- Trials with a EudraCT protocol (412)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
412 result(s) found for: Ulcerative Colitis.
Displaying page 11 of 21.
| EudraCT Number: 2011-004581-14 | Sponsor Protocol Number: A3921139 | Start Date*: 2012-06-29 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: A MULTI-CENTER, OPEN-LABEL STUDY OF CP-690,550 IN SUBJECTS WITH MODERATE TO SEVERE ULCERATIVE COLITIS | |||||||||||||
| Medical condition: Ulcerative colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DK (Completed) HU (Completed) EE (Completed) GB (Completed) LV (Completed) BE (Completed) NL (Completed) ES (Completed) AT (Completed) DE (Completed) SK (Completed) PL (Completed) IT (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004763-31 | Sponsor Protocol Number: CRO.CO.DEX | Start Date*: Information not available in EudraCT |
| Sponsor Name:EryDel S.p.A. | ||
| Full Title: Therapy with dexamethasone intra-erythrocytes in patients with Crohn disease and ulcerative colitis | ||
| Medical condition: patients with Crohn’s Disease and Ulcerative Colitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003123-57 | Sponsor Protocol Number: I6T-MC-AMAC | Start Date*: 2016-02-09 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study of LY3074828 in Subjects with Moderate to Severe Ulcerative Colitis | |||||||||||||
| Medical condition: Ulcerative colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) CZ (Completed) HU (Completed) NL (Completed) LT (Completed) DK (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2019-003334-16 | Sponsor Protocol Number: BUS-5/UCA | Start Date*: 2020-06-26 | |||||||||||
| Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
| Full Title: Randomised, double-blind, placebo-controlled, multicentre study to compare the efficacy and safety of novel 4 mg budesonide suppository in combination with oral mesalazine versus oral mesalazine mo... | |||||||||||||
| Medical condition: acute ulcerative colitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BG (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004572-21 | Sponsor Protocol Number: 1368-0010 | Start Date*: 2017-06-07 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: Proof-of-concept study of BI 655130 add-on treatment in patients with mild-to-moderately active ulcerative colitis during TNF inhibitor therapy | |||||||||||||
| Medical condition: Mild-to-moderately active ulcerative colitis on TNF inhibitor therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) NO (Prematurely Ended) DE (Completed) NL (Completed) ES (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004224-38 | Sponsor Protocol Number: CNTO1275PUC3001 | Start Date*: 2021-02-25 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 3 Study of the Efficacy, Safety and Pharmacokinetics of Ustekinumab as Open-label Intravenous Induction Treatment Followed by Randomized Double-blind Subcutaneous Ustekinumab Maintenance in... | |||||||||||||
| Medical condition: Moderately to Severely Active Ulcerative Colitis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) HU (Trial now transitioned) GB (GB - no longer in EU/EEA) PL (Trial now transitioned) Outside EU/EEA BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004230-28 | Sponsor Protocol Number: 1368-0005 | Start Date*: 2018-02-27 | |||||||||||
| Sponsor Name:Boehringer Ingelheim RCV GmbH & Co KG | |||||||||||||
| Full Title: A Phase II/III Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Safety and Efficacy of BI 655130 (SPESOLIMAB) Induction Therapy in patients with moderate-to-severely ... | |||||||||||||
| Medical condition: Moderate-to-severely active ulcerative colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) BE (Prematurely Ended) DE (Completed) GB (Completed) ES (Prematurely Ended) NL (Prematurely Ended) DK (Prematurely Ended) GR (Prematurely Ended) HU (Completed) CZ (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002063-87 | Sponsor Protocol Number: Protocol Number 291-415 | Start Date*: 2006-03-16 | |||||||||||
| Sponsor Name:PDL BioPharma, Inc | |||||||||||||
| Full Title: A Phase 2/3, Randomized, Double-blind, Placebo-controlled, Multicenter Study of Visilizumab in Subjects with Intravenous Steroid-Refractory Ulcerative Colitis | |||||||||||||
| Medical condition: Intravenous steroid-refractory ulcerative colitis (IVSR-UC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) AT (Prematurely Ended) BE (Completed) CZ (Completed) DE (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001921-15 | Sponsor Protocol Number: BUS-4/UCA | Start Date*: 2017-03-09 | |||||||||||
| Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
| Full Title: Randomised, double-blind, double-dummy, multicentre study to compare the efficacy and safety of once daily novel 4 mg budesonide suppository versus once daily 2 mg budesonide foam in patients with ... | |||||||||||||
| Medical condition: Acute Ulcerative Proctitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) LV (Completed) HU (Completed) SK (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003123-38 | Sponsor Protocol Number: RPC01-202 | Start Date*: 2012-12-11 | |||||||||||
| Sponsor Name:Celgene International II Sàrl (CIS II) | |||||||||||||
| Full Title: A PHASE 2, MULTI-CENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED PARALLEL-GROUP STUDY TO EVALUATE THE CLINICAL EFFICACY AND SAFETY OF INDUCTION THERAPY WITH RPC1063 IN PATIENTS WITH MODERATELY... | |||||||||||||
| Medical condition: Moderately to severely active Ulcerative Colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) HU (Completed) PL (Completed) SK (Completed) BG (Completed) GR (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002485-12 | Sponsor Protocol Number: RP1706 | Start Date*: 2020-07-14 | |||||||||||
| Sponsor Name:Alimentiv Inc. (formerly Robarts Clinical Trials) | |||||||||||||
| Full Title: VERDICT: In actiVE ulcerative colitis, a RanDomIzed Controlled Trial for determination of the optimal treatment target | |||||||||||||
| Medical condition: Ulcerative Colitis (UC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001298-96 | Sponsor Protocol Number: I6T-MC-AMBU | Start Date*: 2019-10-08 | |||||||||||
| Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
| Full Title: Protocol I6T-MC-AMBU A Mulitcenter, Open-Label PK Study of Mirikizumab in Pediatric Patients with Moderately to Severely Active Ulcerative Colitis | |||||||||||||
| Medical condition: Moderately to severely active ulcerative colitis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-003607-40 | Sponsor Protocol Number: GETAID 2006-1 | Start Date*: 2008-11-13 |
| Sponsor Name:Besancon University Hospital | ||
| Full Title: A CONTROLLED, RANDOMISED, DOUBLE-BLIND, MULTICENTER STUDY, COMPARING METHOTREXATE VS PLACEBO IN STEROID-REFRACTORY ULCERATIVE COLITIS | ||
| Medical condition: Steroid-dependent ulcerative colitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) BE (Completed) AT (Completed) FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002108-28 | Sponsor Protocol Number: B7581002 | Start Date*: 2018-03-30 | |||||||||||
| Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, New York 10017 | |||||||||||||
| Full Title: A PHASE 2A, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY, SAFETY, TOLERABILITY AND PHARMACOKINETICS OF PF-06687234 AS ADD-ON THERAPY TO INFLIXIMAB IN ACTIVE ULCERATIV... | |||||||||||||
| Medical condition: Ulcerative colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) ES (Prematurely Ended) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001170-15 | Sponsor Protocol Number: CECUM | Start Date*: 2017-10-19 |
| Sponsor Name:GETECCU (Grupo Español de Trabajo en Enfermedad de Crohn y Colitis ulcerosa) | ||
| Full Title: Efficacy of high-dose corticosteroid pulses added to conventional oral corticosteroid course in comparison with monotherapy oral corticosteroid course for moderate flares of ulcerative colitis: a... | ||
| Medical condition: Moderate flares of Ulcerative Colitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002231-41 | Sponsor Protocol Number: MLN0002-2003 | Start Date*: 2017-11-15 | ||||||||||||||||
| Sponsor Name:Takeda Development Centre Europe, Ltd. | ||||||||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Dose-Ranging Study to Determine the Pharmacokinetics, Safety and Tolerability of Vedolizumab IV in Pediatric Subjects With Ulcerative Colitis or Crohn’s Disease... | ||||||||||||||||||
| Medical condition: Ulcerative Colitis and Crohn’s Disease | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) DE (Completed) BE (Completed) HU (Completed) NL (Completed) PL (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-005697-46 | Sponsor Protocol Number: RCT 06 | Start Date*: 2007-02-12 | |||||||||||
| Sponsor Name:SOFAR SPA | |||||||||||||
| Full Title: Prevention of actinic proctitis by beclomethasone dipropionate. A prospectic,randomised, double blind placebo controlled pilot study | |||||||||||||
| Medical condition: actinic proctitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003649-10 | Sponsor Protocol Number: CA40192 | Start Date*: 2018-03-13 | ||||||||||||||||
| Sponsor Name:Roche Farma S.A. (Soc unipersonal) que realiza el ensayo en España y que actúa como represntante de FHoffmann-La Roche | ||||||||||||||||||
| Full Title: A PHASE I, OPEN–LABEL, RANDOMIZED, PHARMACOKINETIC, PHARMACODYNAMIC, AND SAFETY STUDY OF ETROLIZUMAB FOLLOWED BY OPEN–LABEL EXTENSION AND SAFETY MONITORING IN PEDIATRIC PATIENTS FROM 4 YEARS TO LES... | ||||||||||||||||||
| Medical condition: Moderate to severe ulcerative colitis (UC); moderate to severe Crohn’s disease (CD) | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) GB (GB - no longer in EU/EEA) PL (Prematurely Ended) DE (Completed) BE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-004280-31 | Sponsor Protocol Number: GA29102 | Start Date*: 2014-10-07 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: PHASE III, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY TO EVALUATE THE EFFICACY (MAINTENANCE OF REMISSION) AND SAFETY OF ETROLIZUMAB COMPARED WITH PLACEBO IN PATIENTS WITH MODER... | |||||||||||||
| Medical condition: Ulcerative colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DK (Completed) DE (Completed) HU (Completed) SK (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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