- Trials with a EudraCT protocol (335)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
335 result(s) found for: Breast disorders.
Displaying page 1 of 17.
| EudraCT Number: 2007-007740-10 | Sponsor Protocol Number: TAM-01 | Start Date*: 2008-01-30 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA OSPEDALI GALLIERA | |||||||||||||
| Full Title: Randomized placebo-controlled phase III trial of low-dose tamoxifen women whit IntraEphitelial Neoplasia(IEN) | |||||||||||||
| Medical condition: chemoprevention of breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022065-10 | Sponsor Protocol Number: SABO-2010-01 | Start Date*: 2011-08-02 | |||||||||||
| Sponsor Name:Sahlgrenska University Hospital | |||||||||||||
| Full Title: Effect of angiogenesis inhibiting therapy in patients progressing on endocrine treatment and patients with triple negative breast cancer - a translational phase II study within the Swedish Associa... | |||||||||||||
| Medical condition: Patients with breast cancer who are oestrogen receptor positive but HER2 negative and progressing on endocrine therapy. Patients with locally advanced or recurrent triple negative breast cancer (TN... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: View results | ||||||||||||||||||
| EudraCT Number: 2019-000326-22 | Sponsor Protocol Number: IEO960 | Start Date*: 2020-09-22 | |||||||||||
| Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
| Full Title: The role of Contrast-Enhanced Spectral Mammography (CESM) in the diagnostic process of breast cancer: can it improve specificity of first-line examinations and therefore reduce the suspicious lesio... | |||||||||||||
| Medical condition: Patients with breast lesions undergoing further examination | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-000510-59 | Sponsor Protocol Number: 01012014 | Start Date*: 2014-08-11 | |||||||||||
| Sponsor Name:Dept of Plastic Surgery, Breast Surgery & Burns | |||||||||||||
| Full Title: Fat transplantation enriched with ex vivo expanded adipose-derived autologous mesenchymal stem cells in reconstruction of the breast. | |||||||||||||
| Medical condition: The study will include participants with breast hypoplasia (International Classification of Diseases-10: DQ 838A). | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005518-12 | Sponsor Protocol Number: 2 | Start Date*: 2012-06-25 | |||||||||||
| Sponsor Name:NAMED SRL | |||||||||||||
| Full Title: effect of oral administration of red clover on menopausal symptoms of the syndrome induced by adjuvant hormonal treatment in women diagnosed with breast cancer | |||||||||||||
| Medical condition: - Patients who have undergone surgery for breast cancer: he chose T1-2NO-1MO treated with tamoxifen more or less the same, adjuvant or pre-operative chemotherapy - Premenopausal patients at the ti... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002505-35 | Sponsor Protocol Number: ABCSG_50 | Start Date*: 2018-06-25 | |||||||||||||||||||||
| Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | |||||||||||||||||||||||
| Full Title: BRCA-P: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center, International Phase 3 Study to determine the Preventive Effect of Denosumab on Breast Cancer in Women carrying a BRCA1 Germline... | |||||||||||||||||||||||
| Medical condition: Prevention of breast cancer in women with a BRCA1 germline mutation | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||||||||||||
| Trial protocol: AT (Trial now transitioned) ES (Ongoing) DE (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| 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: 2014-002324-27 | Sponsor Protocol Number: MYL-1401H-3001 | Start Date*: 2015-04-22 | ||||||||||||||||
| Sponsor Name:Mylan GmbH | ||||||||||||||||||
| Full Title: Multicenter, Double-Blind, Randomized, Comparative Efficacy and Safety Study of MYL 1401H and European Sourced Neulasta® in Stage II/III Breast Cancer Patients Receiving Neoadjuvant or Adjuvant Che... | ||||||||||||||||||
| Medical condition: chemotherapy-induced neutropenia in patients with stage II/III breast cancer receiving docetaxel, doxorubicin, and cyclophosphamide (TAC) anti-cancer chemotherapy | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) DE (Completed) BG (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-001930-93 | Sponsor Protocol Number: GC-627-04 | Start Date*: 2017-01-13 | ||||||||||||||||
| Sponsor Name:Generon (Shanghai) Corporation Ltd. | ||||||||||||||||||
| Full Title: A Phase III, Randomized, Multi-Centre, Double-Blind, Placebo Controlled Clinical Trial of F-627 in Women with Breast Cancer Receiving Myelotoxic Chemotherapy | ||||||||||||||||||
| Medical condition: Women, between 18 and 75 years of age that have been diagnosed with Stage II-IV breast cancer in the adjuvant or metastatic setting and are scheduled to undergo chemotherapy. This is a profilaxis ... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: HU (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-003553-15 | Sponsor Protocol Number: GC-627-05 | Start Date*: 2018-06-22 | ||||||||||||||||
| Sponsor Name:Generon (Shanghai) Corporation Ltd. | ||||||||||||||||||
| Full Title: A Phase III, Randomized, Multi-Centre, Open-Label, Fixed Dose, Neulasta Active-Controlled Clinical Trial of F-627 in Women with Breast Cancer Receiving Myelotoxic Chemotherapy | ||||||||||||||||||
| Medical condition: Women, between 18 and 75 years of age that have been diagnosed with Stage I-III breast cancer and are scheduled to undergo chemotherapy. This is a prophylaxis for myleotoxic chemotherapy induced ne... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: LV (Completed) HU (Completed) BG (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2007-005831-27 | Sponsor Protocol Number: EPO PRE TX | Start Date*: 2007-11-09 | |||||||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE NIGUARDA CA' GRANDA (A.O. DI RILIEVO NAZIONALE) | |||||||||||||||||||||||
| Full Title: Use of rHuEpo before autologous hematopoietic stem cell transplantation in patients affected by multiple myeloma, non Hodgkin disease and breast cancer to reduce transfusional requirement after mye... | |||||||||||||||||||||||
| Medical condition: autologous hematopoietic stem cells transplantation in patients affected by multiple myeloma, non Hodgkin disease and breast cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2014-000810-72 | Sponsor Protocol Number: PREDIXLumB | Start Date*: 2014-12-05 | ||||||||||||||||||||||||||
| Sponsor Name:Karolinska University Hospital | ||||||||||||||||||||||||||||
| Full Title: PREDIX Luminal B - Neoadjuvant response-guided treatment of estrogen receptor positive tumors with high proliferation or slow proliferation with metastatic nodes or young patients. Part of a set of... | ||||||||||||||||||||||||||||
| Medical condition: Primary breast cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2006-000703-42 | Sponsor Protocol Number: ML 18742 | Start Date*: 2006-05-17 | |||||||||||
| Sponsor Name:ROCHE | |||||||||||||
| Full Title: A phase III randomized trial of trastuzumab continuation vs discontinuation in combination with 2nd-line chemotherapy after progression on a 1st-line trastuzumab-chemotherapy combination for HER2 ... | |||||||||||||
| Medical condition: Metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000809-12 | Sponsor Protocol Number: PREDIXLumA | Start Date*: 2014-11-17 | ||||||||||||||||||||||||||
| Sponsor Name:Karolinska University Hospital | ||||||||||||||||||||||||||||
| Full Title: PREDIX Luminal A - Neoadjuvant response-guided treatment of slowly proliferating hormone receptor positive tumors. Part of a set of translational phase II trials based on molecular subtypes | ||||||||||||||||||||||||||||
| Medical condition: Primary breast cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2017-004319-37 | Sponsor Protocol Number: 001.4 | Start Date*: 2019-06-19 | |||||||||||
| Sponsor Name:Medical University of Vienna, Department of Surgery | |||||||||||||
| Full Title: A prospective, randomised, single-blind explorative study to investigate the efficacy and safety of fat graft enrichment with autologous platelet lysate in female breast augmentation | |||||||||||||
| Medical condition: Fat grafting e.g. to the breast to restore small tissue defects is a very common and safe surgical procedure. Its main success among other is depended on the survival rate of the transferred fat ti... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000155-16 | Sponsor Protocol Number: CROLT/02 | Start Date*: 2011-10-04 | |||||||||||
| Sponsor Name:FONDAZIONE MICHELANGELO - AVANZAMENTO DELLO STUDIO E CURA DEI TUMORI | |||||||||||||
| Full Title: Modulation of response to hormonal therapy with lapatinib and/or metformin in patients with HER2-negative, ER and/or PgR positive metastatic breast cancer with progressive disease after first-line ... | |||||||||||||
| Medical condition: Female patients with HER2-negative, ER and/or PgR positive breast cancer in progression after first-line hormonal therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-004031-59 | Sponsor Protocol Number: Manta2 | Start Date*: 2004-11-22 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
| Full Title: Weekly maintainance therapy with Paclitaxel vs control arm after first line chemotherapy in patients with metastatic breast carcinoma. Phase III multicentric clinical trial. | |||||||||||||
| Medical condition: breast cancer | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012738-65 | Sponsor Protocol Number: CTC PLATINUM | Start Date*: 2008-10-15 | |||||||||||
| Sponsor Name:AZIENDA USL 4 PRATO | |||||||||||||
| Full Title: CLINICAL ACTIVITY OF DNA DAMAGING AND NON-DAMAGING CHEMIOTHERAPY REGIMENS IN ADVANCED BREAST CANCER PATIENTS WITH DIFFERENT BIOLOGICAL SUB-TYPES DEFINED BY BIOMARKERS EVALUATION ON CIRCULATING TUMO... | |||||||||||||
| Medical condition: METASTATIC BREAST CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005397-31 | Sponsor Protocol Number: GONAL | Start Date*: 2007-08-21 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA CAREGGI | |||||||||||||
| Full Title: EFFECT OF FSH TREATMENT ON ANEUPLOIDIC RATE IN OLIGOASTENOZOOSPERMIC PATIENTS | |||||||||||||
| Medical condition: couple infertility | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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