- Trials with a EudraCT protocol (10,210)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (712)
10,210 result(s) found for: cancer.
Displaying page 183 of 511.
EudraCT Number: 2020-000819-67 | Sponsor Protocol Number: MTW_2020_KC01 | Start Date*: 2020-07-28 |
Sponsor Name:Maidstone and Tunbridge Wells NHS Trust | ||
Full Title: SENTINUS: Technical feasibility and diagnostic accuracy of intradermal microbubbles and contrast enhanced ultrasound to identify sentinel lymph node metastases in breast cancer patients following t... | ||
Medical condition: Breast Cancer - Using SonoVue injected intradermally into the breast and contrast enhanced ultrasound to see if the cancer has spread via lymphatic channels to sentinel lymph nodes in the axilla. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000520-29 | Sponsor Protocol Number: MSC_apceth_111/1 | Start Date*: 2015-11-05 | |||||||||||
Sponsor Name:apceth GmbH & Co. KG | |||||||||||||
Full Title: Treatment of Advanced Gastrointestinal Adenocarcinoma in a Phase I/II trial with modified allogeneic MSC_apceth_111 | |||||||||||||
Medical condition: Patients suffering from advanced, recurrent or metastatic gastrointestinal adenocarcinoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003932-38 | Sponsor Protocol Number: 50797 | Start Date*: 2016-03-30 | |||||||||||
Sponsor Name:VU University medical center (VUmc) | |||||||||||||
Full Title: Advanced imaging in laparoscopic HIPEC for peritoneal carcinomatosis of colorectal orgin to improve cytoreduction; a feasibility study | |||||||||||||
Medical condition: Peritoneal carcinomatosis from colorectal origin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005530-21 | Sponsor Protocol Number: AGO/2006/010 | Start Date*: 2007-01-12 | |||||||||||
Sponsor Name:University Hospital Gent | |||||||||||||
Full Title: Comparison of dynamic contrast enhanced magnetic resonance imaging (DCE-MRI) with gadofosveset trisodium (Vasovist, Schering, Berlin, Germany) to gadopentetate dimeglumine (GD-DTPA, Magnevist, Sche... | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004574-11 | Sponsor Protocol Number: CS1008-A-E202 | Start Date*: 2009-05-26 | |||||||||||||||||||||
Sponsor Name:Daiichi Sankyo Development Limited | |||||||||||||||||||||||
Full Title: RANDOMISED, DOUBLE-BLINDED, PLACEBO- CONTROLLED PHASE 2 STUDY OF CS-1008 IN COMBINATION WITH CARBOPLATIN/PACLITAXEL IN CHEMOTHERAPY NAÏVE SUBJECTS WITH METASTATIC OR UNRESECTABLE NON-SMALL CELL LU... | |||||||||||||||||||||||
Medical condition: Treatment of metastatic or unresectable non small cell lung cancer (NSCLC) with CS 1008 or placebo first in combination with carboplatin/paclitaxel then as monotherapy in the first line setting | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002104-40 | Sponsor Protocol Number: CNIO-CP-2019-01 | Start Date*: 2019-11-12 | |||||||||||||||||||||
Sponsor Name:Centro Nacional de Investigaciones Oncológicas (CNIO) | |||||||||||||||||||||||
Full Title: A phase II, open-label, biomarker-guided study of Carboplatin efficacy in pretreated metastatic castration-resistant Prostate Cancer (mCRPC)-BioChiP | |||||||||||||||||||||||
Medical condition: metastatic prostate cancer castration resistant | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003971-37 | Sponsor Protocol Number: PRIMUS004 | Start Date*: 2020-08-19 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde Health Board [...] | |||||||||||||
Full Title: PRIMUS 004: A multi-arm non-comparative signal seeking phase II platform trial of biomarker-directed novel second-line treatments in metastatic pancreatic cancer | |||||||||||||
Medical condition: Pancreatic Cancer | |||||||||||||
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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: 2016-003287-39 | Sponsor Protocol Number: PRO-105 | Start Date*: 2017-07-05 |
Sponsor Name:NuCana plc | ||
Full Title: A Phase II Open-Label Study of NUC-1031 in Patients with Platinum-Resistant Ovarian Cancer | ||
Medical condition: Platinum-resistant epithelial cancer of the ovary, fallopian tube or primary peritoneum (here termed ‘ovarian cancer’), who have been treated with 3 or more prior chemotherapy regimens. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004151-79 | Sponsor Protocol Number: TRIO030 | Start Date*: 2017-05-08 | |||||||||||
Sponsor Name:Translational Research in Oncology (TRIO) | |||||||||||||
Full Title: A Presurgical Tissue-Acquisition Study to Evaluate Molecular Alterations in Human Breast Cancer Tissue Following Short-Term Exposure to the Androgen Receptor Antagonist Darolutamide (ODM-201) | |||||||||||||
Medical condition: Early Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000259-17 | Sponsor Protocol Number: PazTo_2010 | Start Date*: 2012-04-20 | |||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: A phase I/II study of Pazopanib and weekly Topotecan in patients with platinum-resistant or intermediate-sensitive recurrent ovarian cancer | |||||||||||||
Medical condition: This study is a prospective single-arm, open-label, multicenter phase I/II trial. The phase I-trial is a dose-escalation trial to determine the maxium tolerated dose (MTD) of pazopanib in combinati... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023207-10 | Sponsor Protocol Number: S+M/10/10 | Start Date*: 2011-01-26 | |||||||||||
Sponsor Name:hameln rds a.s. | |||||||||||||
Full Title: A multicentre, randomized, open label, parallel group pilot study comparing efficacy and safety of sufentanil transdermal delivery system (TDS) to oral sustained release morphine sulphate in ... | |||||||||||||
Medical condition: Chronic cancer pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000777-38 | Sponsor Protocol Number: SOAP | Start Date*: 2014-06-19 | |||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori | |||||||||||||
Full Title: Activity and safety of second line SOrafenib After Pazopanib in patients with metastatic renal cell carcinoma (SOAP Study) | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002105-39 | Sponsor Protocol Number: SUT-EXE-08 | Start Date*: 2009-01-08 | |||||||||||
Sponsor Name:Instituto Catalán de Oncología | |||||||||||||
Full Title: Estudio Piloto/Fase II aleatorizado, multicéntrico, doble ciego en neoadyuvancia de la combinación de exemestano y sunitinib en mujeres postmenopaúsicas con cáncer de mama primario, receptores horm... | |||||||||||||
Medical condition: Pacientes con cáncer de mama primario hormonosensible | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001270-24 | Sponsor Protocol Number: A3671014 | Start Date*: 2007-02-13 | |||||||||||
Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
Full Title: Phase 2, single arm study of ticilimumab in patients with refractory metastatic adenocarcinoma of the colon or rectum | |||||||||||||
Medical condition: Refractory meatstatic adenocarcinoma of the colon or rectum | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005395-14 | Sponsor Protocol Number: MOT07/01 | Start Date*: 2008-01-03 | |||||||||||
Sponsor Name:RICARDO MORENO OTERO/MARIA CHAPARRO SANCHEZ | |||||||||||||
Full Title: EFECTO DE SORAFENIB SOBRE LA MODULACION DE LOS FACTORES SOLUBLES ANGIOGIOGÉNICOS EN PACIENTES CON CARCINOMA HEPATOCELULAR IRRESECABLE | |||||||||||||
Medical condition: carcinoma hepatocelular no resecable | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008013-19 | Sponsor Protocol Number: MAMA2009 | Start Date*: 2009-05-21 | |||||||||||
Sponsor Name:Joan Xavier Fontdevila Font | |||||||||||||
Full Title: Estudio aleatorizado para determinar la utilidad de la teicoplanina en la reducción de la colonización bacteriana de la superficie del expansor mamario en cirugía reconstructiva de mama | |||||||||||||
Medical condition: Disminución de la colonización bacteriana en la cirugía reconstructiva de mama con la técnica en 2 tiempos (expansor-prótesis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000661-12 | Sponsor Protocol Number: OCTO_022 | Start Date*: 2011-08-23 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: A randomised double blind phase 2 trial of whole brain radiotherapy with or without vandetanib in metastatic melanoma with brain metastases | |||||||||||||
Medical condition: Metastatic melanoma with brain metastases. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002162-21 | Sponsor Protocol Number: JECF-VITD-2011-01 | Start Date*: 2012-04-24 |
Sponsor Name:José Esteban Castelao Fernández | ||
Full Title: A phase II randomized, prospective, multicenter, placebo-controlled clinical trial to evaluate the chemopreventive effect of vitamin D in women at high risk of breast cancer. | ||
Medical condition: Women at high risk of developing breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001364-22 | Sponsor Protocol Number: ML25625 | Start Date*: 2011-05-25 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: A multi-center, open-label clinical trial to evaluate the objective response rate of bevacizumab in combination with modified FOLFOX-6 followed by one year of maintenance with bevacizumab alone in ... | |||||||||||||
Medical condition: Metastatic colorectal cancer: histologically confirmed adenocarcinoma of the colon or rectum and metastatic disease confined to the liver (with initially not or borderline resectable liver metastas... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003496-11 | Sponsor Protocol Number: EN3348-303 | Start Date*: 2012-02-08 | |||||||||||
Sponsor Name:Endo Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Active-Controlled, Open-Label, Multicenter Study to Evaluate the Efficacy and Safety of EN3348 (MCC) as Compared with Mitomycin C in the Intravesical Treatment of Subjects wi... | |||||||||||||
Medical condition: BCG Recurrent or Refractory Non-Muscle Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
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