- Trials with a EudraCT protocol (765)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
765 result(s) found for: colon cancer.
Displaying page 16 of 39.
EudraCT Number: 2006-002887-25 | Sponsor Protocol Number: 2601 | Start Date*: 2006-06-27 | |||||||||||
Sponsor Name:GOIM GRUPPO ONCOLOGICO MERIDIONALE | |||||||||||||
Full Title: Bevacizumab+folfiri in untreated patients with advanced colorectal cancer. A phase II multicenter study of the Gruppo Oncologico dell'Italia Meridionale. (GOIM). | |||||||||||||
Medical condition: untreated patients with advanced colorectal cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004285-35 | Sponsor Protocol Number: CA224-123 | Start Date*: 2022-07-12 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Open-label (Sponsor Blinded) Study of Relatlimab-nivolumab Fixed-dose Combination Versus Regorafenib or Trifluridine + Tipiracil (TAS-102) for Participants with Later-lines o... | ||||||||||||||||||
Medical condition: Metastatic Colorectal Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) DE (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) NL (Trial now transitioned) CZ (Trial now transitioned) BE (Trial now transitioned) | ||||||||||||||||||
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: 2005-000331-14 | Sponsor Protocol Number: ICORG 05-02/NSABP C-08 | Start Date*: 2005-04-08 |
Sponsor Name:All Ireland Cooperative Oncology Research Group | ||
Full Title: A phase III clinical trial comparing infusional 5-Fluorouracil (5-FU), Leucovorin and Oxaliplatin (mFOLFOX -6) every 2 weeks with Bevacizumab to the same regimen without Bevacizumab for the treatme... | ||
Medical condition: Resected stage II or stage III adenocarcinoma of the colon | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001105-13 | Sponsor Protocol Number: STREAM | Start Date*: 2015-06-19 | ||||||||||||||||
Sponsor Name:ISTITUTO NAZIONALE TUMORI - IRCCS FONDAZIONE PASCALE | ||||||||||||||||||
Full Title: Regorafenib monotherapy as second-line treatment of patients with RAS-mutant advanced colorectal cancer: a multicentre, single-arm, two-stage, phase 2 study. | ||||||||||||||||||
Medical condition: patients with RAS-mutant advanced colorectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003737-25 | Sponsor Protocol Number: STX0206-SIRFLOXstudy | Start Date*: 2008-11-26 | |||||||||||
Sponsor Name:Sirtex Technology Pty Ltd | |||||||||||||
Full Title: Randomised comparative study of folfox6m plus SIR-Spheres microspheres versus folfox6m alone as first line treatment in patients with non-resectable liver metastases from primary colorectal carcinoma | |||||||||||||
Medical condition: Non-resectable liver metastasis from primary colorectal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013756-79 | Sponsor Protocol Number: VECTOX | Start Date*: 2010-09-28 | ||||||||||||||||
Sponsor Name:Anticancer Informing "Me Gnosi Nika" | ||||||||||||||||||
Full Title: VECTIBIX PLUS OXALIPLATIN-BASED ADJUVANT TREATMENT OF RECTAL CANCER | ||||||||||||||||||
Medical condition: Rectal cancer stage 2-3 includes neoadjuvant chemo radiation, followed by resection, followed by adjuvant chemotherapy. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019236-12 | Sponsor Protocol Number: GEMCAD-1002 | Start Date*: 2010-10-13 | ||||||||||||||||
Sponsor Name:Grupo Español Multidisciplinar en Cáncer Digestivo (GEMCAD) | ||||||||||||||||||
Full Title: Ensayo clínico fase II de un solo brazo, multicéntrico y prospectivo para la validación de biomarcadores en pacientes con cáncer colorrectal avanzado y/o metastásico con gen KRAS no mutado tratados... | ||||||||||||||||||
Medical condition: Cancer colorrectal avanzado y/o metastásico | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-017432-40 | Sponsor Protocol Number: MGN1703-C02 | Start Date*: 2010-04-13 | |||||||||||
Sponsor Name:MOLOGEN AG | |||||||||||||
Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled, Multi-Center Clinical Study to Evaluate Efficacy and Safety of a Maintenance Therapy with Immunomodulator MGN1703 in Patients with Advanced ... | |||||||||||||
Medical condition: Patients with advanced colorectal carcinoma (AJCC Stage IV) with disease control after initial first-line therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) GB (Completed) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005422-30 | Sponsor Protocol Number: AIO-KRK-0212 | Start Date*: 2014-01-09 | |||||||||||
Sponsor Name:AIO Studien gGmbH | |||||||||||||
Full Title: Randomized Phase II study for evaluation of efficacy and safety of maintenance treatment with 5-FU/FA plus panitumumab vs. 5-FU/FA alone after prior induction treatment with mFOLFOX6 plus panitumum... | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-005215-29 | Sponsor Protocol Number: 03-CoFactor | Start Date*: 2005-06-03 | |||||||||||
Sponsor Name:ADVENTRX Pharmaceuticals Inc | |||||||||||||
Full Title: A Multi-Center, Open Label, Parallel Group, Randomised, Phase IIB Clinical Trial to Evaluate the Safety and Efficacy of CoFactor and 5-FU versus Leucovorin and 5-FU in Subjects with Metastatic Colo... | |||||||||||||
Medical condition: Metastatic Colorectal Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2018-002250-79 | Sponsor Protocol Number: CCR4938 | Start Date*: 2018-11-29 |
Sponsor Name:The Royal Marsden NHS Foundation Trust | ||
Full Title: iSCORE: Immunotherapy Sequencing in COlon and REctal Cancer. | ||
Medical condition: Metastatic RAS wild-type colorectal cancer which has previously responded to FOLFIRI chemotherapy and Cetuximab treatment but then progressed | ||
Disease: | ||
Population Age: | Gender: | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000894-11 | Sponsor Protocol Number: IRST153.04 | Start Date*: 2016-04-13 | ||||||||||||||||
Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI (IRST) S.R.L. IRCCS | ||||||||||||||||||
Full Title: Vaccination with autologous dendritic cells loaded with autologous tumour homogenate after curative resection for stage IV colorectal cancer: a phase II study | ||||||||||||||||||
Medical condition: colorectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001194-16 | Sponsor Protocol Number: DDD17CRCP2 | Start Date*: 2017-12-11 |
Sponsor Name:KU Leuven | ||
Full Title: Pharmacokinetics of celecoxib for the prevention/treatment of colorectal cancer: optimization of intestinal sampling for celecoxib in healthy volunteers | ||
Medical condition: Colorectal cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005154-44 | Sponsor Protocol Number: OPERA | Start Date*: 2006-03-02 | |||||||||||
Sponsor Name:Universitätsklinikum Hamburg-Eppendorf | |||||||||||||
Full Title: OPERA: OXALIPLATIN AND CETUXIMAB IN FIRST-LINE TREATMENT OF mCRC Open, non-controlled, multicenter phase II study evaluating 5-FU/FA plus oxaliplatin (FOLFOX-4) plus cetuximab as first-line treatme... | |||||||||||||
Medical condition: metastasized colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006700-32 | Sponsor Protocol Number: 80013 | Start Date*: 2022-07-13 |
Sponsor Name:Meander Medical Centre | ||
Full Title: A pilot study to assess the safety and feasibility of fluorescent sentinel lymph node identification in colon carcinoma using submucosal bevacizumab-800CW. | ||
Medical condition: Colon carcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006796-41 | Sponsor Protocol Number: 80117 | Start Date*: 2022-07-13 |
Sponsor Name:Meander Medical Centre | ||
Full Title: A pilot study to assess the safety and feasibility of fluorescent sentinel lymph node identification in colon carcinoma using intravenous bevacizumab-800CW | ||
Medical condition: Colon carcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000834-50 | Sponsor Protocol Number: MGN1703-C06 | Start Date*: 2014-07-09 | |||||||||||
Sponsor Name:MOLOGEN AG | |||||||||||||
Full Title: IMPALA-Trial: Evaluation of an immunomodulatory maintenance treatment in patients with metastatic colorectal cancer with tumor reduction during induction treatment - A phase III trial | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Completed) BE (Prematurely Ended) IT (Ongoing) EE (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004866-42 | Sponsor Protocol Number: AIO KRK 0107 | Start Date*: 2009-07-27 | |||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||
Full Title: An Open-label Randomized Phase II Study of Panitumumab Plus Oral Capecitabine and Infusional Oxaliplatin (XELOX) or XELOX alone for Second-line Treatment of Patients with Metastatic Clororectal Can... | |||||||||||||
Medical condition: Metastatic colorectal cancer (mCRC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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