- Trials with a EudraCT protocol (10,218)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10,218 result(s) found for: Cancer.
Displaying page 201 of 511.
| EudraCT Number: 2005-001680-57 | Sponsor Protocol Number: HDP 603 | Start Date*: 2005-09-22 |
| Sponsor Name:Heidelberg Pharma GmbH | ||
| Full Title: Phase II study of fosfluridine tidoxil in an oral multiple dose schedule given once-a-day for 7 consecutive days every 2 weeks in patients with advanced breast and colorectal cancer | ||
| Medical condition: Patiens with confirmed metastatic breast or colorectal cancer. Breast:Pats should have received/failed at least 1 but no more than 2 lines of chemotherapy with taxanes and/or anthracyclines for me... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-011377-33 | Sponsor Protocol Number: 08_CLPHA_55 | Start Date*: 2009-06-25 | |||||||||||
| Sponsor Name:The Christie NHS Foundation Trust | |||||||||||||
| Full Title: AN ASSESSMENT OF IMAGING AND CIRCULATING BIOMARKERS IN PATIENTS WITH METASTATIC COLORECTAL CARCINOMA TREATED WITH THE ANTI-VEGF MONOCLONAL ANTIBODY BEVACIZUMAB | |||||||||||||
| Medical condition: Metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002385-20 | Sponsor Protocol Number: CAO/ARO/AIO-04 | Start Date*: 2006-06-28 | |||||||||||
| Sponsor Name:Strahlenklinik, Universitätsklinikum Erlangen, insoweit handelnd für den Freistaat Bayern | |||||||||||||
| Full Title: Prospective randomised multicenter phase-III-study: Preoperative radiochemotherapy and adjuvant chemotherapy with 5-Fluorouracil plus oxaliplatin versus preoperative radiochemotherapy and adjuvant... | |||||||||||||
| Medical condition: Male or femal patients suffering from histologically proven carcinoma of the rectum (tumor ≤ 12cm from the anal verge, with clinically staged T3/4 or any node-positive disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003785-33 | Sponsor Protocol Number: 20060100 | Start Date*: 2006-12-05 | |||||||||||
| Sponsor Name:Amgen Inc | |||||||||||||
| Full Title: A Global, Multicenter, Open-label, Single Agent, Two-stage Phase 2 Study to Evaluate the Efficacy and Safety of AMG 102 in Subjects With Advanced Renal Cell Carcinoma | |||||||||||||
| Medical condition: Advanced Renal Cell Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-003323-20 | Sponsor Protocol Number: CP4055-204 | Start Date*: 2008-05-30 |
| Sponsor Name:Clavis Pharma ASA | ||
| Full Title: A Phase I/II Study of CP-4055 in Patients with Platinum Resistant Ovarian Cancer | ||
| Medical condition: A phase I/II clinical study of CP4055 in patients with platinum resistant ovarian cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-006072-38 | Sponsor Protocol Number: HEPATICA | Start Date*: 2007-11-07 |
| Sponsor Name:the Dutch Colorectal Cancer Group | ||
| Full Title: A Randomised Two Arm Phase III Study in Patients Post Radical Resection of Liver Metastasis of Colorectal Cancer to Investigate Bevacizumab (q3w) in Combination With Capecitabine Plus Elaoxantin (X... | ||
| Medical condition: Liver metastatis of colorectal cancer. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-020621-40 | Sponsor Protocol Number: OCTO_021 | Start Date*: 2010-09-30 |
| Sponsor Name:The University of Oxford | ||
| Full Title: SONATINA: A Phase II Multi-Centre Randomised Controlled Study of Nelfinavir Addition to Radiotherapy Treatment in Neo-Adjuvant Therapy for Rectal Cancer | ||
| Medical condition: inoperable rectal cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-004683-30 | Sponsor Protocol Number: KRAS2011 | Start Date*: 2012-05-02 |
| Sponsor Name:VU University Medical | ||
| Full Title: A phase II study of sorafenib and metformin in patients with locally advanced and/or metastatic non-smal cell lung cancer (NSCLC) with a K-Ras mutation | ||
| Medical condition: Patients with advanced non small cell lung cancer that harbours a K-Ras mutation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-007652-10 | Sponsor Protocol Number: BRD 08/11-A | Start Date*: 2009-04-06 |
| Sponsor Name:Centre René Gauducheau | ||
| Full Title: Etude de phase II ouverte évaluant en fonction du polymorphisme du CYP2D6, le taux de réponse biologique au traitement par tamoxifène (TAM) administré en situation pré-opératoire chez des patientes... | ||
| Medical condition: Cancer du sein | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-005289-31 | Sponsor Protocol Number: LF-PB/14/05 | Start Date*: 2015-08-04 | |||||||||||
| Sponsor Name:CHEMI S.P.A. | |||||||||||||
| Full Title: A multicentre, double blind, randomized placebo controlled trial to assess the effect of LF-PB on seroma formation in women with breast cancer undergoing Axillary Lymph Node Dissection | |||||||||||||
| Medical condition: Woman with Breast Cancer Undergoing Axillary Lymph Node Dissection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004509-42 | Sponsor Protocol Number: CTL-101-023 | Start Date*: 2018-04-23 | |||||||||||||||||||||
| Sponsor Name:Celleron Therapeutics Ltd | |||||||||||||||||||||||
| Full Title: A Phase Ib/ II Trial to Assess the Safety and Efficacy of CXD101 in Combination with the PD-1 Inhibitor Nivolumab in Patients with Metastatic, Previously-Treated, Microsatellite-Stable Colorectal C... | |||||||||||||||||||||||
| Medical condition: Metastatic, Previously-Treated, Microsatellite-Stable Colorectal Carcinoma | |||||||||||||||||||||||
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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: 2008-006051-40 | Sponsor Protocol Number: Beva2007 | Start Date*: 2008-09-09 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
| Full Title: A PHASE II STUDY: UNOPERABLE NON NON SQUAMOUS NON SMALL CELL LUNG CANCER METRONOMIC BIOCHEMOTHERAPY WITH WEEKLY CISPLATIN, DAILY ORAL ETOPOSIDE AND BEVACIZUMAB (mPEBev regimen) | |||||||||||||
| Medical condition: Patients with UNOPERABLE NON NON SQUAMOUS NON SMALL CELL LUNG CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-018324-13 | Sponsor Protocol Number: CRLOT/01 | Start Date*: 2011-11-09 | |||||||||||
| Sponsor Name:CONSORZIO PER LA RICERCA ONCOLOGICA | |||||||||||||
| Full Title: Open phase II randomized study to assess safety, tolerability and efficacy of trastuzumab combined with vinorelbine in patients with HER2 positive metastatic breast cancer and cardiac diseases | |||||||||||||
| Medical condition: HER2 positive breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-005215-29 | Sponsor Protocol Number: 03-CoFactor | Start Date*: 2005-06-03 | |||||||||||
| Sponsor Name:ADVENTRX Pharmaceuticals Inc | |||||||||||||
| Full Title: A Multi-Center, Open Label, Parallel Group, Randomised, Phase IIB Clinical Trial to Evaluate the Safety and Efficacy of CoFactor and 5-FU versus Leucovorin and 5-FU in Subjects with Metastatic Colo... | |||||||||||||
| Medical condition: Metastatic Colorectal Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-000686-19 | Sponsor Protocol Number: MO05/6844 | Start Date*: 2005-04-28 |
| Sponsor Name:University of Leeds | ||
| Full Title: PACT (Patient Preferences in Adjuvant Colorectal Cancer Therapy) - A randomised crossover clinical trial comparing Bolus Fluorouracil/Leucovorin to Capecitabine as treatment for moderate to high ri... | ||
| Medical condition: Moderate to high risk resected colorectal cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-009461-33 | Sponsor Protocol Number: AV-IT-001 | Start Date*: 2009-06-04 | |||||||||||
| Sponsor Name:AISAR ASSOCIAZIONE ITALIANA PER LO STUDIO DEGLI ANTIMICROBICI E DELLE RESISTENZE | |||||||||||||
| Full Title: A Phase IIa, Open-Label, Dose-Escalating Study to Evaluate the Safety of AV-951 in Combination with Everolimus in Subjects with Metastatic Renal Cell Carcinoma | |||||||||||||
| Medical condition: Metastatic Renal Cell Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-009194-99 | Sponsor Protocol Number: 2008002 | Start Date*: 2009-07-15 |
| Sponsor Name:Agensys Inc | ||
| Full Title: A Global, Multi-center, Open-label, Phase 2 Study of AGS-1C4D4 Given in Combination With Gemcitabine in Subjects with Metastatic Pancreatic Cancer ?Estudio global, multicéntrico, abierto, de fase ... | ||
| Medical condition: Metastatic Pancreatic Cancer. To evaluate AGS-1C4D4 administered in combination with gemcitabine as measured by the survival rate at 6 months post-randomization Cancer de páncreas metástasico. Eva... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-003478-29 | Sponsor Protocol Number: VIDAFACT | Start Date*: 2014-03-21 |
| Sponsor Name:Maria Nabal Vicuña (Paliative Care Supportive Team-Hospital Universitari Arnau de Vilanova de Lleida) | ||
| Full Title: The effect on quality of life of Vitamin D administration for advanced cancer treatment. A randomized controlled trial | ||
| Medical condition: The effect on quality of life of Vitamin D administration for advanced cancer treatment. A randomized controlled trial | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003760-47 | Sponsor Protocol Number: 2018-14 | Start Date*: 2020-04-06 |
| Sponsor Name:Assistance Publique Hôpitaux de Marseille | ||
| Full Title: Evaluation of 68Ga-PSMA PET-CT in the initial extension assessment of advanced renal cell carcinoma a prospective, multicenter, open study | ||
| Medical condition: renal cell cancer (RCC) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-005605-36 | Sponsor Protocol Number: SCI-Ta1-NSCLC-CHEMOP2-001 | Start Date*: 2016-07-07 | |||||||||||
| Sponsor Name:SCICLONE PHARMACEUTICALS ITALY S.R.L. | |||||||||||||
| Full Title: Thymosin alpha 1 plus maintenance therapy with the Standard of Care (SoC) chemotherapy plus cisplatin (or carboplatin) in patients with metastatic Non-Small Cell Lung Cancer (NSCLC), EGFR wild type | |||||||||||||
| Medical condition: metastatic Non-Small Cell Lung Cancer (NSCLC), EGFR wild type | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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