- 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 AND Cancer.
Displaying page 32 of 93.
EudraCT Number: 2005-004941-33 | Sponsor Protocol Number: A6191007 | Start Date*: 2006-03-02 | |||||||||||
Sponsor Name:PFIZER | |||||||||||||
Full Title: A Phase 2 Study of the Efficacy and Safety of SU-014813 in Patients with Metastatic Breast Cancer | |||||||||||||
Medical condition: Locally Recurrent or Metastatic Breast Cancer MBC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005186-10 | Sponsor Protocol Number: EGF105485 | Start Date*: 2006-09-12 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Randomized, Double-blind, Multicenter, Placebo-controlled Study of Adjuvant Lapatinib in Women with Early-Stage ErbB2 Overexpressing Breast Cancer | |||||||||||||
Medical condition: Women with early-stage ErbB2-overexpressing breast cancer. Eligible women must have had an initial diagnosis of histologically or cytologically confirmed invasive breast cancer (Stage I through St... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (Completed) LT (Completed) ES (Completed) BE (Completed) DK (Completed) LV (Completed) GR (Completed) SK (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005488-18 | Sponsor Protocol Number: 8628-006 | Start Date*: 2016-05-12 | |||||||||||||||||||||
Sponsor Name:Oncoethix GmbH, a wholly owned subsidiary of Merck Sharp & Dohme Corp. | |||||||||||||||||||||||
Full Title: A Phase IB Dose Exploration Trial with MK-8628, a Small Molecule Inhibitor of the Bromodomain and Extra-Terminal (BET) Proteins, in Subjects with Selected Advanced Solid Tumors | |||||||||||||||||||||||
Medical condition: NUT Midline Carcinoma Non-Small Cell Lung Cancer Triple-Negative Breast Cancer Castration-Resistant Prostate Cancer | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Completed) BE (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002385-11 | Sponsor Protocol Number: BIG01−01/BO16348B | Start Date*: 2002-05-16 | |||||||||||
Sponsor Name:F. HOFFMANN - LA ROCHE LTD. | |||||||||||||
Full Title: - | |||||||||||||
Medical condition: - | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003928-35 | Sponsor Protocol Number: EGF30008 | Start Date*: 2005-06-16 | |||||||||||
Sponsor Name:GLAXO SMITH KLINE RESEARCH & DEVELOPMENT LTD | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase III Study Comparing GW572016 and Letrozole versus Letrozole in Subjects with Estrogen/Progesterone Receptor-Positive Advanced or M... | |||||||||||||
Medical condition: Solid tumor treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004216-31 | Sponsor Protocol Number: IB 2007-26 | Start Date*: 2007-09-25 | |||||||||||
Sponsor Name:Institut Bergonié | |||||||||||||
Full Title: Réponse au traitement néoadjuvant par l'anti-aromatase anastrozole et l'anti-oestrogène pur fulvestrant : étude de phase II randomisée chez des patientes ménopausées atteintes d'un cancer du sein n... | |||||||||||||
Medical condition: Cancer du sein non métastatique hormono-sensible. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002643-89 | Sponsor Protocol Number: PALO-05-02 | Start Date*: 2005-12-14 |
Sponsor Name:Helsinn Healthcare SA | ||
Full Title: Double-blind Study to Compare the Efficacy of Palonosetron with or without the use of Dexamethasone on Days 2 and 3, in the Prevention of Nausea and Vomiting Induced by Moderately Emetogenic Chemot... | ||
Medical condition: This is a non-inferiority study in chemotherapy-naïve female patients with breast cancer, age 18 years or older, who are scheduled to receive Moderately Emetogenic Chemotherapy (MEC). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) ES (Completed) AT (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003774-76 | Sponsor Protocol Number: 1.0 | Start Date*: 2012-10-09 |
Sponsor Name:CUSL | ||
Full Title: Perioperative ketorolac in high risk breast cancer patients with and without inflammation. A prospective randomized placebo-controlled trial. | ||
Medical condition: Breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002371-13 | Sponsor Protocol Number: TENEO | Start Date*: 2007-11-06 | |||||||||||
Sponsor Name:Centre Jean Perrin | |||||||||||||
Full Title: A Pilot Phase II combination study of Taxotere (Docetaxel) and Erbitux (Cetuximab) as a NEOadjuvant therapy in patients with “triple-negative” (HR and Her2 negative) operable breast cancer. TENEO S... | |||||||||||||
Medical condition: Cancer du sein opérable RH- et Her2-, en situation néoadjuvante | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000173-77 | Sponsor Protocol Number: 2013-000173-77 | Start Date*: 2014-02-12 | ||||||||||||||||
Sponsor Name:Institut Jules Bordet | ||||||||||||||||||
Full Title: TRIUMPH Trial A phase II TRial evalUating the Menstrual and ovarian function of young breast cancer patients treated with a cycloPHosphamide-free regimen composed of doxorubicin and paclitaxel | ||||||||||||||||||
Medical condition: Primary breast cancer (adjuvant or neoadjuvant) | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001484-23 | Sponsor Protocol Number: Triple-B | Start Date*: 2013-05-24 | |||||||||||
Sponsor Name:BOOG Study Center | |||||||||||||
Full Title: Biomarker discovery randomized phase IIb trial with carboplatin-cyclophosphamide versus paclitaxel with or without atezolizumaB as first-line treatment in advanced triple negative Breast cancer | |||||||||||||
Medical condition: Metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003508-39 | Sponsor Protocol Number: SMR-3475 | Start Date*: 2018-02-28 | |||||||||||
Sponsor Name:Oncology Venture Aps | |||||||||||||
Full Title: Phase II, open label clinical study to investigate anti-tumour effect and tolerability of the PARP inhibitor 2X-121 in patients with metastatic breast cancer selected by the 2X-121 DRP®. | |||||||||||||
Medical condition: Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004057-71 | Sponsor Protocol Number: BC-P2-2020 | Start Date*: 2021-01-12 | |||||||||||
Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCCS | |||||||||||||
Full Title: miRNA100 as predictor of response to anti-endocrine treatment in luminal-HER2 negative breast cancer. a prospective validation clinical trial | |||||||||||||
Medical condition: HER2 NEGATIVE/LUMINAL BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000441-19 | Sponsor Protocol Number: H3E-EW-S098 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Eli lilly and Company Limited | |||||||||||||
Full Title: A randomised Phase II study of two chemotherapy regimens, Pemetrexed-Carboplatin, and Gemcitabine-vinorelbine, in Anthracycline and Taxane pretreated Advanced Breast cancer patients. | |||||||||||||
Medical condition: advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004008-71 | Sponsor Protocol Number: ELDORADO | Start Date*: 2017-01-19 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: The effect of curcumin and piperine on the pharmacokinetics of tamoxifen in patients with estrogen receptor positive breast cancer ‘the ELDORADO study’ | ||
Medical condition: Estrogen receptor positive breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002123-15 | Sponsor Protocol Number: GEICAM/2019-01 | Start Date*: 2020-06-15 | |||||||||||
Sponsor Name:GEICAM (Fundación Grupo Español de Investigación en Cáncer de Mama) | |||||||||||||
Full Title: Phase II, randomized, open-label, international, multicenter study to compare efficacy of standard chemotherapy vs. letrozole plus abemaciclib as neoadjuvant therapy in HR-positive/HER2-negative hi... | |||||||||||||
Medical condition: High/intermediate risk hormone receptor (HR) positive/human epidermal growth factor receptor 2 (HER2) negative breast cancer patients with indication of neoadjuvant therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005081-17 | Sponsor Protocol Number: ARV-471-BC-201 | Start Date*: 2023-01-20 | ||||||||||||||||
Sponsor Name:Arvinas Estrogen Receptor, Inc. (Arvinas) | ||||||||||||||||||
Full Title: An Open-Label, Randomized, Non-Comparative Phase 2 Study of ARV-471 or Anastrozole in Post-Menopausal Women With ER+/HER2– Breast Cancer in the Neoadjuvant Setting | ||||||||||||||||||
Medical condition: Post-menopausal women with ER+ HER2– breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000568-28 | Sponsor Protocol Number: GO28888 | Start Date*: 2014-10-16 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A phase II randomized, double-blind study of neoadjuvant letrozole plus GDC-0032 versus letrozole plus placebo in postmenopausal women with ER-positive/HER2-negative, early stage breast cancer | |||||||||||||
Medical condition: WOMEN WITH ER-POSITIVE/HER2-NEGATIVE, EARLY STAGE BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) AT (Completed) CZ (Completed) PT (Completed) HU (Completed) IT (Completed) GB (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003773-25 | Sponsor Protocol Number: A6181067 | Start Date*: 2006-01-03 | |||||||||||
Sponsor Name:PFIZER S.A | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PHASE 2 STUDY OF SU011248 IN COMBINATION WITH TRASTUZUMAB AS FIRST-LINE TREATMENT FOR METASTATIC DISEASE IN PATIENTS WITH BREAST CANCER | |||||||||||||
Medical condition: Histologically or cytologically proven diagnosis of breast cancer with evidence of 1) unresectable, locally recurrent, or 2) metastatic disease. Locally recurrent disease must not be amenable to r... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005200-19 | Sponsor Protocol Number: I-CONIC | Start Date*: 2022-05-09 |
Sponsor Name:Västra Götalandsregionen/Onkologiska kliniken | ||
Full Title: Use of Imatinib to convert triple negative breast cancer into ER-positive breast cancer - "I-CONIC" | ||
Medical condition: Early Triple Negative Breast Cancer planned for surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
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