- Trials with a EudraCT protocol (103)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
103 result(s) found for: colitis ulcerosa.
Displaying page 1 of 6.
EudraCT Number: 2009-010065-23 | Sponsor Protocol Number: P05553 | Start Date*: 2009-08-17 | ||||||||||||||||||||||||||
Sponsor Name:Essex Pharma GmbH | ||||||||||||||||||||||||||||
Full Title: Conventional Step-Up versus Infliximab Monotherapy in Patients with Active Moderate to Severe Ulcerative Colitis. A Randomized, Open Label, Prospective, Multicenter Study (Phase 3, Protocol No. P05... | ||||||||||||||||||||||||||||
Medical condition: Active Moderate to Severe Ulcerative Colitis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-007928-18 | Sponsor Protocol Number: Repha_1328 | Start Date*: 2008-06-04 | |||||||||||
Sponsor Name:REPHA GmbH | |||||||||||||
Full Title: Evaluation of efficacy and safety of the herbal drug Myrrhinil-Intest vs. mesalazine in maintaining clinical remission of ulcerative colitis - a 12-month, multicenter, randomized, prospective, doub... | |||||||||||||
Medical condition: ulcerative colitis patients in clinical remission | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004768-23 | Sponsor Protocol Number: SIC002 | Start Date*: 2013-06-12 | |||||||||||
Sponsor Name:STELIC INSTITUTE & CO. | |||||||||||||
Full Title: A Phase 2a Trial of STNM01 by a Single Submucosal Injection to Investigate the Mucosal Healing Efficacy in Patients with Ulcerative Colitis | |||||||||||||
Medical condition: Ulcerative Colitis with active endoscopic lesion(s), ranging in severity from moderate to severe in endoscopic score not responding sufficiently to conventional treatment | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017839-18 | Sponsor Protocol Number: PG09-PUR 0210-002 | Start Date*: 2010-05-14 | |||||||||||
Sponsor Name:PurGenesis Techonologies Inc. | |||||||||||||
Full Title: A 2-WEEK EXPLORATORY RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, DOSE-RANGING, PLACEBO-CONTROLLED SAFETY, TOLERABILITY, BIOMARKER AND EFFICACY CLINICAL STUDY OF PUR 0110 RECTAL ENEMA IN MILD-TO-MODER... | |||||||||||||
Medical condition: Active mild-to-moderate distal ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003113-34 | Sponsor Protocol Number: CLYS006X2202 | Start Date*: 2020-02-19 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A randomized, multi-center, subject and investigator blinded, placebo controlled, parallel group study to assess the efficacy, safety and tolerability of LYS006 in patients with mild to moderate ul... | ||||||||||||||||||
Medical condition: Mild to moderate ulcerative colitis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) HU (Prematurely Ended) NO (Prematurely Ended) SK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002350-36 | Sponsor Protocol Number: GA39925 | Start Date*: 2018-09-27 | |||||||||||||||||||||||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||||||||||||||||||||||
Full Title: A PHASE II, RANDOMIZED, PARALLEL-GROUP, DOUBLE-BLIND, DOUBLE-DUMMY, PLACEBO-CONTROLLED, MULTICENTER STUDY TO EVALUATE THE EFFICACY, SAFETY, AND PHARMACOKINETICS OF UTTR1147A COMPARED WITH PLACEBO A... | |||||||||||||||||||||||||||||||||
Medical condition: Ulcerative colitis (UC) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) IE (Completed) HU (Completed) NL (Completed) BG (Completed) ES (Ongoing) GR (Completed) IT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002542-38 | Sponsor Protocol Number: CAEB071A2210 | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double blind, placebo controlled, parallel group design study to explore the efficacy, safety and tolerability of AEB071 in patients with active, moderate to severe ulcerative colitis. | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002013-19 | Sponsor Protocol Number: ACT12688 | Start Date*: 2013-07-19 | |||||||||||
Sponsor Name:Sanofi aventis Recherche&Développement | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter study evaluating efficacy and safety of SAR339658 in patients with active moderate to severe Ulcerative Colitis (UC). | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) AT (Completed) IT (Prematurely Ended) DE (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001830-32 | Sponsor Protocol Number: SAT-25/UCA | Start Date*: 2013-01-15 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, double-dummy, randomised, multi-centre, comparative phase III clinical study on the efficacy and tolerability of an 8 week oral treatment with three times daily 1000 mg mesalazine ver... | |||||||||||||
Medical condition: Active ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) LV (Completed) LT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001012-30 | Sponsor Protocol Number: LTS12593 | Start Date*: 2013-09-30 | |||||||||||
Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Multicenter Single-Arm Open Label Extension Study Evaluating The Long Term Safety And Tolerability Of SAR339658 In Patients With Ulcerative Colitis (UC) | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) AT (Completed) BE (Prematurely Ended) PL (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004878-26 | Sponsor Protocol Number: IM011-127 | Start Date*: 2021-01-05 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study of the Safety, Efficacy, and Biomarker Response of BMS-986165 in Subjects with 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: DE (Completed) NL (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003409-36 | Sponsor Protocol Number: GA27927 | Start Date*: 2011-11-14 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A Phase II Open-Label Extension Study to Evaluate the Long-Term Safety of rhuMAb Beta7 in Patients 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) DE (Completed) CZ (Completed) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001686-12 | Sponsor Protocol Number: 20210210 | Start Date*: 2023-02-17 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Phase 2 Long-Term Extension (LTE) Study to Evaluate The Safety and Efficacy of Efavaleukin Alfa in Subjects with Moderately to Severely Active Ulcerative Colitis | |||||||||||||
Medical condition: Moderate to Severe Active Ulcerative Colitis (UC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) AT (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) LV (Trial now transitioned) SK (Trial now transitioned) BG (Trial now transitioned) DK (Trial now transitioned) FR (Trial now transitioned) HU (Trial now transitioned) FI (Trial now transitioned) GR (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004576-57 | Sponsor Protocol Number: BUX-4/UCA | Start Date*: 2019-04-26 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Randomised, double-blind, double-dummy, active-controlled, phase III clinical trial on the efficacy and safety of an 8-week add-on treatment with budesonide 9 mg capsules vs. budesonide 6 mg capsul... | |||||||||||||
Medical condition: Patients with active ulcerative colitis refractory to standard treatment with mesalazine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LV (Completed) HU (Completed) SK (Completed) LT (Prematurely Ended) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005635-14 | Sponsor Protocol Number: BUX-3/UCA | Start Date*: 2015-06-08 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Open-label, multi-centre, proof of concept phase IIa clinical trial on the efficacy and tolerability of an 8 week oral treatment with once daily 9 mg budesonide in patients with active ulcerative c... | |||||||||||||
Medical condition: Patients with active ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LV (Completed) HU (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
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: 2011-000897-80 | Sponsor Protocol Number: ABS4986g | Start Date*: 2011-08-16 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: PHASE II RANDOMIZED DOUBLE-BLIND PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF rhuMAb BETA7 IN PATIENTS 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) CZ (Completed) GB (Prematurely Ended) ES (Prematurely Ended) DE (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005232-30 | Sponsor Protocol Number: AMUC-2023 | Start Date*: 2021-06-21 | |||||||||||
Sponsor Name:Salix Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blinded, Placebo-Controlled, Parallel Group Study Evaluating the Efficacy and Safety of Amiselimod (MT-1303) in Subjects with Mild to Moderate Ulcerative Colitis (UC) | |||||||||||||
Medical condition: Ulcerative Colitis (UC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) EE (Completed) DE (Completed) CZ (Completed) BG (Completed) SK (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004469-41 | Sponsor Protocol Number: PN-943-03 | Start Date*: 2020-05-11 | |||||||||||
Sponsor Name:Protagonist Therapeutics, Inc | |||||||||||||
Full Title: A Phase 2 Randomized, Double-blind, Placebo-controlled, Parallel-group, Multi-center Study to Evaluate the Safety and Efficacy of Oral PN-943 in Subjects with Moderate to Severe Active Ulcerative C... | |||||||||||||
Medical condition: Ulcerative colitis (US) is a chronic relapsing inflammatory bowel disease of the large intestine characterized by bloody diarrhoea, abdominal cramps and fatigue. UC is characterized by inflammation... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) AT (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004565-15 | Sponsor Protocol Number: FE 999907 CS003 | Start Date*: 2005-04-06 | |||||||||||
Sponsor Name:Ferring BV | |||||||||||||
Full Title: Pentasa® Once Daily In Ulcerative colitis for Maintenance of remission: PODIUM An International multi-centre investigator blinded randomised controlled study of Pentasa ® Sachet comparing one gra... | |||||||||||||
Medical condition: Ulcerative collitis (UC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) DK (Completed) SE (Completed) CZ (Completed) FI (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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