- Trials with a EudraCT protocol (413)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
413 result(s) found for: Crohn's disease.
Displaying page 7 of 21.
| 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: 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: 2005-003337-40 | Sponsor Protocol Number: final version 2.0 | Start Date*: 2006-02-13 |
| Sponsor Name:European Group for Blood and Marrow Transplantation (EMBT) | ||
| Full Title: Autologous Stem Cell Transplantation for Crohn's Disease ('ASTIC'-Trial: Autologous Stem Cell Transplantation International Crohn's Disease Trial) | ||
| Medical condition: Patients with Crohn's disease who have not responded to immunosupressant medication | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) IT (Ongoing) BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-000854-44 | Sponsor Protocol Number: 170CDT01 | Start Date*: 2011-05-02 | |||||||||||
| Sponsor Name:Toray Industries Inc | |||||||||||||
| Full Title: A Two Part, Multi Centre, Randomized, Placebo Controlled, Double Blind Study of TRK 170 for the Treatment of Crohn's Disease | |||||||||||||
| Medical condition: Crohn's disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) BE (Completed) NO (Completed) HU (Completed) NL (Completed) PL (Completed) CZ (Completed) BG (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-018431-18 | Sponsor Protocol Number: REMICADECRD3001 | Start Date*: 2010-08-23 | |||||||||||
| Sponsor Name:Janssen Biologics B.V. | |||||||||||||
| Full Title: Prospective, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Comparing REMICADE® (infliximab) and Placebo in the Prevention of Recurrence in Crohn’s Disease Patients Undergoing Surg... | |||||||||||||
| Medical condition: Crohn’s disease (CD) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) GB (Completed) FR (Completed) BE (Completed) NL (Completed) IT (Completed) HU (Completed) CZ (Completed) | |||||||||||||
| 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: 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: 2016-002939-15 | Sponsor Protocol Number: V56502 | Start Date*: 2017-01-24 | |||||||||||
| Sponsor Name:VHsquared Ltd | |||||||||||||
| Full Title: A Phase 2 study to investigate the efficacy, safety, and tolerability of six weeks treatment with V565 in subjects with active Crohn’s disease. | |||||||||||||
| Medical condition: Active Crohn's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) AT (Completed) HU (Completed) SK (Completed) NL (Completed) NO (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004108-31 | Sponsor Protocol Number: RHB-104-03 | Start Date*: 2015-08-27 | |||||||||||
| Sponsor Name:RedHill Biopharma Ltd. | |||||||||||||
| Full Title: A Phase III Randomized, Double Blind, Placebo-controlled, Multicenter, Parallel Group Study to Assess the Efficacy and Safety of Fixed-dose Combination RHB-104 in Subjects with Moderately Active Cr... | |||||||||||||
| Medical condition: Moderately Active Crohn's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001295-65 | Sponsor Protocol Number: TXC-CD-002-2011 | Start Date*: 2014-11-28 | |||||||||||
| Sponsor Name:TxCell | |||||||||||||
| Full Title: A phase IIb, multicentre, randomised, double-blinded (DB), placebo-controlled, single-dose and parallel-group study to evaluate the efficacy and the safety of Ovasave (ovalbumin-specific autologous... | |||||||||||||
| Medical condition: Moderately to severely active Crohn's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) AT (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002001-65 | Sponsor Protocol Number: RG_17-258 | Start Date*: 2018-12-13 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: A Phase Ib/IIb, Randomised, Double Blind, Placebo-Controlled Trial to Investigate the Safety, Tolerability and Clinical Activity of Humanised Antibody GSK1070806 in the Treatment of Patients with M... | |||||||||||||
| Medical condition: Crohn's disease | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002556-77 | Sponsor Protocol Number: MT-1303-E13 | Start Date*: 2014-11-27 | |||||||||||
| Sponsor Name:Mitsubishi Tanabe Pharma Corporation (MTPC) | |||||||||||||
| Full Title: A Phase II, Multicentre, Randomised, Double-Blind, Parallel Group, Placebo Controlled Study to Evaluate Safety, Tolerability and Clinical Efficacy of MT 1303 in Subjects with Moderate to Severe Act... | |||||||||||||
| Medical condition: Subjects with moderate to severe crohn's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) HU (Completed) SK (Completed) NL (Completed) IT (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002981-19 | Sponsor Protocol Number: IM129-008 | Start Date*: 2012-02-14 | ||||||||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
| Full Title: A Phase IIa, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Clinical Efficacy and Safety of Induction and Maintenance Therapy with BMS-936557 in Subjects with Active Crohn's Dis... | ||||||||||||||||||
| Medical condition: CROHN’S DISEASE | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) HU (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-001892-30 | Sponsor Protocol Number: GLPG1205-CL-201 | Start Date*: 2014-12-08 | |||||||||||
| Sponsor Name:Galapagos NV | |||||||||||||
| Full Title: Phase II, Randomized, Double-Blind, Placebo-Controlled, Proof-of-Concept Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of GLPG1205 in Patients With Moderate Crohn’s Dis... | |||||||||||||
| Medical condition: Crohn’s Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002545-30 | Sponsor Protocol Number: IRAS220495 | Start Date*: 2017-11-06 | |||||||||||
| Sponsor Name:Barts Health NHS Trust | |||||||||||||
| Full Title: Autologous Stem cell Transplantation In refractory Crohn's disease - Low Intensity Therapy Evaluation | |||||||||||||
| Medical condition: Refractory Crohn's Disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001956-22 | Sponsor Protocol Number: CNTO1275CRD1001 | Start Date*: 2017-01-25 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: A Randomized Double-blind Pharmacokinetic study of Ustekinumab in Pediatric Subjects with Moderately to Severely Active Crohn's Disease | |||||||||||||
| Medical condition: Moderately to severely active Crohn's disease | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) PL (Completed) FR (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004784-58 | Sponsor Protocol Number: MRI-0143 | Start Date*: 2007-06-22 | |||||||||||
| Sponsor Name:University of Leuven | |||||||||||||
| Full Title: Effect of infliximab on inflammatory and fibrous lesions in patients with intestinal Crohn’s disease | |||||||||||||
| Medical condition: Crohn's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) FR (Completed) GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000481-58 | Sponsor Protocol Number: MLN0002SC-3031 | Start Date*: 2016-01-22 | |||||||||||
| Sponsor Name:Takeda Development Centre Europe, Ltd. | |||||||||||||
| Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Vedolizumab Subcutaneous as Maintenance Therapy in Subjects With Moderately to Severely Active Cr... | |||||||||||||
| Medical condition: Crohn’s Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) CZ (Completed) NL (Completed) BG (Completed) GB (Completed) DE (Completed) BE (Completed) SE (Completed) DK (Completed) LT (Completed) HU (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001693-18 | Sponsor Protocol Number: GED-0301-CD-005 | Start Date*: 2016-01-29 | |||||||||||
| Sponsor Name:CELGENE CORPORATION | |||||||||||||
| Full Title: A Phase 2, Open-Label Study to Explore the Pharmacodynamic and Clinical Effects of Mongersen (GED-0301) in Subjects with Active Crohn's Disease | |||||||||||||
| Medical condition: Active Crohn's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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