- Trials with a EudraCT protocol (86)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
86 result(s) found for: Therapeutic endoscopy.
Displaying page 4 of 5.
EudraCT Number: 2017-001100-30 | Sponsor Protocol Number: 1334hew16ct | Start Date*: 2018-10-24 | |||||||||||
Sponsor Name:Fachingen Heil- und Mineralbrunnen GmbH | |||||||||||||
Full Title: Investigation of efficacy and tolerability of the healing water Staatl. Fachingen STILL in patients for symptomatic treatment of heartburn in comparison to placebo | |||||||||||||
Medical condition: Efficacy and tolerability investigations of a healing water in symptomatic treatment of heartburn | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003371-13 | Sponsor Protocol Number: IM101084 | Start Date*: 2007-07-17 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Multi-Center, Randomized, Placebo-Controlled Study to Evaluate the Clinical Efficacy and Safety of Induction and Maintenance Therapy with Abatacept in Subjects with Active Crohn’s Diseas... | |||||||||||||
Medical condition: Crohn's disease, NOS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) NL (Prematurely Ended) GB (Prematurely Ended) BE (Completed) IE (Completed) DK (Prematurely Ended) CZ (Completed) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2013-003199-11 | Sponsor Protocol Number: 2013-1 | Start Date*: 2015-09-25 |
Sponsor Name:GETAID - Groupe d'Etude Thérapeutique des Affections Inflammatoires Digestives | ||
Full Title: Changing the coUrse of cRohn's disease with an Early use of adalimumab: The CURE study. | ||
Medical condition: Crohn's disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) FR (Ongoing) | ||
Trial results: (No results available) |
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: 2017-001737-85 | Sponsor Protocol Number: 80-84800-98-81014 | Start Date*: 2018-07-17 | |||||||||||
Sponsor Name:academic medical centre | |||||||||||||
Full Title: Efficacy of AlbenDazole to inDuce mUcosal healing in Patients with Crohn's disease on anti-TNF monotherapy | |||||||||||||
Medical condition: Crohn's disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005260-41 | Sponsor Protocol Number: SA652012 | Start Date*: 2016-10-13 | |||||||||||
Sponsor Name:Academic Medical Centre | |||||||||||||
Full Title: Efficacy of optimized thiopurine therapy in ulcerative colitis. | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002702-51 | Sponsor Protocol Number: 010951201207 | Start Date*: 2012-09-24 | |||||||||||
Sponsor Name:Department of medical gastroenterology S, Odense University Hospital | |||||||||||||
Full Title: Discontinuation of infliximab therapy in patients with Crohn’s disease during sustained complete remission: A Nordic multi-center, double blinded, randomized, placebo controlled study | |||||||||||||
Medical condition: Patients with Crohn's disease with absence of disease activity during biologic therapy (infliximab) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) FI (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000091-11 | Sponsor Protocol Number: PR200-102 | Start Date*: 2021-09-21 | |||||||||||
Sponsor Name:Prometheus Biosciences, Inc. | |||||||||||||
Full Title: A Phase 2, Multi-Center, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Induction Therapy with PRA023 in Subjects with Moderately to Severely Activ... | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) PL (Trial now transitioned) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003604-19 | Sponsor Protocol Number: IM101108 | Start Date*: 2007-08-06 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase III, Multi-Center, Randomized, Placebo-Controlled Study to Evaluate the Clinical Efficacy and Safety of Induction and Maintenance Therapy with Abatacept in Subjects with Active Ulcerative C... | |||||||||||||
Medical condition: ULCERATIVE COLITIS,NOS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Completed) IE (Prematurely Ended) BE (Completed) GB (Prematurely Ended) CZ (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004209-41 | Sponsor Protocol Number: CNTO1275CRD3007 | Start Date*: 2018-06-21 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 3b, Multicenter, Randomized, Blinded, Active-Controlled Study to Compare the Efficacy and Safety of Ustekinumab to that of Adalimumab in the Treatment of Biologic Naïve Subjects with Modera... | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) FR (Completed) PL (Completed) DE (Completed) GB (GB - no longer in EU/EEA) NL (Completed) BG (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003983-32 | Sponsor Protocol Number: CB-17-01/06 | Start Date*: 2013-10-02 |
Sponsor Name:Cosmo Technologies Ltd | ||
Full Title: The safety and efficacy of Methylene Blue MMX® modified release tablets administered to subjects undergoing screening or surveillance colonoscopy. | ||
Medical condition: Polyp and adenoma detection during colonoscopy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) BE (Completed) DE (Completed) NL (Ongoing) LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004282-14 | Sponsor Protocol Number: GA29103 | Start Date*: 2014-09-29 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: PHASE III, RANDOMIZED, MULTICENTER DOUBLE-BLIND, DOUBLE-DUMMY STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ETROLIZUMAB COMPARED WITH INFLIXIMAB IN PATIENTS WITH MODERATE TO SEVERE ACTIVE ULCERATIVE... | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) CZ (Completed) AT (Completed) PT (Completed) NL (Completed) NO (Completed) ES (Completed) BE (Completed) IT (Completed) HU (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002576-14 | Sponsor Protocol Number: TZP-102-CL-G004 | Start Date*: 2012-08-23 | |||||||||||
Sponsor Name:Tranzyme, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Evaluation of the Efficacy and Safety of TZP-102 Given Orally Three Times a Day for the Treatment of Symptoms Associate... | |||||||||||||
Medical condition: The medical condition to be investigated is symptomatic gastroparesis due to diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002061-38 | Sponsor Protocol Number: S53299 | Start Date*: 2011-06-29 | ||||||||||||||||
Sponsor Name:Katholieke Universiteit Leuven | ||||||||||||||||||
Full Title: A randomised prospective trough level monitoring study with real-time therapeutic adaptations: Trough level Adapted infliXImab Treatment scheme (TAXIT). | ||||||||||||||||||
Medical condition: 2) Crohn's disease and ulcerative colitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000725-27 | Sponsor Protocol Number: 2020-000725-27 | Start Date*: 2020-05-28 | ||||||||||||||||||||||||||
Sponsor Name:Center for Surgical Science, Department of Surgery, Zealand University Hospital | ||||||||||||||||||||||||||||
Full Title: Intratumoral Influenza Vaccine for Early Colorectal Cancer | ||||||||||||||||||||||||||||
Medical condition: Patients with colorectal cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016488-12 | Sponsor Protocol Number: C13011 | Start Date*: 2011-07-12 | |||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Placebo-Controlled, Blinded, Multicenter Study of the Induction of Clinical Response and Remission by Vedolizumab in Patients With Moderate to Severe Crohn’s Disease | |||||||||||||
Medical condition: Moderate to Severe Crohn's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) SK (Completed) HU (Completed) DE (Completed) AT (Completed) BE (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002182-21 | Sponsor Protocol Number: Vedolizumab-2005 | Start Date*: 2017-11-16 | ||||||||||||||||
Sponsor Name:Takeda Development Centre Europe, Ltd. | ||||||||||||||||||
Full Title: A Phase 2b, Extension Study to Determine the Long-term Safety of Vedolizumab IV in Pediatric Subjects With Ulcerative Colitis or Crohn’s Disease. (Long-term Safety With Vedolizumab IV in Pediatric... | ||||||||||||||||||
Medical condition: Ulcerative Colitis or Crohn’s Disease | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) HU (Trial now transitioned) DE (Prematurely Ended) BE (Completed) NL (Completed) PL (Trial now transitioned) FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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: 2008-002783-33 | Sponsor Protocol Number: C13007 | Start Date*: 2009-03-02 | |||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Placebo-Controlled, Blinded, Multicenter Study of the Induction and Maintenance of Clinical Response and Remission by MLN0002 in Patients with Moderate to Severe Crohn?s Dise... | |||||||||||||
Medical condition: Moderate to Severe Crohn's Disease Enfermedad de Crohn moderada o grave | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) EE (Completed) HU (Completed) SK (Completed) AT (Completed) IE (Completed) LV (Completed) CZ (Completed) NL (Completed) IS (Completed) PT (Prematurely Ended) DK (Completed) FR (Completed) BE (Completed) MT (Completed) GB (Completed) BG (Completed) SE (Completed) IT (Completed) DE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002981-64 | Sponsor Protocol Number: CC-10004-UC-001 | Start Date*: 2015-08-13 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, PLACEBO-CONTROLLED, MULTICENTER STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) FOR TREATMENT OF SUBJECTS WITH ACTIVE ULCERATIVE COLITIS | |||||||||||||
Medical condition: Subjects with active ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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