- Trials with a EudraCT protocol (28)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28 result(s) found for: Gastrointestinal inflammatory conditions.
Displaying page 1 of 2.
| EudraCT Number: 2018-003998-96 | Sponsor Protocol Number: AXAGIST | Start Date*: 2019-04-03 | |||||||||||
| Sponsor Name:Centrum Onkologii – Instytut im. Marii Skłodowskiej - Curie | |||||||||||||
| Full Title: A Phase II, single arm Study of avelumab In combination with Axitinib in Patients With unresectable/metastatic Gastrointestinal Stromal Tumor after failure of standard therapy - AXAGIST | |||||||||||||
| Medical condition: GIST - unresectable/metastatic Gastrointestinal Stromal Tumor after failure of standard therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002586-34 | Sponsor Protocol Number: STEROID_MC_1 | Start Date*: 2020-11-12 | |||||||||||||||||||||||||||||||
| Sponsor Name:Department of Anesthesiology, Copenhagen University Hospital Hvidovre, Capital Region of Denmark | |||||||||||||||||||||||||||||||||
| Full Title: The effects of preoperative high-dose Dexamethasone on inflammatory response and recovery after emergency laparotomy, a randomized, double-blind, placebo-controlled clinical trial - AHA STEROID ... | |||||||||||||||||||||||||||||||||
| Medical condition: Patients undergoing emergency laparotomy due to either Intestinal obstruction or perforated abdominal viscus. | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2012-000729-28 | Sponsor Protocol Number: GA28084 | Start Date*: 2012-06-13 | |||||||||||
| Sponsor Name:Genentech, Inc. | |||||||||||||
| Full Title: MULTICENTER STUDY IN PATIENTS WITH CROHN?S DISEASE FOR CHARACTERIZATION OF MAGNETIC RESONANCE ENTEROGRAPHY ASSAYS FOR ASSESSMENT OF DISEASE ACTIVITY | |||||||||||||
| Medical condition: Investigation of magnetic resonance enterography (MRE) with/without dye for evaluation of disease status in Crohn's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003662-40 | Sponsor Protocol Number: UKER-AMGEVITA-CED-NOVO-01 | Start Date*: 2019-12-18 | |||||||||||
| Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
| Full Title: Prospective, open-label, single-arm, single-center phase IV clinical trial to evaluate efficacy and safety of the adalimumab biosimilar Amgevita in subjects with moderate to severe active chronic i... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001833-29 | Sponsor Protocol Number: 202152 | Start Date*: 2016-09-07 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A multicentre, randomised, double-blind (sponsor-unblinded), placebo-controlled study with open label extension to investigate the safety and tolerability, pharmacokinetics, pharmacodynamics, and... | |||||||||||||
| Medical condition: Active ulcerative colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) GB (Completed) PL (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001518-25 | Sponsor Protocol Number: P-Monofer-IDA-02 | Start Date*: 2014-11-21 | |||||||||||
| Sponsor Name:Pharmacosmos A/S | |||||||||||||
| Full Title: A Phase III, Randomised, Double-blind, Comparative Study of Intravenous Iron Isomaltoside 1000 (Monofer®) against Placebo in Subjects with Iron Deficiency Anaemia and who are Intolerant or Unrespon... | |||||||||||||
| Medical condition: Subjects with iron deficiency anaemia (IDA) caused by different aetiologies such as abnormal uterine bleeding, gastrointestinal diseases (e.g. inflammatory bowel disease), cancer, preoperative anae... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001991-39 | Sponsor Protocol Number: NIR-DT-301 | Start Date*: 2019-07-26 |
| Sponsor Name:SpringWorks Subsidiary 2, PBC | ||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial of Nirogacestat Versus Placebo in Adult Patients with Progressing Desmoid Tumors/Aggressive Fibromatosis (DT/AF). | ||
| Medical condition: Desmoid Tumors/Aggressive Fibromatosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) NL (Completed) DE (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-004457-76 | Sponsor Protocol Number: CNTO1275ISD3001 | Start Date*: 2021-11-09 | |||||||||||||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||||||||||||
| Full Title: A Phase 3, Multicenter, Open-label, Basket, Long-term Extension Study of Ustekinumab in Pediatric Clinical Study Participants (2 to <18 Years of Age) | |||||||||||||||||||||||
| Medical condition: Paediatric conditions in - Moderately to Severely Active Crohn's Disease - Moderately to Severely Active Ulcerative Colitis - Juvenile Psoriatic Arthritis | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) HU (Trial now transitioned) DE (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2019-002856-18 | Sponsor Protocol Number: Mannitol_03-2018 | Start Date*: 2020-06-04 | |||||||||||
| Sponsor Name:NTC s.r.l. | |||||||||||||
| Full Title: Efficacy and Safety of mAnniTol in bowel preparation: assessment of adequacy and presence of Intestinal levelS of hydrogen and methane during elective colonoscopy aFter mAnnitol or standard split 2... | |||||||||||||
| Medical condition: Subjects scheduled for elective colonoscopy to be prepared and performed according to ESGE (European Society of Gastrointestinal Endoscopy - ESGE) guidelines. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-001234-17 | Sponsor Protocol Number: A3191084 | Start Date*: 2006-06-15 | |||||||||||
| Sponsor Name:Pfizer Limited | |||||||||||||
| Full Title: Double-blind, triple dummy, parallel-group, randomized, six-month study to compare celecoxib (200 mg BID) with diclofenac SR (75 mg BID) plus omeprazole (20 mg QD) for gastrointestinal events in su... | |||||||||||||
| Medical condition: Treatment of osteoarthritis (OA) and/or rheumatoid arthritis (RA) in high GI risk patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) BE (Completed) SE (Completed) CZ (Completed) LT (Completed) DE (Suspended by CA) EE (Completed) PT (Completed) GR (Completed) IE (Completed) LV (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: 2014-001295-65 | Sponsor Protocol Number: TXC-CD-002-2011 | Start Date*: 2014-11-28 | |||||||||||
| Sponsor Name:TxCell | |||||||||||||
| Full Title: A phase IIb, multicentre, randomised, double-blinded (DB), placebo-controlled, single-dose and parallel-group study to evaluate the efficacy and the safety of Ovasave (ovalbumin-specific autologous... | |||||||||||||
| Medical condition: Moderately to severely active Crohn's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) AT (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004254-33 | Sponsor Protocol Number: IFH-2014-002 | Start Date*: 2015-02-26 | |||||||||||
| Sponsor Name:Infirst+ HEALTHCARE Ltd | |||||||||||||
| Full Title: A Three Arm Double blind, Randomised Multicentre Study to Investigate the Non-Inferiority of a Soft Gel Capsule of Ibuprofen Lipid Formulation (total daily dose 1200 mg) versus a Standard Soft Gel ... | |||||||||||||
| Medical condition: Episodic knee arthralgia/flaring knee pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000319-18 | Sponsor Protocol Number: FW-UC-001 | Start Date*: 2018-02-07 | |||||||||||||||||||||
| Sponsor Name:FIRST WAVE BIOPHARMA INCORPORATION | |||||||||||||||||||||||
| Full Title: A phase I/IIa, open-label, three-stage, study to investigate the safety, the efficacy and the pharmacokinetics of Niclosamide enemas in subjects with active Ulcerative Proctitis or Ulcerative Proct... | |||||||||||||||||||||||
| Medical condition: Active ulcerative proctitis or ulcerative procto-sigmoiditis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Completed) DE (Prematurely Ended) AT (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2022-000719-30 | Sponsor Protocol Number: GLPG0634-CL-341 | Start Date*: 2022-08-30 | |||||||||||
| Sponsor Name:Galapagos NV | |||||||||||||
| Full Title: A randomized, double-blind, controlled, multi-center study to evaluate the efficacy and safety of dose de-escalation of orally administered filgotinib in subjects with ulcerative colitis in clinica... | |||||||||||||
| Medical condition: ulcerative colitis (UC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) CZ (Prematurely Ended) FR (Completed) ES (Prematurely Ended) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006311-21 | Sponsor Protocol Number: CBAF312A2202 | Start Date*: 2009-07-28 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: A multi-centre, double-blind, placebo controlled, proof of concept study to evaluate the efficacy and tolerability of BAF312 in patients with polymyositis and dermatomyositis | ||||||||||||||||||
| Medical condition: Polymyositis and dermatomyositis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Prematurely Ended) SE (Prematurely Ended) HU (Completed) CZ (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-000087-83 | Sponsor Protocol Number: 2929 | Start Date*: 2008-12-19 | ||||||||||||||||
| Sponsor Name:University of Liverpool [...] | ||||||||||||||||||
| Full Title: EUROPAC2 trial to investigate the efficacy of ANTOX(vers) 1.2 and MGCT (magnesiocard) for the treatment of hereditary pancreatitis and idiopathic chronic pancreatitis. | ||||||||||||||||||
| Medical condition: Hereditary Pancreatitis and Idiopathic Chronic Pancreatitis | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-003596-19 | Sponsor Protocol Number: CHS1221 | Start Date*: 2020-07-29 | |||||||||||||||||||||||||||||||
| Sponsor Name:Cristcot HCA LLC | |||||||||||||||||||||||||||||||||
| Full Title: A Three-Arm, Randomized, Placebo-Controlled, Double-Blind Phase 3 Study to Evaluate the Safety and Efficacy of Once-Daily and Twice-Daily Dosing of a Novel Hydrocortisone Acetate 90 mg Suppository ... | |||||||||||||||||||||||||||||||||
| Medical condition: Ulcerative Colitis of the Rectum | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) IT (Prematurely Ended) RO (Completed) DK (Completed) BG (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-003157-27 | Sponsor Protocol Number: Sobi.PEGCET-201 | Start Date*: 2021-12-17 | |||||||||||
| Sponsor Name:SWEDISH ORPHAN BIOVITRUM AB (PUBL) | |||||||||||||
| Full Title: An Open-label, Single-arm, Multicenter Pilot Study to Evaluate the Pharmacokinetics, Pharmacodynamics and Safety of Pegcetacoplan in Patients with Transplant-associated Thrombotic Microangiopathy (... | |||||||||||||
| Medical condition: Transplant-Associated Thrombotic Microangiopathy (TA-TMA) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) FR (Trial now transitioned) GR (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-005521-73 | Sponsor Protocol Number: GLPG0974-CL-201 | Start Date*: 2013-03-20 | |||||||||||
| Sponsor Name:Galapagos NV | |||||||||||||
| Full Title: Exploratory, Phase II, Randomized, Double-blind, Placebo-controlled, Proof-of-Concept study to evaluate the safety, tolerability, efficacy, pharmacokinetics and pharmacodynamics of GLPG0974 in sub... | |||||||||||||
| Medical condition: Mild to moderate Ulcerative Colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) LV (Completed) | |||||||||||||
| Trial results: Removed from public view | |||||||||||||
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