- Trials with a EudraCT protocol (122)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
122 result(s) found for: Mucosal tissue.
Displaying page 1 of 7.
EudraCT Number: 2008-003696-43 | Sponsor Protocol Number: KUN 2008-4198 | Start Date*: 2008-11-25 |
Sponsor Name:KWF Kankerbestrijding | ||
Full Title: Prevention of progression of duodenal adenomas to cancer in patients with familial adenomatous polyposis | ||
Medical condition: Familial Adenomatous Polyposis Duodenal adenomas and carcinomas | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001183-37 | Sponsor Protocol Number: n.a. | Start Date*: 2008-06-02 |
Sponsor Name:Erasmus MC | ||
Full Title: PROSPECTIVE RANDOMIZED COMPARISON OF EMR VERSUS EMR FOLLOWED BY PHOTODYNAMIC THERAPY FOR THE TREATMENT OF EARLY BARRETT’S CANCER | ||
Medical condition: high grade dysplasia and early carcinoma in Barrett Esophagus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001557-31 | Sponsor Protocol Number: ALKS4230-006 | Start Date*: 2022-01-31 | |||||||||||
Sponsor Name:Alkermes, Inc. | |||||||||||||
Full Title: A Phase 2, Open-label, Multicenter, Cohort Study of Nemvaleukin Alfa (ALKS 4230) Monotherapy Administered Subcutaneously in Patients With Advanced Cutaneous Melanoma or Intravenously in Patients Wi... | |||||||||||||
Medical condition: Advanced cutaneous melanoma and Advanced mucosal melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003532-71 | Sponsor Protocol Number: MC/Ph.III-2019 | Start Date*: 2019-10-29 | |||||||||||
Sponsor Name:MukoCell GmbH | |||||||||||||
Full Title: Efficacy and safety of a tissue-engineered oral mucosa (MukoCell®) vs. native oral mucosa graft urethroplasty in male patients with urethral stricture | |||||||||||||
Medical condition: Urethral stricture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018085-35 | Sponsor Protocol Number: 4682724 | Start Date*: 2010-05-21 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Regionalhospital Silkeborg | ||||||||||||||||||||||||||||||||||||||
Full Title: Intestinal Inflammation in Ankylosing Spondylitis assessed by Fecal Calprotectin, Capsular Endoscopy and Colonoscopy and the effects of Adalimumab on mucosal healing | ||||||||||||||||||||||||||||||||||||||
Medical condition: Ankylosing spondylitis Inflammatory bowel disease | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001032-54 | Sponsor Protocol Number: 19PH192 | Start Date*: 2019-07-23 | ||||||||||||||||
Sponsor Name:CHU de Saint Etienne | ||||||||||||||||||
Full Title: Impact of anti-cytomegalovirus (valganciclovir) treatment in the management of relapsing ulcerative colitis (UC) requiring vedolizumab therapy: a randomized clinical trial comparing a strategy with... | ||||||||||||||||||
Medical condition: Patient with active ulcerative colitis who failed to anti-TNF with endoscopic active disease with an endoscopic Mayo score> 1 and 2 biopsies of the inflammatory tissue and presence of a CMV infect... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001826-23 | Sponsor Protocol Number: MMP-Clob1 | Start Date*: 2023-05-31 | ||||||||||||||||
Sponsor Name:Dipartimento di Scienze della Salute dell'Università degli Studi di Firenze | ||||||||||||||||||
Full Title: A prospective, non controlled, phase 2 pilot study to assess the safety and efficacy of a new topical formulation of clobetasol 0.05% for mucosal use in patients with mucous membrane pemphigoid | ||||||||||||||||||
Medical condition: Mucous membrane pemphigoid | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001628-23 | Sponsor Protocol Number: 2017/2558 | Start Date*: 2017-10-17 | ||||||||||||||||
Sponsor Name:Gustave Roussy | ||||||||||||||||||
Full Title: Phase II multicentric study: efficacy evaluation of neo-adjuvant treatment associated with maintenance therapy by anti-PD1 immunotherapy on disease-free-survival (DFS) in patients with resectable h... | ||||||||||||||||||
Medical condition: Resectable head and neck mucosal melanoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004666-26 | Sponsor Protocol Number: 2015/208/HP | Start Date*: 2017-07-19 | |||||||||||||||||||||
Sponsor Name:CHU-Hôpitaux de Rouen | |||||||||||||||||||||||
Full Title: Randomised double blind double dummy control trial comparing the safety and efficacy of rituximab versus oral cyclophosphamide in severe forms of mucous membrane pemphigoid | |||||||||||||||||||||||
Medical condition: severe forms of mucous membrane pemphigoid | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002833-13 | Sponsor Protocol Number: AMT-101-203 | Start Date*: 2021-02-05 | |||||||||||
Sponsor Name:Applied Molecular Transport Inc. | |||||||||||||
Full Title: A Randomized, Placebo-controlled, Double-blind, Parallel-group, Exploratory, Phase 2 Study of the Efficacy and Safety of Oral AMT-101 in Combination with Adalimumab in Subjects with Moderate to Sev... | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000048-73 | Sponsor Protocol Number: AMT-101-201 | Start Date*: 2020-09-24 | |||||||||||
Sponsor Name:Applied Molecular Transport Inc. | |||||||||||||
Full Title: A Combined Phase 2/3 12-week, Randomized, Double-blind, Placebo-controlled Study Investigating the Efficacy of AMT-101 in Subjects with Chronic Antibiotic-resistant Pouchitis | |||||||||||||
Medical condition: Pouchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) HU (Completed) DE (Completed) NL (Completed) BE (Completed) IT (Completed) IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003450-28 | Sponsor Protocol Number: CL009_282 | Start Date*: 2007-09-04 | |||||||||||
Sponsor Name:ChemoCentryx, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase II Study Testing CCX282-B in the Treatment of Celiac Disease | |||||||||||||
Medical condition: Celiac Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019996-32 | Sponsor Protocol Number: TNF-K-005 | Start Date*: 2011-01-12 | |||||||||||
Sponsor Name:Neovacs SA | |||||||||||||
Full Title: A phase II, randomized, double-blind, placebo-controlled study to evaluate the clinical efficacy, safety and immunogenicity of Neovacs’TNFα-Kinoid in adult subjects with Crohn’s Disease | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) CZ (Completed) HU (Completed) BG (Completed) NL (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2021-000271-36 | Sponsor Protocol Number: KKS288 | Start Date*: 2021-09-20 | |||||||||||
Sponsor Name:Philipps University Marburg | |||||||||||||
Full Title: Guselkumab in Patients with Oral Lichen Planus - An open label, parallel, randomized, multi- center, phase II trial | |||||||||||||
Medical condition: severe oral lichen planus (LP) with variable phenotype (erosive, ulcerating, hyperplastic/leucoplastic, and combined forms) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000133-31 | Sponsor Protocol Number: AGO/2017/001 | Start Date*: 2017-07-31 |
Sponsor Name:UZ Gent | ||
Full Title: Combined hypofractionated stereotactic body radiotherapy with immunomodulating systemic therapy for inoperable recurrent head and neck cancer: detection of the maximum tolerated dose. | ||
Medical condition: local, regional or combined locoregional recurrence of squamous cell carcinoma of the oral cavity, oropharynx, hypopharynx or larynx in previously irradiated tissue, with former irradiation with cu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002970-36 | Sponsor Protocol Number: 54508 | Start Date*: 2016-06-06 |
Sponsor Name:Maastricht University Medical Center | ||
Full Title: Human intestinal ischemia and reperfusion | ||
Medical condition: The participants enrolled in this study will all undergo major upper abdominal surgery (i.e. mostly Pylorus Preserving Pancreatico Duodenectomy or whipple procedure) mostly for pancreatic cancer, p... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005703-39 | Sponsor Protocol Number: IB2020-05 | Start Date*: 2021-07-27 | |||||||||||
Sponsor Name:Institut Bergonié | |||||||||||||
Full Title: Bintrafusp alfa and Doxorubicin Hydrochloride in Treating Patients With Advanced Sarcoma. | |||||||||||||
Medical condition: soft-tissue sarcoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003647-19 | Sponsor Protocol Number: CELIM-NRCD-001 | Start Date*: 2016-02-22 |
Sponsor Name:Celimmune LLC | ||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of AMG 714 in Adult Patients with Celiac Disease. | ||
Medical condition: Celiac disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
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