- Trials with a EudraCT protocol (2,264)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,264 result(s) found for: Cancer incidence.
Displaying page 1 of 114.
EudraCT Number: 2020-003890-23 | Sponsor Protocol Number: Cisplatin | Start Date*: 2021-02-23 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: The nephroprotective effect of short hydration during cisplatin treatment in head and neck cancer patients. | ||
Medical condition: Cisplatin induced nephrotoxicity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002407-25 | Sponsor Protocol Number: 16996 | Start Date*: 2014-11-25 | |||||||||||||||||||||
Sponsor Name:Bayer AG | |||||||||||||||||||||||
Full Title: A Phase 4 long-term follow-up study to define the safety profile of radium-223 dichloride | |||||||||||||||||||||||
Medical condition: Castrate Resistant Prostate Cancer/Hormone-Refractory Prostate Cancer, breast cancer or multiple myeloma patients with bone metastasis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) ES (Completed) FR (Completed) BE (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) FI (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000661-20 | Sponsor Protocol Number: ICO | Start Date*: 2019-05-31 |
Sponsor Name:Vilnius University Hospital Santaros klinikos | ||
Full Title: Ivabradine to prevent anthracycline-induced cardiotoxicity: a prospective randomized open label clinical trial. | ||
Medical condition: Cancers treated with anthracyclines: leukemias, limphomas, breast, stomach, uterine, ovarian, lung. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-010260-41 | Sponsor Protocol Number: IEO S462/109 | Start Date*: 2009-11-13 |
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | ||
Full Title: Breast cancer prevention with fenretinide in young women at genetic and familial risk. A phase III randomized clinical trial | ||
Medical condition: prevention in patients with high risk for breast cancer | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001559-38 | Sponsor Protocol Number: GEICAM/2018-06 | Start Date*: 2022-01-20 | ||||||||||||||||
Sponsor Name:GEICAM (Fundación Grupo Español de Investigación en Cáncer de Mama) | ||||||||||||||||||
Full Title: A Randomized Phase II Study to Evaluate the Incidence of Discontinuations due to Diarrhoea at 3 Cycles in patients with Early-stage HER2-positive (HER2+), Hormone Receptor-positive (HR+) Breast Can... | ||||||||||||||||||
Medical condition: HER2+, HR+ Early stage Breast Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001191-30 | Sponsor Protocol Number: IISR-2015-101127 | Start Date*: 2017-04-25 | |||||||||||
Sponsor Name:Department of Obstetrics & Gynecology, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: Use of TachoSil® for the prevention of postoperative complications after groin dissection in vulva cancer patients | |||||||||||||
Medical condition: Vulva cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003115-34 | Sponsor Protocol Number: V1 | Start Date*: 2012-06-06 |
Sponsor Name:Medizinische Universität Wien | ||
Full Title: A Collagen-Fibrin Patch (Tachosil®) for the Prevention of Symptomatic Lymphoceles after Pelvic Lymphadenectomy in Women with Gynecologic Malignancies: a Randomized Clinical Trial | ||
Medical condition: endometrial cancer, cervical cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002668-32 | Sponsor Protocol Number: OAS-07OVA | Start Date*: 2009-04-16 | |||||||||||||||||||||
Sponsor Name:Oasmia Pharmaceutical AB | |||||||||||||||||||||||
Full Title: An Open, Randomized, Multicenter Study in Patients with Recurrent Epithelial Ovarian Cancer, Primary Peritoneal Cancer or Fallopian Tube Cancer to Compare the Efficacy and Safety of paclitaxel (mic... | |||||||||||||||||||||||
Medical condition: Histological or cytological confirmed epithelial ovarian cancer, primary peritoneal cancer or fallopian tube cancer. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) BE (Completed) CZ (Completed) HU (Completed) LV (Completed) SK (Completed) LT (Completed) DK (Completed) BG (Completed) FI (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-004438-25 | Sponsor Protocol Number: 20060342 | Start Date*: 2008-10-21 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo Controlled, Phase 2 Trial of Paclitaxel in Combination With AMG 386 in Subjects With Advanced Recurrent Epithelial Ovarian or Primary Peritoneal Cancer | |||||||||||||
Medical condition: Advanced Recurrent Epithelial Ovarian or Primary Peritoneal Cance | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001908-38 | Sponsor Protocol Number: R5093-ONC-1863 | Start Date*: 2020-09-28 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A PHASE 1/2 STUDY OF REGN5093 IN PATIENTS WITH MET-ALTERED ADVANCED NON-SMALL CELL LUNG CANCER | |||||||||||||
Medical condition: Non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001755-45 | Sponsor Protocol Number: OX4325 | Start Date*: 2016-09-12 | |||||||||||||||||||||
Sponsor Name:Mateon Therapeutics, Inc. | |||||||||||||||||||||||
Full Title: FOCUS: A Multicenter, Multinational, Double-blind, 2-Arm, Randomized, Phase 2/3, Study of Physician’s Choice Chemotherapy (PCC) (Weekly Paclitaxel or Pegylated Liposomal Doxorubicin [PLD]) Plus Bev... | |||||||||||||||||||||||
Medical condition: Platinum-resistant, recurrent, epithelial ovarian, primary peritoneal or fallopian tube cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017946-30 | Sponsor Protocol Number: 20060517 | Start Date*: 2011-01-19 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind Trial of Pegylated Liposomal Doxorubicin (PLD) Plus AMG 386 or Placebo in Women With Recurrent Partially Platinum Sensitive or Resistant Epithelial Ovarian, Prim... | |||||||||||||
Medical condition: Recurrent partially platinum sensitive or resistant epithelial ovarian, primary peritoneal, or fallopian tube cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) SK (Completed) AT (Prematurely Ended) BE (Completed) IT (Completed) DK (Completed) DE (Completed) PL (Completed) GR (Completed) LV (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001965-98 | Sponsor Protocol Number: PGFN-001 | Start Date*: 2017-01-10 | |||||||||||
Sponsor Name:Prolong Pharmaceuticals, LLC | |||||||||||||
Full Title: A randomized and open-label dose-finding, phase 2, efficacy, safety, and pharmacokinetic study of once-per-cycle prophylactic injections of ANF-RHO™ versus pegfilgrastim (Neulasta®) in non-metastat... | |||||||||||||
Medical condition: chemotherapy-induced neutropenia (CIN) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024468-16 | Sponsor Protocol Number: BO25460 | Start Date*: 2011-06-29 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled Phase III study of first-line maintenance Tarceva vs Tarceva at the time of disease progression in patients with advanced non-small cell lung cancer (... | ||||||||||||||||||
Medical condition: Advanced (Stage IIIB or IV) NSCLC previously treated with 4 cycles of a platinum-based chemotherapy (for Traceva®). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) HU (Completed) CZ (Completed) LV (Completed) LT (Completed) NL (Completed) FR (Completed) BG (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002910-37 | Sponsor Protocol Number: TEA | Start Date*: 2019-10-07 |
Sponsor Name:Erasmus MC | ||
Full Title: Study on the pharmacokinetic interaction between green tea and tamoxifen in patients with breast cancer. “the TEA study” | ||
Medical condition: Breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002853-11 | Sponsor Protocol Number: GO42501 | Start Date*: 2022-04-04 | |||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||
Full Title: A PHASE II, OPEN-LABEL, MULTICENTER STUDY EVALUATING THE SAFETY AND EFFICACY OF NEOADJUVANT AND ADJUVANT TIRAGOLUMAB PLUS ATEZOLIZUMAB, WITH OR WITHOUT PLATINUM-BASED CHEMOTHERAPY, IN PATIENTS WITH... | |||||||||||||||||||||||
Medical condition: Non-Small Cell Lung Cancer. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) PL (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022810-26 | Sponsor Protocol Number: PERCAT01 Version 10, 31.01.2011 | Start Date*: 2011-03-16 | |||||||||||||||||||||
Sponsor Name:University Witten/Herdecke | |||||||||||||||||||||||
Full Title: MULTICENTER, OPEN-LABEL PHASE II STUDY TO EVALUATE THE EFFICACY OF A 2-CYCLE IMMUNOTHERAPY WITH THE TRI FUNCTIONAL BISPECIFIC ANTIBODY CATUMAXOMAB (ANTI EPCAM X ANTI-CD3) IN ADDITION TO SYSTEMIC CH... | |||||||||||||||||||||||
Medical condition: PERITONEAL CARCINOMATOSIS FROM GASTRIC OR COLORECTAL ADENOCARCINOMA | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005479-42 | Sponsor Protocol Number: A301226 | Start Date*: 2014-06-04 | ||||||||||||||||
Sponsor Name:Erasmus MC, Dept. Urology | ||||||||||||||||||
Full Title: Pilot study: Toxicity of oestradiol for adjuvant endocrine therapy in locally confined prostate cancer | ||||||||||||||||||
Medical condition: Prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011899-30 | Sponsor Protocol Number: 20080259 | Start Date*: 2009-12-18 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study of Pegfilgrastim Administered to Subjects With Newly Diagnosed, Locally-advanced or Metastatic Colorectal Cancer Treated With Bevacizum... | |||||||||||||
Medical condition: Locally-advanced or Metastatic Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) HU (Completed) CZ (Completed) BE (Completed) IE (Completed) IT (Completed) FR (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003078-21 | Sponsor Protocol Number: XTX202-01/02-001 | Start Date*: 2023-03-28 | |||||||||||||||||||||||||||||||
Sponsor Name:Xilio Development, Inc | |||||||||||||||||||||||||||||||||
Full Title: A First-in-Human, Multicenter, Phase 1/2, Open-Label Study of XTX202 in Patients with Advanced Solid Tumors | |||||||||||||||||||||||||||||||||
Medical condition: Advanced solid tumors | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: HU (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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