- Trials with a EudraCT protocol (815)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
815 result(s) found for: prostate cancer OR breast cancer.
Displaying page 4 of 41.
| EudraCT Number: 2007-007666-38 | Sponsor Protocol Number: BR1-127 | Start Date*: 2008-11-28 | |||||||||||
| Sponsor Name:Bracco Imaging SPA | |||||||||||||
| Full Title: A phase III study to compare SonoVue guided prostate biopsy with systematic biopsy in the detection of prostate malignant lesions in patients with suspected prostate cancer | |||||||||||||
| Medical condition: Patients with suspected prostate cancer (For the optimization part: patients with a diagnosis of prostate cancer). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Prematurely Ended) NL (Completed) GB (Completed) AT (Completed) FR (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004426-10 | Sponsor Protocol Number: MO28072 | Start Date*: 2012-05-11 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:F. Hoffman-La Roche Ltd. | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: An open-label, phase II study of vemurafenib in patients with BRAF V600 mutation-positive cancers | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients with cancers (excluding melanoma and papillary thyroid cancer) harboring BRAF V600 mutations as identified by the routinely performed mutation analysis assays at each individual partici... | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) ES (Completed) DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2013-005479-42 | Sponsor Protocol Number: A301226 | Start Date*: 2014-06-04 | ||||||||||||||||
| Sponsor Name:Erasmus MC, Dept. Urology | ||||||||||||||||||
| Full Title: Pilot study: Toxicity of oestradiol for adjuvant endocrine therapy in locally confined prostate cancer | ||||||||||||||||||
| Medical condition: Prostate cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-001650-77 | Sponsor Protocol Number: FE200486 CS18 | Start Date*: 2007-05-14 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: An Open-Label, Multi-Centre, Randomised Parallel-Group Dose-Finding Study, Investigating Efficacy and Safety of Two Degarelix Three-Month Dosing Regimens in Patients with Prostate Cancer Requiring ... | |||||||||||||
| Medical condition: Patients with prostate cancer requiring androgen ablation therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001530-40 | Sponsor Protocol Number: HEC WST06 1276N/WST 2.24 | Start Date*: 2006-07-18 | |||||||||||
| Sponsor Name:STEBA FRANCE | |||||||||||||
| Full Title: Vascular targeted photodynamic therapy using WST09 for patients with untreated localised prostate cancer - Repeat procedure – Phase IIa, Single centre, open-label study. | |||||||||||||
| Medical condition: Localised Prostate Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-019632-12 | Sponsor Protocol Number: A-94-5214-178 | Start Date*: 2010-10-19 | |||||||||||
| Sponsor Name:IPSEN Pharma GmbH | |||||||||||||
| Full Title: A phase II, multicentre, open, prospective, randomised, parallel-group, pharmacodynamic equivalence study on intramuscular versus subcutaneous applications of Triptorelin pamoate (Pamorelin® LA 11.... | |||||||||||||
| Medical condition: advanced prostate cancer (locally advanced or metastatic) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003165-15 | Sponsor Protocol Number: FACBC-STAGING-2014 | Start Date*: 2014-12-02 | |||||||||||
| Sponsor Name:AOU di Bologna Policlinico S.Orsola-Malpighi | |||||||||||||
| Full Title: 18F-FACBC PET/CT FOR STAGING HIGH RISK PROSTATE CANCER | |||||||||||||
| Medical condition: Patients affected by moderate to high risk primary prostate cancer who are scheduled for surgery with a planned, elective lymph node dissection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002345-29 | Sponsor Protocol Number: T83/2017 | Start Date*: 2018-08-10 | |||||||||||
| Sponsor Name:Turku University Hospital | |||||||||||||
| Full Title: The effect of androgen deprivation therapy on the expression of prostate specific membrane antigen (PSMA) in prostate cancer | |||||||||||||
| Medical condition: Prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022064-12 | Sponsor Protocol Number: EFC11784 | Start Date*: 2011-03-23 | |||||||||||
| Sponsor Name:sanofi-aventis R&D | |||||||||||||
| Full Title: Randomized, Open Label, Multi-Center Study comparing Cabazitaxel at 25 mg/m2 and at 20 mg/m² in Combination with Prednisone Every 3 Weeks to Docetaxel in Combination with Prednisone in Patients wit... | |||||||||||||
| Medical condition: metastatic Castration Resistant Prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: SE (Completed) CZ (Completed) ES (Completed) FI (Completed) DK (Completed) PT (Completed) IT (Completed) DE (Completed) RO (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002880-98 | Sponsor Protocol Number: CRO-04-62 / GP/C/03/PRO | Start Date*: 2005-11-25 | |||||||||||
| Sponsor Name:GP-Pharm s.a. | |||||||||||||
| Full Title: Efficacy and safety of a new Leuprolide acetate 3.75 mg depot formulation, GP-Pharm s.a., when given as palliative treatment to prostate cancer patients | |||||||||||||
| Medical condition: prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: AT (Completed) GB (Completed) CZ (Completed) HU (Completed) IT (Completed) DE (Completed) SK (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-006827-29 | Sponsor Protocol Number: FE200486CS34 | Start Date*: 2009-04-27 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: Ensayo clínico fase IIIb, no aleatorizado, abierto, multicéntrico, de seguimiento de la seguridad de dosis mensuales de degarelix en pacientes con cáncer de próstata. A Phase 3b, Non-randomized, O... | |||||||||||||
| Medical condition: Cáncer de próstata | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: ES (Completed) FR (Completed) BE (Completed) FI (Completed) SE (Completed) PT (Completed) GR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001034-18 | Sponsor Protocol Number: PETMR-Staging-PCa1 | Start Date*: 2020-03-04 | |||||||||||
| Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
| Full Title: Phase II monocentric study to evaluate a novel approach for staging prostate cancer patients by using a fully integrated hybrid PET/MRI | |||||||||||||
| Medical condition: Patient diagnosed with prostatic carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012786-58 | Sponsor Protocol Number: 8-79-52014-168 | Start Date*: 2009-12-07 | |||||||||||
| Sponsor Name:Ipsen Pharma SAS | |||||||||||||
| Full Title: PROSTATE CANCER ANTIGEN-3 (PCA-3) AND TMPRSS2-ERG (T2-ERG) SCORE CHANGES DURING INITIATION OF ANDROGEN DEPRIVATION THERAPY (ADT) WITH TRIPTORELIN 22.5MG IN PATIENTS WITH ADVANCED PROSTATE CANCER (P... | |||||||||||||
| Medical condition: Locally advanced or metastatic prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) LV (Completed) FR (Completed) NL (Completed) LT (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001361-81 | Sponsor Protocol Number: ICO-N-2016-01 | Start Date*: 2017-02-10 | |||||||||||
| Sponsor Name:INSTITUT DE CANCEROLOGIE DE L'OUEST | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002511-99 | Sponsor Protocol Number: IOV-PR-CH-PET-1-2013 | Start Date*: 2013-11-25 | |||||||||||
| Sponsor Name:ISTITUTO ONCOLOGICO VENETO | |||||||||||||
| Full Title: Role of PET/ CT with 18F-fluorocholine in the staging of patients with intermediate/high risk prostate cancer. Phase III, randomized, open-label clinical trial | |||||||||||||
| Medical condition: Histologically proven prostate cancer with Gleason score =7 and PSA>=10ng/ml or Gleason score >=8 and any PSA level or cT2-T3 and any PSA level or any Gleason score and PSA>=20ng/ml and indication ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-010079-25 | Sponsor Protocol Number: LPC-002 | Start Date*: 2009-05-11 | |||||||||||
| Sponsor Name:LIDDS AB | |||||||||||||
| Full Title: An open, single and multiple dose, efficacy and safety Proof of Principle study of Liproca® Depot, a controlled release formulation of 2-hydroxyflutamide, injected into the prostate in patients wi... | |||||||||||||
| Medical condition: prostate cancer (T1-T2), Gleason ≤ 3+4 at the time of diagnose in prostate biopsy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004782-40 | Sponsor Protocol Number: PEM-PRO | Start Date*: 2020-09-24 | |||||||||||
| Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
| Full Title: An open label, single-arm, phase 2 study of neoadjuvant PEMbrolizumab before radical PROstatectomy (PEM-PRO) in high-risk prostate cancer patients | |||||||||||||
| Medical condition: High-risk prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000860-32 | Sponsor Protocol Number: UMCN-AKF-14.17 | Start Date*: 2015-04-28 | |||||||||||||||||||||
| Sponsor Name:Radboud University Medical Center | |||||||||||||||||||||||
| Full Title: Personalizing enzalutamide (Xtandi®) therapy by understanding the relation between the decrease in the expression profile of a panel of preselected microRNAs, tumor related mRNAs and treatment resp... | |||||||||||||||||||||||
| Medical condition: Metastatic Castration Resistant Prostate Cancer (mCRPC) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2008-004355-30 | Sponsor Protocol Number: 20070611 | Start Date*: 2009-01-05 | |||||||||||
| Sponsor Name:Amgen Inc | |||||||||||||
| Full Title: A Phase 1b/2 Study to Assess the Safety and Efficacy of AMG 102 in Combination with Mitoxantrone and Prednisone in Subjects with Previously Treated Castrate Resistant Prostate Cancer | |||||||||||||
| Medical condition: Previously Treated Castrate Resistant Prostate Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: CZ (Completed) FR (Completed) NL (Completed) FI (Completed) SE (Completed) BE (Completed) GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-008301-22 | Sponsor Protocol Number: 1661/08 | Start Date*: 2010-03-05 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: PHASE II CLINICAL STUDY OF THE DIAGNOSTIC EFFICACY OF [18F]FLUOROETHYILCHOLINE ([18F]FECh) IN PATIENTS WITH PROSTATE CANCER | |||||||||||||
| Medical condition: PROSTATE CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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