- Trials with a EudraCT protocol (443)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (90)
443 result(s) found for: CRC.
Displaying page 17 of 23.
| EudraCT Number: 2019-003029-83 | Sponsor Protocol Number: OSAS_UCBH | Start Date*: 2020-12-03 | |||||||||||
| Sponsor Name:Service de Neurologie, CHU Liège | |||||||||||||
| Full Title: Assessment of changes in regional brain synaptic density in patients with Obstructive Sleep Apnea (OSA) measured by positron emission tomography and 18F-UCB-H. | |||||||||||||
| Medical condition: Obstructive sleep apnea syndrome | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004434-26 | Sponsor Protocol Number: AIO-KRK-0216 | Start Date*: 2017-04-25 | |||||||||||||||||||||
| Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||
| Full Title: Avelumab and cetuximab in combination with FOLFOX in patients with previously untreated metastatic colorectal cancer – The phase II AVETUX-CRC trial. | |||||||||||||||||||||||
| 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: 2015-002773-38 | Sponsor Protocol Number: AIO-KRK-0214 | Start Date*: 2016-12-20 | |||||||||||||||||||||
| Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||
| Full Title: mFOLFOX6 vs. mFOLFOX6 + aflibercept as neoadjuvant treatment in MRI-defined T3-rectal cancer: a randomized phase-II-trial | |||||||||||||||||||||||
| Medical condition: Patients with locally advanced rectal or rectosigmoid cancer staged cT3 CRM-negative with MRI | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2020-003132-24 | Sponsor Protocol Number: RXC004/0002 | Start Date*: 2021-07-26 | |||||||||||
| Sponsor Name:Redx Pharma Plc | |||||||||||||
| Full Title: A Multi-arm, Phase II, Open-Label, Multicentre Study to Assess the Preliminary Efficacy of RXC004 in Monotherapy and in Combination with Nivolumab, in Patients with Ring Finger Protein 43 (RNF43) o... | |||||||||||||
| Medical condition: Patients with Ring Finger Protein 43 (RNF43) or R-spondin (RSPO) Aberrated, Metastatic, Microsatellite Stable, Colorectal Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002767-98 | Sponsor Protocol Number: UCDCRC/19/01 | Start Date*: 2020-05-28 | |||||||||||
| Sponsor Name:University College Dublin | |||||||||||||
| Full Title: A Pilot Study of Combined Immune Checkpoint Inhibition in combination with ablative therapies in Subjects with Hepatocellular Carcinoma (HCC) | |||||||||||||
| Medical condition: Patients with Hepatocellular Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005694-87 | Sponsor Protocol Number: UCDCRC/21/01 | Start Date*: 2022-10-25 | |||||||||||
| Sponsor Name:University College Dublin | |||||||||||||
| Full Title: A Randomised Pilot Study of the Safety and Efficacy of Tofacitinib (Xeljanz) in Improving Endoscopic Outcomes in Subjects with Ulcerative Colitis with Active, Chronic, Antibiotic Dependent or Refra... | |||||||||||||
| Medical condition: Subjects with Ulcerative Colitis with Active, Chronic, Antibiotic Dependent or Refractory Idiopathic Pouchitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (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 | |||||||||||||
| EudraCT Number: 2014-001208-23 | Sponsor Protocol Number: 2014/VCC/0013 | Start Date*: 2015-01-15 |
| Sponsor Name:Velindre NHS Trust | ||
| Full Title: A randomised, double blind, placebo controlled, phase II study of fulvestrant with or without the addition of vandetanib as treatment for patients with metastatic breast cancer resistant to aromata... | ||
| Medical condition: Metastatic breast cancer that has become resistant to aromatase inhibitor therapy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-012040-16 | Sponsor Protocol Number: EMR62242–004 | Start Date*: 2009-10-06 | |||||||||||
| Sponsor Name:Merck KGaA | |||||||||||||
| Full Title: An open-label, randomized, controlled, multi-center, Phase I/II trial investigating 2 EMD 525797 doses in combination with cetuximab + irinotecan versus cetuximab + irinotecan alone, as second-line... | |||||||||||||
| Medical condition: Subjects with k-ras WT, metastatic colorectal cancer who have failed a fist line chemotherapy with an oxaliplatin-containing regimen will be eligible for this trial. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) BE (Completed) CZ (Completed) GB (Completed) HU (Completed) GR (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004154-41 | Sponsor Protocol Number: ISO-CC-007 | Start Date*: 2018-11-07 | |||||||||||
| Sponsor Name:Isofol Medical AB | |||||||||||||
| Full Title: A randomized, multicenter, parallel-group, Phase III study to compare the efficacy of arfolitixorin versus leucovorin in combination with 5 fluorouracil, oxaliplatin, and bevacizumab in patients wi... | |||||||||||||
| Medical condition: First line advanced Colorectal patients eligible for treatment with 5-FU, oxaliplatin, and bevacizumab. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) DE (Prematurely Ended) FR (Prematurely Ended) AT (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003502-24 | Sponsor Protocol Number: 4130-CL-0201 | Start Date*: 2012-01-03 | |||||||||||
| Sponsor Name:Astellas Pharma Global Development, Inc. | |||||||||||||
| Full Title: A Phase 2, Open Label, Multicenter, Randomized Trial Comparing Tivozanib in Combination with mFOLFOX6 with Bevacizumab in Combination with mFOLFOX6 in Stage IV Metastatic Corectal Cancer (mCRC) Sub... | |||||||||||||
| Medical condition: Metastatic colorectal cancer (CRC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) CZ (Completed) ES (Completed) AT (Completed) HU (Completed) FI (Completed) NL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2008-004093-40 | Sponsor Protocol Number: 08-PIR-03 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:Nektar Therapeutics | ||||||||||||||||||
| Full Title: A Multicenter, Open-Label, Randomized, Phase 2 Study to Evaluate the Efficacy and Safety of NKTR-102 (PEG-Irinotecan) Versus Irinotecan in Patients with Second-Line, Irinotecan-Naïve, KRAS-Mutant, ... | ||||||||||||||||||
| Medical condition: Refractory Solid Tumors (Colorectal Cancer) Tumores sólidos refractarios (Cáncer colorrectal) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) BE (Prematurely Ended) DE (Completed) GB (Completed) SK (Completed) LV (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-000550-12 | Sponsor Protocol Number: 2014-PT026 | Start Date*: 2014-07-23 | |||||||||||
| Sponsor Name:XBiotech Germany GmbH | |||||||||||||
| Full Title: A Double Blind, Placebo Controlled, Pivotal Phase III Study Evaluating Xilonix™ in Symptomatic Colorectal Cancer Patients Refractory To Standard Therapy | |||||||||||||
| Medical condition: Symptomatic Colorectal Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) GB (Completed) PL (Completed) DE (Prematurely Ended) CZ (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000305-76 | Sponsor Protocol Number: CMEK162X2111 | Start Date*: 2012-09-03 | |||||||||||||||||||||
| Sponsor Name:Novartis Farmacéutica S.A. | |||||||||||||||||||||||
| Full Title: A phase Ib/II open-label, multi-center study of the combination of MEK162 plus AMG 479 (ganitumab) in adult patients with selected advanced solid tumors | |||||||||||||||||||||||
| Medical condition: colorectal adenocarcinoma. metastatic pancreatic adenocarcinoma melanoma | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Completed) GB (Prematurely Ended) BE (Completed) FR (Completed) DE (Completed) IT (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2020-004721-23 | Sponsor Protocol Number: 20190135 | Start Date*: 2022-01-28 |
| Sponsor Name:Amgen Inc. | ||
| Full Title: A Phase 1b, Master Protocol Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Sotorasib (AMG 510) in Subjects With Advanced Solid Tumors With KRAS p.G12C Mutation (CodeBreaK 101) | ||
| Medical condition: Advanced Solid Tumors with KRAS p.G12C Mutation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Trial now transitioned) ES (Temporarily Halted) AT (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-004188-65 | Sponsor Protocol Number: KFE-11.17 | Start Date*: 2012-03-05 | |||||||||||||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||||||||||||
| Full Title: Potentially resectable metastatic colorectal cancer with wild-type KRAS and BRAF: alternating chemotherapy plus cetuximab - A randomised phase II trial - Nordic 7.6 | |||||||||||||||||||||||
| Medical condition: Metastatic colorectal cancer with wild-type KRAS and BRAF | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: SE (Completed) DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2016-003644-37 | Sponsor Protocol Number: HE6B/16 | Start Date*: 2017-08-01 | |||||||||||
| Sponsor Name:Hellenic Cooperative Oncology Group (HeCOG) | |||||||||||||
| Full Title: Single-arm phase II study of panitumumab rechallenge in combination with oxaliplatin or irinotecan-based chemotherapy in patients with RAS wild type advanced colorectal cancer. | |||||||||||||
| Medical condition: RAS wild type advanced colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) CY (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004240-19 | Sponsor Protocol Number: ALASCCA | Start Date*: 2016-03-02 |
| Sponsor Name:Karolinska Institutet, Department of Molecular medicine and Surgery | ||
| Full Title: A randomized double-blind placebo-controlled study with ASA treatment in colorectal cancer patients with mutations in the PI3K signaling pathway. | ||
| Medical condition: Colon or rectal cancer tumor stage II-III, tumor with somatic alterations in PIK3CA, PIK3R1 or PTEN. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) DK (Trial now transitioned) FI (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-005464-42 | Sponsor Protocol Number: 2335/2015 | Start Date*: 2016-06-16 | |||||||||||||||||||||
| Sponsor Name:Gustave Roussy | |||||||||||||||||||||||
| Full Title: A phase II study to assess the efficacy of the anti-PD-L1 antibody atezolizumab (MPDL3280A) administered with stereotactic ablative radiotherapy (SABR) in patients with metastatic tumours | |||||||||||||||||||||||
| Medical condition: Patients with one of following metastatic tumours: - Metastatic colorectal cancer - Metastatic non-small lung cancer - Metastatic renal cell carcinoma | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
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