- Trials with a EudraCT protocol (113)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
113 result(s) found for: Ulcerative Colitis AND Crohn's Disease.
Displaying page 1 of 6.
EudraCT Number: 2020-004461-40 | Sponsor Protocol Number: IM011-077 | Start Date*: 2021-08-04 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: An Open-label, Multi-center Extension Study to Evaluate the Long-term Safety and Efficacy of BMS-986165 in Participants with Moderate to Severe Crohn’s Disease or Moderate to Severe Ulcerative Colitis | ||||||||||||||||||
Medical condition: moderate to severe Crohn’s Disease (CD), moderate to severe Ulcerative Colitis (UC) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) IT (Prematurely Ended) ES (Ongoing) PT (Prematurely Ended) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001467-10 | Sponsor Protocol Number: IBDVit3 | Start Date*: 2008-04-30 | ||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||
Full Title: Trial of Adjuvant Vitamin D with Standard Maintenance Therapy in Preventing Relapse of Inflammatory Bowel Disease | ||||||||||||||||||
Medical condition: Ulcerative colitis - in remission Crohn's Disease - in remission | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003141-10 | Sponsor Protocol Number: AGO/2014/004 | Start Date*: 2014-09-29 | ||||||||||||||||
Sponsor Name:Ghent University Hospital | ||||||||||||||||||
Full Title: Invloed van UDCA op fecale galzoutensamenstelling van IBD patiënten: piloot studie. | ||||||||||||||||||
Medical condition: Crohn's disease or colitis ulcerosa | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002651-15 | Sponsor Protocol Number: 000001 | Start Date*: 2014-03-03 | ||||||||||||||||
Sponsor Name:Zon MW | ||||||||||||||||||
Full Title: Adjusting infliximab dose in IBD patients in remission, based on infliximab trough levels: the study on Infliximab Levels in IBD patients Steering Treatment, the ILIST pilot | ||||||||||||||||||
Medical condition: Crohns disease Ulcerative colitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023797-39 | Sponsor Protocol Number: 2 | Start Date*: 2011-08-12 | ||||||||||||||||
Sponsor Name:Barts Health NHS Trust | ||||||||||||||||||
Full Title: TREATMENT OF IRON DEFICIENCY ANAEMIA IN ADOLESCENTS WITH INFLAMMATORY BOWEL DISEASE USING FERROUS SULPHATE OR COSMOFER: TOLERANCE AND EFFECTS ON HAEMOGLOBIN, DISEASE ACTIVITY, MOOD, QUALITY OF LIFE... | ||||||||||||||||||
Medical condition: Inflammatory bowel disease | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008285-12 | Sponsor Protocol Number: 1655/08 | Start Date*: 2009-10-14 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: PROSPECTIVE STUDY IBDISC: Regeneration and Immunity in patients affected by IBD undergoing immunomodulatory treatment and adjuvant role of G-CSF and/or plasmapheresis (Inflammatory Bowel Disease... | ||||||||||||||||||
Medical condition: Inflammatory bowel disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013680-19 | Sponsor Protocol Number: 541/09 | Start Date*: 2009-12-18 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Phase II, Open, Monocenter Study to investigate the efficacy of Propionyl-L-carnitine (ST 261) Colon Release Tablets in Patients Affected by Inflammatory Bowel Disease (IBD) under Oral Stable Trea... | ||||||||||||||||||
Medical condition: IBD | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004997-32 | Sponsor Protocol Number: GA40209 | Start Date*: 2018-12-10 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Roche Farma, S.A por delegación de Genentech, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A PHASE II OPEN LABEL EXTENSION STUDY TO EVALUATE THE LONG TERM SAFETY AND TOLERABILITY OF UTTR1147A IN PATIENTS WITH MODERATE TO SEVERE ULCERATIVE COLITIS OR CROHN'S DISEASE | ||||||||||||||||||||||||||||||||||||||
Medical condition: Ulcerative Colitis (UC) or Crohn's Disease (CD) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Completed) GB (GB - no longer in EU/EEA) NL (Prematurely Ended) IE (Prematurely Ended) DE (Completed) HU (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-006692-37 | Sponsor Protocol Number: VitDIBD1 | Start Date*: 2008-04-10 | ||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||
Full Title: The Immunomodulatory Role of Vitamin D in Inflammatory Bowel Disease (IBDVit): IBDVit1 - Trial of Adjuvant Vitamin D with Corticosteroids in Active Crohn’s Disease; IBDVit2 - Trial of Adjuvant Vita... | ||||||||||||||||||
Medical condition: IBDVit1 - Active Crohn's Disease IBDVit2 - Active Crohn's Disease IBDVit3 - Crohn's Disease in remission / Ulcerative Colitis in remission | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001332-29 | Sponsor Protocol Number: IFX2.0 | Start Date*: 2013-12-02 | ||||||||||||||||
Sponsor Name:Universitätsklinik für Innere Medizin III, Klinische Abteilung für Gastroenterologie und Hepatologie | ||||||||||||||||||
Full Title: Pharmacokinetics of Infliximab | ||||||||||||||||||
Medical condition: Inflammatory bowel disease (Ulcerative Colitis, Crohn's disease) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001278-13 | Sponsor Protocol Number: PROSIBD | Start Date*: 2016-06-08 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Taina Sipponen | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Immunologic, genetic and microbiomic predictors of the treatment response for TNFalpha-blocking drugs – prospective follow-up cohort of patients with Crohn’s disease or ulcerative colitis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Ulcerative colitis and Crohn's disease | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FI (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006084-22 | Sponsor Protocol Number: 4242 | Start Date*: 2012-10-04 | ||||||||||||||||
Sponsor Name:Royal Liverpool University Hospital | ||||||||||||||||||
Full Title: Utilising drug levels and anti-drug antibodies to predict response to treatment in patients with Inflammatory Bowel Disease | ||||||||||||||||||
Medical condition: Inflammatory bowel disease | ||||||||||||||||||
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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: 2011-002061-38 | Sponsor Protocol Number: S53299 | Start Date*: 2011-06-29 | ||||||||||||||||
Sponsor Name:Katholieke Universiteit Leuven | ||||||||||||||||||
Full Title: A randomised prospective trough level monitoring study with real-time therapeutic adaptations: Trough level Adapted infliXImab Treatment scheme (TAXIT). | ||||||||||||||||||
Medical condition: 2) Crohn's disease and ulcerative colitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004457-76 | Sponsor Protocol Number: CNTO1275ISD3001 | Start Date*: 2021-11-09 | |||||||||||||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Open-label, Basket, Long-term Extension Study of Ustekinumab in Pediatric Clinical Study Participants (2 to <18 Years of Age) | |||||||||||||||||||||||
Medical condition: Paediatric conditions in - Moderately to Severely Active Crohn's Disease - Moderately to Severely Active Ulcerative Colitis - Juvenile Psoriatic Arthritis | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) HU (Trial now transitioned) DE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002182-21 | Sponsor Protocol Number: Vedolizumab-2005 | Start Date*: 2017-11-16 | ||||||||||||||||
Sponsor Name:Takeda Development Centre Europe, Ltd. | ||||||||||||||||||
Full Title: A Phase 2b, Extension Study to Determine the Long-term Safety of Vedolizumab IV in Pediatric Subjects With Ulcerative Colitis or Crohn’s Disease. (Long-term Safety With Vedolizumab IV in Pediatric... | ||||||||||||||||||
Medical condition: Ulcerative Colitis or Crohn’s Disease | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) HU (Trial now transitioned) DE (Prematurely Ended) BE (Completed) NL (Completed) PL (Trial now transitioned) FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002784-14 | Sponsor Protocol Number: C13008 | Start Date*: 2009-04-28 | ||||||||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 3, Open-label Study to Determine the Long-Term Safety and Efficacy of Vedolizumab (MLN0002) in Patients with Ulcerative Colitis and Crohn’s Disease | ||||||||||||||||||
Medical condition: Ulcerative Colitis and Crohn’s Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: EE (Completed) HU (Completed) AT (Completed) SK (Completed) IE (Completed) LV (Completed) CZ (Completed) NL (Completed) IS (Completed) PT (Prematurely Ended) FR (Completed) BE (Completed) ES (Completed) MT (Completed) BG (Completed) SE (Completed) IT (Completed) DE (Completed) GR (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000678-40 | Sponsor Protocol Number: Vedolizumab-4013 | Start Date*: 2016-08-19 | ||||||||||||||||
Sponsor Name:Takeda Development Centre Europe Limited | ||||||||||||||||||
Full Title: Entyvio (Vedolizumab IV) Extended Access Program in Ulcerative Colitis and Crohn’s Disease | ||||||||||||||||||
Medical condition: Ulcerative Colitis and Crohn’s Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LV (Completed) CZ (Completed) HU (Completed) EE (Completed) BG (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001954-14 | Sponsor Protocol Number: 1 | Start Date*: 2015-09-14 | ||||||||||||||||
Sponsor Name:Santeon | ||||||||||||||||||
Full Title: SIMILAR Trial: Santeon InflixMab biosimILAr Research A randomized, controlled, double blind, phase 4 noninferiority trial to assess efficacy of Infliximab-biosimilar (Inflectra) compared to Inflix... | ||||||||||||||||||
Medical condition: ulcerative colitis and Crohn’s disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002925-47 | Sponsor Protocol Number: GIS-2018-BioIBD | Start Date*: 2018-12-28 | ||||||||||||||||
Sponsor Name:Fundación de Investigación Biomédica del Hospital Universitario de La Princesa | ||||||||||||||||||
Full Title: Identification of predictive biomarkers for response to biologic therapies in inflammatory bowel disease by proteomic and mass cytometry approaches | ||||||||||||||||||
Medical condition: Inflammatory bowel disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003169-19 | Sponsor Protocol Number: CYC-201 | Start Date*: 2009-11-09 | |||||||||||
Sponsor Name:Sigmoid Pharma Ltd | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study of a Controlled Release Minicapusle Formulation of Ciclosporin (CyCol™) in the Treatment of Ulcerative Colitis | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
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