- Trials with a EudraCT protocol (412)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
412 result(s) found for: ulcerative colitis.
Displaying page 5 of 21.
EudraCT Number: 2014-002579-27 | Sponsor Protocol Number: UC-GOL | Start Date*: 2015-03-03 | |||||||||||
Sponsor Name:Istituto Clinico Humanitas | |||||||||||||
Full Title: Pilot study on the efficacy of golimumab in the induction and maintenance of clinical and endoscopic remission in patients with steroid-dependent ulcerative colitis. | |||||||||||||
Medical condition: active steroid-dependent ulcerative colitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000656-29 | Sponsor Protocol Number: MK8259-027 | Start Date*: 2014-06-13 | |||||||||||
Sponsor Name:MSD Belgium BVBA/SPRL | |||||||||||||
Full Title: Preference for a prefilled syringe or Smartject™ device for delivering SIMPONI (golimumab) in patients suffering from moderate to severe ulcerative colitis | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003023-14 | Sponsor Protocol Number: CSUC-02/21 | Start Date*: 2021-09-02 | |||||||||||
Sponsor Name:InDex Pharmaceuticals AB | |||||||||||||
Full Title: Pharmacokinetics of Cobitolimod Enemas in Participants with active Ulcerative Colitis | |||||||||||||
Medical condition: Moderate to Severe Active Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004890-28 | Sponsor Protocol Number: WI239830 | Start Date*: 2019-10-09 | |||||||||||
Sponsor Name:DIP. MEDICINA DEI SISTEMI UNIVERSITà DEGLI STUDI DI ROMA TOR VERGATA | |||||||||||||
Full Title: (A)nalysis of immunological (VA)riables in ex vivo (T)ofacitinib-treated human biopsies from (A)ctive ulcerative colitis patients to predict clinical (R)esponse (the AVATAR study). | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2016-000516-15 | Sponsor Protocol Number: 5-ASA/12/2015 | Start Date*: 2016-05-30 | |||||||||||
Sponsor Name:CONSORZIO UNIVERSITARIO UNIFARM | |||||||||||||
Full Title: Intestinal mucosal concentrations from three mesalazine pharmaceutical formulations and correlation with efficacy in patients with mild/moderate ulcerative colitis | |||||||||||||
Medical condition: Ulcerative colites | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004812-40 | Sponsor Protocol Number: D2211C00001 | Start Date*: 2012-01-26 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A phase IIa, randomised, double-blind, placebo-controlled, parallel-arm, multicenter study to evaluate the efficacy and safety of tralokinumab (CAT-354), a recombinant human monoclonal antibody dir... | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Prematurely Ended) CZ (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004732-23 | Sponsor Protocol Number: EMET 001 | Start Date*: 2007-10-22 | |||||||||||
Sponsor Name:EMET Pharmaceuticals LLC | |||||||||||||
Full Title: A Multicenter, Randomized, Partially Blinded, Placebo Controlled, Parallel Design, Three-Arm, Bioequivalence Study With Clinical Endpoints Comparing Mesalamine Delayed Release Tablets 400mg To The ... | |||||||||||||
Medical condition: Mild to moderately active ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LV (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001653-99 | Sponsor Protocol Number: I6T-MC-AMBI | Start Date*: 2021-01-15 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3b, Randomized, Double-Blind, Parallel-Arm, Placebo- and Active- Controlled Treat-Through Study of Mirikizumab and Vedolizumab in Participants with Moderately to Severely Active Ulcerativ... | |||||||||||||
Medical condition: Moderately to Severely Active Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) LT (Prematurely Ended) DE (Prematurely Ended) FR (Completed) LV (Prematurely Ended) AT (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001644-10 | Sponsor Protocol Number: D5272C00002 | Start Date*: 2022-10-05 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase 2 Open-label, Long-term Extension Safety Study of Brazikumab in Participants with Moderately to Severely Active Ulcerative Colitis (EXPEDITION OLE) | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) AT (Prematurely Ended) IT (Prematurely Ended) PL (Prematurely Ended) FR (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000197-69 | Sponsor Protocol Number: AP IBD 02-02 | Start Date*: 2006-05-30 |
Sponsor Name:AM-Pharma B.V. | ||
Full Title: A pilot, open-label, multi-center clinical trial to investigate the safety and efficacy of Bovine-Calf Intestinal Alkaline Phosphatase in patients with moderate to severe ulcerative colitis | ||
Medical condition: Inflammatory Bowel Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005520-32 | Sponsor Protocol Number: CUC111342 | Start Date*: 2008-10-01 | |||||||||||
Sponsor Name:GlaxoSmithKline R&D Ltd | |||||||||||||
Full Title: An open label, 7-day repeat dose study to evaluate the pharmacodynamics of SB-656933-AAA in patients with Ulcerative Colitis. | |||||||||||||
Medical condition: ulcerative colitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013890-16 | Sponsor Protocol Number: P06120 | Start Date*: 2010-05-28 | |||||||||||
Sponsor Name:GEDII - Grupo de Estudo da Doença inflamatória Intestinal | |||||||||||||
Full Title: Herica - Histological and Endoscopic evaluation of Remission induced by Infliximab in moderately to severely active ulcerative Colitis Patients | |||||||||||||
Medical condition: This national, multi-centre, open-label pilot study will assess the histologic remission in patients with moderate to severe active ulcerative colitis under infliximab treatment who have had an ina... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005702-49 | Sponsor Protocol Number: 2007017 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Procter & Gamble Pharmaceuticals | |||||||||||||
Full Title: A Randomized, Double-blind, Parallel-group Study to Assess the Safety and Efficacy of Asacol® (1.2 to 4.8 g/day) Administered as 400 mg Delayed-release Tablets Given Every 12 Hours for 6 Weeks to C... | |||||||||||||
Medical condition: Mildly-to-Moderately Active Ulcerative Colitis in Children and Adolescents | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003556-33 | Sponsor Protocol Number: BBT401-UC-005 | Start Date*: 2021-04-19 | |||||||||||
Sponsor Name:Bridge Biotherapeutics, Inc. | |||||||||||||
Full Title: A Randomised, Double-blind, Placebo-controlled Study of Orally Administered BBT-401-1S in Subjects with Moderate to Severe Ulcerative Colitis, Incorporating a Response-Adaptive, Double-blind Extens... | |||||||||||||
Medical condition: Moderate to severe ulcerative colitis. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003006-31 | Sponsor Protocol Number: ASPIRE | Start Date*: 2021-02-08 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: Predictive value of colonic mucosal and synovial tissues profiles for response to JAKs inhibitor in patients affected by ulcerative colitis and concomitant peripheral arthritis | |||||||||||||
Medical condition: Ulcerative colitis and concomitant peripheral arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003420-16 | Sponsor Protocol Number: SPRINT | Start Date*: 2021-08-11 | |||||||||||
Sponsor Name:Instituto Clinico Humanitas | |||||||||||||
Full Title: SPRINT: AN OPEN-LABEL, MULTICENTER STUDY TO EVALUATE STEP-UP VS TOP-DOWN TREATMENT ALGORITHMS IN MODERATE TO SEVERE ULCERATIVE COLITIS | |||||||||||||
Medical condition: Moderate to severe ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) BE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004230-32 | Sponsor Protocol Number: CMA-0402-PR-0005 | Start Date*: 2007-12-07 | |||||||||||
Sponsor Name:Chiesi Farmaceutici SpA | |||||||||||||
Full Title: EFFICACY AND SAFETY OF BECLOMETHASONE DIPROPIONATE GASTRO-RESISTANT, PROLONGED RELEASE TABLETS (CHF 1514) COMPARED WITH ORAL PREDNISONE, IN A 8-WEEK TREATMENT PERIOD, IN PATIENTS WITH ACTIVE ULCERA... | |||||||||||||
Medical condition: Ulcerative Colitis extending proximally beyond the rectum with bleeding, verified by endoscopic examination | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) ES (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004278-88 | Sponsor Protocol Number: GA28950 | Start Date*: 2014-06-19 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: PHASE III, DOUBLE BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY OF THE EFFICACY AND SAFETY OF ETROLIZUMAB DURING INDUCTION AND MAINTENANCE IN PATIENTS WITH MODERATE TO SEVERE ACTIVE ULCERATIVE COLIT... | |||||||||||||
Medical condition: Ulcerative colitis (UC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) GR (Completed) DE (Completed) CZ (Completed) DK (Completed) BE (Completed) HU (Completed) AT (Completed) ES (Completed) NL (Completed) IT (Completed) FR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004776-12 | Sponsor Protocol Number: CB-01-02/02 | Start Date*: 2008-06-02 | |||||||||||
Sponsor Name:COSMO Technologies Ltd | |||||||||||||
Full Title: Efficacy and safety of oral budesonide-MMX™ (CB-01-02) 6 mg and 9 mg extended release tablets in patients with mild or moderate active ulcerative colitis. A multicentre, randomised, double-blind, ... | |||||||||||||
Medical condition: Mild or moderate active ulcerative colitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) LT (Completed) GB (Completed) LV (Completed) FR (Completed) EE (Completed) BE (Completed) SK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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