- Trials with a EudraCT protocol (189)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
189 result(s) found for: Prostate specific antigen test.
Displaying page 3 of 10.
EudraCT Number: 2012-004331-23 | Sponsor Protocol Number: 212082-PCR-2023 | Start Date*: 2013-07-22 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized Phase 2 Study Evaluating Abiraterone Acetate With Different Steroid Regimens for Preventing Symptoms Associated With Mineralocorticoid Excess in Asymptomatic, Chemotherapy-Naïve and Me... | |||||||||||||
Medical condition: Metastatic Castration-Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) IT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000123-12 | Sponsor Protocol Number: 2020110469 | Start Date*: 2021-06-22 |
Sponsor Name:Odense University Hospital | ||
Full Title: PRISMA-PET – Primary Staging of Prostate Cancer: A Randomized Controlled Trial Comparing 18F-PSMA-1007 PET/CT to Conventional Imaging. | ||
Medical condition: Newly diagnosed prostate cancer, PET/CT scan used to stage newly diagnosed prostate cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001193-26 | Sponsor Protocol Number: C_30050_P3_02 | Start Date*: 2011-12-21 | |||||||||||
Sponsor Name:Acino Supply AG | |||||||||||||
Full Title: An open label, one-arm, multiple dose study in patients with prostate cancer to demonstrate efficacy of a one month goserelin 3.6 mg implant in a two months treatment (2 application periods) and PK... | |||||||||||||
Medical condition: Locally advanced, recurrent, or metastatic carcinoma of the prostate indicated for endocrine therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) CZ (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002987-34 | Sponsor Protocol Number: CA184-437 | Start Date*: 2014-12-22 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind Study of Ipilimumab Administered at 3 mg/kg vs 10 mg/kg in Adult Subjects with Metastatic Chemotherapy-Naïve Castration Resistant Prostate Cancer Who are Asympto... | |||||||||||||
Medical condition: Metastatic Chemotherapy-Naïve Castration Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Completed) IT (Prematurely Ended) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001891-35 | Sponsor Protocol Number: D4200C00080 | Start Date*: 2007-06-22 | |||||||||||
Sponsor Name:AstraZeneca SAS | |||||||||||||
Full Title: A randomized, double-blind phase II trial to assess the efficacy and safety of bicalutamide (Casodex® ) associated to ZD6474 (Zactima™ ) or to placebo in patients with castration-refractory metasta... | |||||||||||||
Medical condition: Metastatic prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004489-32 | Sponsor Protocol Number: CV-9104-007 | Start Date*: 2014-03-05 | |||||||||||
Sponsor Name:CureVac AG | |||||||||||||
Full Title: An open label Randomised Phase II Trial of RNActive® Cancer Vaccine (CV9104) in high risk and intermediate risk patients with prostate cancer | |||||||||||||
Medical condition: prostate carcinoma (intermediate and high risk) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001790-25 | Sponsor Protocol Number: FP01C-13-001 | Start Date*: 2014-09-01 | |||||||||||
Sponsor Name:Foresee Pharmaceuticals Co., Ltd. | |||||||||||||
Full Title: An Open-Label, Single-Arm Study of the Safety, Efficacy, and Pharmacokinetic Behavior of Leuprolide Mesylate for Injectable Suspension (LMIS 50 mg) in Subjects with Advanced Prostate Carcinoma | |||||||||||||
Medical condition: Advanced Prostate Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) CZ (Completed) SK (Completed) LT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003680-22 | Sponsor Protocol Number: BC1-04 | Start Date*: 2006-02-01 | |||||||||||
Sponsor Name:Algeta ASA | |||||||||||||
Full Title: A double blind, randomised, dose finding, repeat dose, phase II, multicentre study of Alpharadin TM for the treatment of patients with hormone refractory prostate cancer and skeletal metastases. | |||||||||||||
Medical condition: Hormone refractory prostate cancer and skeletal metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002338-31 | Sponsor Protocol Number: 47 | Start Date*: 2008-08-29 | |||||||||||
Sponsor Name:Hannover Medical School | |||||||||||||
Full Title: Prospektive randomisierte Phase II Studie zur Behandlung von Patienten mit fortgeschrittenem hormonrefraktären Prostatakarzinom mittels LHRH-Analoga und Somatostatin-Analoga unter Berücksichtigung ... | |||||||||||||
Medical condition: Patients with hormone - independent non metastatic prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001746-34 | Sponsor Protocol Number: 56021927PCR3011 | Start Date*: 2019-04-02 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Phase 3 Study of Apalutamide in Subjects with High-risk, Localized or Locally Advanced Prostate Cancer Who are Candidates for Radical Prostatectomy | |||||||||||||
Medical condition: High-risk localized or locally advanced prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001626-17 | Sponsor Protocol Number: CA209-9KD | Start Date*: 2018-04-18 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 2 Study of Nivolumab in Combination with Either Rucaparib, Docetaxel, or Enzalutamide in Men with Castration-resistant Metastatic Prostate Cancer | ||||||||||||||||||
Medical condition: Castration-resistant Metastatic Prostate Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000951-14 | Sponsor Protocol Number: RhoVac-002 | Start Date*: 2019-08-26 | |||||||||||
Sponsor Name:RhoVac ApS | |||||||||||||
Full Title: A Phase 2, Double-Blind, Placebo Controlled Study of RV001V in Men with Biochemical Failure following Curatively Intended Therapy for Localized Prostate Cancer | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) FI (Completed) SE (Completed) DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002100-42 | Sponsor Protocol Number: ARD-0301-003 | Start Date*: 2005-08-24 |
Sponsor Name:Ardana Bioscience Ltd | ||
Full Title: A Phase II single centre, open-label study investigating the pharmacokinetics, pharmacodynamics, efficacy and safety of a loading dose regimen of a new GnRH antagonist, Teverelix, long-acting formu... | ||
Medical condition: advanced prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003046-17 | Sponsor Protocol Number: BAY88-8223/16506 | Start Date*: 2013-10-25 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A re-treatment safety study of radium-223 dichloride in subjects with castration-resistant prostate cancer with bone metastases who received an initial course of six doses of radium-223 dichloride ... | |||||||||||||
Medical condition: Castration Resistant Prostate cancer patients with bone metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) NO (Completed) FI (Completed) IT (Completed) ES (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003461-34 | Sponsor Protocol Number: UR1840 | Start Date*: 2019-07-09 | |||||||||||||||||||||
Sponsor Name:Department of Oncology, Herlev & Gentofte Hospital | |||||||||||||||||||||||
Full Title: Randomised phase 2 trial of stereotactic body radiation therapy, SBRT, in combination with checkpoint inhibitors in metastatic castration-resistant prostate cancer | |||||||||||||||||||||||
Medical condition: metastatic castration-resistant prostate cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000625-37 | Sponsor Protocol Number: BED-004 | Start Date*: 2015-08-28 | |||||||||||
Sponsor Name:Blue Earth Diagnostics Limited | |||||||||||||
Full Title: A phase 3, open-label study to assess the clinical utility of fluciclovine (18F) PET/CT in patients with prostate cancer with biochemical recurrence after radical treatment | |||||||||||||
Medical condition: Prostate cancer with biochemical recurrence after radical treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003386-22 | Sponsor Protocol Number: PRX302-2-07 | Start Date*: 2015-01-19 |
Sponsor Name:Sophiris Bio Corp | ||
Full Title: A Single Centre, Open Label, Phase IIa Study, Evaluating the Safety and Tolerability of Targeted Intraprostatic Administration of PRX302 to Treat Men with Histologically Proven, Clinically Signific... | ||
Medical condition: Prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002725-74 | Sponsor Protocol Number: COU-AA-004 | Start Date*: 2007-07-16 | |||||||||||
Sponsor Name:Cougar Biotechnology, Inc | |||||||||||||
Full Title: A Phase II Open Label Study of CB7630 (Abiraterone Acetate) and Prednisone in Patients with Advanced Prostate Cancer Who Have Failed Androgen Deprivation and Docetaxel-Based Chemotherapy | |||||||||||||
Medical condition: HRPC (Hormone refractory prostate cancer) refractory to androgen deprivation and Docetaxel based chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002940-26 | Sponsor Protocol Number: 212082PCR3011 | Start Date*: 2013-05-24 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Comparative Study of Abiraterone Acetate Plus Low-dose Prednisone Plus Androgen Deprivation Therapy (ADT) Versus ADT Alone in Newly Diagnosed Subjects With High-Risk, Me... | |||||||||||||
Medical condition: Metastatic Hormone-Naive Prostate Cancer (mHNPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) FR (Completed) SE (Completed) HU (Completed) PT (Completed) FI (Completed) ES (Completed) IT (Completed) SK (Completed) DK (Completed) DE (Completed) BE (Completed) PL (Completed) BG (Completed) NL (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003578-24 | Sponsor Protocol Number: FE 200486 CS25 | Start Date*: 2008-06-30 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A single-centre, open-label, randomised explorative pharmacokinetic/pharmacodynamic study of the gonadotropin-releasing hormone receptor antagonist degarelix (FE 200486) in patients with benign pro... | |||||||||||||
Medical condition: Patients with Benign Prostata Hypertropia (BPH) who fulfil the following criteria: a prostate volume of more than 30 mL, maximal uroflow of 12 mL/s or less; International Prostate Symptom Score (IP... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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