- Trials with a EudraCT protocol (596)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
596 result(s) found for: "prostate cancer" OR "breast cancer".
Displaying page 5 of 30.
| 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: 2008-001916-18 | Sponsor Protocol Number: 20080331 | Start Date*: 2008-11-05 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA ORDINE MAURIZIANO | ||||||||||||||||||
| Full Title: A phase II, randomized trial with single agent trastuzumab or lapatinib in women with metastatic breast cancer iperexpressing HER2 | ||||||||||||||||||
| Medical condition: women with metastatic breast cancer iperexpressing HER2 | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2006-006236-22 | Sponsor Protocol Number: MET/TEST1106 | Start Date*: 2007-01-31 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA O.I.R.M. - S. ANNA | |||||||||||||
| Full Title: Use of Metformin to reduce serum level of Testosterone and improve the metabolic picture in women treated for breast cancer | |||||||||||||
| Medical condition: Menopausal women on treatment for BC, with higher risk of recurrence due to augmented level of T | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004836-76 | Sponsor Protocol Number: Suprefact1 | Start Date*: 2012-01-25 | |||||||||||
| Sponsor Name:Urologkliniken USÖ | |||||||||||||
| Full Title: Suprefact1 Can Suprefact be administrated every forth month with good castration effect. | |||||||||||||
| Medical condition: Prostate cancer that need hormone treatment by LHRH-agoniste. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: SE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004513-27 | Sponsor Protocol Number: MedOPP127 | Start Date*: 2017-09-04 | |||||||||||
| Sponsor Name:Medica Scientia Innovation Research (MedSIR) | |||||||||||||
| Full Title: A phase II study of pembrolizumab and eribulin in patients with HR-positive/HER2-negative metastatic breast cancer previously treated with anthracyclines and taxanes | |||||||||||||
| Medical condition: Hormone receptor-(HR)positive/HER2-negative metastatic breast cancer (MBC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002289-35 | Sponsor Protocol Number: SGNLVA-002 | Start Date*: 2018-04-02 | |||||||||||||||||||||
| Sponsor Name:Seattle Genetics, Inc. | |||||||||||||||||||||||
| Full Title: Single Arm, Open Label Phase 1b/2 Study of SGN-LIV1A in Combination with Pembrolizumab for First-Line Treatment of Patients with Unresectable Locally-Advanced or Metastatic Triple-Negative Breast C... | |||||||||||||||||||||||
| Medical condition: Unresectable Locally-Advanced or Metastatic Triple-Negative Breast Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2016-004091-21 | Sponsor Protocol Number: UCL/16/0587 | Start Date*: 2017-08-23 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: Nivolumab and ipilimumab treatment in prostate cancer with an immunogenic signature | |||||||||||||
| Medical condition: Metastatic castrate resistant prostate cancer (prostate adenocarcinoma) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-020681-16 | Sponsor Protocol Number: LO-10-01 | Start Date*: 2010-10-12 | |||||||||||
| Sponsor Name:Lunamed Operations AG | |||||||||||||
| Full Title: A PILOT STUDY TO INVESTIGATE THE SAFETY, TOLERABILITY AND EFFICACY OF A DAILY DOSE OF 500MG. LU901 (4PHENYL-BUTYRATE, CONTROLLED RELEASE TABLETS) IN ADDITION TO STANDARD HORMONAL TREATMENT IN PATIE... | |||||||||||||
| Medical condition: Patients suffering from prostate carcinoma with progression under first line hormonal treatment. Patients entering the study should have a life expectancy prognosis of at least 6 months. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001146-34 | Sponsor Protocol Number: 1301 | Start Date*: 2015-02-20 | |||||||||||
| Sponsor Name:Centre Oscar Lambret | |||||||||||||
| Full Title: Impact of a treatment with zoledronic acid on bone mineral density in patients with metastatic castration-resistant prostate cancer, chemo-naïve and receiving abiraterone acetate | |||||||||||||
| Medical condition: Metastatic castration-resistant prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003007-19 | Sponsor Protocol Number: MK-7339-002 | Start Date*: 2018-11-29 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
| Full Title: A Phase 2 Study of Olaparib Monotherapy in Participants with Previously Treated, Homologous Recombination Repair Mutation (HRRm) or Homologous Recombination Deficiency (HRD) Positive Advanced Cancer | |||||||||||||
| Medical condition: Homologous recombination repair mutation (HRRm) or Homologous recombination deficiency (HRD) positive cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) IE (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001587-19 | Sponsor Protocol Number: UHSM0315 | Start Date*: 2015-07-15 | |||||||||||||||||||||
| Sponsor Name:Manchester University NHS Foundation Trust | |||||||||||||||||||||||
| Full Title: A pilot prevention study of the effects of the anti-progestin Ulipristal Acetate (UA) on surrogate markers of breast cancer risk | |||||||||||||||||||||||
| Medical condition: We seek to investigate the breast cancer risk reducing properties of ulipristal acetate | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2011-001998-10 | Sponsor Protocol Number: Create-01 | Start Date*: 2011-10-17 | |||||||||||
| Sponsor Name:Department of Oncology University Hospital Uppsala | |||||||||||||
| Full Title: An International Randomized Phase II Study Comparing Early Electrochemotherapy to Delayed or No Electrochemotherapy in Patients with Cutaneous Breast Cancer Metastases | |||||||||||||
| Medical condition: Breast cancer that has spread to the skin | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000120-14 | Sponsor Protocol Number: ASL605LIOM01 MYTA | Start Date*: 2006-10-11 | |||||||||||
| Sponsor Name:AZIENDA USL 6 LIVORNO ZONA LIVORNESE | |||||||||||||
| Full Title: Study of the association of docetaxel and liposomial doxorubicin Myocet in metastatic breast cancer phase II clinical trial | |||||||||||||
| Medical condition: Patiens with metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-018795-24 | Sponsor Protocol Number: APREC S-2010-01 | Start Date*: 2010-06-01 | |||||||||||
| Sponsor Name:Alliance pour la recherche en cancérologie | |||||||||||||
| Full Title: Evaluation of the effect of pasireotide LAR administration in the lymphocele prevention after axillary node dissection for breast cancer | |||||||||||||
| Medical condition: BREAST CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003734-32 | Sponsor Protocol Number: BXCL701-201 | Start Date*: 2019-07-02 | |||||||||||
| Sponsor Name:BioXcel Therapeutics, Inc | |||||||||||||
| Full Title: A Phase 1b/2 Study of BXCL701, a Small Molecule Inhibitor of Dipeptidyl Peptidases (DPP), Administered in Combination with the Anti-Programmed Cell Death 1 (PD-1) Monoclonal Antibody Pembrolizumab ... | |||||||||||||
| Medical condition: Small Cell Neuroendocrine Prostate Cancer | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004450-24 | Sponsor Protocol Number: PHIX-IT | Start Date*: 2019-08-01 |
| Sponsor Name:Tergooi Hospital, dep of internal medicine | ||
| Full Title: A pharmacokinetic study of edoxaban in patients with breast cancer using the P-glycoprotein inhibitor tamoxifen | ||
| Medical condition: If there are increased plasma levels of edoxaban when used concomitantly with the P-glycoproteïne inhibitor tamoxifen for the treatment of venous thromboembolism in patients with breast cancer. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-003212-39 | Sponsor Protocol Number: LPM-008 | Start Date*: 2019-12-17 | |||||||||||
| Sponsor Name:Lightpoint Medical Ltd | |||||||||||||
| Full Title: Evaluation of the LightPath Imaging System and the PET tracer 68Ga-RM2 in wide local excision (WLE) for breast cancer | |||||||||||||
| Medical condition: Wide local excision (WLE) for 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: 2015-003106-16 | Sponsor Protocol Number: B2 | Start Date*: 2016-08-03 |
| Sponsor Name:Antonis Valachis | ||
| Full Title: Immunogenicity of influenza vaccination among breast cancer patients treated with trastuzumab in adjuvant setting | ||
| Medical condition: Efficacy of vaccination against influenza in patients with breast cancer treated with Trastuzumab as adjuvant therapy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-009921-28 | Sponsor Protocol Number: PLOTINA | Start Date*: 2010-05-15 |
| Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | ||
| Full Title: The Effect of Metformin, an insulin-sensitizing drug, on Breast Cancer Primary Prevention: The Plotina Breast Cancer Prevention Randomized, Placebo Controlled Trial | ||
| Medical condition: Breast cancer chemoprevention | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: IT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-002616-16 | Sponsor Protocol Number: NL49061.031.14 | Start Date*: 2014-07-10 |
| Sponsor Name:NKI-AVL | ||
| Full Title: Pilot for high-resolution SPECT imaging of breast cancer lumpectomy specimens for 3D identification and quantification of resection margins | ||
| Medical condition: Patients with breast cancer, IDC (n=3) and DCIS (n=3) scheduled for a lumpectomy. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
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