- Trials with a EudraCT protocol (10,211)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10,211 result(s) found for: Cancer.
Displaying page 22 of 511.
EudraCT Number: 2005-003929-22 | Sponsor Protocol Number: ICON7 | Start Date*: 2006-12-15 | |||||||||||
Sponsor Name:Medical Research Council | |||||||||||||
Full Title: ICON7 - A randomised, two-arm, multicentre Gynaecologic Cancer InterGroup trial of adding bevacizumab to standard chemotherapy (carboplatin and paclitaxel) in patients with epithelial ovarian cancer. | |||||||||||||
Medical condition: Following initial surgery (either debulking cytoreductive surgery or a biopsy if the patient has FIGO stage IV disease and there is no planned surgery before disease progression) patients with new... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) FI (Completed) DE (Completed) DK (Completed) SE (Completed) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024631-16 | Sponsor Protocol Number: EFC10260 | Start Date*: 2011-04-26 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Phase 2, Multi-Center, Double-Blind, placebo controlled, Randomized Study of Ombrabulin in Patients with Platinum-Sensitive Recurrent Ovarian Cancer treated with Carboplatin/Paclitaxel | |||||||||||||
Medical condition: Ovarian Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) CZ (Prematurely Ended) PL (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013838-25 | Sponsor Protocol Number: IMCLCP11-0806 | Start Date*: 2009-10-21 | |||||||||||
Sponsor Name:ImClone LLC | |||||||||||||
Full Title: A Randomized, Multicenter, Open-Label, Phase 3 Study of Gemcitabine-Cisplatin Chemotherapy Plus Necitumumab (IMC-11F8) Versus Gemcitabine-Cisplatin Chemotherapy Alone in the First-Line Treatment of... | |||||||||||||
Medical condition: Advanced squamous non small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) DE (Completed) HU (Completed) PT (Completed) ES (Ongoing) GR (Ongoing) SK (Completed) IT (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001943-21 | Sponsor Protocol Number: IFG-08-2019 | Start Date*: 2021-05-14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Institut für Frauengesundheit GmbH | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: NeoOn – Neoadjuvant treatment of Ontruzant® (SB3) in patients with HER2-positive early breast cancer: An open-label, multicenter, phase IV study | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Female patients with early HER2positive breast cancer, neoadjuvantly treated. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020408-31 | Sponsor Protocol Number: I2I-MC-JMMG | Start Date*: 2010-11-10 | ||||||||||||||||
Sponsor Name:Eli Lilly and Company | ||||||||||||||||||
Full Title: A Phase 1/Randomized Phase 2 Study to Evaluate LY2603618 in Combination with Pemetrexed and Cisplatin in Patients with Stage IV Non-small Cell Lung Cancer | ||||||||||||||||||
Medical condition: • Histological diagnosis of Stage IV NSCLC other than predominantly squamous cell histology. • Mesothelioma in advanced or metastatic stage for whom the combination with pemetrexed and cisplatin i... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024046-29 | Sponsor Protocol Number: GEP 11/1010 | Start Date*: 2013-05-28 | |||||||||||
Sponsor Name:FNCLCC | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000703-40 | Sponsor Protocol Number: KFE10.08 | Start Date*: 2011-06-24 | ||||||||||||||||||||||||||
Sponsor Name:Odense University Hospital | ||||||||||||||||||||||||||||
Full Title: Clinical trial with chemotherapy for patients with non-resectable, locally advanced pancreatic cancer and addition of chemo-radiotherapy for patients with borderline resectable pancreatic cancer. ... | ||||||||||||||||||||||||||||
Medical condition: Patients with non-resectable or resectable pancreatic cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020664-38 | Sponsor Protocol Number: HE 21/10 | Start Date*: 2010-09-28 | |||||||||||
Sponsor Name:Hellenic Cooperative Oncology Group | |||||||||||||
Full Title: Efficacy and safety of Bevacizumab/Temsirolimus combination after first-line Bevacizumab/IFN combination in advanced renal cell carcinoma | |||||||||||||
Medical condition: Advanced renal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003939-30 | Sponsor Protocol Number: CA209-142 | Start Date*: 2014-03-21 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 2 Clinical Trial of Nivolumab and Nivolumab Plus Ipilimumab in Recurrent and Metastatic Microsatellite High (MSI-H) Colon Cancer | |||||||||||||
Medical condition: MSI Positive Colorectal Cancer MSI Negative Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) BE (Trial now transitioned) IE (Completed) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000559-15 | Sponsor Protocol Number: FB2012 | Start Date*: 2012-09-14 |
Sponsor Name:FinnBladder | ||
Full Title: TREATMENT OF Ta BLADDER CANCER WITH HIGH RISK OF RECURRENCE – FLUORESCENCE CYSTOSCOPY WITH OPTIMIZED ADJUVANT MITOMYCIN-C | ||
Medical condition: bladder cancer (non-invasive Ta urothelial bladder cancer) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000366-36 | Sponsor Protocol Number: TLK286.3025 | Start Date*: 2006-06-07 | |||||||||||
Sponsor Name:Telik, Inc. | |||||||||||||
Full Title: Phase 3 randomized study of TLK286 (Telcyta™) in combination with liposomal doxorubicin (Doxil®/Caelyx®) versus liposomal doxorubicin (Doxil®/Caelyx®) as second-line therapy in platinum refractory ... | |||||||||||||
Medical condition: platinum refractory or resistant ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005782-59 | Sponsor Protocol Number: 08/0136 | Start Date*: 2010-09-29 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: ARISTOTLE - A phase III trial comparing standard versus novel CRT as pre-operative treatment for MRI defined locally advanced rectal cancer. | ||||||||||||||||||
Medical condition: Locally advanced rectal 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: 2017-000490-36 | Sponsor Protocol Number: CHUBX2016/38 | Start Date*: 2018-02-19 | ||||||||||||||||
Sponsor Name:CHU de Bordeaux | ||||||||||||||||||
Full Title: Etude monocentrique, exploratoire, comparant la TEP/TDM au 68Ga-RM2 à la TEP/TDM au 68Ga-PSMA-617 chez des patients atteints de cancers de la prostate de différents risques métastatiques, candidats... | ||||||||||||||||||
Medical condition: Prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001603-32 | Sponsor Protocol Number: iOM-04318 | Start Date*: 2016-06-14 | |||||||||||||||||||||
Sponsor Name:iOMEDICO AG | |||||||||||||||||||||||
Full Title: An open-label, multi-center, sINGlE arm clinical study to evaluate treatment efficacy and quality of life in women with hormone-receptor-positive, HER2-negative loco-regionally recurrent or metast... | |||||||||||||||||||||||
Medical condition: The study population includes postmenopausal patients with advanced (locally recurrent, inoperable and/or metastatic), HR+, HER2- breast cancer. For peri-/premenopausal patients, endocrine therapy ... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003057-42 | Sponsor Protocol Number: CAO/ARO/AIO-16 | Start Date*: 2018-02-23 | ||||||||||||||||
Sponsor Name:Univeristy Hospital Tuebingen | ||||||||||||||||||
Full Title: Organ preservation in locally advanced rectal cancer by radiochemotherapy followed by consolidation chemotherapy. A prospective phase II pilot trial of the German Rectal Cancer Study Group | ||||||||||||||||||
Medical condition: Locally advanced rectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001219-22 | Sponsor Protocol Number: SGNTV-002 | Start Date*: 2019-10-25 | |||||||||||||||||||||
Sponsor Name:Seattle Genetics, Inc. | |||||||||||||||||||||||
Full Title: Open Label Phase 2 Study of Tisotumab Vedotin for Patients with Platinum-Resistant Ovarian Cancer with a Safety Run-in of a Dose-Dense Regimen | |||||||||||||||||||||||
Medical condition: Patients with epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer (hereafter collectively referred to as platinum-resistant ovarian cancer and abbreviated as PROC) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) IE (Prematurely Ended) BE (Completed) DK (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003300-23 | Sponsor Protocol Number: EMR100070-007 | Start Date*: 2016-06-13 | |||||||||||||||||||||||||||||||
Sponsor Name:Merck KGaA | |||||||||||||||||||||||||||||||||
Full Title: A Phase III open-label, multicenter trial of maintenance therapy with avelumab (MSB0010718C) versus continuation of first-line chemotherapy in subjects with unresectable, locally advanced or metas... | |||||||||||||||||||||||||||||||||
Medical condition: Advanced (unresectable, locally advanced or metastatic) adenocarcinoma of the stomach, or of the gastro-esophageal junction (GEJ) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) HU (Completed) RO (Completed) DE (Completed) ES (Completed) FR (Completed) IT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-002708-33 | Sponsor Protocol Number: POP 01 | Start Date*: 2007-07-19 | |||||||||||
Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | |||||||||||||
Full Title: RANDOMIZED PHASE III TRIAL OF PREOPERATIVE VERSUS POSTOPERATIVE CHEMOTHERAPY WITH CISPLATIN AND GEMCITABINE IN STAGE IB-IIIA NON-SMALL CELL LUNG CANCER NSCLC | |||||||||||||
Medical condition: Neoadjuvant treatmento for early stage non small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010079-25 | Sponsor Protocol Number: LPC-002 | Start Date*: 2009-05-11 | |||||||||||
Sponsor Name:LIDDS AB | |||||||||||||
Full Title: An open, single and multiple dose, efficacy and safety Proof of Principle study of Liproca® Depot, a controlled release formulation of 2-hydroxyflutamide, injected into the prostate in patients wi... | |||||||||||||
Medical condition: prostate cancer (T1-T2), Gleason ≤ 3+4 at the time of diagnose in prostate biopsy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004503-23 | Sponsor Protocol Number: CS-2015-1 | Start Date*: 2015-12-17 | |||||||||||
Sponsor Name:Rigshospitalet, Department of Clinical Physiology, Nucelar Medicine and PET | |||||||||||||
Full Title: Phase II trial: uPAR-PET for preoperative staging of breast cancer patients | |||||||||||||
Medical condition: breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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