- 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 20 of 93.
| EudraCT Number: 2011-001024-38 | Sponsor Protocol Number: AIO-MAM-0110 | Start Date*: 2011-07-27 | |||||||||||
| Sponsor Name:AIO-Studien-gGmbH | |||||||||||||
| Full Title: Vinorelbine In Combination with the mTOR Inhibitor Everolimus vs Vinorelbine monotherapy in Advanced breast cancer | |||||||||||||
| Medical condition: local advanced metastatic breat cancer, second line therapy for patients who did not respond to treatment with anthracyclines or taxanes or are not suitable for such treatment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001040-62 | Sponsor Protocol Number: GBG78/BIG1-13 | Start Date*: 2013-11-14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:GBG Forschungs GmbH | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Phase III study evaluating palbociclib (PD-0332991), a cyclin-dependent kinase (CDK) 4/6 inhibitor, in patients with hormone-receptor positive, HER2 normal primary breast cancer with high relapse r... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: About one-third of patient with hormone-receptor positive, HER2 negative breast cancer and residual disease after standard of care - including adequate surgery - have a substantial risk of relapse ... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) ES (Completed) AT (Completed) IE (Completed) FR (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-002114-36 | Sponsor Protocol Number: 20110113 | Start Date*: 2011-10-04 | |||||||||||||||||||||
| Sponsor Name:Amgen Inc | |||||||||||||||||||||||
| Full Title: Open-Label Access Protocol of Denosumab for Subjects with Advanced Cancer | |||||||||||||||||||||||
| Medical condition: Bone Metastases in Subjects with Advanced Breast Cancer and Bone Metastases in Men with Hormone-Refractory Prostate Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) AT (Completed) FR (Completed) ES (Completed) PL (Completed) BE (Completed) LV (Completed) LT (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2020-000960-52 | Sponsor Protocol Number: 107CS-6 | Start Date*: 2020-11-20 | ||||||||||||||||
| Sponsor Name:Daehwa Pharmaceutical Co., Ltd. | ||||||||||||||||||
| Full Title: A Multi-national, Multi-center, Open-label, Phase 2 Clinical Trial to Evaluate the Efficacy, Safety and Pharmacokinetics of DHP107 (Liporaxel®, Oral Paclitaxel) Compared to IV Paclitaxel in Patient... | ||||||||||||||||||
| Medical condition: Recurrent or metastatic HER2 negative Breast Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: CZ (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-001864-12 | Sponsor Protocol Number: IRFMN-BRC-6992 | Start Date*: 2018-02-09 | ||||||||||||||||||||||||||
| Sponsor Name:IRCCS - Istituto di Ricerche Farmacologiche Mario Negri | ||||||||||||||||||||||||||||
| Full Title: International, multicenter, phase II, randomized, parallel-arm trial investigating the role of two different metronomic chemotherapy regimens in locally advanced or metastatic triple negative breas... | ||||||||||||||||||||||||||||
| Medical condition: Locally advanced or metastatic triple negative breast cancer (TNBC) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2010-019216-20 | Sponsor Protocol Number: AZ2010 | Start Date*: 2010-05-01 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | |||||||||||||
| Full Title: "Effects of drug treatment with bisphosphonates (zoledronic acid) in the prevention of skeletal events in breast cancer patients with osteoporosis. Significant correlation with some biological para... | |||||||||||||
| Medical condition: Breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003442-32 | Sponsor Protocol Number: ML28589 | Start Date*: 2013-01-08 | |||||||||||
| Sponsor Name:ROCHE SAS | |||||||||||||
| Full Title: AN OPEN-LABEL, RANDOMIZED, MULTICENTER PHASE III STUDY IN PATIENTS WITH HER2-POSITIVE METASTATIC BREAST CANCER RESPONDING TO FIRST LINE TREATMENT WITH INTRAVENOUS TRASTUZUMAB FOR AT LEAST 3 YEARS A... | |||||||||||||
| Medical condition: HER2-positive metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006252-21 | Sponsor Protocol Number: 3160A6-2207-WW | Start Date*: 2009-05-28 | |||||||||||
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc | |||||||||||||
| Full Title: A Phase 2, Randomized, Open-label Study of Bosutinib Administered in Combination With Letrozole Versus Letrozole Alone as First Line Therapy in Post-Menopausal Women With Locally Advanced or Metast... | |||||||||||||
| Medical condition: Locally advanced or metastatic ER+/PgR+/erbB2-breast cancer in post-menopausal women | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: HU (Completed) BE (Completed) GB (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-006109-19 | Sponsor Protocol Number: STM01-102 | Start Date*: 2006-09-08 | |||||||||||
| Sponsor Name:Sopherion Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase III Randomized, Controlled Trial of Myocet, Trastuzumab and Paclitaxel versus Trastuzumab and Paclitaxel for First line Therapy of Metastatic Breast Cancer | |||||||||||||
| Medical condition: HER2+ Metastatic Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: PT (Completed) DE (Completed) ES (Prematurely Ended) GB (Completed) IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004734-22 | Sponsor Protocol Number: WO39392 | Start Date*: 2017-09-06 | ||||||||||||||||
| Sponsor Name:F. Hoffman-La Roche Ltd. | ||||||||||||||||||
| Full Title: A PHASE III RANDOMIZED STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF ATEZOLIZUMAB (ANTI-PD-L1 ANTIBODY) IN COMBINATION WITH NEOADJUVANT ANTHRACYCLINE/NAB-PACLITAXEL-BASED CHEMOTHERAPY COMPARED WI... | ||||||||||||||||||
| Medical condition: Triple-negative breast cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) BE (Completed) PL (Completed) ES (Ongoing) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-001765-41 | Sponsor Protocol Number: 1200.137 | Start Date*: 2012-02-13 | |||||||||||
| Sponsor Name:Medizinische Fakultät der Otto-von-Guericke Universität Magdeburg Universitätsklinikum Magdeburg A.ö.R. | |||||||||||||
| Full Title: Single-arm, open-label, multicentre phase II study evaluating the efficacy and safety of BIBW 2992 (Afatinib) in combination with vinorelbine for the treatment of patients with metastatic breast ca... | |||||||||||||
| Medical condition: Metastatic breast cancer patients with intermediate HER2 expression (IHC 2+, HER2 FISH-negative) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002924-18 | Sponsor Protocol Number: CYC065-101 | Start Date*: 2021-10-08 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Cyclacel Pharmaceuticals | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 1/2, Open-Label, Multicenter Study to Investigate the Safety, Pharmacokinetics, and Efficacy of Fadraciclib (CYC065), an Oral CDK2/9 Inhibitor, in Subjects with Advanced Solid Tumors and Ly... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Endometrial cancer, Ovarian cancer, Biliary tract cancer, Hepatocellular carcinoma, B-cell lymphoma, T-cell lymphoma, Metastatic colorectal cancer, Breast cancer (metastatic HER-2 refractory, Horm... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2008-004988-19 | Sponsor Protocol Number: fides | Start Date*: 2008-07-31 | |||||||||||
| Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | |||||||||||||
| Full Title: A PHASE II STUDY, COMPARING A DOSE-TITRATION REGIMEN OF FULVESTRANT WITH THE APPROVED DOSING REGIMEN IN POSTMENOPAUSAL PATIENTS WITH HORMONE-RESPONSIVE ADVANCED BREAST CANCER (ABC) | |||||||||||||
| Medical condition: Post-menopausal women with advanced breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-014662-26 | Sponsor Protocol Number: IRST 174.04 | Start Date*: 2009-11-06 | |||||||||||
| Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI | |||||||||||||
| Full Title: Phase II comparative study of Myocet plus Cyclophosphamide plus metformin versus Myocet plus Cyclophosphamide in first line treatment of HER2 negative metastatic breast cancer patients. | |||||||||||||
| Medical condition: HER2 negative metastatic breast cancer patients | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000380-13 | Sponsor Protocol Number: CP-MGAH22-04 | Start Date*: 2015-09-02 | |||||||||||||||||||||
| Sponsor Name:MacroGenics, Inc. | |||||||||||||||||||||||
| Full Title: A Phase 3, Randomized Study of Margetuximab Plus Chemotherapy vs Trastuzumab Plus Chemotherapy in the Treatment of Patients with HER2+ Metastatic Breast Cancer Who Have Received Prior Anti-HER2 The... | |||||||||||||||||||||||
| Medical condition: Metastatic or Locally Advanced HER2-positive Breast Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) PT (Completed) CZ (Completed) AT (Completed) FI (Completed) ES (Completed) DK (Completed) FR (Ongoing) PL (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2012-000677-23 | Sponsor Protocol Number: CLCL161A2201 | Start Date*: 2012-10-24 |
| Sponsor Name:Novartis Pharma Services AG | ||
| Full Title: A Phase II, multi-center, open-label, neoadjuvant, randomized study of weekly paclitaxel with or without LCL161 in patients with triple negative breast cancer | ||
| Medical condition: Triple negative breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (Completed) ES (Completed) IE (Completed) IT (Completed) BE (Completed) CZ (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000579-12 | Sponsor Protocol Number: D4200L00009 | Start Date*: 2008-12-03 | |||||||||||
| Sponsor Name:ASTRAZENECA | |||||||||||||
| Full Title: A randomised, double-blind, parallel-group, multicentre, phase ii study to evaluate the safety and pharmacological activity of the combination of Vandetanib (100 or 300 mg/daily or placebo) with Fu... | |||||||||||||
| Medical condition: Postmenopausal women with advanced breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006026-10 | Sponsor Protocol Number: IEOS381/607 | Start Date*: 2008-04-02 | |||||||||||
| Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
| Full Title: PREOPERATIVE ENDOCRINE TREATMENT WITH LETROZOLE ± TRIPTORELIN IN PATIENTS WITH ER AND PgR POSITIVE LOCALLY ADVANCED BREAST CANCER | |||||||||||||
| Medical condition: LOCALLY ADVANCED BREAST CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023763-17 | Sponsor Protocol Number: GDC4950g | Start Date*: 2012-05-18 | |||||||||||
| Sponsor Name:Genentech, Inc. | |||||||||||||
| Full Title: A phase II double-blind placebo-controlled randomized study of GDC-0941 or GDC-0980 with Fulvestrant versus Fulvestrant in advanced or metastatic breast cancer in patients resistant to aromatase in... | |||||||||||||
| Medical condition: Advanced or metastatic breast cancer resistant to aromatase inhibitor therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) GB (Prematurely Ended) DK (Prematurely Ended) HU (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001267-33 | Sponsor Protocol Number: A6181107 | Start Date*: 2006-10-11 | |||||||||||
| Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
| Full Title: Phase III Randomized, Multi Center Study of Sunitinib Malate (SU 011248) or Capecitabine in Subjects with Advanced Breast Cancer who failed both a taxane and an anthracycline chemotherapy regimen o... | |||||||||||||
| Medical condition: Histologically or cytologically proven diagnosis of breast adenocarcinoma that is not amenable to surgery, radiation, or combined modality therapy with curative intent | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) FR (Completed) IT (Prematurely Ended) GB (Completed) BG (Completed) ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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