- Trials with a EudraCT protocol (433)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
433 result(s) found for: Male breast cancer.
Displaying page 1 of 22.
EudraCT Number: 2014-004226-18 | Sponsor Protocol Number: 20140930 | Start Date*: 2014-10-27 | |||||||||||
Sponsor Name:Szegedi Tudományegyetem Szent-Györgyi Albert Klinikai Központ Onkotrápiás Klinika | |||||||||||||
Full Title: Metasztatikus ER+ HER2- férfi emlőrák fulvestant és CKD 4/6 inhibitor palbociclib kezelésae többszörös megelőző kemoterápia, endokrin terápia és molekuláris célzott terápia után | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006262-28 | Sponsor Protocol Number: IEO S438/508 | Start Date*: 2009-06-03 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Allogeneic Haematopoietic Cell Transplantation Using a Non-myeloablative Preparative Regimen of Total Lymphoid Irradiation and Anti-Thymocyte Globulin for Patients with Refractory Triple Negative... | |||||||||||||
Medical condition: Patients with Refractory Triple Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004194-16 | Sponsor Protocol Number: IRFMN-BRC-6591 | Start Date*: 2015-01-19 | |||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | |||||||||||||
Full Title: A multicenter, single-arm, phase II study to evaluate the activity of pre-operative zoledronate in triple negative breast cancer patients, according to p53 level | |||||||||||||
Medical condition: Newly diagnosed, untreated, operable triple negative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004610-35 | Sponsor Protocol Number: AL-2001 | Start Date*: 2021-03-16 | |||||||||||
Sponsor Name:Allarity Therapeutics Europe Aps | |||||||||||||
Full Title: Phase II, open label, single arm study to investigate anti-tumor effect of ixabepilone in patients with locally recurrent metastatic breast cancer (mBC) selected by the ixabepilone Drug Response Pr... | |||||||||||||
Medical condition: Locally recurrent or metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) PL (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003995-23 | Sponsor Protocol Number: GBG52 | Start Date*: 2009-03-31 | |||||||||||
Sponsor Name:GBG Forschungs GmbH | |||||||||||||
Full Title: An investigational randomized phase II-(III) study on epirubicin plus cyclophospamide (or CMF) vs nab-paclitaxel plus capecitabine as adjuvant chemotherapy for elderly non frail patients with an in... | |||||||||||||
Medical condition: Primary breast cancer at non-frail, eldery male and female patients | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003194-28 | Sponsor Protocol Number: PULSION-001 | Start Date*: 2011-10-24 | |||||||||||
Sponsor Name:PULSION Medical Systems SE | |||||||||||||
Full Title: Determination of the sensitivity of ICG fluorescence technique for the detection of Sentinel Lymph Nodes in breast cancer – a monocenter, prospective open-label clinical trial | |||||||||||||
Medical condition: Breast cancer with indicated sentinel lymph node biopsy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001054-34 | Sponsor Protocol Number: D0816C00018 | Start Date*: 2018-01-11 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: LUCY - Lynparza Breast Cancer Real-World Utility, Clinical Effectiveness and Safety Study A Phase IIIb, Single-arm, Open-label Multicentre Study of Olaparib Monotherapy in the Treatment of HER2-... | |||||||||||||
Medical condition: Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) HU (Completed) FR (Completed) PL (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002173-28 | Sponsor Protocol Number: C4391002 | Start Date*: 2023-01-25 | ||||||||||||||||
Sponsor Name:Pfizer Inc. | ||||||||||||||||||
Full Title: PHASE 1B/2, OPEN-LABEL, MULTICENTER, DOSE ESCALATION AND DOSE EXPANSION STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, PHARMACODYNAMICS, AND ANTITUMOR ACTIVITY OF PF-07220060 IN COMB... | ||||||||||||||||||
Medical condition: HR-positive HER2-negative metastatic/advanced BC | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012439-14 | Sponsor Protocol Number: 155-CL-036 | Start Date*: 2010-01-26 | |||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. (APGD) | |||||||||||||
Full Title: A Phase II, Multicenter, Open-Label, Randomized Study of YM155 Plus Docetaxel as First-Line Treatment in Subjects with HER2 Negative Metastatic Breast Cancer | |||||||||||||
Medical condition: Adenocarcinoma of the breast that is HER2 negative. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) CZ (Completed) BE (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000075-13 | Sponsor Protocol Number: GBG65 | Start Date*: 2011-06-20 | |||||||||||
Sponsor Name:GBG Forschungs GmbH | |||||||||||||
Full Title: A multicenter non-randomized phase II study to evaluate nab-paclitaxel in metastatic breast cancer patients failing a solvent based taxane as (neo-)adjuvant treatment | |||||||||||||
Medical condition: Evaluate nab-paclitaxel in metastatic breast cancer patients failing a solvent based taxane as (neo-)adjuvant treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (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: 2018-002998-21 | Sponsor Protocol Number: CLEE011O12301C | Start Date*: 2019-02-25 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A phase III, multicenter, randomized, open-label trial toevaluate efficacy and safety of ribociclib with endocrine therapy as an adjuvant treatment in patients with hormone receptor-positive, HER2-... | ||||||||||||||||||
Medical condition: hormone receptor-positive, HER2-negative, early breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) IE (Trial now transitioned) HU (Trial now transitioned) AT (Trial now transitioned) BE (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
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: 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: 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: 2008-000062-24 | Sponsor Protocol Number: D0810C00021 | Start Date*: 2008-10-27 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: Ensayo fase I/II, abierto, multicéntrico, de AZD2281 oral en combinación con Cisplatino, para valorar la seguridad y tolerabilidad en pacientes con tumores sólidos avanzados, y para valorar la efic... | |||||||||||||
Medical condition: Tumores sólidos avanzados, cáncer de mama triple negativo Advanced Solid Tumours, Triple Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004358-32 | Sponsor Protocol Number: IJB–TNBC–1–RHEA | Start Date*: 2015-05-07 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: Biomarker Research Study for PF-03084014 in cHEmoresistant triple negative breast cAncer - “RHEA” study | |||||||||||||
Medical condition: patients with chemoresistant, triple-negative breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002324-27 | Sponsor Protocol Number: MYL-1401H-3001 | Start Date*: 2015-04-22 | ||||||||||||||||
Sponsor Name:Mylan GmbH | ||||||||||||||||||
Full Title: Multicenter, Double-Blind, Randomized, Comparative Efficacy and Safety Study of MYL 1401H and European Sourced Neulasta® in Stage II/III Breast Cancer Patients Receiving Neoadjuvant or Adjuvant Che... | ||||||||||||||||||
Medical condition: chemotherapy-induced neutropenia in patients with stage II/III breast cancer receiving docetaxel, doxorubicin, and cyclophosphamide (TAC) anti-cancer chemotherapy | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) DE (Completed) BG (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-000810-72 | Sponsor Protocol Number: PREDIXLumB | Start Date*: 2014-12-05 | ||||||||||||||||||||||||||
Sponsor Name:Karolinska University Hospital | ||||||||||||||||||||||||||||
Full Title: PREDIX Luminal B - Neoadjuvant response-guided treatment of estrogen receptor positive tumors with high proliferation or slow proliferation with metastatic nodes or young patients. Part of a set of... | ||||||||||||||||||||||||||||
Medical condition: Primary breast cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005209-23 | Sponsor Protocol Number: CA163139 | Start Date*: 2008-03-21 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: Randomized Phase II of Ixabepilone Alone and Ixabepilone Plus Cetuximab as First-Line Treatment for Female Subjects with Triple Negative (ER, PR, Her2 negative) Locally Advanced non-resectable and/... | |||||||||||||
Medical condition: BREAST CANCER, FIRST LINE | |||||||||||||
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Population Age: | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) AT (Completed) CZ (Completed) ES (Completed) IT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
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