- Trials with a EudraCT protocol (647)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
647 result(s) found for: Metastatic Colorectal Cancer.
Displaying page 18 of 33.
| EudraCT Number: 2017-002442-72 | Sponsor Protocol Number: C17-01 | Start Date*: 2017-10-23 | |||||||||||
| Sponsor Name:GERCOR | |||||||||||||
| Full Title: RECIST 1.1 and iRECIST evaluation for patients with deficient MMR and/or MSI Metastatic Colorectal Cancer treated with nivolumab and ipilimumab. A GERCOR open-label phase II study NIPICOL C17-01 | |||||||||||||
| Medical condition: Patients with deficient MMR and/or MSI Metastatic Colorectal Cancer treated with nivolumab and ipilimumab | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002435-29 | Sponsor Protocol Number: CR6086-1-04 | Start Date*: 2021-09-28 | |||||||||||
| Sponsor Name:ROTTAPHARM BIOTECH S.R.L. | |||||||||||||
| Full Title: An open-label, single-arm, phase Ib/IIa trial to evaluate the safety and efficacy of the EP4 receptor antagonist CR6086 in combination with the PD-1 inhibitor balstilimab (AGEN2034), in patients wi... | |||||||||||||
| Medical condition: Pretreated mismatch-repair-proficient and microsatellite stable metastatic colorectal cancer (pMMR–MSS metastatic CRC). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004065-34 | Sponsor Protocol Number: TUD-COFI06-014 | Start Date*: 2006-11-24 |
| Sponsor Name:Technical University Dresden | ||
| Full Title: Open labeled, multicenter phase I / II study evaluating the dose escalation/ safety of Cetuximab and Oxaliplatin/ 5-FU/FA/ Irinotecan as first-line treatment of metastatic colorectal cancer | ||
| Medical condition: first-line treatment of metastatic colorectal cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004200-36 | Sponsor Protocol Number: BRTA-0100-014 | Start Date*: 2005-12-02 | |||||||||||
| Sponsor Name:NERVIANO MEDICAL SCIENCES | |||||||||||||
| Full Title: Phase II exploratory study of brostallicin PNU-166196A as third/fourth line chemoterapy in adult patients with advanced/metastatic colorectal cancer CRC . | |||||||||||||
| Medical condition: Use for the treatment of advanced/metastatic colorectal cancer, as third/fourth line chemioterapy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001414-15 | Sponsor Protocol Number: REVOLUTION | Start Date*: 2018-07-27 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE TUMORI - IRCCS FONDAZIONE PASCALE | |||||||||||||
| Full Title: Randomized phasE 2 study of Valproic acid in combination with bevacizumab and Oxaliplatin/fLUoropyrimidine regimens in patients with ras-mutated metastaTIc cOlorectal caNcer | |||||||||||||
| Medical condition: patients with ras-mutated metastaTIc 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: 2020-004636-25 | Sponsor Protocol Number: ACOTAS_G098 | Start Date*: 2021-06-17 | ||||||||||||||||
| Sponsor Name:GERCOR | ||||||||||||||||||
| Full Title: A phase II study to evaluate the rate of cardiovascular events during trifluridine/tipiracil +/-oxaliplatin treatment in colorectal/oesogastric adenocarcinoma patients that have experienced a pas... | ||||||||||||||||||
| Medical condition: colorectal or oesogastric adenocarcinoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-002797-56 | Sponsor Protocol Number: C04-2 | Start Date*: 2007-08-28 | |||||||||||
| Sponsor Name:Gercor | |||||||||||||
| Full Title: Phase III study of an optimized chemotherapy + Avastin strategy +/- Tarceva in metastatic colorectal cancer. | |||||||||||||
| Medical condition: Metastatic Colorectal Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-002849-11 | Sponsor Protocol Number: FIRE-5 | Start Date*: 2019-06-17 | |||||||||||
| Sponsor Name:Klinikum der Universität München, Ludwig-Maximilians-Universität München, represented by the managing medical director | |||||||||||||
| Full Title: Optimal anti-EGFR Treatment of mCRC Patients with Low-Frequency RAS Mutation | |||||||||||||
| Medical condition: RAS-mutant metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-005758-64 | Sponsor Protocol Number: INCA06-FT/STIC-AVASTIN | Start Date*: 2007-01-16 | |||||||||||
| Sponsor Name:CHRU TOURS | |||||||||||||
| Full Title: Evaluation médico-économique de l'échographie de contraste pour l'appréciation précoce de l'effet du bevacizumab sur les métastases hépatiques de cancer colorectal | |||||||||||||
| Medical condition: cancer colorectal avancé avec au moins une métastase hépatique | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005003-32 | Sponsor Protocol Number: ORCHESTRA | Start Date*: 2012-06-14 | |||||||||||
| Sponsor Name:VU University Medical Center, Department of Medical Oncology | |||||||||||||
| Full Title: A randomized multicenter clinical trial for patients with multi-organ, colorectal cancer metastases comparing the combination of chemotherapy and maximal tumor debulking versus chemotherapy alone. | |||||||||||||
| Medical condition: multi-organ metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001017-61 | Sponsor Protocol Number: MO29112 | Start Date*: 2014-11-08 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A MULTI-CENTRE RANDOMISED CLINICAL TRIAL OF BIOMARKER-DRIVEN MAINTENANCE TREATMENT FOR FIRST-LINE METASTATIC COLORECTAL CANCER (MODUL) | |||||||||||||
| Medical condition: METASTATIC COLORECTAL CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) GB (GB - no longer in EU/EEA) DE (Completed) PT (Completed) DK (Completed) SK (Prematurely Ended) NL (Completed) FR (Completed) SE (Completed) BE (Completed) GR (Completed) ES (Temporarily Halted) SI (Completed) CY (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-001459-17 | Sponsor Protocol Number: NuTide:323 | Start Date*: 2023-03-27 | |||||||||||
| Sponsor Name:NuCana plc | |||||||||||||
| Full Title: A randomised, open-label, Phase II, dose/schedule optimisation study of NUC-3373/leucovorin/irinotecan plus bevacizumab (NUFIRI-bev) versus 5-FU/leucovorin/irinotecan plus bevacizumab (FOLFIRI-bev)... | |||||||||||||
| Medical condition: Relapsed, unresectable, histologically or cytologically confirmed metastatic adenocarcinoma of colon or rectum with radiologically measurable disease. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DE (Prematurely Ended) IT (Prematurely Ended) FR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000490-79 | Sponsor Protocol Number: AB12006 | Start Date*: 2015-09-18 | |||||||||||
| Sponsor Name:AB Science | |||||||||||||
| Full Title: A prospective, multicenter, randomized, double blind, placebo-controlled, 2-parallel groups, phase 3 study to compare the efficacy and safety of masitinib in combination with FOLFIRI (irinotecan, 5... | |||||||||||||
| Medical condition: Metastatic colorectal cancer after 1 previous line of treatment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Prematurely Ended) ES (Completed) CZ (Completed) SK (Prematurely Ended) HU (Completed) GB (Prematurely Ended) FR (Completed) CY (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-003258-14 | Sponsor Protocol Number: 20070307 | Start Date*: 2008-11-14 | |||||||||||
| Sponsor Name:Amgen Inc | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Placebo Controlled Study of AMG 386 in Combination with FOLFIRI in Subjects with Previously Treated Metastatic Colorectal Carcinoma | |||||||||||||
| Medical condition: Metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) BE (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002071-34 | Sponsor Protocol Number: ALLOCATE | Start Date*: 2019-10-31 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Vejle Hospital | ||||||||||||||||||||||||||||||||||||||
| Full Title: Allocation of patients with pre-treated solid tumors to anti-cancer therapy based on gene expression drug response prediction - a phase II basket trial | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Breast cancer Ovarian cancer Lung cancer Colorectal cancer Prostate cancer Pancreatic cancer | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| 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: 2011-005547-27 | Sponsor Protocol Number: GO28074 | Start Date*: 2012-10-24 | |||||||||||||||||||||
| Sponsor Name:Genentech, Inc. | |||||||||||||||||||||||
| Full Title: A PHASE II, MULTICENTER, OPEN-LABEL, RANDOMIZED STUDY EVALUATING THE EFFICACY AND SAFETY OF FOLFIRI + MEHD7945A VERSUS FOLFIRI + CETUXIMAB IN SECOND LINE IN PATIENTS WITH KRAS WILD-TYPE METASTATIC ... | |||||||||||||||||||||||
| Medical condition: Colorectal cancer that does not carry mutation in the KRAS gene | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) BE (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2010-023695-91 | Sponsor Protocol Number: SoMore version 2.0 | Start Date*: 2010-12-29 | |||||||||||||||||||||
| Sponsor Name:Institut Jules Bordet | |||||||||||||||||||||||
| Full Title: Sorafenib plus capecitabine activity assesment in patients with advanced pre-treated colorectal cancer | |||||||||||||||||||||||
| Medical condition: Histologically confirmed colorectal cancer that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective. Age >18 years. Life exp... | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-004849-11 | Sponsor Protocol Number: AIO-KRK-0116 | Start Date*: 2016-09-29 | |||||||||||
| Sponsor Name:University Clinic od Munich-Großhadern (represented by the medical management) | |||||||||||||
| Full Title: Randomised study to investigate FOLFOXIRI plus cetuximab or FOLFOXIRI plus bevacizumab as first-line treatment of BRAF-mutated metastatic colorectal cancer (FIRE-4.5) | |||||||||||||
| Medical condition: Histologically confirmed, UICC stage IV adenocarcinoma of the colon or rectum with metastases (metastatic colorectal cancer, mCRC), primarily non-resectable or surgery refused by the patient; RAS ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001210-15 | Sponsor Protocol Number: MOU-2017-02 | Start Date*: 2018-11-19 |
| Sponsor Name:Masarykův onkologický ústav | ||
| Full Title: Rational Anti-EGFR therapy Selection for the first-line treatment of patients with metastatic KRAS/NRAS wild type colorectal cancer based on the use of molecular predictor miR-31-5p (RASmiR) | ||
| Medical condition: inoperable, untreated, wild type RAS (wt KRAS/wtNRAS), metastatic colorectal cancer (mCRC) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Prematurely Ended) | ||
| Trial results: (No results available) | ||
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