- Trials with a EudraCT protocol (179)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
179 result(s) found for: Inflammatory Bowel Disease AND Crohn's Disease.
Displaying page 1 of 9.
EudraCT Number: 2014-004399-42 | Sponsor Protocol Number: C87037 | Start Date*: 2015-03-05 | |||||||||||
Sponsor Name:UCB Japan Co., Ltd. | |||||||||||||
Full Title: A Phase II, Multi-center, Double-blind, Placebo-controlled, Parallel-group, Dose-response Study to Assess the Safety and Efficacy of CDP870/Certolizumab Pegol, Dosed Subcutaneously in Patients With... | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006165-11 | Sponsor Protocol Number: CNTO1959CRD3004 | Start Date*: 2022-04-19 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of Guselkumab Subcutaneous Induction Therapy in Participants with Moderately t... | |||||||||||||
Medical condition: Moderately to Severely Active Crohn's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) LT (Trial now transitioned) NL (Prematurely Ended) IT (Trial now transitioned) PL (Trial now transitioned) DE (Trial now transitioned) SK (Trial now transitioned) BE (Completed) NO (Completed) DK (Prematurely Ended) HR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004354-34 | Sponsor Protocol Number: C87047 | Start Date*: 2015-02-27 | |||||||||||
Sponsor Name:UCB Japan Co., Ltd. | |||||||||||||
Full Title: A 26-week, multi-center, open-label study to investigate the efficacy and safety of CDP870 in active Crohn’s disease patients, who showed clinical efficacy in a remission induction study (Study C87... | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005966-39 | Sponsor Protocol Number: TJT1123 | Start Date*: 2012-03-08 | ||||||||||||||||||||||||||
Sponsor Name:CHU-ULg | ||||||||||||||||||||||||||||
Full Title: Mesenchymal stem cell therapy for the treatment of severe or refractory inflammatory and/or autoimmune disorders. | ||||||||||||||||||||||||||||
Medical condition: Crohn's disease | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002716-26 | Sponsor Protocol Number: C87088 | Start Date*: 2008-01-22 | |||||||||||
Sponsor Name:UCB Celltech | |||||||||||||
Full Title: A phase IIIb, multinational, open-label, follow-on trial to C87085 designed to assess the long-term safety of certolizumab pegol, a pegylated Fab' fragment of a humanized anti TNF alpha monoclonal ... | |||||||||||||
Medical condition: Crohn's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FI (Prematurely Ended) HU (Completed) LV (Completed) EE (Completed) IT (Completed) CZ (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
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: 2012-002432-93 | Sponsor Protocol Number: NN8828-4004 | Start Date*: 2013-01-18 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, parallel-group trial to assess clinical efficacy and safety of NNC0114-0006 in subjects with active Crohn’s disease | |||||||||||||
Medical condition: Crohns disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) BG (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002389-33 | Sponsor Protocol Number: CNTO1959CRD3007 | Start Date*: 2023-04-07 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study Evaluating the Safety and Efficacy of Guselkumab for the Treatment of Participants with Crohn’s Disease After Surgical Resection | |||||||||||||
Medical condition: Crohn’s Disease After Surgical Resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) BE (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: 2006-005526-23 | Sponsor Protocol Number: NSP/0002/07 | Start Date*: 2009-01-29 | |||||||||||
Sponsor Name:Provexis Plc | |||||||||||||
Full Title: Randomised controlled trial of soluble plantain fibre for maintenance of health during periods of remission in Crohn's disease v2 | |||||||||||||
Medical condition: Crohn's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002882-41 | Sponsor Protocol Number: AIBDSG_002 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Medical University of Vienna (MUW) | |||||||||||||
Full Title: Sono-Response-Study A Pilot Study on the use of contrast enhanced ultrasound in Crohn’s disease | |||||||||||||
Medical condition: Inflammatory bowel disease (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: 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: 2005-005414-20 | Sponsor Protocol Number: 14/05 | Start Date*: 2006-03-06 | |||||||||||
Sponsor Name:ISTITUTO PER L INFANZIA BURLO GAROFOLO | |||||||||||||
Full Title: Randomized controlled double-blind Vs. placebo multicentre study on the safety and effectiveness of thalidomide in the treatment of refractory Crohn s disease and ulcerative colitis. | |||||||||||||
Medical condition: Inflammatory Bowel Disease Crohn Disease, Ulcerative Colitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 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: 2014-004400-30 | Sponsor Protocol Number: C87048 | Start Date*: 2015-02-27 | |||||||||||
Sponsor Name:UCB Japan Co., Ltd. | |||||||||||||
Full Title: A multi-center, open-label study to investigate the efficacy and safety of CDP870 in active Crohn’s Disease patients, who showed no clinical efficacy in a remission induction study (Study C87037) b... | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004098-26 | Sponsor Protocol Number: CD-IA-MEDI2070-1147/D5170C00001 | Start Date*: 2013-04-17 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase 2a Study to Evaluate the Efficacy and Safety of MEDI2070 in Subjects with Moderate to Severe Crohn’s Disease Who Have Failed or Are Intolerant to Anti-tumor Necrosis Factor-alpha Therapy ... | |||||||||||||
Medical condition: Crohn's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (Completed) IT (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000786-24 | Sponsor Protocol Number: NET-2013-02355002 | Start Date*: 2017-03-07 | |||||||||||
Sponsor Name:IRCCS Burlo Garofolo | |||||||||||||
Full Title: Thalidomide, a novel immunological treatment to modify the natural history of paediatric Crohn's disease: a new proposal from a well-established paediatric research network | |||||||||||||
Medical condition: Crohn's Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003855-76 | Sponsor Protocol Number: GA29145 | Start Date*: 2015-08-12 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: AN OPEN-LABEL EXTENSION AND SAFETY MONITORING STUDY OF PATIENTS WITH MODERATELY TO SEVERELY ACTIVE CROHN’S DISEASE PREVIOUSLY ENROLLED IN THE ETROLIZUMAB PHASE III PROTOCOL GA29144 | |||||||||||||
Medical condition: Crohn`s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) EE (Prematurely Ended) LT (Prematurely Ended) LV (Prematurely Ended) HU (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) SK (Prematurely Ended) CZ (Prematurely Ended) BE (Prematurely Ended) AT (Completed) FR (Ongoing) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022215-19 | Sponsor Protocol Number: GHIGF1/2011 | Start Date*: 2011-07-21 | |||||||||||
Sponsor Name:Greater Glasgow & Clyde NHS | |||||||||||||
Full Title: A Pharmacokinetic Study Of The Combined Use Of Recombinant Human GH And IGF-1 In Children With Inflammatory Bowel (Crohn’s) Disease | |||||||||||||
Medical condition: Impaired growth in Paediatric Crohn's disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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