- 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 4 of 41.
EudraCT Number: 2008-004351-29 | Sponsor Protocol Number: 2008-02-IMP-5 | Start Date*: 2008-12-18 | |||||||||||
Sponsor Name:HEXAL AG | |||||||||||||
Full Title: OPEN LABEL, MULTICENTER STUDY ON PHARMACOKINETICS, PHARMACODYNAMICS, EFFICACY AND SAFETY OF GOSERELIN 10.8 mg IMPLANT HEXAL IN PATIENTS WITH ADVANCED HORMONE DEPENDENT PROSTATE CANCER | |||||||||||||
Medical condition: Palliative treatment of advanced hormone dependent prostate cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
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) |
EudraCT Number: 2016-003185-26 | Sponsor Protocol Number: 2016-NUK-01 | Start Date*: 2016-10-20 | ||||||||||||||||
Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
Full Title: Qualification of 82Rb PET for measurement of tumor perfusion. Uptake in primary prostate cancer vs healthy prostate | ||||||||||||||||||
Medical condition: Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-004846-39 | Sponsor Protocol Number: N-20200025 | Start Date*: 2023-04-26 | ||||||||||||||||
Sponsor Name:Aalborg University Hospital | ||||||||||||||||||
Full Title: 68Ga-PSMA PET/CT vs. 18F-PSMA PET/CT for the diagnosis of metastases in newly diagnosed high-risk prostate cancer patients undergoing radical prostatectomy | ||||||||||||||||||
Medical condition: Prostate Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007072-42 | Sponsor Protocol Number: 20599 | Start Date*: 2008-07-08 | |||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||
Full Title: Double-blind placebo-controlled randomized study to determine the effectiveness of magnesium oxide to reduce the prostate motion. | |||||||||||||
Medical condition: Prostate cancer patients who are being treated with external beam radiotherapy using fiducial marker-based position verification. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001506-96 | Sponsor Protocol Number: TCD12128 | Start Date*: 2012-03-27 | |||||||||||
Sponsor Name:sanofi-aventis recherche et développement | |||||||||||||
Full Title: A Phase I/II Study of Cabazitaxel Combined with Abiraterone Acetate and Prednisone in Patients with Metastatic Castrate-Resistant Prostate Cancer (CRPC) whose Disease has Progressed after Docetaxe... | |||||||||||||
Medical condition: prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005964-24 | Sponsor Protocol Number: CRO-06-78 / DSC/06/LEU15/01 | Start Date*: 2007-04-03 | |||||||||||
Sponsor Name:Italfarmaco S.p.A. | |||||||||||||
Full Title: Pharmacokinetics, pharmacodynamics and safety of a new Leuprolide acetate 22.5 mg depot formulation, when given as palliative treatment to prostate cancer patients | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003183-68 | Sponsor Protocol Number: PSMA-RGS | Start Date*: 2020-12-10 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: The Role of Imaging Guided Surgery to Improve the Detection of LymphNode metastases in Prostate Cancer Patients Treated with Radical Prostatectomy and Extended Pelvic Lymph Node Dissection | |||||||||||||
Medical condition: Patients with prostate cancer (PCa) who are candidate to undergo surgical treatment with robot-assisted radical prostatectomy with a risk of lymph nodal invasion > 5% according to preoperative data | |||||||||||||
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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: 2008-003525-16 | Sponsor Protocol Number: DOCRTPC | Start Date*: 2007-05-02 | |||||||||||
Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | |||||||||||||
Full Title: Neoadjuvant chemotherapy with weekly docetaxel followed from concomitant docetaxel-RT in patients with high risk locally advanced prostate cancer | |||||||||||||
Medical condition: high risk locally advanced prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022037-29 | Sponsor Protocol Number: AFU-GETUG 20/0310 | Start Date*: 2011-01-31 | |||||||||||
Sponsor Name:FNCLCC (Fédération Nationale des Centres de Lutte Contre le Cancer) | |||||||||||||
Full Title: Phase III randomised trial to evaluate the benefit of adjuvant hormonal treatment with leuprorelin acetate (Eligard® 45 mg) for 24 months after radical prostatectomy in patients with high risk of r... | |||||||||||||
Medical condition: PROSTATIC ADENOCARCINOMA WITH HIGH RISK OF RECURRENCE. | |||||||||||||
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Population Age: | Gender: Male | ||||||||||||
Trial protocol: FR (Trial now transitioned) SK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004419-69 | Sponsor Protocol Number: P070129 | Start Date*: 2008-04-02 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Impact de la TEP-TDM à la Fluorométhylcholine-(18F) sur la prise en charge de la récidive biologique occulte du cancer de la prostate. Etude multicentrique nationale de phase III. (ICHOROPRO) | |||||||||||||
Medical condition: Récidive biologique occulte du cancer de la prostate | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009114-40 | Sponsor Protocol Number: 2009/01 | Start Date*: 2009-03-16 | |||||||||||
Sponsor Name:Hopital Foch | |||||||||||||
Full Title: Impact de la technique anesthésique et analgésique sur le risque de récidive biologique de cancer de la prostate | |||||||||||||
Medical condition: prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001685-15 | Sponsor Protocol Number: ANTI-3-18F-FACBC | Start Date*: 2012-05-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: ANTI-3-18F-FACBC IN COMPARISON TO 11C-CHOLINE PET/CT IN THE EVALUATION OF PATIENTS WITH SUSPECT PROSTATE CANCER RELAPSE | |||||||||||||
Medical condition: Patients with prostate cancer treated with radical prostatectomy or radiotherapy presenting with suspect progression(rising PSA) of local or distant (lymphnodes or bones) already scheduled for a ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005232-33 | Sponsor Protocol Number: FE200486 CS30 | Start Date*: 2009-04-15 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, parallel arm, open-label trial comparing degarelix with goserelin plus anti-androgen flare protection (bicalutamide), in terms of prostate size reduction in prostate cancer patients o... | |||||||||||||
Medical condition: Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) FR (Completed) ES (Completed) GB (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001703-38 | Sponsor Protocol Number: ARI109924 | Start Date*: 2007-09-25 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled Trial Assessing the Efficacy and Safety of Dutasteride (AVODART™) 0.5 mg in Extending the Time to PSA Doubling in Men with Prostate Cancer and Biochem... | |||||||||||||
Medical condition: Clinically localised prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) FR (Completed) ES (Completed) LT (Prematurely Ended) LV (Prematurely Ended) NL (Completed) GB (Completed) EE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006595-38 | Sponsor Protocol Number: SU/2006/2424 | Start Date*: 2007-08-03 | |||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||
Full Title: A Phase II, Open-Label, Single-Arm Study to Assess the Efficacy and Safety of Decapeptyl® SR (3 mg and 11.25 mg formulations) when administered by subcutaneous injection | |||||||||||||
Medical condition: Enrolled patients will be those who have a diagnosis of prostate cancer and for whom medical castration by means of Luteinising Hormone Releasing Hormone analogue (LHRHa) injection is indicated. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005165-11 | Sponsor Protocol Number: GETUG 16/0504 | Start Date*: 2006-06-16 | |||||||||||
Sponsor Name:Fédération Nationale des Centres de Lutte Contre le Cancer | |||||||||||||
Full Title: Etude randomisée multicentrique comparant l'efficacité d'une hormonothérapie courte par Zoladex® concomitante à une radiothérapie versus une radiothérapie exclusive dans le traitement de rattrapage... | |||||||||||||
Medical condition: Avec 40 000 nouveaux cas par an en France, le cancer de la prostate est le second cancer pour l’ensemble de la population française et le premier chez l’homme. L'hormonothérapie est le traitement ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000566-38 | Sponsor Protocol Number: GETUG-AFU_23_/_UC-0160/1202 | Start Date*: 2014-07-23 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: A randomized Phase III, factorial design, of cabazitaxel and pelvic radiotherapy in patients with localized prostate cancer and high-risk features of relapse | |||||||||||||
Medical condition: localized prostate cancer with high-risk features of relapse | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) IT (Prematurely Ended) BE (Trial now transitioned) DE (Completed) PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004628-21 | Sponsor Protocol Number: SAMDOCET | Start Date*: 2008-12-02 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: A multicenter phase III randomized study of 153Sm-EDTMP and Docetaxel + Prednisone versus Docetaxel + Prednisone in Taxane-naive patients with metastatic hormone-refractory prostate cancer. | |||||||||||||
Medical condition: Taxane-naive patients with metastatic hormone-refractory prostate cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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