- Trials with a EudraCT protocol (1,113)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,113 result(s) found for: Metastatic Breast Cancer.
Displaying page 8 of 56.
| EudraCT Number: 2010-020101-32 | Sponsor Protocol Number: OAM4861g | Start Date*: 2010-10-21 | |||||||||||
| Sponsor Name:GENENTECH, Inc. | |||||||||||||
| Full Title: A RANDOMIZED, PHASE II, MULTICENTER, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE SAFETY AND EFFICACY OF METMAB IN COMBINATION WITH PACLITAXEL AND BEVACIZUMAB IN PATIENTS WITH METASTATIC, ... | |||||||||||||
| Medical condition: Metastatic, triple-negative breast cancer Cáncer de mama metastásico triple negativo | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) FR (Completed) BE (Completed) DE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005161-12 | Sponsor Protocol Number: OAS-12DOC-BIO | Start Date*: 2015-10-22 | |||||||||||||||||||||||||||||||
| Sponsor Name:Oasmia Pharmaceutical AB | |||||||||||||||||||||||||||||||||
| Full Title: A multi-country, multicenter, randomized, open-label, parallel group study to assess the efficacy and safety of Docecal compared with Taxotere® | |||||||||||||||||||||||||||||||||
| Medical condition: adenocarcinoma of the breast | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
| Trial protocol: LV (Prematurely Ended) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-005238-40 | Sponsor Protocol Number: EQ132-201 | Start Date*: 2022-05-11 | ||||||||||||||||||||||||||
| Sponsor Name:EQRx, Inc. | ||||||||||||||||||||||||||||
| Full Title: A Phase 2 Study to Evaluate the Safety and Efficacy of Lerociclib in Participants with Advanced Breast Cancer | ||||||||||||||||||||||||||||
| Medical condition: Metastatic Breast Cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
| 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: 2007-006060-29 | Sponsor Protocol Number: FARM6N78KN | Start Date*: 2008-11-21 | |||||||||||
| Sponsor Name:IST - ISTITUTO NAZIONALE PER LA RICERCA SUL CANCRO | |||||||||||||
| Full Title: Efficacy and toxicity of Trastuzumab at the maintaining dose of 1 mg/kg/week versus the standard dose of 2 mg/kg/week in combination with chemotherapy in metastatic breast cancer patients. A phase ... | |||||||||||||
| Medical condition: HER-2 positive metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001246-36 | Sponsor Protocol Number: ACE-Breast-03 | Start Date*: 2022-02-22 | ||||||||||||||||
| Sponsor Name:Ambrx, Inc. | ||||||||||||||||||
| Full Title: A Global, Phase 2 Study of ARX788 in HER2-positive Metastatic Breast Cancer Patients Whose Disease is Resistant or Refractory to T-DM1, and/or T-DXd, and/or Tucatinib-containing Regimens | ||||||||||||||||||
| Medical condition: Metastatic Breast Cancer Resistant or Refractory | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) ES (Prematurely Ended) IT (Prematurely Ended) DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-001916-18 | Sponsor Protocol Number: 20080331 | Start Date*: 2008-11-05 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA ORDINE MAURIZIANO | ||||||||||||||||||
| Full Title: A phase II, randomized trial with single agent trastuzumab or lapatinib in women with metastatic breast cancer iperexpressing HER2 | ||||||||||||||||||
| Medical condition: women with metastatic breast cancer iperexpressing HER2 | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-002707-18 | Sponsor Protocol Number: EFFECT | Start Date*: 2012-11-14 | |||||||||||
| Sponsor Name:FONDAZIONE SANDRO PITIGLIANI PER LA LOTTA CONTRO I TUMORI-ONLUS | |||||||||||||
| Full Title: EFFECT: A randomized phase II study to evaluate the EFficacy and impact on Function of two different doses of nab-paclitaxEl in elderly patients with advanCed breasT cancer | |||||||||||||
| Medical condition: Patients aged 65 years or older with histologically or cytologically confirmed breast cancer, locally recurrent and/or metastatic; any estrogen/progesterone receptor status; HER2 receptor negative ... | |||||||||||||
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| Population Age: Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005335-97 | Sponsor Protocol Number: GO25632 | Start Date*: 2012-10-11 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A phase III, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of bevacizumab, and associated biomarkers, in combination with paclitaxel compared w... | |||||||||||||
| Medical condition: HER2-negative metastatic breast cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) BE (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002669-38 | Sponsor Protocol Number: 0822-016 | Start Date*: 2006-12-07 | |||||||||||
| Sponsor Name:Merck & Co Inc. | |||||||||||||
| Full Title: A Phase II Study to Assess the Safety, Tolerability, and Efficacy of MK-0822 (Cathepsin-K Inhibitor) in the Treatment of Women with Breast Cancer and Established Bone Metastases (MBD) | |||||||||||||
| Medical condition: Metastatic Bone Disease (MBD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) NO (Completed) DK (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000572-14 | Sponsor Protocol Number: EFC6088 (XRP9881B/2001) | Start Date*: 2004-10-08 | |||||||||||
| Sponsor Name:Aventis Pharmaceuticals, Inc. (a subsidiary of sanofi-aventis group) | |||||||||||||
| Full Title: Phase II multicenter, open label, non-randomized study of intravenous RPR109881 q 3 weeks in patients with metastatic breast cancer progressing after therapy with anthracyclines, taxanes, and capec... | |||||||||||||
| Medical condition: Metastatic breast cancer patients after failure to anthracyclines, taxanes and capecitabine. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) IT (Completed) ES (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003283-20 | Sponsor Protocol Number: MO21926 | Start Date*: 2009-02-09 | |||||||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||
| Full Title: Estudio de fase II abierto, con un solo grupo de tratamiento, de bevacizumab en combinación con trastuzumab y capecitabina como tratamiento en primera línea de pacientes con cáncer de mama localmen... | |||||||||||||||||||||||
| Medical condition: Tratamiento de pacientes con cáncer de mama localmente recurrente o metastásico HER2- positivo que no han recibido previamente quimioterapia para enfermedad localmente recurrente o metastásica. H... | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) FR (Ongoing) SE (Completed) SK (Completed) DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-001765-41 | Sponsor Protocol Number: 1200.137 | Start Date*: 2012-02-13 | |||||||||||
| Sponsor Name:Medizinische Fakultät der Otto-von-Guericke Universität Magdeburg Universitätsklinikum Magdeburg A.ö.R. | |||||||||||||
| Full Title: Single-arm, open-label, multicentre phase II study evaluating the efficacy and safety of BIBW 2992 (Afatinib) in combination with vinorelbine for the treatment of patients with metastatic breast ca... | |||||||||||||
| Medical condition: Metastatic breast cancer patients with intermediate HER2 expression (IHC 2+, HER2 FISH-negative) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003435-13 | Sponsor Protocol Number: MARLENE | Start Date*: 2021-05-27 | |||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
| Full Title: Metronomic vinorelbin, cyclophosphamide and capecitabine after progression to cyclin-dependent kinase 4/6 inhibitors for hormone receptors positive HER2 negative metastatic breast cancer | |||||||||||||
| Medical condition: HER2 negative hormone receptors positive metastatic breast cancer progressed after CDK 4/6 inhibitors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000245-13 | Sponsor Protocol Number: SOLTI-1907 | Start Date*: 2021-03-04 | |||||||||||
| Sponsor Name:SOLTI | |||||||||||||
| Full Title: A Phase II with 2 parallel cohorts clinical trial targeting estrogen receptor negative or PAM50 non-luminal disease with Atezolizumab in combination with Trastuzumab and Vinorelbine in HER2-positiv... | |||||||||||||
| Medical condition: Pre- and post-menopausal women with locally advanced or metastatic HER2-positive breast cancer who have progressed to trastuzumab/pertuzumab and T-DM1. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005021-30 | Sponsor Protocol Number: FARM5P8YFC | Start Date*: 2007-10-31 | |||||||||||
| Sponsor Name:REGIONE LOMBARDIA - DIREZIONE GENERALE SANITA' | |||||||||||||
| Full Title: TOP TRIAL. A RANDOMISED PHASE III CLINICAL TRIAL OF TRASTUZUMAB (HERCEPTIN) OPTIMIZATION IN PATIENTS WITH LOCALLY ADVANCED AND/OR METASTATIC BREAST CANCER OVEREXPRESSING HER2 AFTER A FIRST LINE CHE... | |||||||||||||
| Medical condition: Women with locally advanced or metastatic breast cancer over expressing HER2 who have been previously treated with a first line chemotherapy plus trastuzumab. | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2005-006109-19 | Sponsor Protocol Number: STM01-102 | Start Date*: 2006-09-08 | |||||||||||
| Sponsor Name:Sopherion Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase III Randomized, Controlled Trial of Myocet, Trastuzumab and Paclitaxel versus Trastuzumab and Paclitaxel for First line Therapy of Metastatic Breast Cancer | |||||||||||||
| Medical condition: HER2+ Metastatic Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: PT (Completed) DE (Completed) ES (Prematurely Ended) GB (Completed) IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003994-28 | Sponsor Protocol Number: VinCaT | Start Date*: 2006-11-10 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE "G. PASCALE" | |||||||||||||
| Full Title: VINORELBINE, CARBOPLATIN AND TRASTUZUMAB IN ADVANCED HER-2 POSITIVE BREAST CANCER. A PHASE 2 STUDY | |||||||||||||
| Medical condition: BREAST CANCER | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| 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) | |||||||||||||
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