- Trials with a EudraCT protocol (99)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
99 result(s) found for: Inflammatory breast cancer.
Displaying page 1 of 5.
EudraCT Number: 2009-016453-17 | Sponsor Protocol Number: IEO S504/409 | Start Date*: 2009-12-17 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Phase II study of preoperative bevacizumab plus weekly paclitaxel, carboplatin and metronomic cyclophosphamide � trastuzumab and endocrine therapy for inflammatory breast cancer | |||||||||||||
Medical condition: Inflammatory breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005858-23 | Sponsor Protocol Number: PROMIX | Start Date*: 2008-03-12 | |||||||||||||||||||||
Sponsor Name:PROMIX Trial Group | |||||||||||||||||||||||
Full Title: Preoperative treatment of breast cancer with a combination of epirubicin, docetaxel and bevacizumab. A translational trial on molecular markers and functional imaging to predict response early | |||||||||||||||||||||||
Medical condition: Patients diagnosed with breast cancer who are candidates for preoperative (neoadjuvant) chemotherapy due to localized primary breast cancer including inflammatory breast cancer suitable for primary... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003291-35 | Sponsor Protocol Number: ML 19884 | Start Date*: 2007-11-26 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Phase II, open label, neoadjuvant study of Bevacizumab in patients with inflammatory or locally advanced breast cancer | |||||||||||||
Medical condition: Patients with inflammatory or locally advanced operable breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007257-31 | Sponsor Protocol Number: GIC/468 | Start Date*: 2008-11-07 | |||||||||||
Sponsor Name:IPOLFG | |||||||||||||
Full Title: Open-label, single arm, phase II study for evaluation of complete response rate at surgery after NEOadjuvant treatment with SUnitinib and docetaxel in patients with newly diagnosed large operable o... | |||||||||||||
Medical condition: large operable and locally advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: PT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006381-29 | Sponsor Protocol Number: EXPRESSION | Start Date*: 2009-11-12 | ||||||||||||||||||||||||||
Sponsor Name:Universitätsmedizin Mainz | ||||||||||||||||||||||||||||
Full Title: Neoadjuvant, sequential chemotherapy with docetaxel followed by Fluorouracil, Epirubicin, and Cyclophosphamid every 3 weeks - genome wide expression analysis for identification of a predictive gene... | ||||||||||||||||||||||||||||
Medical condition: Eligible will be only females between 18 - 70 years of age, suffering from histologically confirmed primary breast cancer, nodal status positive or negative, phase cT2, cT3, or cT4 including inflam... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007326-19 | Sponsor Protocol Number: BO22227 | Start Date*: 2009-06-19 | |||||||||||||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||||||||||||
Full Title: A phase III, randomized, open-label study to compare pharmacokinetics, efficacy and safety of subcutaneous (SC) trastuzumab with intravenous (IV) trastuzumab administered in women with HER2 positiv... | |||||||||||||||||||||||||||||||||
Medical condition: Locally advanced, inflammatory or early stage HER2 positive breast cancer | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) ES (Completed) CZ (Completed) EE (Completed) DE (Completed) GB (Prematurely Ended) SE (Completed) IT (Completed) SK (Completed) HU (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001943-21 | Sponsor Protocol Number: IFG-08-2019 | Start Date*: 2021-05-14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Institut für Frauengesundheit GmbH | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: NeoOn – Neoadjuvant treatment of Ontruzant® (SB3) in patients with HER2-positive early breast cancer: An open-label, multicenter, phase IV study | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Female patients with early HER2positive breast cancer, neoadjuvantly treated. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001906-29 | Sponsor Protocol Number: EGF103009 | Start Date*: 2005-08-18 | |||||||||||
Sponsor Name:GlaxoSmithKline R&D Ltd | |||||||||||||
Full Title: Phase II study to evaluate the efficacy, safety and pharmacodynamics of lapatinib in patients with relapsed or refractory inflammatory breast cancer | |||||||||||||
Medical condition: Relapsed or refractory infammatory breast cancer (IBC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014619-11 | Sponsor Protocol Number: Kotoe_01 | Start Date*: 2009-10-09 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Pirkanmaan sairaanhoitopiiri | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The effect of dexmedetomidine on reactivity of a propofol-anaesthetized patient | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Surgical patients scheduled for elective surgery under general anaesthesia. Otherwise in stable medical condition (ASA status 1 or 2). | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000783-16 | Sponsor Protocol Number: ML21531 | Start Date*: 2008-06-18 | ||||||||||||||||
Sponsor Name:ROCHE SAS | ||||||||||||||||||
Full Title: Multicenter, phase II trial assessing the efficacy and safety of bevacizumab (Avastin®) combined to trastuzumab (Herceptin®) based chemotherapy in patients with primary inflammatory HER2+ breast ca... | ||||||||||||||||||
Medical condition: Primary inflammatory HER2+ breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024454-10 | Sponsor Protocol Number: 1200.89 | Start Date*: 2011-07-21 | |||||||||||
Sponsor Name:Boehringer Ingelheim | |||||||||||||
Full Title: An open label, phase II trial of afatinib with or without vinorelbine for the treatment of HER2-overexpressing Inflammatory Breast Cancer | |||||||||||||
Medical condition: Locally advanced or metastic Inflammatory Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000435-41 | Sponsor Protocol Number: GOIRC-01-2016 | Start Date*: 2016-09-23 | |||||||||||
Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA CLINICA (GOIRC) | |||||||||||||
Full Title: Phase II, Open Label, Randomized, Biomarker Study of Immune-mediated Mechanism of Action of Neoadjuvant Subcutaneous (SC) Trastuzumab in Patients with Operable or Locally Advanced/Inflammatory HER2... | |||||||||||||
Medical condition: HER2-positive Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2017-003343-37 | Sponsor Protocol Number: IEO675 | Start Date*: 2019-01-23 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Combination of pembrolizumab with oral metronomic cyclophosphamide in patients with chest wall breast cancer (PERICLES): A phase II study. | |||||||||||||
Medical condition: Locally recurrent, inoperable, and/or metastatic inflammatory breast cancer with lymphangitic spread to the chest wall | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001105-13 | Sponsor Protocol Number: WO20697 | Start Date*: 2007-09-24 | ||||||||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||||||||||||
Full Title: Estudio de fase II multicéntrico, internacional, randomizado de trastuzumab y docetaxel frente a trastuzumab, docetaxel y pertuzumab, comparado con trastuzumab y pertuzumab en pacientes con cáncer ... | ||||||||||||||||||||||||||||
Medical condition: Cáncer de mama localmente avanzado, inflamatorio o precoz HER2 positivo. Locally advanced, inflammatory or early stage HER2 positive breast cancer. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: ES (Completed) AT (Completed) IT (Completed) PL (Completed) GB (Completed) SE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003064-19 | Sponsor Protocol Number: NeoTEC | Start Date*: 2008-12-30 | |||||||||||
Sponsor Name:Universität Leipzig | |||||||||||||
Full Title: Phase-IIb-Study to Evaluate the Effect of a Neoadjuvant Chemotherapy with Docetaxel, Epirubicine and Cyclphosphamide (TEC) in Patients with primary HER-2 neu Negative Mammacarcinoma | |||||||||||||
Medical condition: Primary mamma carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000864-94 | Sponsor Protocol Number: EORTC protocol 10054 | Start Date*: 2007-01-15 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer (EORTC) | |||||||||||||
Full Title: A phase I-II study of lapatinib and docetaxel as neoadjuvant treatment for HER-2 positive locally advanced/inflammatory or large operable breast cancer. | |||||||||||||
Medical condition: Locally advanced/inflammatory or large operable brest cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) GB (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001905-93 | Sponsor Protocol Number: EGF102580 | Start Date*: 2005-07-11 |
Sponsor Name:GlaxoSmithKline R&D Ltd | ||
Full Title: A Phase II study to evaluate the efficacy, safety and pharmacodynamics of lapatinib in combination with paclitaxel as neoadjuvant therapy in patients with newly diagnosed inflammatory breast cancer | ||
Medical condition: Newly diagnosed infammatory breast cancer (IBC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003509-41 | Sponsor Protocol Number: GBG90 | Start Date*: 2016-08-01 | |||||||||||
Sponsor Name:GBG Forschungs GmbH | |||||||||||||
Full Title: A randomized phase II trial to assess the efficacy of paclitaxel and olaparib in comparison to paclitaxel / carboplatin followed by epirubicin/cyclophosphamide as neoadjuvant chemotherapy in patien... | |||||||||||||
Medical condition: Patients with triple negative or HRpositive, early breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001949-34 | Sponsor Protocol Number: E7389-G000-305 | Start Date*: 2006-10-02 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Phase III Open Label, Randomized Parallel Two-Arm Multi Center Study of E7389 versus ‘Treatment of Physician’s Choice’ in Patients with Locally Recurrent or Metastatic Breast Cancer, Previously T... | |||||||||||||
Medical condition: Locally recurrent or metastatic breast cancer after failure of multiple prior chemotherapy regimens | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) DE (Completed) GB (Completed) CZ (Completed) FR (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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