- Trials with a EudraCT protocol (412)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
412 result(s) found for: 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 (Ongoing) PL (Trial now transitioned) DE (Trial now transitioned) SK (Trial now transitioned) BE (Ongoing) NO (Completed) DK (Prematurely Ended) HR (Ongoing) | |||||||||||||
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: (No results available) |
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 (Temporarily Halted) | |||||||||||||
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 (Ongoing) 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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