- Trials with a EudraCT protocol (1,850)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
1,850 result(s) found for: Breast cancer.
Displaying page 7 of 93.
EudraCT Number: 2017-002930-22 | Sponsor Protocol Number: IOM-050371 | Start Date*: 2018-02-14 | ||||||||||||||||||||||||||
Sponsor Name:iOMEDICO AG | ||||||||||||||||||||||||||||
Full Title: A randomized, open-label, multicenter, two-arm, phase III study to evaluate efficacy and quality of life in patients with metastatic hormone receptor-positive HER2-negative breast cancer receiving ... | ||||||||||||||||||||||||||||
Medical condition: The study will include adult women with HR-positive, HER2-negative advanced breast cancer with visceral metastases, who received no prior therapy for advanced disease. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001949-34 | Sponsor Protocol Number: E7389-G000-305 | Start Date*: 2006-10-02 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Phase III Open Label, Randomized Parallel Two-Arm Multi Center Study of E7389 versus ‘Treatment of Physician’s Choice’ in Patients with Locally Recurrent or Metastatic Breast Cancer, Previously T... | |||||||||||||
Medical condition: Locally recurrent or metastatic breast cancer after failure of multiple prior chemotherapy regimens | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) DE (Completed) GB (Completed) CZ (Completed) FR (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004100-35 | Sponsor Protocol Number: GBG102-SASCIA | Start Date*: 2020-10-09 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GBG Forschungs GmbH | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Phase III postneoadjuvant study evaluating Sacituzumab Govitecan, an Antibody Drug Conjugate in primary HER2-negative breast cancer patients with high relapse risk after standard neoadjuvant treat... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: HER2-negative breast cancer patients with high relapse risk after standard neoadjuvant treatment | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) IE (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) AT (Trial now transitioned) IT (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017671-22 | Sponsor Protocol Number: E7389-G000-398 | Start Date*: 2010-07-15 | ||||||||||||||||
Sponsor Name:Eisai Limited | ||||||||||||||||||
Full Title: An Open-Label, Multi-Center, Expanded Access Program With Eribulin for the Treatment of Advanced Breast Cancer Refractory to All Other Commercially Available Therapies | ||||||||||||||||||
Medical condition: Advanced and/or metastatic breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002714-72 | Sponsor Protocol Number: GBG89 | Start Date*: 2016-03-08 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GBG Forschungs GmbH | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomized phase II study to investigate the addition of PD-L1 antibody MEDI4736 to a taxane-anthracycline containing chemotherapy in triple negative breast cancer. (GeparNuevo) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with triple negative, early breast cancer | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002080-25 | Sponsor Protocol Number: NBG-19-01 | Start Date*: 2019-06-26 | |||||||||||
Sponsor Name:Skåne University Hospital | |||||||||||||
Full Title: A TRANSLATIONAL RANDOMIZED PHASE III STUDY EXPLORING THE EFFECT OF THE ADDITION OF CAPECITABINE TO CARBOPLATINUM BASED CHEMOTHERAPY IN EARLY “TRIPLE NEGATIVE” BREAST CANCER. | |||||||||||||
Medical condition: Early triple negative breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004848-23 | Sponsor Protocol Number: 89/2006/O/Sper | Start Date*: 2006-09-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Sequential Oral Therapy (SOT trial) in elderly patients with metastatic breast cancer: a phase IV randomized trial | |||||||||||||
Medical condition: breast cancer | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007057-12 | Sponsor Protocol Number: ML21846 | Start Date*: 2009-04-06 | ||||||||||||||||
Sponsor Name:ROCHE | ||||||||||||||||||
Full Title: A Randomized open label study of the effect of first line combination treatment with Avastin (bevacizumab) plus paclitaxel and gemcitabine Compared With Avastin (bevacizumab) plus paclitaxel on... | ||||||||||||||||||
Medical condition: Metastatic breast cancer, HER2-negative patients who have not received prior chemotherapy for mBC | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004220-34 | Sponsor Protocol Number: TNPET01 | Start Date*: 2012-01-19 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: A randomised phase II trial of [18F]fluorothymidine and the standard tracer [18F]Fluorodeoxyglucose in the assessment of systemic therapy response in triple negative breast cancer and their utility... | |||||||||||||
Medical condition: Triple Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006381-29 | Sponsor Protocol Number: EXPRESSION | Start Date*: 2009-11-12 | ||||||||||||||||||||||||||
Sponsor Name:Universitätsmedizin Mainz | ||||||||||||||||||||||||||||
Full Title: Neoadjuvant, sequential chemotherapy with docetaxel followed by Fluorouracil, Epirubicin, and Cyclophosphamid every 3 weeks - genome wide expression analysis for identification of a predictive gene... | ||||||||||||||||||||||||||||
Medical condition: Eligible will be only females between 18 - 70 years of age, suffering from histologically confirmed primary breast cancer, nodal status positive or negative, phase cT2, cT3, or cT4 including inflam... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000418-31 | Sponsor Protocol Number: IKP275 | Start Date*: 2019-04-01 | ||||||||||||||||||||||||||
Sponsor Name:Robert Bosch Gesellschaft für medizinische Forschung mbH | ||||||||||||||||||||||||||||
Full Title: GENOTYPE AND PHENOTYPE GUIDED SUPPLEMENTATION OF TAMOXIFEN STANDARD THERAPY WITH ENDOXIFEN IN BREAST CANCER PATIENTS. | ||||||||||||||||||||||||||||
Medical condition: Patients with ductal carcinoma in situ (DCIS) or early stage breast cancer. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001889-14 | Sponsor Protocol Number: Bubble2012 | Start Date*: 2012-10-15 | ||||||||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | ||||||||||||||||||
Full Title: MicroBubble detection and Ultrasound guided Biopsy of axillary Lymph nodes in patients with Early breast cancer. | ||||||||||||||||||
Medical condition: Diagnosis of lymph node metastases in patients with newly diagnosed breast cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021587-15 | Sponsor Protocol Number: ICORG10-04NSABP-B46I | Start Date*: 2010-09-08 | |||||||||||
Sponsor Name:ICORG | |||||||||||||
Full Title: A Phase III Clinical Trial Comparing TC to TAC for Women with Node-Positive or High-Risk Node-Negative, HER2-Negative Breast Cancer | |||||||||||||
Medical condition: Adjuvant Breast Cancer: Node positive or high risk node negative and HER 2 negative | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003992-35 | Sponsor Protocol Number: MREC02/8/71 | Start Date*: 2009-12-16 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: International Breast Cancer Intervention Study II (DCIS). An international multi-centre trial of tamoxifen v anastrozole in post-menopausal women with ductal carcinoma in situ. | |||||||||||||
Medical condition: Ductal carcinoma in situ | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001545-42 | Sponsor Protocol Number: B9E-IT-S376 | Start Date*: 2005-07-13 | |||||||||||
Sponsor Name:ELI LILLY | |||||||||||||
Full Title: A Randomized Phase III Trial of Gemcitabine and Docetaxel versus Gemcitabine and Paclitaxel in Patients with Metastatic Breast Cancer: a comparison of different schedules | |||||||||||||
Medical condition: Metatstatic breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016062-82 | Sponsor Protocol Number: ML22373 | Start Date*: 2009-11-23 | ||||||||||||||||
Sponsor Name:SOUTH EASTERN EUROPEAN RESEARCH ONCOLOGY GROUP | ||||||||||||||||||
Full Title: Phase II clinical study of bevacizumab in combination with capecitabine as first-line treatment in elderly patients with metastatic breast cancer | ||||||||||||||||||
Medical condition: Metastatic or locally recurrent HER2-negative breast cancer | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001456-36 | Sponsor Protocol Number: EGF100151 | Start Date*: 2004-09-06 | |||||||||||
Sponsor Name:GLAXO SMITHKLINE | |||||||||||||
Full Title: A phase III, randomized, open-label, multicenter study comparing GW572016 and Capecitabile (Xeloda) versus Capecitabile in women with refractory advanced or metastatic breast cancer. | |||||||||||||
Medical condition: Solid tumor treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004989-23 | Sponsor Protocol Number: G200901 | Start Date*: 2015-08-20 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:GTx, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 2 Open Label, Multi-Center, Multinational Study Investigating The Efficacy and Safety Of GTx-024 On Advanced, Androgen Receptor-Positive Triple Negative Breast Cancer (AR+ TNBC) | ||||||||||||||||||||||||||||||||||||||
Medical condition: Androgen Receptor-Positive Triple Negative Breast Cancer (AR+ TNBC) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: LT (Completed) GB (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-006168-71 | Sponsor Protocol Number: SF2- Gem/tax | Start Date*: 2006-02-16 | |||||||||||
Sponsor Name:A.S.L. 2 | |||||||||||||
Full Title: Phase II study with gemcitabine/docetaxel first line in women with metastatic breast cancer | |||||||||||||
Medical condition: oncological patients only | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005683-87 | Sponsor Protocol Number: VNBCAPTAX | Start Date*: 2006-02-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. LUIGI GONZAGA | |||||||||||||
Full Title: VINORELBINA CAPECITABIME PACLITAXEL AS FIRST LINE THERAPY IN ADVANCED BREAST CANCER PATIENTS PRETREATED WITH ADJUVANT ANTHRACYCLINES | |||||||||||||
Medical condition: METASTATIC BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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