- Trials with a EudraCT protocol (1,850)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,850 result(s) found for: Breast cancer.
Displaying page 6 of 93.
EudraCT Number: 2014-004112-11 | Sponsor Protocol Number: C/31/2014 | Start Date*: 2015-05-20 | ||||||||||||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||||||||||||
Full Title: ALERT: A phase II study of alternating eribulin and hormonal therapy in pre-treated ER+ve breast cancer | ||||||||||||||||||||||||||||
Medical condition: Patients with locally advanced or metastatic oestrogen receptor positive (ER+ve) breast cancer who have received at least one hormonal therapy and at least one chemotherapy in the metastatic setting. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015999-10 | Sponsor Protocol Number: XM22-03 | Start Date*: 2010-03-02 | |||||||||||||||||||||
Sponsor Name:BioGeneriX AG | |||||||||||||||||||||||
Full Title: Efficacy and Safety of XM22 compared to pegfilgrastim in patients with breast cancer receiving chemotherapy. A multinational, multicentre, randomised, double-blind controlled study | |||||||||||||||||||||||
Medical condition: Breast cancer high risk stage II, III or IV according to AJCC classification | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BG (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-018090-30 | Sponsor Protocol Number: 09SEIN09 | Start Date*: 2010-01-27 | |||||||||||
Sponsor Name:Institut Claudius Regaud | |||||||||||||
Full Title: Hormonothérapie adjuvante du cancer du sein : Pharmacocinétique du tamoxifène et des anti-aromatases, corrélation avec les caractéristiques pharmacogénétiques Protocole PHACS (Pharmacologie de l’Ho... | |||||||||||||
Medical condition: Cancer du sein en situation adjuvante | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (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: 2006-007089-12 | Sponsor Protocol Number: 2606 B | Start Date*: 2007-02-07 | |||||||||||
Sponsor Name:GOIM GRUPPO ONCOLOGICO MERIDIONALE | |||||||||||||
Full Title: Liposomial pegylate doxorubicine and trasuzumab in the first line treatment of the metastatised Her2 positive breast cancer for senior women | |||||||||||||
Medical condition: Metastased breast cancer, first line treatment, for women with age>70 years old,Her2 positive | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003620-11 | Sponsor Protocol Number: SBG-2-01 | Start Date*: 2006-10-10 | |||||||||||
Sponsor Name:Biotec Pharmacon ASA | |||||||||||||
Full Title: A phase I/II study to assess the effect of soluble beta-1,3/1,6-glucan in combination with standard therapy in patients with breast cancer | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002759-15 | Sponsor Protocol Number: XEL-CONT-VS ESTANDAR | Start Date*: 2004-11-15 | |||||||||||
Sponsor Name:Dr. Miguel Martín | |||||||||||||
Full Title: Randommized Phase II study of the continuous treatment vs. standard treatment with capecitabine in metastatic breast cancer patients | |||||||||||||
Medical condition: METASTATIC BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000900-34 | Sponsor Protocol Number: VA 2007-09 | Start Date*: 2007-07-10 | |||||||||||
Sponsor Name:Centre Val d'Aurelle - Paul Lamarque | |||||||||||||
Full Title: Essai randomisé, en double aveugle, chez les femmes ménopausées ayant un cancer du sein RE+ comparant deux traitements néo-adjuvants : un anti-aromatase (Letrozole) VS un SERM (Tamoxifène). Effet ... | |||||||||||||
Medical condition: Le cancer du sein est le cancer féminin le plus fréquent en Europe représentant 28% de tous les cancers féminins. Son incidence y est de l’ordre de 70 pour 100 000 femmes. Sa fréquence est stable (... | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002018-37 | Sponsor Protocol Number: BO27938 | Start Date*: 2013-04-09 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: A RANDOMIZED, MULTICENTER, OPEN LABEL PHASE III STUDY TO EVALUATE THE EFFICACY AND SAFETY OF TRASTUZUMAB EMTANSINE VERSUS TRASTUZUMAB AS ADJUVANT THERAPY FOR PATIENTS WITH HER2-POSITIVE PRIMARY BRE... | ||||||||||||||||||
Medical condition: HER2-positive primary breast cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) SE (Prematurely Ended) AT (Prematurely Ended) CZ (Completed) DE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) IE (Prematurely Ended) ES (Ongoing) GR (Completed) FR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-006943-29 | Sponsor Protocol Number: 2006.453/46 | Start Date*: 2009-01-07 | |||||||||||||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||||||||||||
Full Title: ESSAI RANDOMISE, EN DOUBLE AVEUGLE CONTRE PLACEBO EVALUANT L’EFFICACITE DU RISEDRONATE ORAL 35 MG PAR SEMAINE DANS LA PREVENTION DE LA PERTE OSSEUSE CHEZ LA FEMME ATTEINTE D’UN CANCER DU SEIN TRAIT... | |||||||||||||||||||||||
Medical condition: Cancer du sein | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003620-32 | Sponsor Protocol Number: MNEMOSYNE-0712 | Start Date*: 2008-11-20 | |||||||||||
Sponsor Name:Centre Oscar Lambret | |||||||||||||
Full Title: Etude Prospective Randomisée Ouverte et Multicentrique évaluant les effets sur les fonctions cognitives de l’hormonothérapie adjuvante dans le cancer du sein de la femme ménopausée | |||||||||||||
Medical condition: Cancer du sein non métastatique | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005885-36 | Sponsor Protocol Number: 0007 | Start Date*: 2006-02-09 | |||||||||||
Sponsor Name:AZIENDA USL DI FORLI | |||||||||||||
Full Title: Dose finding study of Liposomal Doxorubicin Myocet in combination with Capecitabine Xeloda in the treatment of metastatic breast cancer patients | |||||||||||||
Medical condition: Metastatic breast cancer pretreated | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002736-28 | Sponsor Protocol Number: GINECO-BR106 | Start Date*: 2007-09-19 | |||||||||||
Sponsor Name:ARCAGY-GINECO | |||||||||||||
Full Title: A multicentre study DOGMES: Liposomal doxorubicin in geriatric oncology - Metastatic breast cancer - first line treatment by pegylated liposomal doxorubicin in patients of more than 70 years old wi... | |||||||||||||
Medical condition: Breast cancer metastatic | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (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: 2010-018389-22 | Sponsor Protocol Number: LAP113957 / SOLTI-1001 | Start Date*: 2010-09-07 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A randomized, multicentre, open-label, Phase II study of the efficacy and safety of lapatinib plus epirubicin and cyclophosphamide (EC90-L) followed by weekly paclitaxel and lapatinib (PX-L) compar... | |||||||||||||
Medical condition: patients with previously untreated ErbB2-overexpressing Stage I - IIIA invasive breast cancer with primary tumour size > 1cm. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) AT (Prematurely Ended) FR (Completed) NO (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014773-40 | Sponsor Protocol Number: AVASTEM/IPC2009-001 | Start Date*: 2010-01-04 | |||||||||||
Sponsor Name:Institut Paoli-Calmettes | |||||||||||||
Full Title: Essai de phase II de preuve du concept : Evaluation de l’activité anti-cellules souches cancéreuses du bevacizumab administré en combinaison à la chimiothérapie néoadjuvante dans les cancers du sein | |||||||||||||
Medical condition: Tumeurs du sein localement avancées ou inflammatoires candidates à un traitement néo-adjuvant par une association séquentielle FEC/docetaxel . | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005173-56 | Sponsor Protocol Number: GOG/2007-01 | Start Date*: 2008-03-06 | |||||||||||
Sponsor Name:Grupo Oncológico Gallego (GOG) | |||||||||||||
Full Title: ENSAYO CLÍNICO ABIERTO, NO ALEATORIZADO, EN FASE II, DE TRATAMIENTO SECUENCIAL CON TAXOTERE® (T) SEGUIDO DE MYOCET® Y CICLOFOSFAMIDA (MC), COMO TRATAMIENTO ANTINEOPLASICO PRIMARIO EN PACIENTES CON ... | |||||||||||||
Medical condition: Cáncer de mama localizado (estadio II y IIIa). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011037-27 | Sponsor Protocol Number: ML22197/2009-01 | Start Date*: 2009-05-27 | |||||||||||
Sponsor Name:Instituto Científico Tecnológico de Navarra (ICTN) | |||||||||||||
Full Title: Estudio fase II, multicéntrico, para evaluar los marcadores predictores de respuesta en cáncer de mama localmente avanzado, tratado con bevacizumab en combinación con quimioterapia neoadyuvante. | |||||||||||||
Medical condition: Cancer Mama localmente avanzado | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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: 2007-004169-16 | Sponsor Protocol Number: ML20382 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:Roche Farma, S.A. | |||||||||||||
Full Title: Estudio fase II multicéntrico, abierto, no aleatorizado para evaluar la eficacia de una combinación con bevacizumab y quimioterapia secuencial, como tratamiento de pacientes con cáncer de mama oper... | |||||||||||||
Medical condition: Adenocarcinoma de mama operable HER2 negativo, de más de 2 cm de tamaño, no tratado previamente. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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