- Trials with a EudraCT protocol (1,850)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
1,850 result(s) found for: Breast cancer.
Displaying page 2 of 93.
EudraCT Number: 2009-017788-40 | Sponsor Protocol Number: KEO09069EST | Start Date*: 2010-10-20 | |||||||||||
Sponsor Name:CRLCC Alexis Vautrin | |||||||||||||
Full Title: Etude de phase II randomisée multicentrique évaluant l'efficacité d’estramustine phosphate (Estracyt ®) chez des patientes présentant un cancer du sein métastatique HER2- / RH+ ayant déjà reçu un t... | |||||||||||||
Medical condition: Metastases breast cancer in women already treated with aromatase inhibitors. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024067-41 | Sponsor Protocol Number: COLTONE | Start Date*: 2011-04-28 | |||||||||||
Sponsor Name:F.A.R.O. FONDAZIONE PER LE ATTIVITA' DI RICERCA IN ONCOLOGIA | |||||||||||||
Full Title: Pilot study of sequential adjuvant chemotherapy regimen including non-pegylated Liposomal Doxorubicin (MYOCET) in combination with Cyclophosphamide and Paclitaxel in elderly patients with diagnosis... | |||||||||||||
Medical condition: Elderly patients with diagnosis of early breast Cancer candidate to adjuvant chemotherapy. | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004326-25 | Sponsor Protocol Number: Shother 2007-004326-25 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: SHORT-HER: MULTICENTRIC RANDOMISED PHASE III TRIAL OF ADJUVANT CHEMOTHERAPY PLUS 3 VS 12 MONTHS OF TRASTUZUMAB IN BREAST CANCER PATIENTS WITH HER2 POSITIVE DISEASE | |||||||||||||
Medical condition: carcinoma mammario con iperespressione di Her 2 o amplificazione dei geni codificanti per il recettore stesso. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023776-52 | Sponsor Protocol Number: Lisette-1 | Start Date*: 2011-01-19 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Optimizing tamoxifen therapy through the induction of CYP3A4, CYP2C and CYP2D6 mediated metabolism | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019001-42 | Sponsor Protocol Number: NEUGR-003 | Start Date*: 2010-07-08 | |||||||||||
Sponsor Name:Teva Pharmaceutical Works Private Limited Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Active Comparator, Non-Inferiority Study of Subcutaneously Administered Neugranin (Recombinant Human Albumin-Human Granulocyte Colony Stimulating Factor) or Pegfilgrasti... | |||||||||||||
Medical condition: breast cancer patients receiving myelosupressive chemotherapy (doxorubicin/docetaxel) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006262-28 | Sponsor Protocol Number: IEO S438/508 | Start Date*: 2009-06-03 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Allogeneic Haematopoietic Cell Transplantation Using a Non-myeloablative Preparative Regimen of Total Lymphoid Irradiation and Anti-Thymocyte Globulin for Patients with Refractory Triple Negative... | |||||||||||||
Medical condition: Patients with Refractory Triple Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006236-22 | Sponsor Protocol Number: MET/TEST1106 | Start Date*: 2007-01-31 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA O.I.R.M. - S. ANNA | |||||||||||||
Full Title: Use of Metformin to reduce serum level of Testosterone and improve the metabolic picture in women treated for breast cancer | |||||||||||||
Medical condition: Menopausal women on treatment for BC, with higher risk of recurrence due to augmented level of T | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000520-14 | Sponsor Protocol Number: IEO S291/106 | Start Date*: 2006-10-26 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: A PHASE II STUDY OF GW572016 LAPATINIBTM ON CELL PROLIFERATION IN HER-2/neu ErbB2 POSITIVE BREAST CANCER BEFORE SURGERY. | |||||||||||||
Medical condition: Primary breast cancer T1-3 N0-1 M0 Histologically-confirmed HER 2 positive | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006025-27 | Sponsor Protocol Number: IEOS380/607 | Start Date*: 2008-11-10 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: A phase II study of metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with bevacizumab and erlotinib (BEXE), plus trastuzumab in HER2/neu positive tumors (BEXET), in adv... | |||||||||||||
Medical condition: advanced or metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006430-10 | Sponsor Protocol Number: CTKI258A2202 | Start Date*: 2009-06-22 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, open label Phase II trial of TKI258 in FGFR1 amplified and non-amplified metastatic HER2 negative breast cancer. | |||||||||||||
Medical condition: In female patients with FGFR1 amplified and non-amplified metastatic HER2 negative breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) ES (Prematurely Ended) FR (Completed) GB (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018795-24 | Sponsor Protocol Number: APREC S-2010-01 | Start Date*: 2010-06-01 | |||||||||||
Sponsor Name:Alliance pour la recherche en cancérologie | |||||||||||||
Full Title: Evaluation of the effect of pasireotide LAR administration in the lymphocele prevention after axillary node dissection for breast cancer | |||||||||||||
Medical condition: BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005184-42 | Sponsor Protocol Number: CLEE011A2412B | Start Date*: 2022-04-15 | ||||||||||||||||
Sponsor Name:NOVARTIS PHARMA AG | ||||||||||||||||||
Full Title: A post-trial access roll-over study to allow access to ribociclib (LEE011) for patients who are on ribociclib treatment in Novartis-sponsored study | ||||||||||||||||||
Medical condition: HR+, HER2- advanced or metastatic breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) PT (Trial now transitioned) FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000398-10 | Sponsor Protocol Number: EFC16133 | Start Date*: 2022-04-19 | |||||||||||
Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
Full Title: A randomized, multicenter, double-blind, Phase 3 study of amcenestrant (SAR439859) versus tamoxifen for the treatment of patients with hormone receptor-positive, human epidermal growth factor 2-neg... | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) HU (Prematurely Ended) EE (Prematurely Ended) BE (Prematurely Ended) PT (Prematurely Ended) DK (Prematurely Ended) IT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003576-19 | Sponsor Protocol Number: I07015 | Start Date*: 2007-10-18 | |||||||||||
Sponsor Name:CHU de LIMOGES | |||||||||||||
Full Title: Evaluation de l'efficacité et de la tolérance du Lanreotide LP 90 mg versus placebo dans la diminution de la lyphorrhée post curage axillaire dans les cancers du sein. | |||||||||||||
Medical condition: cancer du sein | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002120-83 | Sponsor Protocol Number: ICO-N-2016-02 | Start Date*: 2016-10-05 | |||||||||||
Sponsor Name:INSTITUT DE CANCEROLOGIE DE L'OUEST RENE GAUDUCHEAU | |||||||||||||
Full Title: Study evaluation of 2nd hormone line response by -[18F]fluoro-17β-œstradiol (FES) PET/CT in metastatic breast cancer patients | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011113-25 | Sponsor Protocol Number: SA2009 | Start Date*: 2009-05-29 | |||||||||||
Sponsor Name:Per Honore | |||||||||||||
Full Title: Populationsbaseret farmakokinetisk og farmakodynamisk doseringsmodel af epirubicin, cyklofosfamid og docetaxel til brystkræft | |||||||||||||
Medical condition: brystcancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004234-41 | Sponsor Protocol Number: 4102000 | Start Date*: 2006-11-23 | |||||||||||
Sponsor Name:Otto-von-Guericke Universität Magdeburg | |||||||||||||
Full Title: Dosisdichte 1st-line Therapie des metastasierten Mammakarzinoms mit Paclitaxel und liposomalem Doxorubicin (Myocet®) | |||||||||||||
Medical condition: metastasiertes Mammakarzinom | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017402-36 | Sponsor Protocol Number: DEND/CM | Start Date*: 2010-11-12 | |||||||||||
Sponsor Name:Instituto Científico y Tecnológico de Navarra | |||||||||||||
Full Title: Estudio prospectivo fase II de la vacunación con células dendríticas autólogas en pacientes con cáncer de mama triple negativo en estadios II-III | |||||||||||||
Medical condition: Cáncer de mama triple negativo en estadíos II-III | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008698-69 | Sponsor Protocol Number: CRAD001Y2301 | Start Date*: 2009-07-28 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A Randomized Double-Blind, Placebo-Controlled Study of Everolimus in Combination with Exemestane in the Treatment of Postmenopausal Women with Estrogen Receptor Positive Locally Advanced or Metasta... | |||||||||||||
Medical condition: estrogen receptor positive locally advanced or metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) CZ (Completed) NL (Completed) FR (Completed) BE (Completed) GB (Completed) DE (Completed) SE (Completed) ES (Completed) HU (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002061-12 | Sponsor Protocol Number: SBG2004-1/ABCSG25/GBG53 | Start Date*: 2007-08-17 | |||||||||||
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | |||||||||||||
Full Title: PANTHER (The SBG 2004-1/ABCSG 25/GBG53 Protocol) - a randomised phase III study: Comparing two weekly and tailored epirubicin + cyclophosphamide followed by two weekly tailored docetaxel (dtEC->dtT... | |||||||||||||
Medical condition: lymph node positive breast cancer patients | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) FI (Prematurely Ended) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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