- Trials with a EudraCT protocol (73)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
73 result(s) found for: Breast cancer management.
Displaying page 1 of 4.
EudraCT Number: 2018-003559-39 | Sponsor Protocol Number: ICO-A-2018-10 | Start Date*: 2018-12-11 | |||||||||||
Sponsor Name:INSTITUT DE CANCEROLOGIE DE L'OUEST | |||||||||||||
Full Title: multicentric Study , open, randomized, comparing the topical treatment by patch of capsaïcine with 8 % ( Qutenza) to the oral prégabaline treatment in the early treatment of the neuropathic pains a... | |||||||||||||
Medical condition: men and /or women older than 18 years with breast cancer for which a surgical operation was realized. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004430-26 | Sponsor Protocol Number: 010207QM | Start Date*: 2015-06-08 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Queen Mary University of London | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: FEASIBILITY of IBIS 3. An International Breast Intervention Study investigating Prevention Of Late Recurrence in ER+ breast cancer survivors following 5 years of adjuvant treatment | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Late recurrence of hormone receptor positive breast cancer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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: 2012-001889-14 | Sponsor Protocol Number: Bubble2012 | Start Date*: 2012-10-15 | ||||||||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | ||||||||||||||||||
Full Title: MicroBubble detection and Ultrasound guided Biopsy of axillary Lymph nodes in patients with Early breast cancer. | ||||||||||||||||||
Medical condition: Diagnosis of lymph node metastases in patients with newly diagnosed breast cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003575-18 | Sponsor Protocol Number: ICO-2020-06 | Start Date*: 2020-12-08 | |||||||||||
Sponsor Name:INSTITUT DE CANCEROLOGIE DE L'OUEST | |||||||||||||
Full Title: Impact of Neoadjuvant Hormonal Therapy on the Surgical Management of Extensive Ductal Carcinomas in Situ | |||||||||||||
Medical condition: Patients with extensive ductal carcinoma in situ with an indication for total mastectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005954-22 | Sponsor Protocol Number: VEG108843 | Start Date*: 2008-06-03 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter Phase II study to compare the efficacy and tolerability of pazopanib administered in combination with exemestane versus exemestane plus p... | |||||||||||||
Medical condition: Advanced or metastatic hormone receptor positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004652-35 | Sponsor Protocol Number: GIM22-ERICA | Start Date*: 2018-02-22 | ||||||||||||||||
Sponsor Name:CONSORZIO ONCOTECH | ||||||||||||||||||
Full Title: Second line ERIbulin followed by CApecitabine or the reverse sequence in HER2-negative Metastatic Breast Cancer (MBC) patients: a randomized phase II study – ERICA trial | ||||||||||||||||||
Medical condition: HER2-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: 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: 2021-003601-21 | Sponsor Protocol Number: ZX-2021-FES-ESTROTIMP-4. | Start Date*: 2021-09-22 | |||||||||||
Sponsor Name:Zionexa | |||||||||||||
Full Title: Impact of 18F-FES TEP on therapeutical management in patients with metastatic breast cancer, ER positive and HER2 negative, in relapse after a first line of treatment combining hormonal therapy | |||||||||||||
Medical condition: Patients with metastatic breast cancer initially presenting with overexpression of estrogen receptors (ERs) and absence of overexpression of HER2, relapsing after a first therapeutic line combining... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001139-98 | Sponsor Protocol Number: IC2021-07 | Start Date*: 2022-06-13 | ||||||||||||||||
Sponsor Name:Institut Curie | ||||||||||||||||||
Full Title: Opioid-Free versus Opioid-Based Anaesthesia for secondary free-flap reconstruction surgery of the breast: A phase III multicentric randomized controlled study | ||||||||||||||||||
Medical condition: Anaesthesia during secondary free flap reconstruction surgery of the breast. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016743-18 | Sponsor Protocol Number: ICG10 | Start Date*: 2010-02-02 |
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | ||
Full Title: A feasibility study of indocyanine green (ICG) fluorescence mapping for sentinel lymph node detection in early breast cancer | ||
Medical condition: Primary breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003212-39 | Sponsor Protocol Number: LPM-008 | Start Date*: 2019-12-17 | |||||||||||
Sponsor Name:Lightpoint Medical Ltd | |||||||||||||
Full Title: Evaluation of the LightPath Imaging System and the PET tracer 68Ga-RM2 in wide local excision (WLE) for breast cancer | |||||||||||||
Medical condition: Wide local excision (WLE) for breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
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: 2016-001087-11 | Sponsor Protocol Number: 15112SMcI-SS | Start Date*: 2016-06-23 | ||||||||||||||||||||||||||
Sponsor Name:Belfast Health and Social Care Trust | ||||||||||||||||||||||||||||
Full Title: Chemoprevention in BRCA1 mutation carriers - a proof of concept study | ||||||||||||||||||||||||||||
Medical condition: BRCA1 mutation carrier Breast Cancer | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002455-42 | Sponsor Protocol Number: WO41554 | Start Date*: 2020-08-21 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE III, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE EFFICACY AND SAFETY OF INAVOLISIB PLUS PALBOCICLIB AND FULVESTRANT VERSUS PLACEBO PLUS PALBOCICLIB AND FULVESTRANT IN ... | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) BE (Trial now transitioned) PT (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Completed) HU (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004398-28 | Sponsor Protocol Number: AA01 | Start Date*: 2016-06-17 | ||||||||||||||||||||||||||
Sponsor Name:Medical Research Council Clinical Trials Unit at UCL [...] | ||||||||||||||||||||||||||||
Full Title: A phase III double-blind placebo-controlled randomised trial assessing the effects of aspirin on disease recurrence and survival after primary therapy in common non-metastatic solid tumours. | ||||||||||||||||||||||||||||
Medical condition: Cancer (breast, colorectal, gastro-oesophageal and prostate) | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004426-10 | Sponsor Protocol Number: MO28072 | Start Date*: 2012-05-11 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | |||||||||||||||||||||||||||||||||||||||||||
Full Title: An open-label, phase II study of vemurafenib in patients with BRAF V600 mutation-positive cancers | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with cancers (excluding melanoma and papillary thyroid cancer) harboring BRAF V600 mutations as identified by the routinely performed mutation analysis assays at each individual partici... | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005037-37 | Sponsor Protocol Number: 10-005 | Start Date*: 2013-10-02 | |||||||||||||||||||||
Sponsor Name:Puma Biotechnology, Inc. | |||||||||||||||||||||||
Full Title: A Phase I/II Trial of Temsirolimus Plus Neratinib for Patients with Metastatic HER2-Amplified or Triple-Negative Breast Cancer | |||||||||||||||||||||||
Medical condition: advanced breast carcinoma in patients with trastuzumab-refractory HER2-amplified disease | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) ES (Completed) DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004424-38 | Sponsor Protocol Number: 011604QM | Start Date*: 2017-11-16 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: A phase II study investigating preoperative combination strategies for immunotherapy in patients with untreated, operable ER+, HER2-negative primary breast cancer. | |||||||||||||
Medical condition: Untreated, operable ER+, HER2-negative primary breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001698-89 | Sponsor Protocol Number: Monet | Start Date*: 2006-06-08 |
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | ||
Full Title: Molecular profiling of postmenopausal women with breast cancer on neoadjuvant exemestane or tamoxifen | ||
Medical condition: Early or locally advanced breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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