- Trials with a EudraCT protocol (231)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
231 result(s) found for: Triple negative breast cancer.
Displaying page 4 of 12.
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: 2015-003693-33 | Sponsor Protocol Number: CDX011-04 | Start Date*: 2016-01-18 | |||||||||||
Sponsor Name:Celldex Therapeutics, Inc. | |||||||||||||
Full Title: A Randomized Multicenter Pivotal Study of CDX-011 (CR011-vcMMAE) in Patients with Metastatic, GPNMB Over-Expressing, Triple-Negative Breast Cancer | |||||||||||||
Medical condition: Metastatic, GPNMB Over-Expressing, Triple-Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Completed) AT (Prematurely Ended) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004384-39 | Sponsor Protocol Number: ABCSG-45 | Start Date*: 2018-12-18 | |||||||||||
Sponsor Name:Austrian Breast & Colorectal Cancer Study Group (ABCSG) | |||||||||||||
Full Title: A prospective, open, randomized, phase II study of carboplatin/olaparib in the pre-operative treatment of patients with triple-negative primary breast cancer which exhibit the features of positive ... | |||||||||||||
Medical condition: Early invasive triple negative breast cancer with positive HRD status (acc. to Myriad mychoice© test) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000189-45 | Sponsor Protocol Number: | Start Date*: 2018-03-26 |
Sponsor Name:University of Padova | ||
Full Title: Adjuvant treatment for high-risk triple negative breast cancer patients with the anti-pd-l1 antibody Avelumab: A phase III randomized trial | ||
Medical condition: High risk triple negative (ER negative, PR negative, HER2 negative) breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) IT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003330-16 | Sponsor Protocol Number: GBG74 | Start Date*: 2013-02-26 | |||||||||||
Sponsor Name:GBG Forschungs GmbH (German Breast Group) | |||||||||||||
Full Title: Randomized, open-label, phase II study comparing the efficacy and the safety of cabazitaxel versus weekly paclitaxel given as neo-adjuvant treatment in patients with operable Triple Negative or lum... | |||||||||||||
Medical condition: Breast Cancer in patients with operable Triple Negative or luminal B/HER2 normal patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000553-23 | Sponsor Protocol Number: GBG66 | Start Date*: 2011-09-29 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:German Breast Group GBG Forschungsgesellschaft mbH (Sponsor nach GCP) | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomized phase II trial investigating the addition of carboplatin to neoadjuvant therapy for triple-negative and HER2-positive early breast cancer | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: patients with triple-negative breast cancer, patients with HER2-positive early breast cancer | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004734-22 | Sponsor Protocol Number: WO39392 | Start Date*: 2017-09-06 | ||||||||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | ||||||||||||||||||
Full Title: A PHASE III RANDOMIZED STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF ATEZOLIZUMAB (ANTI-PD-L1 ANTIBODY) IN COMBINATION WITH NEOADJUVANT ANTHRACYCLINE/NAB-PACLITAXEL-BASED CHEMOTHERAPY COMPARED WI... | ||||||||||||||||||
Medical condition: Triple-negative breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) BE (Completed) PL (Completed) ES (Ongoing) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-003203-14 | Sponsor Protocol Number: TUXEDO-2 | Start Date*: 2023-05-02 |
Sponsor Name:Med. Univ. Wien, Klinik f. Innere Medizin I, Onkologie | ||
Full Title: Phase II Study of daTopotamab-derUXtecan (Dato-DXd; DS-1026a) in triple-negative brEast cancer patients with newly Diagnosed or prOgressing brain metastases | ||
Medical condition: triple negative breast cancer with newly diagnosed or progressing brain metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001484-23 | Sponsor Protocol Number: Triple-B | Start Date*: 2013-05-24 | |||||||||||
Sponsor Name:BOOG Study Center | |||||||||||||
Full Title: Biomarker discovery randomized phase IIb trial with carboplatin-cyclophosphamide versus paclitaxel with or without atezolizumaB as first-line treatment in advanced triple negative Breast cancer | |||||||||||||
Medical condition: Metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001287-35 | Sponsor Protocol Number: SHH-CM | Start Date*: 2015-03-12 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Clínica Universidad de Navarra/Universidad de Navarra | ||||||||||||||||||||||||||||||||||||||
Full Title: A randomized phase II pilot study to evaluate safety and efficacy of the addition of vismodegib to standard neoadjuvant chemotherapy in triple negative breast cancer patients. | ||||||||||||||||||||||||||||||||||||||
Medical condition: Breast cancer | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005017-23 | Sponsor Protocol Number: FM-14-B02 | Start Date*: 2016-01-26 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Fondazione Michelangelo - Avanzamento dello studio e cura dei tumori | ||||||||||||||||||||||||||||||||||||||
Full Title: Neo-Adjuvant study with the PDL1-directed antibody in Triple Negative, Early High-Risk and Locally Advanced Breast Cancer undergoing treatment with nab-paclitaxel and carboplatin | ||||||||||||||||||||||||||||||||||||||
Medical condition: Women with a diagnosis of invasive unilateral, early high-risk and locally advanced or inflammatory, triple negative (HER2-negative and ER-negative and PgRnegative) breast cancer of high proliferat... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) ES (Completed) IE (Completed) IT (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003465-18 | Sponsor Protocol Number: BCT1902 | Start Date*: 2021-10-06 |
Sponsor Name:Breast Cancer Trials | ||
Full Title: A randomised phase II trial evaluating the efficacy of a nivolumab monotherapy lead in “window” or commencement of nivolumab concurrently with paclitaxel and carboplatin as neoadjuvant therapy in e... | ||
Medical condition: Early stage triple negative breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001432-35 | Sponsor Protocol Number: 3475-355 | Start Date*: 2016-08-02 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Phase III Study of Pembrolizumab (MK-3475) plus Chemotherapy vs Placebo plus Chemotherapy for Previously Untreated Locally Recurrent Inoperable or Metastatic Triple Nega... | |||||||||||||
Medical condition: Triple-Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) IE (Completed) ES (Completed) CZ (Completed) HU (Completed) BE (Completed) NL (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003570-40 | Sponsor Protocol Number: ML39079 | Start Date*: 2018-09-07 | |||||||||||
Sponsor Name:Oslo University Hospital (OUS) | |||||||||||||
Full Title: ALICE: A randomized placebo-controlled phase II study evaluating atezolizumab combined with immunogenic chemotherapy in patients with metastatic triple-negative breast cancer. | |||||||||||||
Medical condition: Triple-negative breast cancer patients With matasteses | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006106-23 | Sponsor Protocol Number: 2020/3210 | Start Date*: 2021-07-21 | |||||||||||
Sponsor Name:Gustave Roussy | |||||||||||||
Full Title: Short-term Pre-OPerative Durvalumab (MEDI 4736) in early small triple negative breast cancer patients | |||||||||||||
Medical condition: Untreated operable small triple negative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000794-31 | Sponsor Protocol Number: ET-B-027-06 | Start Date*: 2007-08-01 | |||||||||||
Sponsor Name:Pharma Mar, S.A. | |||||||||||||
Full Title: Phase II, multicenter, open-label, clinical trial of Trabectedin (Yondelis®) in Metastatic Breast Cancer Patients with triple negative profile (ER-, PR-, HER2-), HER2 overexpressing tumors and BRCA... | |||||||||||||
Medical condition: Progressive metastatic breast cancer previously treated in the following subpopulation of patients: Group A: Triple negative phenotype: Estrogen Receptor, Progesterone Receptor and HER-2 negative s... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) IT (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002771-25 | Sponsor Protocol Number: NSABP_B-59/GBG96 | Start Date*: 2018-04-03 | |||||||||||
Sponsor Name:NSABP Foundation Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Phase III Clinical Trial of Neoadjuvant Chemotherapy with Atezolizumab or Placebo in Patients with Triple-Negative Breast Cancer Followed by Adjuvant Continuation of At... | |||||||||||||
Medical condition: Patients with early breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000298-11 | Sponsor Protocol Number: ISS22810078 | Start Date*: 2015-09-02 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "ISTITUTI OSPITALIERI" DI CREMONA | |||||||||||||
Full Title: A phase II, open label, controlled study of olaparib in locally advanced ER, PgR and HER2 negative (Triple Negative) and in locally advanced germline BRCA mutation-positive breast cancer patients: ... | |||||||||||||
Medical condition: Locally advanced breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002608-25 | Sponsor Protocol Number: D0810C00011 | Start Date*: 2009-03-13 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase I/II randomised, double-blind, multi-centre study to assess the efficacy of AZD2281 when given in combination with paclitaxel in the 1st or 2nd line treatment of patients with metastatic Tr... | |||||||||||||
Medical condition: Metastatic Triple Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) CZ (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000113-20 | Sponsor Protocol Number: ABI-007-MBC-001 | Start Date*: 2013-07-23 | ||||||||||||||||
Sponsor Name:Abraxis BioScience, LLC, a wholly-owned subsidiary of Celgene Corporation | ||||||||||||||||||
Full Title: A PHASE 2/3, MULTI-CENTER, OPEN-LABEL, RANDOMIZED STUDY OF WEEKLY nab®-PACLITAXEL IN COMBINATION WITH GEMCITABINE OR CARBOPLATIN, COMPARED TO GEMCITABINE/CARBOPLATIN, AS FIRST LINE TREATMENT IN SUB... | ||||||||||||||||||
Medical condition: ER, PgR, and HER2 negative (triple negative) metastatic breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: AT (Prematurely Ended) ES (Completed) DE (Prematurely Ended) GB (Prematurely Ended) IT (Completed) PT (Prematurely Ended) GR (Prematurely Ended) FR (Completed) | ||||||||||||||||||
Trial results: View results |
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