- Trials with a EudraCT protocol (917)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
917 result(s) found for: Colorectal Cancer.
Displaying page 5 of 46.
| EudraCT Number: 2013-002308-15 | Sponsor Protocol Number: PR001 | Start Date*: 2013-11-11 | |||||||||||
| Sponsor Name:Guys & St. Thomas' NHS Foundation Trust | |||||||||||||
| Full Title: A phase I/II dose finding study evaluating the safety and tolerability of CAPecitabine and AflIbercept in patients with unresectable metasTAtic colorectaL cancer deemed unsuitable for doublet/ trip... | |||||||||||||
| Medical condition: Colorectal Cancer | |||||||||||||
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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: 2022-001534-11 | Sponsor Protocol Number: GIT-PRo-2022-02 | Start Date*: 2022-10-11 | ||||||||||||||||
| Sponsor Name:Grupo Gallego de Investigación en Tumores Digestivos (GITuD) | ||||||||||||||||||
| Full Title: Prophylaxis of venous thromboembolic disease with LMWH (TINzaparin) in patients with metastatic colorectal cancer who start the first line of treatment. | ||||||||||||||||||
| Medical condition: Metastatic colorectal cancer (mCRC), stage IV that initiates the first-line systemic treatment in the metastatic setting | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-001016-30 | Sponsor Protocol Number: NODAGA-RGD-2 | Start Date*: 2018-12-11 |
| Sponsor Name:Department of Nuclear Medicine, Medical University Innsbruck | ||
| Full Title: PROSPECTIVE STUDY OF 68GA-NODAGA-RGD-PET FOR THE NON-INVASIVE DETERMINAITON OF THE INTEGRIN αvβ3 EXPRESSION IN PATIENTS WITH UNTREATED OR RECURRENT BREAST CANCER, COLORECTAL CANCER, NON-SMALL CELL ... | ||
| Medical condition: Patient with untreated or reccurent breast cancer, non-small cell lung cancer, colorectal cancer and neuroendocrine tumors | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-015952-11 | Sponsor Protocol Number: 0923 | Start Date*: 2009-11-17 | |||||||||||
| Sponsor Name:Department of OncologyHerlev University Hospital | |||||||||||||
| Full Title: Phase Fase II examination of irinotecan, cetuximab and everolimus for patients resistente to chemoptherapy with metastatic colorectal cancer and KRAS mutation or with KRAS wildtype after progressio... | |||||||||||||
| Medical condition: Patient with metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002211-28 | Sponsor Protocol Number: 36713 | Start Date*: 2012-11-07 | ||||||||||||||||
| Sponsor Name:VU medical center | ||||||||||||||||||
| Full Title: Perioperative selective decontamination of the digestive tract (SDD) in elective colorectal cancer patients: a multicenter randomized clinical trial | ||||||||||||||||||
| Medical condition: Post-operative infective complications and long term oncological outcome in patients undergoing surgery for colorectal cancer | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-003460-24 | Sponsor Protocol Number: 82914 | Start Date*: 2023-02-23 | |||||||||||
| Sponsor Name:Radboud University Medical Center | |||||||||||||
| Full Title: Pilot study to determine the intraTUMORal OsImertinib concentration in patients with peritoneal metastasizeD colorectal cancer (TUMOROID study) | |||||||||||||
| Medical condition: Colorectal cancer | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000092-24 | Sponsor Protocol Number: 56286 | Start Date*: 2016-05-02 | |||||||||||
| Sponsor Name:University Medical Center Utrecht | |||||||||||||
| Full Title: The PLCRC substudy Ultra high field 7.0 Tesla MR Spectroscopy to monitor capecitabine metabolism in liver metastases – a proof of concept study | |||||||||||||
| Medical condition: Colorectal carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005690-59 | Sponsor Protocol Number: Genmab A/S | Start Date*: 2008-02-11 | |||||||||||
| Sponsor Name:Genmab A/S | |||||||||||||
| Full Title: A Dose-Escalation, Randomized Phase I/II trial of Zalutumumab - a Human Monoclonal Anti-EGF receptor Antibody - With or Without Irinotecan chemotherapy in Cetuximab refractory Colorectal Cancer pat... | |||||||||||||
| Medical condition: Refractory Colorectal Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000394-39 | Sponsor Protocol Number: KFEAC14.01 | Start Date*: 2014-05-05 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: Full dose S-1 monotherapy compared to reduced dose S-1/oxaliplatin combination therapy as first-line treatment for older patients with metastatic colorectal cancer | |||||||||||||
| Medical condition: Treatment of older (≥ 70 years) patients with metastatic colorectal cancer | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) NO (Completed) FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004299-37 | Sponsor Protocol Number: CA209-8U4 | Start Date*: 2019-01-24 | ||||||||||||||||
| Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | ||||||||||||||||||
| Full Title: NIVOLUMAB plus IPILIMUMAB and TEMOZOLOMIDE in combination in microsatellite stable (MSS), MGMT silenced metastatic colorectal cancer (mCRC): the MAYA study. | ||||||||||||||||||
| Medical condition: Microsatellite stable (MSS), MGMT-silenced metastatic colorectal carcinoma (mCRC). | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-000109-66 | Sponsor Protocol Number: TPU-TAS-102-301 | Start Date*: 2012-12-10 | |||||||||||
| Sponsor Name:Taiho Oncology, Inc. | |||||||||||||
| Full Title: RANDOMIZED, DOUBLE-BLIND, PHASE 3 STUDY OF TAS-102 PLUS BEST SUPPORTIVE CARE (BSC) VERSUS PLACEBO PLUS BSC IN PATIENTS WITH METASTATIC COLORECTAL CANCER REFRACTORY TO STANDARD CHEMOTHERAPIES | |||||||||||||
| Medical condition: Refractory metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) SE (Completed) AT (Completed) ES (Completed) IE (Completed) CZ (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000460-24 | Sponsor Protocol Number: TT1-2007 | Start Date*: 2009-04-07 | |||||||||||
| Sponsor Name:University of Duisburg-Essen | |||||||||||||
| Full Title: Bi-weekly Cetuximab combined with FOLFOX-6 as first-line treatment in metastatic colorectal cancer patients with wild-type k-ras status | |||||||||||||
| Medical condition: Histologically proven metastatic colorectal cancer with k-ras wildtyp status | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-000502-30 | Sponsor Protocol Number: DKFZ-2019-001 | Start Date*: 2020-03-26 | |||||||||||||||||||||
| Sponsor Name:German Cancer Research Center (DKFZ) | |||||||||||||||||||||||
| Full Title: Personalized Vitamin D Supplementation for Reducing or Preventing Fatigue and Enhancing Quality of Life of Patients with Colorectal Tumor: Randomized Intervention Trial | |||||||||||||||||||||||
| Medical condition: Fatigue in patients with colorectal cancer (ICD codes C18-C20 and C21.8) within 12 months after a colorectal cancer therapy (surgery, chemotherapy and/ or radiation) and not optimal vitamin D status | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2006-001815-30 | Sponsor Protocol Number: SGUL/SGH 001 | Start Date*: 2006-06-05 | |||||||||||
| Sponsor Name:St George's, University of London (SGUL) [...] | |||||||||||||
| Full Title: Prevention Of Endometrial Tumours (POET) | |||||||||||||
| Medical condition: Endometrial cancer/tumours in women with Hereditary Non-polyposis Colorectal Cancer (HNPCC) | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000131-13 | Sponsor Protocol Number: DDD17CRCCXB1 | Start Date*: 2017-05-11 |
| Sponsor Name:KU Leuven | ||
| Full Title: Pharmacokinetics of Celebrex for the prevention/treatment of colorectal cancer: Systemic pharmacokinetics and elimination of Celebrex in healthy volunteers | ||
| Medical condition: Colorectal cancer | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-003522-86 | Sponsor Protocol Number: P18.210 | Start Date*: 2019-03-21 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: Imaging tumor angiogenesis using 18F-Fluciclatide PET/CT in patients with colorectal and pancreatic cancer. | ||
| Medical condition: Patient suffering from colorectal or pancreatic adenocarcinoma. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001362-42 | Sponsor Protocol Number: COI-B | Start Date*: 2013-07-08 | |||||||||||
| Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori | |||||||||||||
| Full Title: Perioperative treatment with COI-B (Capecitabine, Oxaliplatin, Irinotecan and Bevacizumab) of high risk or borderline resectable colorectal liver metastases | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-006151-40 | Sponsor Protocol Number: MITOUFT | Start Date*: 2007-12-29 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA S. LUIGI GONZAGA | |||||||||||||
| Full Title: UFT/LEUCOVORIN AND MITOMYCIN C IN THE TREATMENT OF METASTATIC COLORECTAL CANCER OXALIPLATIN AND IRINOTECAN RESISTANT | |||||||||||||
| Medical condition: PATIENTS WITH METASTATIC COLON-RECTAL CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-005428-41 | Sponsor Protocol Number: 02044190615-01 | Start Date*: 2014-12-01 | ||||||||||||||||
| Sponsor Name:Department of experimental and clincial medicine "F. Magrassi" | ||||||||||||||||||
| Full Title: Phase III study of RegorAfenib VErsus placebo as maintenance therapy in RAS wiLd type metastatic coLOrectal cancer | ||||||||||||||||||
| Medical condition: The present proposal is aimed to evaluate the efficacy and safety of regorafenib as maintenance therapy in increasing the efficacy of the best available therapy for first line treatment fluoropirim... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Prematurely Ended) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-001180-11 | Sponsor Protocol Number: ML20514 | Start Date*: 2009-03-16 | |||||||||||
| Sponsor Name:Roche Pharma AG | |||||||||||||
| Full Title: An Open-label, single-arm, Phase II study to evaluate the efficacy and the feasibility of bevacizumab (Avastin®) based on a FOLFOXIRI regimen until progression in patients with previously untreated... | |||||||||||||
| Medical condition: previously untreated metastatic colorectal carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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