- 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 1 of 23.
EudraCT Number: 2008-005584-33 | Sponsor Protocol Number: KUN2009 | Start Date*: 2010-02-09 |
Sponsor Name:Radboud University Nijmegen Medical Centre | ||
Full Title: Dendritic cell vaccination in patients with Lynch Syndrome or colorectal cancer with MSI | ||
Medical condition: In this study our primary objective is to induce or enhance an immune response to tumor antigens in Lynch syndrome mutation carriers (with and without colorectal adenomas or carcinomas) and patient... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004369-42 | Sponsor Protocol Number: BAY73-4506/15983 | Start Date*: 2013-11-28 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Phase-III Study of Adjuvant Regorafenib Versus Placebo for Patients with Stage IV Colorectal Cancer After Curative Treatment of Liver Metastases | |||||||||||||
Medical condition: Metastatic Colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) GB (Completed) IT (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001664-34 | Sponsor Protocol Number: 12028-FC-SS | Start Date*: 2013-08-30 | |||||||||||
Sponsor Name:Belfast HSC Trust [...] | |||||||||||||
Full Title: Vit-D in CRC - A Randomised Double Blind Placebo-Controlled Clinical Trial Of a Single Oral Cholecalciferol Treatment Against Surrogate End Point Biomarkers (SEBs) In Colon Cancer (CRC) Patients | |||||||||||||
Medical condition: Colon cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000973-41 | Sponsor Protocol Number: Etx and portal embolisation | Start Date*: 2008-04-09 |
Sponsor Name:Karolinska University Hospital, Huddinge | ||
Full Title: Efficacy of cetuximab for preventing progression of CRC liver metastases after selective portal embolisation | ||
Medical condition: Patients with colorectal cancer and livermetastases planned for hemihepatectomy following portal embolisation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004061-13 | Sponsor Protocol Number: ESR21-21165 | Start Date*: 2022-06-09 | ||||||||||||||||
Sponsor Name:VHIO Vall d’Hebron Institute of Oncology | ||||||||||||||||||
Full Title: Single cell characterization of persistent cells upon treatment with durvalumab (MEDI4736) with or without tremelimumab in MSS and MSI colorectal and endometrial tumors | ||||||||||||||||||
Medical condition: MSS and MSI colorectal and endometrial tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001400-11 | Sponsor Protocol Number: 20170543 | Start Date*: 2019-11-14 | ||||||||||||||||
Sponsor Name:Amgen Inc. | ||||||||||||||||||
Full Title: A Phase 1/2, Open-label Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of AMG 510 Monotherapy in Subjects With Advanced Solid Tumors With KRAS p.G12C Mu... | ||||||||||||||||||
Medical condition: KRAS p.G12C mutant advanced NSCLC, CRC, and other solid tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) AT (Trial now transitioned) BE (Trial now transitioned) PT (Trial now transitioned) GR (Trial now transitioned) ES (Temporarily Halted) HU (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004418-32 | Sponsor Protocol Number: U31402-A-U202 | Start Date*: 2020-10-30 | |||||||||||
Sponsor Name:DAIICHI SANKYO, INC | |||||||||||||
Full Title: A MULTI-CENTER, OPEN-LABEL, PHASE 2 STUDY TO EVALUATE SAFETY AND EFFICACY OF U3-1402 IN SUBJECTS WITH ADVANCED OR METASTATIC COLORECTAL CANCER (CRC) | |||||||||||||
Medical condition: Advanced or metastatic colorectal cancer (CRC) which is resistant, refractory, or intolerant to at least 2 prior lines of therapy, that must include all of the following agents: fluoropyrimidine, i... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000528-39 | Sponsor Protocol Number: TAK-676-1002 | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:Takeda Development Center Americas, Inc. (TDC Americas) | |||||||||||||
Full Title: An Open-label, Dose Escalation, Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TAK-676 as a Single Agent and in Combination With Pembrolizumab in Ad... | |||||||||||||
Medical condition: Solid Neoplasms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005451-15 | Sponsor Protocol Number: IPR/12 | Start Date*: 2006-12-29 | |||||||||||
Sponsor Name:MOLMED | |||||||||||||
Full Title: NGR006 A phase II study of NGR-hTNF administered as single agent every 3 weeks in patients affected by colorectal cancer CRC , previously treated with fluoropyrimidine, oxaliplatin and irinotecan... | |||||||||||||
Medical condition: Patients affected by advanced or metastatic colorectal cancer CRC. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003656-40 | Sponsor Protocol Number: PCYC-1128-CA | Start Date*: 2016-02-17 | ||||||||||||||||||||||||||
Sponsor Name:Pharmacyclics LLC | ||||||||||||||||||||||||||||
Full Title: A Phase 1b/2 Study of Ibrutinib Combination Therapy in Selected Advanced Gastrointestinal And Genitourinary Tumors | ||||||||||||||||||||||||||||
Medical condition: Metastatic renal cell carcinoma (RCC), advanced urothelial carcinoma, advanced gastric (including gastro-esophageal [GEJ]) adenocarcinoma, and metastatic colorectal adenocarcinoma (CRC) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000613-32 | Sponsor Protocol Number: STEMNESS-CRC | Start Date*: 2020-07-24 | |||||||||||
Sponsor Name:1Globe Health Institute | |||||||||||||
Full Title: A Phase III, Randomized, Open-Label Clinical Study of Napabucasin in Combination with FOLFIRI and Best Supportive Care (BSC) Versus Napabucasin plus BSC (or BSC alone) in Adult Patients with Previo... | |||||||||||||
Medical condition: Histologically confirmed adenocarcinoma of the colon or rectum that is metastatic. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002349-50 | Sponsor Protocol Number: M16TGA | Start Date*: 2017-09-29 |
Sponsor Name:Netherlands Cancer Institute- Antoni van Leeuwenhoek Hospital (NKI-AVL) | ||
Full Title: Phase I/II study with galunisertib (LY2157299) combined with capecitabine in patients with advanced chemotherapy resistant colorectal cancer and an activated TGF-β signature | ||
Medical condition: colorectal carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) BE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002177-25 | Sponsor Protocol Number: 19-255-03 | Start Date*: 2021-11-08 | ||||||||||||||||||||||||||
Sponsor Name:Nektar Therapeutics | ||||||||||||||||||||||||||||
Full Title: A Phase 1b/2, Open-label, Multicenter, Dose Escalation and Dose Expansion Study of NKTR-255 in Combination with Cetuximab as a Salvage Regimen for Solid Tumors | ||||||||||||||||||||||||||||
Medical condition: Relapsed or refractory (R/R) head and neck squamous cell carcinoma (HNSCC) or colorectal carcinoma (CRC) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-003460-24 | Sponsor Protocol Number: 82914 | Start Date*: 2023-02-23 | |||||||||||
Sponsor Name:Radboud University Medical Center | |||||||||||||
Full Title: Pilot study to determine the intraTUMORal OsImertinib concentration in patients with peritoneal metastasizeD colorectal cancer (TUMOROID study) | |||||||||||||
Medical condition: Colorectal cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002001-19 | Sponsor Protocol Number: VHIO-16001 | Start Date*: 2017-11-24 | |||||||||||
Sponsor Name:VHIO | |||||||||||||
Full Title: A phase II open-label study with the anti-PD-L1 Atezolizumab monoclonal antibody in combination with Bevacizumab in patients with advanced chemotherapy resistant colorectal cancer and MSI-like mole... | |||||||||||||
Medical condition: Colorectal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Ongoing) NL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002415-15 | Sponsor Protocol Number: TG-MV-015 | Start Date*: 2016-02-17 | |||||||||||
Sponsor Name:ThromboGenics NV | |||||||||||||
Full Title: A PHASE 2, RANDOMISED, DOUBLE-MASKED, SHAM-CONTROLLED, MULTI-CENTRE STUDY TO EVALUATE THE EFFICACY AND SAFETY OF OCRIPLASMIN IN INDUCING TOTAL POSTERIOR VITREOUS DETACHMENT (PVD) IN SUBJECTS WITH N... | |||||||||||||
Medical condition: Moderately severe to very severe non-proliferative diabetic retinopathy (NPDR) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Completed) CZ (Completed) BE (Completed) HU (Completed) ES (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001852-32 | Sponsor Protocol Number: 3475-164 | Start Date*: 2015-12-11 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
Full Title: A Phase II Study of Pembrolizumab (MK-3475) as Monotherapy in Subjects with Previously Treated Locally Advanced Unresectable or Metastatic (Stage IV) Mismatched Repair Deficient or Microsatellite I... | ||
Medical condition: Colorectal Carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) BE (Completed) ES (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-004167-25 | Sponsor Protocol Number: NKI-AVLM22TGA | Start Date*: 2023-05-04 |
Sponsor Name:Department of Medical Oncology and Clinical Pharmacology, The Netherlands Cancer Institute - Antoni van Leeuwenhoek Hosp | ||
Full Title: Phase I/II study with galunisertib combined with capecitabine in patients with advanced chemotherapy resistant colorectal cancer with peritoneal metastases | ||
Medical condition: Advanced colorectal cancer with peritoneal metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005836-25 | Sponsor Protocol Number: BAY73-4506/15967 | Start Date*: 2012-06-12 |
Sponsor Name:Bayer HealthCare AG | ||
Full Title: An open-label phase IIIb study of regorafenib in patients with metastatic colorectal cancer (CRC) who have progressed after standard therapy | ||
Medical condition: Colorectal neoplasms | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) DE (Completed) CZ (Completed) ES (Completed) GB (Completed) IT (Completed) AT (Completed) NL (Completed) IE (Completed) FR (Completed) PT (Completed) FI (Completed) SE (Completed) GR (Completed) HU (Completed) PL (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002919-18 | Sponsor Protocol Number: AC220-A-U202 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||||||||||||
Full Title: A Phase 1/2, Multicenter, Dose-Escalating Study To Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy Of Quizartinib Administered in Combination with Re-Induction Chemotherapy, a... | |||||||||||||||||||||||
Medical condition: Relapsed or Refractory acute myeloid leukemia (AML) in subjects aged ≥1 month to ≤21 years with FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) mutations following failure of fr... | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IE (Prematurely Ended) FR (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) SE (Trial now transitioned) NL (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
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