- Trials with a EudraCT protocol (343)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
343 result(s) found for: Gastrointestinal Cancer AND Cancer.
Displaying page 13 of 18.
EudraCT Number: 2006-006538-16 | Sponsor Protocol Number: A6181114 | Start Date*: 2007-03-30 | |||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017, US | |||||||||||||
Full Title: AN OPEN-LABEL SUNITINIB MALATE (SU011248) CONTINUATION PROTOCOL FOR PATIENTS WHO HAVE COMPLETED A PRIOR SUNITINIB STUDY AND ARE JUDGED BY THE INVESTIGATOR TO HAVE THE POTENTIAL TO BENEFIT FROM SUNI... | |||||||||||||
Medical condition: Malignant Gastrointestinal Stromal Tumor (GIST), Metastatic Breast Cancer, Metastatic Renal Cell Cancer, Pancreatic Neuroendocrine Tumor, Hepatocellular Carcinoma, Prostate Cancer, Thyroid Cancer, ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) FR (Completed) DK (Prematurely Ended) GB (Completed) NL (Prematurely Ended) BG (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010065-23 | Sponsor Protocol Number: P05553 | Start Date*: 2009-08-17 | ||||||||||||||||||||||||||
Sponsor Name:Essex Pharma GmbH | ||||||||||||||||||||||||||||
Full Title: Conventional Step-Up versus Infliximab Monotherapy in Patients with Active Moderate to Severe Ulcerative Colitis. A Randomized, Open Label, Prospective, Multicenter Study (Phase 3, Protocol No. P05... | ||||||||||||||||||||||||||||
Medical condition: Active Moderate to Severe Ulcerative Colitis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000698-22 | Sponsor Protocol Number: MK-7339-003 | Start Date*: 2020-02-26 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: A Phase 3 Randomized, Open-label Study to Evaluate the Efficacy and Safety of Olaparib Alone or in Combination With Bevacizumab Compared to Bevacizumab with a Fluoropyrimidine in Participants with ... | |||||||||||||
Medical condition: The treatment of participants with unresectable or metastatic CRC that has not progressed following an induction course of FOLFOX + bevacizumab | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) FR (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002741-21 | Sponsor Protocol Number: AAA-Ga-TOC-EU-01 | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:Advanced Accelerator Applications SA | |||||||||||||
Full Title: Safety and tolerability of 68Ga-DOTATOC for injection in patients with proven gastro-entero-pancreatic neuroendocrine tumors (GEP-NETs). | |||||||||||||
Medical condition: Patients with proven gastro-entero-pancreatic neuroendocrine tumours (GEP-NETs) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004373-23 | Sponsor Protocol Number: ROV-BEM-2003-02 | Start Date*: 2007-08-14 | |||||||||||
Sponsor Name:LABORATORIOS FARMACEUTICOS ROVI, S.A. | |||||||||||||
Full Title: MULTICENTRIC, RANDOMISED, DOUBLE BLIND, PLACEBO CONTROLLED CLINICAL TRIAL TO EVALUATE THE EFFICACY AND THE SAFETY OF THE PROPHYLAXIS WITH BEMIPARIN 3,500 IU/day FOR 28 DAYS COMPARED TO 8 DAYS, IN V... | |||||||||||||
Medical condition: VENOUS THROMBOEMBOLIC DISEASE IN PATIENTS UNDERGOING ONCOLOGICAL ABDOMINAL OR PELVIC SURGERY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010921-38 | Sponsor Protocol Number: MDL_2009_27155 | Start Date*: 2009-09-08 | |||||||||||
Sponsor Name:UMC Utrecht | |||||||||||||
Full Title: Chemopreventive effects of 5-ASA and UDCA in Ulcerative Colitis: A Double-blind, Randomized Placebo-controlled Pilot Study | |||||||||||||
Medical condition: Ulcerative Colitis and the risk of developing colorectal cancer. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001185-32 | Sponsor Protocol Number: 38/2007/O/Sper | Start Date*: 2007-03-28 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Protocol for the experimental study about Peritonectomy (CCR) associated with Chemo-Hyperthermic intra-peritonel (CHIP) treatment for primary or secondary peritoneal neoplastic desease (Peritoneal ... | |||||||||||||
Medical condition: Peritoneal Carcinosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022991-29 | Sponsor Protocol Number: SMR/0211OBD-1033 | Start Date*: 2011-02-01 | |||||||||||
Sponsor Name:Sucampo Pharma Americas, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Placebo-controlled, Double-blinded Study of the Efficacy and Safety of Lubiprostone in Patients with Opioid-induced Bowel Dysfunction | |||||||||||||
Medical condition: Opioid-induced Bowel Dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Completed) SE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002182-21 | Sponsor Protocol Number: Vedolizumab-2005 | Start Date*: 2017-11-16 | ||||||||||||||||
Sponsor Name:Takeda Development Centre Europe, Ltd. | ||||||||||||||||||
Full Title: A Phase 2b, Extension Study to Determine the Long-term Safety of Vedolizumab IV in Pediatric Subjects With Ulcerative Colitis or Crohn’s Disease. (Long-term Safety With Vedolizumab IV in Pediatric... | ||||||||||||||||||
Medical condition: Ulcerative Colitis or Crohn’s Disease | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) HU (Trial now transitioned) DE (Prematurely Ended) BE (Completed) NL (Completed) PL (Trial now transitioned) FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003342-33 | Sponsor Protocol Number: STH16359 | Start Date*: 2012-09-28 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Optimising the use of Entonox during screening colonoscopy: an open randomised controlled trial | |||||||||||||
Medical condition: Colonoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004577-12 | Sponsor Protocol Number: BRF116613 | Start Date*: 2015-03-23 | |||||||||||
Sponsor Name:GlaxoSmithKline, S.A. | |||||||||||||
Full Title: Phase II biomarker study evaluating the upfront combination of BRAF inhibitor dabrafenib with MEK inhibitor trametinib versus the combination after eight weeks of monotherapy with dabrafenib or tra... | |||||||||||||
Medical condition: patients with metastatic and unresectable stage III or IV melanoma harbouring an activating BRAF mutation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000927-29 | Sponsor Protocol Number: NL60405.100.17 | Start Date*: 2017-07-31 |
Sponsor Name:Catharina Ziekenhuis | ||
Full Title: Repetitive electrostatic pressurised intraperitoneal aerosol chemotherapy with oxaliplatin as a palliative monotherapy for isolated unresectable colorectal peritoneal metastases: protocol of a mult... | ||
Medical condition: Isolated unresectable colorectal peritoneal metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002453-11 | Sponsor Protocol Number: CFTSp116 | Start Date*: 2018-01-19 | |||||||||||
Sponsor Name:The Christie NHS Foundation Trust | |||||||||||||
Full Title: A multi-centre, randomised, parallel group, open-label, phase II, single-stage selection trial of nanoliposomal irinotecan (nal-IRI) and 5-fluorouracil (5-FU)/folinic acid or docetaxel as second-li... | |||||||||||||
Medical condition: Poorly differentiated extra-pulmonary neuroendocrine carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004637-16 | Sponsor Protocol Number: SLAP | Start Date*: 2009-04-28 | |||||||||||
Sponsor Name:GISCAD | |||||||||||||
Full Title: Folfiri as Second-Line chemotherapy for Advanced Pancreatic cancer: a GISCAD Phase II study | |||||||||||||
Medical condition: Subjects enrolled in this study must have histologically confirmed locally advanced or metastatic pancreatic adenocarcinoma. They must have been received a first-line chemotherapy (one line only) w... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001515-23 | Sponsor Protocol Number: PROICM2019-03MES | Start Date*: 2020-01-29 |
Sponsor Name:Institut Régional du Cancer de Montpellier | ||
Full Title: Phase II multicenter randomized trial evaluating the association of PIPAC and systemic chemotherapy versus systemic chemotherapy alone as 1st-line treatment of Malignant Peritoneal Mesothelioma | ||
Medical condition: Patient with Histologically-confirmed diagnosis of peritoneal malignant mesothelioma and non eligible for cytoreductive surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000560-37 | Sponsor Protocol Number: IOV-CAR-01-2020PIPAC | Start Date*: 2020-11-30 | |||||||||||
Sponsor Name:ISTITUTO ONCOLOGICO VENETO - IRCCS | |||||||||||||
Full Title: Pressurized intraperitoneal aerosol chemotherapy in patients with peritoneal carcinomatosis. PIPAC-IOV study. Single-center, single-arm open-label phase II clinical trial | |||||||||||||
Medical condition: Peritoneal carcinomatosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004730-28 | Sponsor Protocol Number: FFCD1701 | Start Date*: 2019-09-17 | |||||||||||
Sponsor Name:fédération francophone de cancérologie digestive | |||||||||||||
Full Title: Nal-IRI/LV5-FU VERSUS PACLITAXEL AS SECOND-LINE THERAPY IN PATIENTS WITH METASTATIC OESOPHAGEAL SQUAMOUS CELL CARCINOMA | |||||||||||||
Medical condition: METASTATIC OESOPHAGEAL SQUAMOUS CELL CARCINOMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2023-000171-13 | Sponsor Protocol Number: P23 | Start Date*: 2023-08-23 | ||||||||||||||||
Sponsor Name:leiden university medical center | ||||||||||||||||||
Full Title: SGM-101 tumor-targeted fluorescence endoscopy to enable discrimination of malignant from benign tissue in rectal polyps with suspected T1 adenocarcinoma or high grade dysplasia: a feasibility study | ||||||||||||||||||
Medical condition: Early rectal cancer/ big polyps with suspected T1 rectal cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000878-11 | Sponsor Protocol Number: OMO1.01.02 | Start Date*: 2017-06-08 | |||||||||||
Sponsor Name:OCTIMET Oncology NV | |||||||||||||
Full Title: A modular, multi-arm, multi-part, first time in patient study to evaluate the safety and tolerability of OMO-1, alone and in combination with anti-cancer treatments, in patients with locally advanc... | |||||||||||||
Medical condition: Locally advanced, unresectable or metastatic solid malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) NL (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
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