- Trials with a EudraCT protocol (815)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
815 result(s) found for: prostate cancer.
Displaying page 3 of 41.
EudraCT Number: 2016-004210-10 | Sponsor Protocol Number: ASSTBS-BLADE-2540-2016 | Start Date*: 2017-03-29 | ||||||||||||||||
Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | ||||||||||||||||||
Full Title: A PILOT PHASE IV STUDY TO EVALUATE VARIATION IN BONE MINERAL DENSITY, LEAN AND FAT BODY MASS MEASURED BY DUAL-ENERGY X-RAY ABSORPTIOMETRY IN PATIENTS WITH PROSTATE CANCER WITHOUT BONE METASTASIS T... | ||||||||||||||||||
Medical condition: prostate cancer prostate cancer without bone metastases | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001786-18 | Sponsor Protocol Number: CZOL446GDE08 | Start Date*: 2005-03-22 | |||||||||||
Sponsor Name:EAU EUROPEAN ASSOCIATION OF UROLOGY | |||||||||||||
Full Title: Effectiveness of Zometa treatment for the prevention of bone metastases in high risk prostate cancer patients. A randomized, open-label, multicenter study of the European Association of Urology (EA... | |||||||||||||
Medical condition: Prevention of bone metastasis in high risk prostate cancer patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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: 2012-000101-69 | Sponsor Protocol Number: EGD-EC-005 | Start Date*: 2013-07-04 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. (APEL) | |||||||||||||
Full Title: An exploratory, open label, single-arm study to evaluate the effect of Eligard® 6-month on biomarkers of disease in patients with metastatic prostate cancer. | |||||||||||||
Medical condition: Patients with metastatic prostate cancer whom androgen deprivation therapy (ADT) is indicated | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2010-021287-16 | Sponsor Protocol Number: 9785-CL-0321 | Start Date*: 2010-11-29 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A phase 2, open-label, single-arm, efficacy and safety study of MDV3100 in patients with hormone-naïve prostate cancer | |||||||||||||
Medical condition: Hormone-naïve prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) DE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
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: 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: 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: 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: 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: 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: (No results available) |
EudraCT Number: 2008-007028-25 | Sponsor Protocol Number: ON/2008/2781 | Start Date*: 2010-08-17 | |||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||
Full Title: A Randomised Controlled Trial to Determine the Effect of Decapeptyl on Reduction of Prostate Volume Pre-Radiotherapy Compared with Standard Therapy (Zoladex) | |||||||||||||
Medical condition: Enrolled patients will be those with a diagnosis of prostate cancer who require radiotherapy to the prostate, with medical castration by means of Luteneising Hormone Releasing Hormone analogue (LRH... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 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: 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: 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: 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) |
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