- 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 3 of 33.
| EudraCT Number: 2017-000159-15 | Sponsor Protocol Number: PRTK15-TL/SONCHIMIO | Start Date*: 2018-01-12 | ||||||||||||||||
| Sponsor Name:CHRU TOURS | ||||||||||||||||||
| Full Title: Targeted delivery of chemotherapy with ultrasound and microbubbles | ||||||||||||||||||
| Medical condition: Colo-Rectal Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-003668-24 | Sponsor Protocol Number: IPR/11 | Start Date*: 2007-12-20 | |||||||||||
| Sponsor Name:MOLMED | |||||||||||||
| Full Title: NGR005: Pilot study of NGR-hTNF administered at low and high doses in combination with a standard oxaliplatin-based regimen in patients wit metastatic colorectal cancer | |||||||||||||
| Medical condition: Patients with metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004524-41 | Sponsor Protocol Number: KFE-2022 | Start Date*: 2020-12-03 | ||||||||||||||||
| Sponsor Name:Aarhus University Hospital/Karen-Lise Garm Spindler | ||||||||||||||||||
| Full Title: OPTIMISE: OPTIMIzation of treatment SElection and follow up in oligometastatic colorectal cancer - a ctDNA guided phase II randomized approach | ||||||||||||||||||
| Medical condition: | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-000151-40 | Sponsor Protocol Number: SGM-CLIN03 | Start Date*: 2019-06-13 | ||||||||||||||||||||||||||
| Sponsor Name:Surgimab | ||||||||||||||||||||||||||||
| Full Title: Multicenter, semi-blinded, randomized, controlled, parallel arms clinical study on the performance of SGM-101, a fluorochrome-labeled anti-carcino-embryonic antigen (CEA) monoclonal antibody, for t... | ||||||||||||||||||||||||||||
| Medical condition: Patients undergoing curative surgery for colorectal cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) NL (Ongoing) IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| 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: 2009-014452-30 | Sponsor Protocol Number: 30012009 | Start Date*: 2010-03-29 | |||||||||||
| Sponsor Name:Academisch ziekenhuis Leiden acting under the name of Leids Universitair Medisch Centrum | |||||||||||||
| Full Title: Safety and efficacy of the addition of simvastatin to panitumumab in k-ras mutant advanced or metastatic colorectal cancer patients. A single-arm, multicenter, phase II study using a Simon two stag... | |||||||||||||
| Medical condition: k-ras mutant advanced or metastatic colorectal cancer failing prior 5FU, oxaliplatin and irinotecan containing regimens | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002866-65 | Sponsor Protocol Number: M14-217 | Start Date*: 2014-12-05 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: Randomized, Blinded, Multicenter, Phase 2 Study Comparing Veliparib Plus FOLFIRI ± Bevacizumab Versus Placebo Plus FOLFIRI ± Bevacizumab in Previously Untreated Metastatic Colorectal Cancer | |||||||||||||
| Medical condition: Untreated Metastatic Colorectal Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) HU (Completed) DE (Completed) BE (Completed) ES (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-006073-24 | Sponsor Protocol Number: CCR2983 | Start Date*: 2008-05-22 | ||||||||||||||||
| Sponsor Name:Royal Marsden Hospital | ||||||||||||||||||
| Full Title: CINATRA: Chromosomal Instability and Anti-Tubulin Response Assessment: A Phase II Study of Epothilone B in Metastatic Colon Carcinoma in patients with Microsatellite Instability or Chromosomal Inst... | ||||||||||||||||||
| Medical condition: Metastatic or locally recurrent colorectal cancer in genetically unselected patients, followed by recruitment of patients selected for microsatellite positive tumours | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
| 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: 2017-000329-11 | Sponsor Protocol Number: Elderly | Start Date*: 2018-05-02 | ||||||||||||||||
| Sponsor Name:Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest | ||||||||||||||||||
| Full Title: Aflibercept and 5-FU vs. FOLFOX as 1st line treatment for elderly or frail elderly patients with metastatic colorectal cancer | ||||||||||||||||||
| Medical condition: metastatic colorectal cancer | ||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2010-019841-25 | Sponsor Protocol Number: IRST153.03 | Start Date*: 2012-07-12 | |||||||||||
| Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI | |||||||||||||
| Full Title: A Phase II Study to evaluate activity and toxicity of Gemcitabine in Combination with Pemetrexed long term infusion in the Treatment of pretreated Metastatic Colorectal Cancer Patients | |||||||||||||
| Medical condition: Pretreated patients with advanced colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001986-18 | Sponsor Protocol Number: CMEK162X2116 | Start Date*: 2013-11-12 | ||||||||||||||||||||||||||
| Sponsor Name:Array BioPharma Inc. | ||||||||||||||||||||||||||||
| Full Title: A phase Ib/II, open-label, multi-center, dose escalation study of MEK162 in combination with panitumumab in adult patients with mutant RAS or wild-type RAS metastatic colorectal cancer | ||||||||||||||||||||||||||||
| Medical condition: Mutant RAS or wild-type (WT) RAS metastatic colorectal cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: ES (Completed) BE (Completed) IT (Prematurely Ended) NL (Completed) DE (Completed) FR (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2016-005241-23 | Sponsor Protocol Number: 16.37 | Start Date*: 2017-04-19 | |||||||||||
| Sponsor Name:Odense Universitetshospital | |||||||||||||
| Full Title: Lonsurf - RII Lonsurf (TAS-102) with or without bevacizumab in patients with chemo-refractory metastatic colorectal cancer. A randomized phase II study | |||||||||||||
| Medical condition: Metastatic, non-resectable and chemo-refractory colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-005364-14 | Sponsor Protocol Number: 1199.51 | Start Date*: 2009-06-03 | |||||||||||
| Sponsor Name:SCS Boehringer Ingelheim Comm.V | |||||||||||||
| Full Title: A phase I-II study of BIBF 1120 and Folfox compared to Bevacizumab and Folfox in first line metastatic colorectal cancer patients. | |||||||||||||
| Medical condition: Metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) FR (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002393-12 | Sponsor Protocol Number: PRODIGE49 | Start Date*: 2016-08-26 | ||||||||||||||||
| Sponsor Name:Fédération Francophone de Cancérologie Digestive | ||||||||||||||||||
| Full Title: Systemic oxaliplatin or in intra-arterial chemotherapy combined with LV5FU2 and targeted therapy in first-line treatment of metastatic colorectal cancer restricted to the liver | ||||||||||||||||||
| Medical condition: | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) BE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-000644-94 | Sponsor Protocol Number: VA_2012/01 | Start Date*: 2012-06-28 | |||||||||||
| Sponsor Name:Centre Val d’Aurelle - Paul Lamarque | |||||||||||||
| Full Title: A randomized phase II trial assessing Sorafenib (Nexavar®) in combination with irinotecan in metastatic colorectal cancer patients with KRAS mutated tumours after failure of all active drugs known ... | |||||||||||||
| Medical condition: metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000560-28 | Sponsor Protocol Number: ImmunoPeCa | Start Date*: 2014-07-24 | |||||||||||
| Sponsor Name:Oslo University Hospital | |||||||||||||
| Full Title: PHASE I/II TRIAL OF MOC31PE IMMUNOTOXIN IN PERITONEAL CARCINOMATOSIS FROM COLORECTAL CARCINOMA. | |||||||||||||
| Medical condition: Metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004528-35 | Sponsor Protocol Number: 1239.6 | Start Date*: 2007-01-22 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: A multicenter, randomized, open label phase II trial evaluating the efficacy and safety of mFOLFOX7 plus weekly alternating sequential oral administration of BIBF 1120 250 mg twice daily and BIBW 2... | |||||||||||||
| Medical condition: Metastatic colorectal carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) FR (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2005-000970-37 | Sponsor Protocol Number: EMR62202-047 | Start Date*: 2007-07-08 | |||||||||||
| Sponsor Name:Merck KGaA | |||||||||||||
| Full Title: Open, randomized, controlled, multicenter phase II study comparing 5-FU/FA plus oxaliplatin (FOLFOX 4) plus cetuximab versus 5-FU/FA plus oxaliplatin as first-line treatment for epidermal growth fa... | |||||||||||||
| Medical condition: Metastatic colon rectal carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) AT (Completed) PT (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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