis/painful bladder syndrome. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) BE (Completed) ES (Prematurely Ended) DE (Prematurely Ended) FI (Completed) SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000906-12 | Sponsor Protocol Number: AQX-1125-301 | Start Date*: 2016-09-07 | ||||||||||||||||
Sponsor Name:Aquinox Pharmaceuticals (Canada) Inc. | ||||||||||||||||||
Full Title: The LEADERSHIP 301 Trial: A 12-Week, Randomized, Multi-Center, Double-Blind, Placebo-Controlled, 3 Arm, Parallel-Group, Phase 3 Trial to Evaluate the Efficacy and Safety of 2 Doses of AQX-1125 Targ... | ||||||||||||||||||
Medical condition: Interstitial Cystitis/Bladder Pain Syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) HU (Completed) CZ (Completed) LV (Prematurely Ended) GB (Prematurely Ended) BE (Completed) ES (Prematurely Ended) NL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-007800-13 | Sponsor Protocol Number: PIPF-012 | Start Date*: 2008-06-04 | |||||||||||
Sponsor Name:InterMune, Inc. | |||||||||||||
Full Title: An Open-Label Extension Study of the Long-Term Safety of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis (IPF) Who Complete the CAPACITY Studies | |||||||||||||
Medical condition: Idiopathic Pulmonary Fibrosis (IPF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) DE (Completed) FR (Completed) BE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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