- 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 29 of 33.
| EudraCT Number: 2018-004231-72 | Sponsor Protocol Number: IBICCR2018-01 | Start Date*: 2019-06-27 | |||||||||||
| Sponsor Name:Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud (FIMABIS) | |||||||||||||
| Full Title: Randomized study of the detection of RAS / BRAF mutations by BEAMing technology in advance of the radiological diagnosis of progression in patients with metastatic colorectal cancer RAS / BRAF WT a... | |||||||||||||
| Medical condition: Median of the progression-free survival of patients with mCRC who maintains the treatment in conventional 1st line, QT + anti-EFGR, versus patients who withdraw anti-EGFR therapy after detection of... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-002598-49 | Sponsor Protocol Number: CRO1885 | Start Date*: 2012-04-23 |
| Sponsor Name:Imperial College Joint Research Office | ||
| Full Title: The AXitinib MicroBubble UltraSound in metastatic Colorectal cancer trial | ||
| Medical condition: Third line colorectal liver metastases | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-000885-13 | Sponsor Protocol Number: UC-0105/1303 | Start Date*: 2013-07-31 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:UNICANCER | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Secured access to crizotinib for patients with tumors harboring a genomic alteration on one of the biological targets of the drug | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients with metastatic or unresectable locally advanced malignancies harboring specific genomic alterations regarding the biological crizotinib targets, and who are no more amenable to curative t... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-000461-23 | Sponsor Protocol Number: CA209-627 | Start Date*: 2017-03-07 | ||||||||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
| Full Title: An Open-label Phase 2 Multi-cohort Trial of Nivolumab in Advanced or Metastatic Malignancies | ||||||||||||||||||
| Medical condition: Advanced/Metastatic malignancies | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-002565-22 | Sponsor Protocol Number: LOKON002 | Start Date*: 2017-12-21 | |||||||||||
| Sponsor Name:Lokon Pharma AB | |||||||||||||
| Full Title: Phase I/II Trial Investigating an Immunostimulatory Oncolytic Adenovirus for Cancer | |||||||||||||
| Medical condition: Colorectal, ovarian, pancreatic, gallbladder and bile duct cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000318-39 | Sponsor Protocol Number: RG_17-215 | Start Date*: 2019-06-11 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: A phase II trial assessing nivolumab in strong class II expressing microsatellite stable colorectal cancer | |||||||||||||
| Medical condition: Colorectal cancer (CRC) | |||||||||||||
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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: 2009-012942-22 | Sponsor Protocol Number: PRODIGE 18 - ACCORD 22/0906 | Start Date*: 2010-08-30 | |||||||||||
| Sponsor Name:Fédération Nationale des Centres de Lutte Contre le Cancer (FNCLCC) | |||||||||||||
| Full Title: Essai de phase II, randomisé multicentrique, évaluant l'efficacité d'une chimiothérapie standard à base de fluoropyrimidine associée au cétuximab ou au bévacizumab, chez des patients kras sauvage, ... | |||||||||||||
| Medical condition: Cancer colorectal métastatique (CCM), KRAS sauvage, nécessitant un traitement de 2éme ligne. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006254-26 | Sponsor Protocol Number: COMETS | Start Date*: 2009-03-25 | |||||||||||
| Sponsor Name:GISCAD | |||||||||||||
| Full Title: Open-label randomized, parallel group, phase III, multicenter trial comparing two different sequences of therapy (irinotecan/cetuximab followed by fluorouracil/leucovorin with oxaliplat... | |||||||||||||
| Medical condition: Patients with histologically confirmed metastatic colorectal cancer progressed after a first line treatment containing FOLFIRI and BEV. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-003475-42 | Sponsor Protocol Number: GTAEXS617-001 | Start Date*: 2023-05-23 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Exscientia AI Ltd | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 1/2 open-label multicenter study to assess the safety, pharmacokinetics, and anti-tumor activity of GTAEXS617 in patients with advanced solid tumors. | ||||||||||||||||||||||||||||||||||||||
| Medical condition: advanced solid tumors | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: BE (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-005875-17 | Sponsor Protocol Number: CMEK162X2110 | Start Date*: 2012-05-30 |
| Sponsor Name:Array Biopharma Inc | ||
| Full Title: A Phase Ib/II, multicenter, open-label, dose escalation study of LGX818 in combination with MEK162 in adult patients with BRAF V600 - dependent advanced solid tumors | ||
| Medical condition: Patients with solid tumors harboring a BRAF V600 mutation. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) IT (Completed) BE (Completed) FR (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001356-35 | Sponsor Protocol Number: ACO/ARO/AIO-18.2 | Start Date*: 2020-08-04 | |||||||||||
| Sponsor Name:University of Heidelberg | |||||||||||||
| Full Title: ACO/ARO/AIO-18.2 Preoperative FOLFOX versus postoperative risk-adapted chemotherapy in patients with locally advanced rectal cancer and low risk for local failure: A randomized phase III trial of ... | |||||||||||||
| Medical condition: Locally advanced rectal adenocarcinoma localized 0 - 16 cm from the anal verge with low risk of local failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000315-26 | Sponsor Protocol Number: MO18024 | Start Date*: 2004-11-25 |
| Sponsor Name:F.Hoffmann-La Roche Ltd. | ||
| Full Title: First-line Bevacizumab and Chemotherapy in Metastatic Cancer of the Colon or Rectum. An Expanded Access Program. | ||
| Medical condition: Metastatic cancer of the colon or rectum. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SK (Completed) HU (Completed) IT (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-001527-32 | Sponsor Protocol Number: SC105(AURELIO-05) | Start Date*: 2022-10-21 |
| Sponsor Name:SOTIO Biotech AG | ||
| Full Title: A phase 2, open-label, single-arm, multicenter study to evaluate the efficacy and safety of SOT101 in combination with cetuximab in patients with RAS wild-type colorectal cancer (AURELIO-05) | ||
| Medical condition: RAS wild-type colorectal cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) BE (Completed) IT (Prematurely Ended) FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-001700-12 | Sponsor Protocol Number: TTD 04-02 | Start Date*: 2004-12-23 |
| Sponsor Name:Spanish Cooperative Group for Gastrointestinal Tomour therapy | ||
| Full Title: Open-label, phase II, ramdomised, pilot study to evaluate the safety and efficacy of combination therapy with cetuximab and FOLFOX4 or FOLFOX4 alone in patients with EGFR-pos. colorectal cancer and... | ||
| Medical condition: Open-label, phase II, randomised, pilot study to evaluate the safety and efficacy of combination therapy with cetuximab and FOLFOX4 or FOLFOX4 alone in patients with EGFR-positive colorectal cance... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002732-24 | Sponsor Protocol Number: FP2CLI001 | Start Date*: 2018-11-29 | |||||||||||
| Sponsor Name:Faron Pharmaceuticals Ltd | |||||||||||||
| Full Title: A Phase I/II Open–Label, Three-Part, Dose-Finding and Separate Cohort Expansion Trial to Assess the Safety, Tolerability and Preliminary Efficacy of Repeated Doses of CLEVER-1 Antibody FP-1305, in ... | |||||||||||||
| Medical condition: Selected solid tumours; - cutaneous melanoma - pancreatic ductal adenocarcinoma - ovarian cancer - colorectal adenocarcinoma - hepatocellular carcinoma - gallbladder cancer and cholangiocarcinoma... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) GB (GB - no longer in EU/EEA) NL (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001111-12 | Sponsor Protocol Number: 1367.1 | Start Date*: 2015-06-12 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:SCS Boehringer Ingelheim Comm.V | ||||||||||||||||||||||||||||||||||||||
| Full Title: An open label, Phase Ia/Ib dose finding study with BI 894999 orally administered once a day in patients with advanced malignancies, with repeated administration in patients with clinical benefit | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Advanced, unresectable and/or metastatic solid tumours, which have failed with conventional treatment or for which no therapy of proven efficacy exists, or in patients who are not amenable to stand... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2006-006532-21 | Sponsor Protocol Number: 40054-22062 | Start Date*: 2008-10-27 | ||||||||||||||||
| Sponsor Name:EORTC | ||||||||||||||||||
| Full Title: Preoperative chemoradiotherapy and postoperative chemotherapy with capecitabine and oxaliplatin vs. capecitabine alone in locally advanced rectal cancer (PETACC-6) | ||||||||||||||||||
| Medical condition: locally advanced rectal cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) GB (Completed) FR (Completed) DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2022-004122-22 | Sponsor Protocol Number: APHP220097 | Start Date*: 2023-06-02 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Monalizumab and MEDI5752 in patients with MSI and/or dMMR metastatic cancer | |||||||||||||
| Medical condition: adult patients in all MSI/DMMR solid tumor types | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-005282-12 | Sponsor Protocol Number: | Start Date*: 2013-05-14 |
| Sponsor Name:University of Edinburgh [...] | ||
| Full Title: TOFFEE Trial Toxicity OF Fluoropyrimidines: A comparative study of the cardiotoxicity of capEcitabine and tEysuno | ||
| Medical condition: All gastrointestinal and hepatobiliary cancers including colorectal cancer, cancer of unknown primary, pancreatic cancer, stomach cancer and oesophageal cancer. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002344-81 | Sponsor Protocol Number: 1381-0009 | Start Date*: 2019-05-22 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Limited | |||||||||||||
| Full Title: An open-label, Phase II, platform trial evaluating safety and efficacy of multiple BI 754091 anti-PD-1 based combination regimens in PD-(L)1 naïve and PD-(L)1 pretreated patient populations with ad... | |||||||||||||
| Medical condition: Advanced/metastatic solid tumours | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
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