- Trials with a EudraCT protocol (506)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (28)
506 result(s) found for: Inflammatory Bowel Disease.
Displaying page 14 of 26.
| EudraCT Number: 2021-003702-42 | Sponsor Protocol Number: B7981058 | Start Date*: 2022-05-17 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: AN INTERVENTIONAL PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, PARALLEL GROUP STUDY OF THE EFFICACY AND SAFETY OF RITLECITINIB (PF-06651600) IN ADULT PARTICIPANTS WITH MODERATELY TO SEVER... | |||||||||||||
| Medical condition: Moderate to Severe Ulcerative Colitis (UC) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-002100-26 | Sponsor Protocol Number: FE 999907 CS05 | Start Date*: 2009-01-28 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: PENTASA in active Crohn’s Disease: A 10-week, double-blind, multi-centre trial comparing PENTASA Sachet 6 g/day (mesalazine, mesalamine) with placebo | |||||||||||||
| Medical condition: Active mild to moderate crohn's disease. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) SE (Prematurely Ended) DK (Prematurely Ended) GB (Prematurely Ended) FR (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020448-37 | Sponsor Protocol Number: ENC-0303-CL-203 | Start Date*: 2011-12-21 | |||||||||||
| Sponsor Name:Enceladus Pharmaceuticals | |||||||||||||
| Full Title: Randomized placebo-controlled multicenter exploratory Phase IIA study to assess the safety and efficacy of PEG-liposomal prednisolone sodium phosphate (Nanocort) in subjects with active ulcerative ... | |||||||||||||
| Medical condition: Active Ulcerative Colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003257-20 | Sponsor Protocol Number: 10MI28 | Start Date*: 2014-05-02 |
| Sponsor Name:GREAT ORMOND STREET HOSPITAL FOR CHILDREN NHS FOUNDATION TRUST | ||
| Full Title: Evaluation of Treosulfan pharmacokinetics (PK) in children undergoing allogeneic haematopoietic stem cell transplantation (HSCT) | ||
| Medical condition: Any paediatric disease with an indication to an allogeneic stem cell transplantation (inclusing leukaemia, primary immunodeficiencies, metabolic disorders and autoimmune or genetic inflammatory bow... | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-000659-11 | Sponsor Protocol Number: GLPG3970-CL-210 | Start Date*: 2020-09-10 | |||||||||||
| Sponsor Name:Galapagos NV | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, multicenter study to evaluate the safety, tolerability, efficacy, and pharmacokinetics of GLPG3970, administered orally for 6 weeks in adult subjects... | |||||||||||||
| Medical condition: Ulcerative Colitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000854-44 | Sponsor Protocol Number: 170CDT01 | Start Date*: 2011-05-02 | |||||||||||
| Sponsor Name:Toray Industries Inc | |||||||||||||
| Full Title: A Two Part, Multi Centre, Randomized, Placebo Controlled, Double Blind Study of TRK 170 for the Treatment of Crohn's Disease | |||||||||||||
| Medical condition: Crohn's disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) BE (Completed) NO (Completed) HU (Completed) NL (Completed) PL (Completed) CZ (Completed) BG (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001117-42 | Sponsor Protocol Number: DORI-NOS-2001 | Start Date*: 2007-10-18 | ||||||||||||||||
| Sponsor Name:Janssen Cilag International NV | ||||||||||||||||||
| Full Title: A Randomized, Open-Label, Multicenter Study to Assess the Safety and Tolerability of Doripenem Compared With Imipenem in the Treatment of Subjects With Complicated Intra-Abdominal Infections or Ven... | ||||||||||||||||||
| Medical condition: ventilator-associated pneumonia complicated intra-abdominal infections | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) DE (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: 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: 2004-004333-34 | Sponsor Protocol Number: EORTC 55041 | Start Date*: 2005-09-20 | |||||||||||
| Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
| Full Title: A randomized, multicentre, phase III study of Erlotinib versus observation in patients with no evidence of disease progression after first line, platinum-based chemotherapy for high-risk Stage I an... | |||||||||||||
| Medical condition: Histologically confirmed high-risk FIGO stage I (grade 3, or aneuploid grade 1 or 2, or clear cell), or Stages II-IV ovarian epithelial, primary peritoneal, and fallopian tube cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) ES (Completed) IT (Completed) AT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004098-26 | Sponsor Protocol Number: CD-IA-MEDI2070-1147/D5170C00001 | Start Date*: 2013-04-17 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase 2a Study to Evaluate the Efficacy and Safety of MEDI2070 in Subjects with Moderate to Severe Crohn’s Disease Who Have Failed or Are Intolerant to Anti-tumor Necrosis Factor-alpha Therapy ... | |||||||||||||
| Medical condition: Crohn's Disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) HU (Completed) IT (Completed) ES (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002422-23 | Sponsor Protocol Number: twostepala | Start Date*: 2019-01-08 | |||||||||||
| Sponsor Name:Akershus University Hospital | |||||||||||||
| Full Title: Extracorporeal photopheresis of patients with Crohns disease using 5- aminolevulinic acid. | |||||||||||||
| Medical condition: Crohns disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002231-41 | Sponsor Protocol Number: MLN0002-2003 | Start Date*: 2017-11-15 | ||||||||||||||||
| Sponsor Name:Takeda Development Centre Europe, Ltd. | ||||||||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Dose-Ranging Study to Determine the Pharmacokinetics, Safety and Tolerability of Vedolizumab IV in Pediatric Subjects With Ulcerative Colitis or Crohn’s Disease... | ||||||||||||||||||
| Medical condition: Ulcerative Colitis and Crohn’s Disease | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) DE (Completed) BE (Completed) HU (Completed) NL (Completed) PL (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2005-003471-20 | Sponsor Protocol Number: ST261DM01004 | Start Date*: 2005-12-07 | |||||||||||
| Sponsor Name:SIGMA-TAU | |||||||||||||
| Full Title: Phase II, Parallel-group, Placebo Controlled, Double-blind, Randomized, Multicenter Study to investigate the efficacy of Two Dosages of Propionyl-L-carnitine (ST 261) Colon Release Tablets in Patie... | |||||||||||||
| Medical condition: ULCERATIVE COLITIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003913-28 | Sponsor Protocol Number: CB-01-02/04 | Start Date*: 2009-05-25 | |||||||||||
| Sponsor Name:COSMO TECHNOLOGIES LTD | |||||||||||||
| Full Title: Randomised, double-blind,multicentre,12 months extension study to evaluate the safety and the efficacy of daily Budesonide MMX 6mg vs placebo in the maintenance of remission in subjects with ulcera... | |||||||||||||
| Medical condition: Mild to moderate ulcerative colitis. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023798-20 | Sponsor Protocol Number: HLPDIG-2010-01 | Start Date*: 2012-11-29 | |||||||||||
| Sponsor Name:Fundacion para la Investigacion Biomedica Hospital Universitario La Paz | |||||||||||||
| Full Title: A PHASE I/IIA CLINICAL TRIAL TO EVALUATE SAFETY AND EFFICACY OF ADIPOSE TISSUE-DERIVED MESENCHYMAL STEM CELLS (ASC) ON INDUCTION TO REMISSION IN ULCERATIVE COLITIS | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001198-10 | Sponsor Protocol Number: MLN0002/CCT-101 | Start Date*: 2019-05-28 |
| Sponsor Name:Takeda | ||
| Full Title: A Phase 3, Multicenter, Randomized, Double-blinded, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Intravenous MLN0002 (300 mg) Infusion in Induc... | ||
| Medical condition: The purpose of the trial is to examine the efficacy, safety, and pharmacokinetics of intravenous Vedolizumab (300 mg) infusion in induction and maintenance therapy in Japanese patients with moderat... | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000784-41 | Sponsor Protocol Number: 2014010113 | Start Date*: 2015-04-15 | |||||||||||
| Sponsor Name:Department of Medicine and Endocrinology | |||||||||||||
| Full Title: Amino acids in ileal pouch-anal anastomosis for ulcerative colitis: a randomized, double-blind placebo-controlled trial | |||||||||||||
| Medical condition: Ileal pouch-anal anastomosis for ulcerative colitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006780-70 | Sponsor Protocol Number: none | Start Date*: 2008-03-06 | |||||||||||
| Sponsor Name:Tampereen yliopistollinen sairaala | |||||||||||||
| Full Title: METYYLIPREDNISOLONIN IMEYTYMINEN VAIKEAA KOLIITTIA SAIRASTAVILLA Suonensisäistä ja suun kautta tapahtuvaa annostelua vertaileva lääkeainepitoisuusmäärityksiin perustuva tutkimus | |||||||||||||
| Medical condition: Colitis ulcerosan pahenemisvaihe | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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 | ||||||||||||||||||
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