- Trials with a EudraCT protocol (414)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
414 result(s) found for: Crohn Disease AND Crohn's Disease.
Displaying page 1 of 21.
EudraCT Number: 2013-005629-21 | Sponsor Protocol Number: Tech-infliximab2014/1 | Start Date*: 2014-08-14 | |||||||||||
Sponsor Name:First Department of Medicine, University of Szeged | |||||||||||||
Full Title: Diagnostic use of 99mTecnetium labeled infliximab in Crohn’s disease | |||||||||||||
Medical condition: Crohn’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001109-81 | Sponsor Protocol Number: MC/PR/1405/002/02 | Start Date*: 2004-10-04 | |||||||||||
Sponsor Name:Chiesi Farmaceutici SpA | |||||||||||||
Full Title: A randomised, controlled with placebo, double blind, double dummy, parallel group study on the therapeutic efficacy and safety of Beclomethasone dipropionate (BDP) in the treatment of patients with... | |||||||||||||
Medical condition: Active Crohn's ileitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006165-11 | Sponsor Protocol Number: CNTO1959CRD3004 | Start Date*: 2022-04-19 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of Guselkumab Subcutaneous Induction Therapy in Participants with Moderately t... | |||||||||||||
Medical condition: Moderately to Severely Active Crohn's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) LT (Trial now transitioned) NL (Prematurely Ended) IT (Trial now transitioned) PL (Trial now transitioned) DE (Trial now transitioned) SK (Trial now transitioned) BE (Completed) NO (Completed) DK (Prematurely Ended) HR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001466-93 | Sponsor Protocol Number: IBDVit2 | Start Date*: 2008-04-30 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Trial of adjuvant vitamin D with Infliximab in active Crohn's Disease (IBDVit2). | |||||||||||||
Medical condition: Active Crohn's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004034-15 | Sponsor Protocol Number: M14-347 | Start Date*: 2014-10-07 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Open-Label Study to Evaluate the Long Term Efficacy, Safety, and Tolerability of Repeated Administration of Adalimumab in Subjects with Crohn's Disease | |||||||||||||
Medical condition: Crohn's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) DE (Completed) ES (Completed) CZ (Completed) IT (Completed) SK (Completed) DK (Completed) AT (Completed) BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007329-38 | Sponsor Protocol Number: CRODEX01 | Start Date*: 2009-02-06 | |||||||||||
Sponsor Name:ERYDEL S.P.A. | |||||||||||||
Full Title: Multicenter, randomized, double-blind, parallel-group study of intra-erythrocyte dexamethasone versus placebo in patients with steroid-dependent Crohns disease | |||||||||||||
Medical condition: Patients with steroid-dependent Crohns Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002838-20 | Sponsor Protocol Number: NL.45391.018.13 | Start Date*: 2013-11-12 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: The effect of Vitamin D3 to prevent post-operative relapse of Crohn’s Disease: a placebo-controlled randomized trial (DETECT) | |||||||||||||
Medical condition: Crohn's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006484-36 | Sponsor Protocol Number: FARM79YXLN | Start Date*: 2009-04-16 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: MULTICENTER COMPARATIVE STUDY BETWEEN NUTRITIONAL THERAPY ALONE AND ANTI-TNF-alpha MONOCLONAL ANTIBODY IN INDUCING AND MAINTAINING REMISSION IN PEDIATRIC CROHN`S DISEASE: A RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: Moderate-to-severe active Crohn`s disease. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005688-32 | Sponsor Protocol Number: CD-FNB | Start Date*: 2009-07-02 | |||||||||||
Sponsor Name:Univeristy Hospital Na Bulovce | |||||||||||||
Full Title: Biological therapy in the prevention of Crohn`s disease recurrence after resection in ileocecal region. | |||||||||||||
Medical condition: Prevention of Crohn`s disease recurrence after surgery in ileocecal region by postoperative application of infliximab (four infusions). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001014-17 | Sponsor Protocol Number: RETIC/03/06 | Start Date*: 2007-07-26 | |||||||||||
Sponsor Name:Alfa Wassermann S.p.A. | |||||||||||||
Full Title: A Phase II, multicentre, double-blind, randomized, dose range finding placebo controlled study of Rifaximin- EIR tablet: clinical effectiveness and tolerability in the treatment of moderate, active... | |||||||||||||
Medical condition: Treatment of moderate, active Crohn’s disease: induction of remission. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) HU (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000261-51 | Sponsor Protocol Number: PHRC_IR_2013_BOMMELAER | Start Date*: 2014-11-04 | |||||||||||
Sponsor Name:CHU de Clermont-Ferrand | |||||||||||||
Full Title: POPCUR : a randomized, controlled, double bind study, comparing curcuma to placebo, associated with thiopurines, in the prevention of post-operative Crohn's disease recurrence | |||||||||||||
Medical condition: Crohn's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010727-91 | Sponsor Protocol Number: 00695 | Start Date*: 2011-03-01 | |||||||||||
Sponsor Name:LMU München, Campus Großhadern | |||||||||||||
Full Title: Colesevelam for the treatment of bile acid malabsorption in patients with Crohn’s disease (Colesevelam für die Therapie der Gallensäuren-Malabsorption bei M. Crohn-Patienten) | |||||||||||||
Medical condition: Morbus Crohn | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011621-14 | Sponsor Protocol Number: CAIN457A2202E1 | Start Date*: 2009-11-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 52-week open label extension study to evaluate the safety and tolerability of AIN457 (anti IL-17 monoclonal antibody) in patients with moderate to severe Crohn’s disease | |||||||||||||
Medical condition: Moderate to severe Crohn's disease (CDAI ≥ 220 and ≤450) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002716-26 | Sponsor Protocol Number: C87088 | Start Date*: 2008-01-22 | |||||||||||
Sponsor Name:UCB Celltech | |||||||||||||
Full Title: A phase IIIb, multinational, open-label, follow-on trial to C87085 designed to assess the long-term safety of certolizumab pegol, a pegylated Fab' fragment of a humanized anti TNF alpha monoclonal ... | |||||||||||||
Medical condition: Crohn's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FI (Prematurely Ended) HU (Completed) LV (Completed) EE (Completed) IT (Completed) CZ (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024528-12 | Sponsor Protocol Number: HGRWLBKULT1 | Start Date*: 2011-02-14 | |||||||||||
Sponsor Name:Henning Glerup | |||||||||||||
Full Title: Kontrast UltraLydsskanning af Tyndtarmen hos patienter med Crohns sygdom – et pilotstudie (KULT) | |||||||||||||
Medical condition: Morbus Crohn disease with signs of activity in the small bowel. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013348-35 | Sponsor Protocol Number: 7915 | Start Date*: 2009-08-04 | |||||||||||||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||||||||||||
Full Title: (Patho)Physiological aspects of the bile salt-FXR-FGF19-axis: potential consequences in Crohn's disease. | |||||||||||||||||||||||
Medical condition: Patients with quiescent Crohn’s colitis, defined as a Crohn’s Disease Activity Index <150 ; non-IBD patients will serve as disease controls. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002418-39 | Sponsor Protocol Number: DG 01/05 | Start Date*: 2005-10-20 | |||||||||||
Sponsor Name:SOFAR SPA | |||||||||||||
Full Title: Valutation of the efficacy of Lactobacillus casei subspeciae casei DG in prevention of Crohn s disease relapse after induction of clinical remission by antibiotics a multicentric, randomised, doub... | |||||||||||||
Medical condition: prevention of Crohn s disease relapse | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002472-15 | Sponsor Protocol Number: FE999907 CS004 | Start Date*: 2005-09-22 | |||||||||||
Sponsor Name:Ferring Laegemidler A/S | |||||||||||||
Full Title: The effect on mucosal healing with Pentasa® Sachet 4 g in mild to moderate active small bowel Crohn's disease, evaluated with video capsule endoscopy after 6 and 12 weeks treatment. A pilot study. | |||||||||||||
Medical condition: Mild to moderate active Crohn's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005237-30 | Sponsor Protocol Number: REMICADEPIB4002 | Start Date*: 2009-12-01 | |||||||||||
Sponsor Name:Janssen Biologics B.V. | |||||||||||||
Full Title: A Multicenter, Prospective, Long-term Registry of Pediatric Patients with Crohn's Disease or Ulcerative Colitis | |||||||||||||
Medical condition: Pediatric patients with a confirmed diagnosis of CD or UC . | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003759-23 | Sponsor Protocol Number: M14-327 | Start Date*: 2016-11-04 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 2, Multicenter, Open-Label Extension (OLE) Study to Observe the Long-Term Efficacy, Safety, and Tolerability of Repeated Administration of Upadacitinib (ABT-494) in Subjects with Crohn's Di... | |||||||||||||
Medical condition: Crohn's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) NL (Trial now transitioned) SK (Trial now transitioned) CZ (Completed) BE (Completed) ES (Ongoing) FR (Trial now transitioned) HU (Completed) NO (Completed) | |||||||||||||
Trial results: (No results available) |
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