- 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 9 of 93.
EudraCT Number: 2009-015628-27 | Sponsor Protocol Number: CAUY922A2109 | Start Date*: 2010-08-25 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A phase Ib/II, multi-center, open-label study to evaluate the efficacy of AUY922 in combination with Trastuzumab in patients with locally advanced or metastatic HER2-positive breast cancer, that ha... | ||||||||||||||||||
Medical condition: locally advanced or metastatic HER2-positive breast cancer, that has progressed after or during at least one Trastuzumab-containing regimen | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: SE (Completed) FR (Completed) GB (Completed) DE (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005433-35 | Sponsor Protocol Number: DBCG 05 H | Start Date*: 2005-11-30 | |||||||||||
Sponsor Name:Danish Breast Cancer Cooperative Group (DBCG) | |||||||||||||
Full Title: TRASTUZUMAB (HERCEPTIN) SOM ADJUVERENDE BEHANDLING AF PATIENTER MED TIDLIG OPERABEL HER2-POSITIV BRYSTKRÆFT – ET FASE IV-STUDIE | |||||||||||||
Medical condition: Kvinder, som har modtaget definitiv kirurgi for histologisk verificeret operabel ikke-metastatisk HER2-positiv brystkræft stratificeret i gruppen med øget risiko i hht. DBCG´s retningslinier, og so... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001212-44 | Sponsor Protocol Number: GIM-4 | Start Date*: 2005-07-27 | |||||||||||
Sponsor Name:CONSORZIO ONCOTECH | |||||||||||||
Full Title: Letrozole adjuvant therapy duration (LEAD)study: standard versus long treatment. A phase III study in postmenopausal women with early breast cancer | |||||||||||||
Medical condition: Adjuvant therapy with letrozole after 2 or 3 years of tamoxifen for early breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015238-31 | Sponsor Protocol Number: M09TNM | Start Date*: 2009-12-16 | |||||||||||
Sponsor Name:NKI-AVL | |||||||||||||
Full Title: RANDOMIZED PHASE II/III STUDY OF INDIVIDUALIZED NEOADJUVANT CHEMOTHERAPY IN ‘TRIPLE-NEGATIVE’ BREAST TUMORS | |||||||||||||
Medical condition: Triple negative breast cancer treated with neoadjuvant chemotherapy | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003634-42 | Sponsor Protocol Number: TRAS-LIQ-2004 | Start Date*: 2007-12-17 | ||||||||||||||||
Sponsor Name:Klinikum der Universität München, Standort Großhadern | ||||||||||||||||||
Full Title: Prospective phase II trial using Capecitabine and Trastuzumab for therapy of female patients with cerebral metastasizing, HER2-overexpressing breast cancer | ||||||||||||||||||
Medical condition: CNS-metastasizing HER2-overexpressing breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-005231-22 | Sponsor Protocol Number: D931CC00001 | Start Date*: 2022-09-02 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Multicentre, Open-Label Study to Assess the Efficacy and Safety of Olaparib Monotherapy and Olaparib Plus Durvalumab Combination as Neoadjuvant Therapy in Patients with BRCA Mutations a... | |||||||||||||
Medical condition: BRCA Mutations and Early Stage HER2-Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Restarted) DE (Ongoing) AT (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000174-37 | Sponsor Protocol Number: GEICAM/2011-03_S1007 | Start Date*: 2012-04-26 | |||||||||||
Sponsor Name:GEICAM (Fundación Grupo Español de Investigación en Cáncer de Mama) | |||||||||||||
Full Title: A Phase III, Randomized Clinical Trial of Standard Adjuvant Endocrine Therapy +/- Chemotherapy in Patients with 1-3 Positive Nodes, Hormone Receptor-Positive and HER2-Negative Breast Cancer with Re... | |||||||||||||
Medical condition: Patients with confirmed diagnosis of node positive (1-3 nodes) invasive breast carcinoma with positive hormone receptor status, and negative HER-2. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000224-13 | Sponsor Protocol Number: A6181100 | Start Date*: 2006-05-10 | |||||||||||
Sponsor Name:PFIZER AB | |||||||||||||
Full Title: EXPLORATORY EVALUATION OF A SEQUENTIAL ADMINISTRATION OF DOCETAXEL AND SU011248 IN WOMEN WITH ADVANCED BREAST CANCER | |||||||||||||
Medical condition: Advanced Breast Cancer | |||||||||||||
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Population Age: | Gender: | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005186-31 | Sponsor Protocol Number: 01062017 | Start Date*: 2018-06-06 | ||||||||||||||||
Sponsor Name:Department of Plastic Surgery, Breast and Burns Treatment | ||||||||||||||||||
Full Title: Fat Grafting with Ex-Vivo Expanded Adipose-Derived Stem Cells for Breast Reconstruction Following Mastectomy | ||||||||||||||||||
Medical condition: This study will include patients with genetic predisposition to development of breast cancer, who are offered prophylactic bilateral skin-sparring mastectomy. | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002286-30 | Sponsor Protocol Number: A8641020 | Start Date*: 2014-12-12 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: PHASE 2 STUDY OF SINGLE-AGENT PF 03084014 IN PATIENTS WITH ADVANCED TRIPLE-NEGATIVE BREAST CANCER WITH OR WITHOUT GENOMIC ALTERATIONS IN NOTCH RECEPTORS | |||||||||||||
Medical condition: ADVANCED TRIPLE-NEGATIVE BREAST CANCER WITH OR WITHOUT GENOMIC ALTERATIONS IN NOTCH RECEPTORS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) IT (Completed) BE (Prematurely Ended) ES (Completed) DE (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003403-36 | Sponsor Protocol Number: GEMCAPE | Start Date*: 2005-11-10 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Trattamento con Capecitabina e Gemcitabina in pazienti con carcinoma della mammella metastatico pretrattati con Taxani ed Antracicline. Studio di fase II. | |||||||||||||
Medical condition: BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004860-22 | Sponsor Protocol Number: IJB-BCTL:20120306 | Start Date*: 2014-01-16 | |||||||||||
Sponsor Name:Institute Jules Bordet | |||||||||||||
Full Title: The [PEARL] Study : Pet imaging as a biomarker of Everolimus Added value in hormone Refractory postmenopausaL women | |||||||||||||
Medical condition: Locally advanced or metastatic endocrine receptor positive and HER2 negative breast cancer refractory to non-steroidal aromatase inhibitors (NSAI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004532-58 | Sponsor Protocol Number: LA-EP06-301 | Start Date*: 2012-08-20 | |||||||||||
Sponsor Name:Sandoz GmbH | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, multi-center Phase 3 comparative study investigating efficacy and safety of LA-EP2006 and Neulasta® in breast cancer patients treated with myelosuppressi... | |||||||||||||
Medical condition: Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004189-13 | Sponsor Protocol Number: 1 | Start Date*: 2012-02-23 | ||||||||||||||||
Sponsor Name:Medizinische Universität Wien | ||||||||||||||||||
Full Title: ASSESSMENT OF MULTIDRUG RESISTANCE IN BREAST CANCER AND LOW GRADE GLIOMA PATIENTS WITH [11C]TARIQUIDAR PET. A PILOT STUDY | ||||||||||||||||||
Medical condition: Prospective cohort diagnostic test accuracy study in 30 breast cancer patients scheduled for neoadjuvant chemotherapy (15 of which with Pgp-positive and 15 with Pgp-negative tumors) and 10 low grad... | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005209-23 | Sponsor Protocol Number: CA163139 | Start Date*: 2008-03-21 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: Randomized Phase II of Ixabepilone Alone and Ixabepilone Plus Cetuximab as First-Line Treatment for Female Subjects with Triple Negative (ER, PR, Her2 negative) Locally Advanced non-resectable and/... | |||||||||||||
Medical condition: BREAST CANCER, FIRST LINE | |||||||||||||
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Population Age: | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) AT (Completed) CZ (Completed) ES (Completed) IT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004986-18 | Sponsor Protocol Number: DS8201-A-U201 | Start Date*: 2017-11-08 | |||||||||||
Sponsor Name:Daiichi Sankyo Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Open-Label Study of DS-8201a, an Anti-HER2-Antibody Drug Conjugate (ADC) for HER2-Positive, Unresectable and/or Metastatic Breast Cancer Subjects Who are Resistant or Refrac... | |||||||||||||
Medical condition: Unresectable/metastatic breast cancer with HER2 positive expression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) BE (Completed) GB (GB - no longer in EU/EEA) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003530-13 | Sponsor Protocol Number: 18072011 | Start Date*: 2011-12-20 | |||||||||||
Sponsor Name:Brighton & Sussex University Hospitals NHS Trust | |||||||||||||
Full Title: Randomised phase II window study of short-term preoperative treatment with the PI3K inhibitor GDC-0941 plus Anastrozole versus Anastrozole alone in patients with ER-positive primary breast cancer | |||||||||||||
Medical condition: Primary breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005161-12 | Sponsor Protocol Number: OAS-12DOC-BIO | Start Date*: 2015-10-22 | |||||||||||||||||||||||||||||||
Sponsor Name:Oasmia Pharmaceutical AB | |||||||||||||||||||||||||||||||||
Full Title: A multi-country, multicenter, randomized, open-label, parallel group study to assess the efficacy and safety of Docecal compared with Taxotere® | |||||||||||||||||||||||||||||||||
Medical condition: adenocarcinoma of the breast | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: LV (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003262-41 | Sponsor Protocol Number: GO28509 | Start Date*: 2013-05-16 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A PHASE II, RANDOMIZED STUDY OF PACLITAXEL WITH GDC-0941 VERSUS PACLITAXEL WITH PLACEBO IN PATIENTS WITH LOCALLY RECURRENT OR METASTATIC BREAST CANCER | |||||||||||||
Medical condition: Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) CZ (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020966-34 | Sponsor Protocol Number: ICORG10-05 | Start Date*: 2010-08-06 | |||||||||||
Sponsor Name:ICORG | |||||||||||||
Full Title: A phase II neoadjuvant study assessing TCH (Docetaxel, Carboplatin and Trastuzumab) and TCHL (Docetaxel, Carboplatin, Traztuzumab and Lapatinib) in Erb B2 positive breast cancer patients | |||||||||||||
Medical condition: Her 2 positive locally advanced or primary breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
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