- Trials with a EudraCT protocol (1,852)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
1,852 result(s) found for: breast cancer.
Displaying page 11 of 93.
| 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: 2009-011079-57 | Sponsor Protocol Number: BICG26UMCG-NIRF | Start Date*: 2009-05-28 | ||||||||||||||||
| Sponsor Name:University Medical Center Groningen | ||||||||||||||||||
| Full Title: Evaluation of Indocyanine Green (ICG) enhanced Near-InfraRed Fluorescence (NIRF) Imaging for Intra-Operative Sentinel Lymph Node (SLN) detection in Breast Surgery. | ||||||||||||||||||
| Medical condition: Women above the age of 21 with core biopsy or cytology proven breast cancer stage I and II, eligible for lumpectomy and sentinel lymph node procedure | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2005-003217-32 | Sponsor Protocol Number: 0006 | Start Date*: 2005-11-08 | |||||||||||
| Sponsor Name:AZIENDA USL DI FORLI | |||||||||||||
| Full Title: PHASE-II STUDY TO EVALUATE ACTIVITY OF DEXRAZOXANE CARDIOXANE IN ORDER TO PREVENT CARDIAC TOXICITY IN PATIENTS WITH BREAST CANCER AND TREATED WITH ANTHRACYCLINE | |||||||||||||
| Medical condition: To evaluate activity of Dexrazoxane in order to prevent cardiac toxicity in patients with breast cancer and treated with anthracycline | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-005267-21 | Sponsor Protocol Number: IEO 222/604 | Start Date*: 2005-04-04 | |||||||||||
| Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
| Full Title: A RANDOMIZED PHASE II PREVENTION TRIAL IN SUBJECTS AT HIGH RISK FOR HORMONE NON RESPONSIVE BREAST CANCER | |||||||||||||
| Medical condition: PREVENTION TRIAL IN SUBJECTS AT HIGH RISK FOR HORMONE NON-RESPONSIVE BREAST CANCER | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004018-42 | Sponsor Protocol Number: FARM5K3MEE | Start Date*: 2006-09-15 | |||||||||||
| Sponsor Name:UNIVERSITA' DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
| Full Title: A phase III study comparing anastrozole, letrozole and exemestane, upfront (for 5 years) or sequentially (for 3 years after 2 years of tamoxifen), as adjuvant treatment of postmenopausal patients ... | |||||||||||||
| Medical condition: adjuvant hormono-therapy in breast cancer patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-000898-68 | Sponsor Protocol Number: 2013/VCC/0008 | Start Date*: 2014-01-24 | ||||||||||||||||||||||||||
| Sponsor Name:Velindre NHS Trust | ||||||||||||||||||||||||||||
| Full Title: A phase 1b/2 randomised placebo controlled trial of fulvestrant +/- AZD5363 in postmenopausal women with advanced breast cancer previously treated with a third generation aromatase inhibitor. | ||||||||||||||||||||||||||||
| Medical condition: Estrogen receptor positive advanced breast cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2013-003839-30 | Sponsor Protocol Number: D081CC00006 | Start Date*: 2014-06-16 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A randomised, double-blind, parallel group, placebo-controlled multi-centre Phase III study to assess the efficacy and safety of olaparib versus placebo as adjuvant treatment in patients with germl... | |||||||||||||
| Medical condition: Adjuvant breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Trial now transitioned) HU (Trial now transitioned) IT (Trial now transitioned) BE (Trial now transitioned) SE (Trial now transitioned) ES (Ongoing) NL (Ongoing) AT (Trial now transitioned) IS (Trial now transitioned) PL (Trial now transitioned) PT (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-001806-17 | Sponsor Protocol Number: AS1402-C-201 | Start Date*: 2008-11-17 | |||||||||||
| Sponsor Name:Antisoma Research Limited | |||||||||||||
| Full Title: A Phase II, Randomised, Open-Label, Multicentre Study of AS1402 in Combination with Letrozole as First Line Treatment in Postmenopausal Women with Locally Advanced or Metastatic Breast Cancer. | |||||||||||||
| Medical condition: Locally Advanced or Metastatic Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Ongoing) PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-006412-29 | Sponsor Protocol Number: 3144A1-203-WW | Start Date*: 2007-10-18 | |||||||||||
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | |||||||||||||
| Full Title: A Phase 1 / 2 Study of HKI-272 in combination With Paclitaxel in Subjects With Solid Tumors and Breast Cancer | |||||||||||||
| Medical condition: Metastatic breast cancer remains incurable and represents an area of unmet medical need globally. Epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor 2 (HER2) activat... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003399-36 | Sponsor Protocol Number: MK-4214-008 | Start Date*: 2011-10-28 | |||||||||||||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||||||||||||
| Full Title: A Phase III Randomized, Double-Blind, Active-Controlled Clinical Trial to Study the Efficacy and Safety of MK-4214 (filgrastim) and Neupogen™ as an Adjunct to Combination Chemotherapy with Doxorubi... | |||||||||||||||||||||||
| Medical condition: Breast Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: LV (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2012-002556-17 | Sponsor Protocol Number: SAKK22/10/UC-0140/1207 | Start Date*: 2013-02-04 | |||||||||||
| Sponsor Name:UNICANCER | |||||||||||||
| Full Title: A randomized phase II trial of pertuzumab in combination with trastuzumab with or without chemotherapy, both followed by T-DM1 in case of progression, in patients with HER2-positive metastatic brea... | |||||||||||||
| Medical condition: HER2-positive metastatic breast cancer | |||||||||||||
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| Population Age: | Gender: Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-018188-29 | Sponsor Protocol Number: Calendula study | Start Date*: 2010-08-06 | ||||||||||||||||
| Sponsor Name:Dept of Oncology | ||||||||||||||||||
| Full Title: Randomised blinded trial of Calendula Officinalis compared with aqueos cream for the prevention of acute skin toxicity in relation to radiotherapy for breast cancer | ||||||||||||||||||
| Medical condition: Patients operated for breast cancer who undergo postoperative adjuvant radiotherapy will be offered to participate in this randomized trial with the aim to reduce the risk of severe radiation skin ... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: SE (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-004489-17 | Sponsor Protocol Number: IEOS733612 | Start Date*: 2013-08-02 | |||||||||||
| Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
| Full Title: WAVE: Weekly nab-paclitaxel (Abraxane®) Versus Epirubicin in women with early breast cancer who are elderly or unfit for a 3-weekly polychemotherapy regimen: a Phase II Randomized Trial evaluating ... | |||||||||||||
| Medical condition: early breast cancer in elderly patients or patients who are unfit for a polychemotherapy regimen | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005021-30 | Sponsor Protocol Number: FARM5P8YFC | Start Date*: 2007-10-31 | |||||||||||
| Sponsor Name:REGIONE LOMBARDIA - DIREZIONE GENERALE SANITA' | |||||||||||||
| Full Title: TOP TRIAL. A RANDOMISED PHASE III CLINICAL TRIAL OF TRASTUZUMAB (HERCEPTIN) OPTIMIZATION IN PATIENTS WITH LOCALLY ADVANCED AND/OR METASTATIC BREAST CANCER OVEREXPRESSING HER2 AFTER A FIRST LINE CHE... | |||||||||||||
| Medical condition: Women with locally advanced or metastatic breast cancer over expressing HER2 who have been previously treated with a first line chemotherapy plus trastuzumab. | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-024481-22 | Sponsor Protocol Number: EP06-302 | Start Date*: 2012-01-17 | |||||||||||
| Sponsor Name:Sandoz GmbH | |||||||||||||
| Full Title: A randomized, double-blind, parallel-group, multi-center Phase III study comparing the efficacy and safety of EP2006 and Neupogen® in breast cancer patients treated with myelosuppressive chemothe... | |||||||||||||
| Medical condition: Breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: CZ (Completed) HU (Completed) SK (Completed) LT (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2017-001467-20 | Sponsor Protocol Number: COBC | Start Date*: 2017-08-19 | |||||||||||
| Sponsor Name:Dept. of Oncology, Karolinska university hospital | |||||||||||||
| Full Title: Effects of Identifying and Treating Early, Subclinical Cardiotoxicity on the Long- Term Incidence of Clinical Cardiotoxicity in Women with Breast Cancer, a prospective randomised study: The Cardio-... | |||||||||||||
| Medical condition: Women with newly diagnosed breast cancer who are expected to receive neo-adjuvant or adjuvant therapy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: SE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000509-29 | Sponsor Protocol Number: BO25734/TDM4997g | Start Date*: 2011-12-02 | ||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
| Full Title: A Phase III randomized, multicenter, two-arm, open-label trial to evaluate the efficacy of trastuzumab emtansine compared with treatment of physician’s choice in patients with HER2-positive metasta... | ||||||||||||||||||
| Medical condition: HER2-Positive Metastatic Breast Cancer (MBC) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) SE (Completed) DE (Completed) SK (Completed) BE (Completed) CZ (Completed) HU (Completed) NO (Completed) IT (Completed) ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-005000-13 | Sponsor Protocol Number: EMR200027-051 | Start Date*: 2007-03-30 | |||||||||||
| Sponsor Name:Merck KGaA | |||||||||||||
| Full Title: Randomized Phase II trial with cetuximab and cisplatin in the treatment of ER negative, PgR negative, HER2 negative metastatic breast carcinoma (“basal-like”) | |||||||||||||
| Medical condition: Metastatic breast cancer PR-negative, ER-negative and HER-2 negative | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IE (Completed) BE (Completed) ES (Completed) AT (Completed) PT (Completed) DE (Completed) IT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002860-25 | Sponsor Protocol Number: ML19944 | Start Date*: 2006-09-27 | |||||||||||
| Sponsor Name:Roche Hungary Ltd. | |||||||||||||
| Full Title: A multicenter randomized phase II trial to compare trastuzumab (Herceptin®) continuation or discontinuation in combination with 2nd-line chemotherapies after progression on a 1st-line chemotherapy ... | |||||||||||||
| Medical condition: Metastacic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: HU (Completed) EE (Completed) LT (Completed) SK (Completed) LV (Prematurely Ended) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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