- Trials with a EudraCT protocol (655)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
655 result(s) found for: Breast biopsy.
Displaying page 6 of 33.
| EudraCT Number: 2012-003507-35 | Sponsor Protocol Number: AV-951-12-204 | Start Date*: 2013-05-20 | ||||||||||||||||
| Sponsor Name:AVEO Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled, 2-Arm, Multi-Center Study Comparing Tivozanib Hydrochloride In Combination With Paclitaxel Versus Placebo In Combination With Paclitaxel in t... | ||||||||||||||||||
| Medical condition: Locally recurrent and/or metastatic triple negative breast cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-006542-34 | Sponsor Protocol Number: PR3076 | Start Date*: 2007-01-08 |
| Sponsor Name:Pantarhei Bioscience B.V. | ||
| Full Title: Preoperative hormone therapy for pre- and postmenopausal women with ER positive breast cancer: A double blind randomized parallel group phase II trial, comparing the effect of 2 weeks of preoperati... | ||
| Medical condition: breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001938-35 | Sponsor Protocol Number: IFG-06-2019 | Start Date*: 2020-10-02 | |||||||||||
| Sponsor Name:Institut für Frauengesundheit GmbH | |||||||||||||
| Full Title: AIRE: – ASSESSING IMMUNORESPONSE POST ERIBULIN: ERIBULIN AND IMMUNOGENICITY IN ADVANCED BREAST CANCER – A PROSPECTIVELY RANDOMIZED PHASE IV STUDY | |||||||||||||
| Medical condition: Female patients diagnosed with HER2 negative advanced breast cancer, which had received at least one previous chemotherapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-003865-39 | Sponsor Protocol Number: WSG-AM12 | Start Date*: 2023-05-04 | ||||||||||||||||
| Sponsor Name:Westdeutsche Studiengruppe GmbH | ||||||||||||||||||
| Full Title: NeoAdjuvant Dynamic marker - Adjusted Personalized Therapy comparing trastuzumab-deruxtecan versus pacli-/docetaxel+carboplatin+trastuzumab+pertuzumab in HER2+ early breast cancer | ||||||||||||||||||
| Medical condition: HER2+ early breast cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-003996-37 | Sponsor Protocol Number: WSG-AM09 | Start Date*: 2019-12-10 | ||||||||||||||||
| Sponsor Name:Westdeutsche Studiengruppe GmbH (WSG) | ||||||||||||||||||
| Full Title: A prospective, multicenter, open label, neoadjuvant phase II single arm study with pembrolizumab in combination with dual anti-HER2 blockade with trastuzumab and pertuzumab in early breast cancer p... | ||||||||||||||||||
| Medical condition: HER 2+/HR+ and HR- early breast cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-004188-30 | Sponsor Protocol Number: M18BEL | Start Date*: 2019-04-23 | ||||||||||||||||||||||||||
| Sponsor Name:NKI-AVL | ||||||||||||||||||||||||||||
| Full Title: Pre-operative phase II trial for breast cancer with nivolumab in combination with novel IO | ||||||||||||||||||||||||||||
| Medical condition: | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2009-011878-15 | Sponsor Protocol Number: 3160A6-2208-WW | Start Date*: 2009-08-14 | |||||||||||
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc | |||||||||||||
| Full Title: A phase 1/2, open-label study of bosutinib administered in combination with capecitabine in subjects with solid tumor and ErbB2 negative locally advanced or metastatic breast cancer. | |||||||||||||
| Medical condition: Solid tumor and ErbB2 negative locally advanced or metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) ES (Completed) BE (Completed) FR (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002135-33 | Sponsor Protocol Number: MRFF01 | Start Date*: 2008-06-16 |
| Sponsor Name:University Hospital Antwerp | ||
| Full Title: Is it possible to detect a fibrotic focus in a carcinoma with MR mammography with Gadovist 1.0 followed by core biopsy? | ||
| Medical condition: breast carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-004770-10 | Sponsor Protocol Number: IBCSG_45-13/BIG_4-13 | Start Date*: 2014-09-23 | |||||||||||
| Sponsor Name:International Breast Cancer Study Group (IBCSG) | |||||||||||||
| Full Title: A phase Ib/II trial evaluating the efficacy of MK-3475 and trastuzumab in patients with trastuzumab-resistant, HER2-positive metastatic breast cancers | |||||||||||||
| Medical condition: Patients with HER2-positive, PD-L1 expressing, unresectable locoregional or metastatic breast carcinoma which has progressed on prior trastuzumab-based therapy. A parallel cohort of 15 patients wi... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) IT (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005048-19 | Sponsor Protocol Number: IEO S268/505 | Start Date*: 2006-04-10 | |||||||||||
| Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
| Full Title: A phase II randomised study to investigate the effects of Bevacizumab on cell proliferation and on pCR in patients with locally advanced operable breast cancer | |||||||||||||
| Medical condition: histologically proven primary breast cancer 2.0 cm, T2-T3 T4 a-d, N0-2, M0 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003036-31 | Sponsor Protocol Number: 01B | Start Date*: 2012-03-20 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA CAREGGI | |||||||||||||
| Full Title: Ministry of health integrated oncological program n°5/2006: 18F-Fluorometilcholine (18FFCH) PET/CT sensibility in diagnosis of breast cancer metastasis | |||||||||||||
| Medical condition: de novo breast cancer metastasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-002914-10 | Sponsor Protocol Number: 66856 | Start Date*: 2019-09-16 |
| Sponsor Name:Erasmus MC Cancer Institute | ||
| Full Title: FUnctional selection of advanced breast cancer patients for Talazoparib treatment Using the REpair Capacity (RECAP) test: The FUTURE trial | ||
| Medical condition: Advanced or metastatic breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-003098-17 | Sponsor Protocol Number: SOLTI-1402 | Start Date*: 2017-03-29 |
| Sponsor Name:SOLTI | ||
| Full Title: CORALLEEN: A Phase 2 Clinical Trial of multi-agent Chemotherapy or letrozole plus Ribociclib (LEE001) as neoadjuvant treatment for postmenopausal patients with Luminal B/HER2-negative breast cancer. | ||
| Medical condition: Luminal B/HER2-negative breast cancer. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-006161-84 | Sponsor Protocol Number: Version 2.1 | Start Date*: 2009-06-17 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: ARTiST - Aromasin Randomised Trial +/- Sutent as neoadjuvant Therapy for post-menopausal women with breast cancer. | |||||||||||||
| Medical condition: Breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000809-12 | Sponsor Protocol Number: PREDIXLumA | Start Date*: 2014-11-17 | ||||||||||||||||||||||||||
| Sponsor Name:Karolinska University Hospital | ||||||||||||||||||||||||||||
| Full Title: PREDIX Luminal A - Neoadjuvant response-guided treatment of slowly proliferating hormone receptor positive tumors. Part of a set of translational phase II trials based on molecular subtypes | ||||||||||||||||||||||||||||
| Medical condition: Primary breast cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2017-000508-92 | Sponsor Protocol Number: ICR-CTSU/2016/10058 | Start Date*: 2017-06-14 | |||||||||||
| Sponsor Name:The Institute of Cancer Research | |||||||||||||
| Full Title: c-TRAK TN: A clinical trial utilising ctDNA mutation tracking to detect minimal residual disease and trigger intervention in patients with moderate and high risk early stage triple negative breast ... | |||||||||||||
| Medical condition: Early stage triple negative breast cancer | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000168-28 | Sponsor Protocol Number: IBCSG25-02/BIG3-02 | Start Date*: 2005-11-21 | |||||||||||
| Sponsor Name:International Breast Cancer Study Group (IBCSG) | |||||||||||||
| Full Title: A Phase III Trial Evaluating the Role of Exemestane Plus GnRH Analogue as Adjuvant Therapy for Premenopausal Women with Endocrine Responsive Breast Cancer | |||||||||||||
| Medical condition: Premenopausal women with histologically proven, resected breast cancer with ER and/or PgR positive tumors | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: SE (Completed) BE (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000661-19 | Sponsor Protocol Number: CFEM345EGB07 | Start Date*: 2005-11-04 |
| Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
| Full Title: Neoadjuvant hormone therapy for postmenopausal women with ER and/or PgR positive primary breast cancer: A multi-center study to determine the optimum length of treatment with Femara (letrozole 2.5m... | ||
| Medical condition: Postmenopausal women with ER and/or PgR positive primary breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-001669-11 | Sponsor Protocol Number: IFOM-CPT008/2022/PO007 | Start Date*: 2022-09-22 | |||||||||||||||||||||
| Sponsor Name:IFOM - Istituto FIRC di Oncologia Molecolare - Milano | |||||||||||||||||||||||
| Full Title: Restoring sensitivity to immunotherapy in advanced triple negative breast cancer exploiting Ceralasertib priming followed by combined Durvalumab/Nab-paclitaxel: The ATRiBRAVE Trial. | |||||||||||||||||||||||
| Medical condition: Unresectable locally advanced or metastatic triple-negative breast cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2014-000469-35 | Sponsor Protocol Number: GO29227 | Start Date*: 2014-08-12 | ||||||||||||||||
| Sponsor Name:Genentech, Inc. | ||||||||||||||||||
| Full Title: A RANDOMIZED, PHASE II, MULTICENTER, PLACEBO-CONTROLLED STUDY OF IPATASERTIB (GDC-0068), AN INHIBITOR OF AKT, IN COMBINATION WITH PACLITAXEL AS FRONT-LINE TREATMENT FOR PATIENTS WITH METASTATIC TRI... | ||||||||||||||||||
| Medical condition: Inoperable locally advanced or metastatic triple negative breast cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Completed) BE (Completed) ES (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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