- Trials with a EudraCT protocol (1,852)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,852 result(s) found for: Breast Cancer.
Displaying page 33 of 93.
| EudraCT Number: 2004-004223-36 | Sponsor Protocol Number: CFEM345EGB05 | Start Date*: 2005-07-29 |
| Sponsor Name:South Manchester University Hospital | ||
| Full Title: Short term biological study effects of Zoledronate and Letrozole on invasive breast cancer | ||
| Medical condition: Breast Cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-002459-40 | Sponsor Protocol Number: BREAST-AB-01 | Start Date*: 2020-12-17 |
| Sponsor Name:Rigshospitalet | ||
| Full Title: Prophylactic treatment of breast implants with a solution of gentamicin, vancomycin and cefazolin antibiotics for women undergoing breast reconstructive surgery: a randomized controlled trial (The ... | ||
| Medical condition: Implant-based breast reconstruction following mastectomy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DK (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-003183-19 | Sponsor Protocol Number: CA180-261 | Start Date*: 2009-02-16 | |||||||||||
| Sponsor Name:Bristol Myers Squibb International Corporation | |||||||||||||
| Full Title: A Randomized, Double-Blind, Multi-Center Phase 2 Trial of Exemestane (Aromasin®) plus Dasatinib versus Exemestane plus Placebo in Advanced Estrogen Receptor-Positive Breast Cancer after Disease Pro... | |||||||||||||
| Medical condition: Advanced Estrogen Receptor-Positive Breast Cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) IE (Completed) CZ (Completed) IT (Completed) SE (Completed) ES (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004618-36 | Sponsor Protocol Number: CTMX-2009-002 | Start Date*: 2021-03-15 | |||||||||||
| Sponsor Name:CytomX Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase 2, Open-Label Study to Evaluate the Safety and Antitumor Activity of CX-2009 in Advanced HR-Positive/HER2-Negative Breast Cancer and of CX-2009 as Monotherapy and in Combination with CX-072... | |||||||||||||
| Medical condition: HR-positive/HER2-negative breast cancer Triple-negative breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-002371-16 | Sponsor Protocol Number: D6997C00002 (9238IL/0064) | Start Date*: 2004-11-18 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: A Randomised, Double-Blind, Parallel-group, Multicentre, Phase III Study Comparing the Efficacy and Tolerability of Fulvestrant (FASLODEX™) 500 mg with Fulvestrant (FASLODEX™) 250 mg in Postmenopau... | ||
| Medical condition: Postmenopausal women with advanced breast cancer, progressing or relapsing after previous endocrine therapy | ||
| Disease: | ||
| Population Age: Elderly | Gender: Female | |
| Trial protocol: SK (Completed) CZ (Completed) HU (Completed) ES (Completed) IT (Completed) MT (Ongoing) | ||
| Trial results: (No results available) | ||
| 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: View results | ||||||||||||||||||
| EudraCT Number: 2010-024394-39 | Sponsor Protocol Number: CBEZ235B2201 | Start Date*: 2011-05-06 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A Phase II study of orally administered BEZ235 monotherapy in patients with hormone receptor positive, HER2 negative, metastatic breast cancer, with or without PI3K activated pathway | |||||||||||||
| Medical condition: Patients who have experienced progression of disease after first-line antineoplasic treatment of advanced endometrial carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) GB (Prematurely Ended) BE (Prematurely Ended) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-003434-18 | Sponsor Protocol Number: IBCSG 32-05/ BIG 1-05 | Start Date*: 2006-05-04 |
| Sponsor Name:International Breast Cancer Study Group (IBCSG) | ||
| Full Title: Phase III Trials Evaluating the Role of Adjuvant Pegylated Liposomal Doxorubicin (PLD, Caelyx®, Doxil®) for Women (age 66 years or older) with Endocrine Nonresponsive Breast Cancer Who Are NOT Suit... | ||
| Medical condition: Older women (66 years of age or older) with histologically proven, resected breast cancer. The disease must be classified as endocrine nonresponsive and patients must not be candidates for endocrin... | ||
| Disease: | ||
| Population Age: Elderly | Gender: Female | |
| Trial protocol: SE (Prematurely Ended) HU (Completed) SI (Completed) IT (Completed) BE (Completed) FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-016091-80 | Sponsor Protocol Number: TCD11418 | Start Date*: 2010-01-11 | |||||||||||
| Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
| Full Title: Multicenter, randomized, open label study evaluating a poly(ADP-ribose) polymerase-1(PARP-1) inhibitor, SAR240550 (BSI-201), administered twice weekly or weekly, in combination with gemcitabine/car... | |||||||||||||
| Medical condition: Metastatic Triple Negative Breast Cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) ES (Completed) IT (Completed) NL (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: 2009-011118-47 | Sponsor Protocol Number: L00070IN308B0 | Start Date*: 2009-04-24 | |||||||||||
| Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
| Full Title: Phase III trial of IV vinflunine versus an alkylating agent in patients with metastatic breast cancer previously treated with or resistant to an anthracycline, a taxane, an antimetabolite, and a vi... | |||||||||||||
| Medical condition: Metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Completed) PT (Completed) IT (Completed) ES (Completed) BE (Completed) DE (Completed) AT (Completed) HU (Completed) GB (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-004007-37 | Sponsor Protocol Number: CZOL446GDE19 | Start Date*: 2006-03-27 | |||||||||||
| Sponsor Name:Novartis Pharma GmbH | |||||||||||||
| Full Title: Neoadjuvant therapy for postmenopausal women with ER and/or PgR positive breast cancer. A randomized open phase II trial evaluating the efficacy of a 6 months preoperative treatment with Letrozo... | |||||||||||||
| Medical condition: Breast cancer by postmenopausal women | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2006-000339-93 | Sponsor Protocol Number: 20050136 | Start Date*: 2006-05-26 | |||||||||||
| Sponsor Name:Amgen Inc. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Multicenter Study of Denosumab Compared With Zoledronic Acid (Zometa) in the Treatment of Bone Metastases in Subjects with Advanced Breast Cancer. | |||||||||||||
| Medical condition: Treatment of bone metastases in subjects with advanced breast cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) HU (Completed) NL (Completed) SK (Completed) GB (Completed) AT (Completed) ES (Completed) DE (Completed) LT (Completed) EE (Completed) BE (Completed) SE (Completed) LV (Completed) DK (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004879-38 | Sponsor Protocol Number: BO28408 | Start Date*: 2014-08-11 | |||||||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||
| Full Title: A RANDOMIZED, MULTICENTER, OPEN-LABEL, TWO-ARM, PHASE III NEOADJUVANT STUDY EVALUATING TRASTUZUMAB EMTANSINE PLUS PERTUZUMAB COMPARED WITH CHEMOTHERAPY PLUS TRASTUZUMAB AND PERTUZUMAB FOR PATIENTS ... | |||||||||||||||||||||||
| Medical condition: HER2-positive, operable, locally advanced or inflammatory early breast cancer. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) ES (Completed) DE (Completed) FR (Completed) IE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2020-003096-18 | Sponsor Protocol Number: ACT16432 | Start Date*: 2022-02-09 | ||||||||||||||||
| Sponsor Name:Sanofi aventis recherche & développement | ||||||||||||||||||
| Full Title: Open-label, multi-cohort, Phase 2 trial, evaluating the efficacy and safety of SAR408701 in patients with CEACAM5-positive advanced solid tumors | ||||||||||||||||||
| Medical condition: Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) NL (Completed) HU (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-003699-38 | Sponsor Protocol Number: CEDM-MRI | Start Date*: 2021-04-28 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE TUMORI - IRCCS FONDAZIONE PASCALE | |||||||||||||
| Full Title: DETECTION RATE AND CLASSIFICATION OF BREAST LESIONS WITH DIGITAL MAMMOGRAPHY WITH CONTRAST MEDIUM (CEDM) ALONE AND IN COMBINATION WITH TOMOSYNTHESIS COMPARED TO MR IMAGING WITH GADOLINIUM IN DYNAMI... | |||||||||||||
| Medical condition: Breast souspicious lesions | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001463-75 | Sponsor Protocol Number: ICO-2019-04 | Start Date*: 2020-02-03 | |||||||||||
| Sponsor Name:INSTITUT DE CANCEROLOGIE DE L'OUEST | |||||||||||||
| Full Title: Pilot Feasibility Study: Inflammation and presence of M2 macrophages explorations with[18F]-DPA-714 PET/CT in Triple Negative breast cancers | |||||||||||||
| Medical condition: Patients with Triple Negative Breast Cancer prior to surgical treatment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-002625-31 | Sponsor Protocol Number: 10041 | Start Date*: 2006-12-11 | |||||||||||
| Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
| Full Title: Microarray In Node negative and 1 to 3 positive lymph node Disease may Avoid ChemoTherapy. A prospective, randomised study comparing the 70-gene expression signature with common clinical-pathologi... | |||||||||||||
| Medical condition: Lymph-node negative early breast cancer and breast cancer with 1 to 3 positive nodes | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) ES (Completed) SI (Completed) DE (Completed) GB (Completed) IT (Completed) PT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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