- Trials with a EudraCT protocol (210)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
210 result(s) found for: HER2-negative Breast Cancer.
Displaying page 4 of 11.
EudraCT Number: 2011-005524-17 | Sponsor Protocol Number: CBKM120F2302 | Start Date*: 2012-09-13 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase III randomized, double-blind placebo controlled study of BKM120 with fulvestrant, in postmenopausal women with hormone receptor-positive HER2-negative locally advanced or metastatic breast ... | |||||||||||||
Medical condition: This study will evaluate whether the addition of daily BKM120 to fulvestrant is effective and safe in treating patients with hormone receptor-positive HER2 negative locally advanced or metastatic b... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BE (Completed) DE (Prematurely Ended) AT (Prematurely Ended) NL (Completed) IT (Prematurely Ended) HU (Completed) FR (Completed) GR (Completed) CZ (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005590-41 | Sponsor Protocol Number: M14REV | Start Date*: 2015-02-10 | |||||||||||||||||||||
Sponsor Name:Netherlands Cancer Institute | |||||||||||||||||||||||
Full Title: A phase I followed by a randomized phase II trial of two cycles carboplatin-olaparib followed by olaparib monotherapy versus capecitabine in BRCA-1 or -2 mutated Her2 negative advanced breast cance... | |||||||||||||||||||||||
Medical condition: BRCA1 or -2 mutated breast cancer Any other cancer type expected to benefit from olaparib-carboplatin | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
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: 2016-002556-24 | Sponsor Protocol Number: CLEE011XDE01 | Start Date*: 2016-10-14 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A national phase IIIb, multi-center, open label study for women and men with hormone-receptor positive, HER2-negative locally advanced or metastatic breast cancer treated with ribociclib (LEE011) i... | |||||||||||||
Medical condition: HR+, HER2- advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000542-35 | Sponsor Protocol Number: RDD490 | Start Date*: 2013-05-22 | ||||||||||||||||
Sponsor Name:The Clatterbridge Cancer Centre NHS Foundation Trust | ||||||||||||||||||
Full Title: Phase II multicentre study assessing the efficacy of Cabazitaxel in Patients with HER2-negative metastatic breast cancer and having unresectable brain metastases. | ||||||||||||||||||
Medical condition: Her-2 negative breast cancer with brain metastases | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001931-36 | Sponsor Protocol Number: CLEE011E2301 | Start Date*: 2014-12-19 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase III randomized, double-blind, placebo-controlled study of LEE011 or placebo in combination with tamoxifen and goserelin or a non-steroidal aromatase inhibitor (NSAI) and goserelin for the t... | |||||||||||||
Medical condition: premenopausal women with hormone receptor positive, HER2-negative, advanced breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) BE (Completed) IT (Completed) PT (Completed) PL (Completed) BG (Completed) ES (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001603-32 | Sponsor Protocol Number: iOM-04318 | Start Date*: 2016-06-14 | |||||||||||||||||||||
Sponsor Name:iOMEDICO AG | |||||||||||||||||||||||
Full Title: An open-label, multi-center, sINGlE arm clinical study to evaluate treatment efficacy and quality of life in women with hormone-receptor-positive, HER2-negative loco-regionally recurrent or metast... | |||||||||||||||||||||||
Medical condition: The study population includes postmenopausal patients with advanced (locally recurrent, inoperable and/or metastatic), HR+, HER2- breast cancer. For peri-/premenopausal patients, endocrine therapy ... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004744-22 | Sponsor Protocol Number: GERICO11/PACS10 | Start Date*: 2013-05-27 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: Adjuvant systemic treatment for oestrogen-receptor (ER)-positive HER2-negative breast carcinoma in women over 70 according to Genomic Grade (GG): chemotherapy + endocrine treatment versus endocrine... | |||||||||||||
Medical condition: oestrogen-receptor (ER)-positive HER2-negative breast carcinoma in women over 70 | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003384-51 | Sponsor Protocol Number: 20060341 | Start Date*: 2007-12-11 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Randomized, 4-Arm, Placebo-Controlled Phase 2 Trial of AMG 386 in Combination with Bevacizumab and Paclitaxel or AMG386 plus Paclitaxel as First-Line Therapy in Subjects with Her2-Negative, Metas... | |||||||||||||
Medical condition: Her2-Negative, Metastatic or Locally Recurrent Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) AT (Completed) BE (Completed) DK (Completed) FI (Completed) NL (Completed) ES (Completed) HU (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: 2013-003194-10 | Sponsor Protocol Number: GIM11-BERGI | Start Date*: 2014-06-06 | |||||||||||
Sponsor Name:Consorzio Oncotech | |||||||||||||
Full Title: A Phase II Single Arm Trial Evaluating the Efficacy and Safety of Eribulin in Combination With Bevacizumab for Second-Line Treatment of Human Epidermal Growth Factor Receptor 2–Negative Metastatic ... | |||||||||||||
Medical condition: Epidermal Growth Factor Receptor 2–Negative Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001502-18 | Sponsor Protocol Number: I3YMCJPBM | Start Date*: 2014-11-24 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study of Nonsteroidal Aromatase Inhibitors (Anastrozole or Letrozole) Plus LY2835219, a CDK4/6 Inhibitor, or Placebo in Postmenopausal Women ... | |||||||||||||
Medical condition: Hormone Receptor Positive, HER2 negative Locoregionally Recurrent or Metastatic Breast Cancer with No Prior Systemic Therapy in This Disease Setting | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) DE (Completed) ES (Ongoing) IT (Completed) SK (Completed) BE (Completed) GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000568-28 | Sponsor Protocol Number: GO28888 | Start Date*: 2014-10-16 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A phase II randomized, double-blind study of neoadjuvant letrozole plus GDC-0032 versus letrozole plus placebo in postmenopausal women with ER-positive/HER2-negative, early stage breast cancer | |||||||||||||
Medical condition: WOMEN WITH ER-POSITIVE/HER2-NEGATIVE, EARLY STAGE BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) AT (Completed) CZ (Completed) PT (Completed) HU (Completed) IT (Completed) GB (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001090-15 | Sponsor Protocol Number: MADONNA | Start Date*: 2008-09-10 |
Sponsor Name:Universitätsklinikum Heidelberg | ||
Full Title: Randomized, double-blind Phase II study of Docetaxel + Sorafenib (Nexavar®) versus Docetaxel + Placebo in First-Line treatment of patients with HER2-negative, metastatic breast cancer. | ||
Medical condition: metastatic HER2-negative breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005828-32 | Sponsor Protocol Number: CECOG/BC 1.3.005 | Start Date*: 2008-04-03 | ||||||||||||||||
Sponsor Name:CECOG | ||||||||||||||||||
Full Title: A randomized phase III 2-arm trial of paclitaxel plus bevacizumab vs. capecitabine plus bevacizumab for the first-line treatment of HER2-negative locally recurrent or metastatic breast cancer | ||||||||||||||||||
Medical condition: First-line treatment of patients with locally recurrent or metastatic, HER2-negative breast cancer who have not received prior chemotherapy for locally recurrent or metastatic disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) CZ (Completed) HU (Completed) LV (Completed) SK (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004728-13 | Sponsor Protocol Number: I3Y-MC-JPBL | Start Date*: 2014-07-09 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study of Fulvestrant with or without LY2835219, a CDK4/6 Inhibitor, for Women with Hormone Receptor Positive, HER2 Negative Locally Advanced ... | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) BE (Trial now transitioned) ES (Ongoing) DE (Completed) FI (Completed) GR (Trial now transitioned) RO (Ongoing) DK (Completed) PL (Trial now transitioned) FR (Completed) | |||||||||||||
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: 2015-003612-20 | Sponsor Protocol Number: C31006 | Start Date*: 2016-06-09 | |||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited | |||||||||||||
Full Title: An Open-Label Phase 2 Study of MLN0128 (A TORC1/2 Inhibitor) in Combination With Fulvestrant in Women With ER-Positive/HER2-Negative Advanced or Metastatic Breast Cancer That Has Progressed During ... | |||||||||||||
Medical condition: Advanced or Metastatic Breast Cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003058-10 | Sponsor Protocol Number: IBCSG_42-12/BIG_2-12 | Start Date*: 2013-04-03 | |||||||||||
Sponsor Name:International Breast Cancer Study Group (IBCSG) | |||||||||||||
Full Title: A randomized phase II study evaluating different schedules of nab-Paclitaxel in metastatic breast cancer | |||||||||||||
Medical condition: Patients with histologically or cytologically confirmed HER2-negative metastatic (stage IV) breast cancer who have not received chemotherapy for metastatic breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) SI (Completed) IE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003779-37 | Sponsor Protocol Number: IOM-080-2 | Start Date*: 2009-02-05 | |||||||||||
Sponsor Name:iOMEDICO AG | |||||||||||||
Full Title: Capecitabine and bevacizumab ± vinorelbine as 1st line treatment in HER2/neu-negative metastatic or locally advanced inoperable breast cancer patients | |||||||||||||
Medical condition: HER-2/neu negative metastatic or locally advanced inoperable breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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