- Trials with a EudraCT protocol (181)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
181 result(s) found for: Androgen deprivation therapy.
Displaying page 1 of 10.
EudraCT Number: 2018-004853-26 | Sponsor Protocol Number: T315/2018 | Start Date*: 2019-03-25 | ||||||||||||||||
Sponsor Name:Turku University Hospital | ||||||||||||||||||
Full Title: The effect of androgen deprivation therapy on the expression of prostate specific membrane antigen (PSMA) in treatment naive metastatic prostate cancer | ||||||||||||||||||
Medical condition: Metastatic prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: FI (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002415-10 | Sponsor Protocol Number: PROCoMBO | Start Date*: 2014-02-11 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: [18F]-labelled FDHT in PET/CT for detection and staging of bone metastases in hormone naïve prostate cancer | ||
Medical condition: Hormone naive prostate cancer, metastasized to bone (2 or more bone metastases). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002815-20 | Sponsor Protocol Number: MET07 | Start Date*: 2007-10-09 | ||||||||||||||||
Sponsor Name:Royal Surrey County Hospital | ||||||||||||||||||
Full Title: A Prospective Randomised Pilot Study of Metformin and Lifestyle Intervention in the Prevention of Metabolic Syndrome due to Androgen Deprivation Therapy in Prostate Cancer | ||||||||||||||||||
Medical condition: Patients with prostate cancer on androgen deprivation therapy (ADT). Randomisation between standard treatment with ADT only, and the additional use of metformin with dietary and exercise advice. Ai... | ||||||||||||||||||
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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: 2010-019004-24 | Sponsor Protocol Number: PON-PC-02 | Start Date*: 2010-04-30 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. LUIGI GONZAGA | |||||||||||||
Full Title: ANDROGEN DEPRIVATION THERAPY WITHDRAWAL VERSUS MAINTENANCE AND INTERMITTENT DOCETAXEL THERAPY VERSUS CONTINUOUS ADMINISTRATION IN PATIENTS WITH PROSTATE CANCER RESISTANT TO CHEMICAL CASTRATION | |||||||||||||
Medical condition: PROSTATIC ADENOCARCINOMA CHEMICAL CASTRATION RESISTANT | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002120-29 | Sponsor Protocol Number: 0822-030 | Start Date*: 2008-08-13 | |||||||||||
Sponsor Name:Merck&Co.,Inc | |||||||||||||
Full Title: A Phase III Study to Assess the Safety, Tolerability, and Efficacy of MK-0822 (Odanacatib) in Prolonging Bone Metastasis-Free Survival in Men with Castration-Resistant Prostate Cancer | |||||||||||||
Medical condition: Prevention of bone metastases in men with prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005325-23 | Sponsor Protocol Number: SGB_HF_MEN | Start Date*: 2014-06-20 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Short-term Efficacy of Stellate Ganglion Block in Men to reduce Hot Flushes related to Androgen Deprivation Therapy | ||
Medical condition: Hot flushes due to androgen deprivation therapy | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002027-13 | Sponsor Protocol Number: DPSA05 | Start Date*: 2005-07-22 |
Sponsor Name:Royal Marsden NHS FOundation Trust | ||
Full Title: A phase I/II study of docetaxel plus prednisolone plus diethylstilbestrol plus aspirin in androgen-independent prostate cancer | ||
Medical condition: Hormone refractory prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-000160-15 | Sponsor Protocol Number: MVT-601-3201 | Start Date*: 2017-07-25 | |||||||||||
Sponsor Name:Myovant Sciences GmbH | |||||||||||||
Full Title: HERO: A Multinational Phase 3 Randomized, Open-label, Parallel Group Study to Evaluate the Safety and Efficacy of Relugolix in Men with Advanced Prostate Cancer | |||||||||||||
Medical condition: Androgen-sensitive advanced prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) SE (Completed) GB (GB - no longer in EU/EEA) BE (Completed) AT (Completed) SK (Completed) DK (Completed) FI (Completed) ES (Completed) DE (Completed) PL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004774-17 | Sponsor Protocol Number: ESTO2 | Start Date*: 2018-08-23 | |||||||||||||||||||||||||||||||
Sponsor Name:Pirkanmaan sairaanhoitopiiri | |||||||||||||||||||||||||||||||||
Full Title: Impact of atorvastatin on prostate cancer progression after initiation of androgen deprivation therapy – lipid metabolism as a novel biomarker to predict prostate cancer progression – phase 3, doub... | |||||||||||||||||||||||||||||||||
Medical condition: Metastatic prostate cancer managed with androgen deprivation therapy | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||||||||||||
Trial protocol: FI (Trial now transitioned) NO (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020821-41 | Sponsor Protocol Number: MDV3100-03 | Start Date*: 2011-02-10 | |||||||||||
Sponsor Name:Medivation, Inc., a wholly owned subsidiary of Pfizer Inc. | |||||||||||||
Full Title: PREVAIL: A Multinational Phase 3, Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Oral MDV3100 in Chemotherapy-Naïve Patients with Progressive Metastatic Prostate Cancer W... | |||||||||||||
Medical condition: Chemotherapy-Naïve Patients with Progressive Metastatic Prostate Cancer Who Have Failed Androgen Deprivation Therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) NL (Completed) ES (Completed) SE (Completed) AT (Completed) FI (Completed) DK (Completed) SK (Completed) IT (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004094-25 | Sponsor Protocol Number: EGD-EC-003 | Start Date*: 2006-01-05 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A phase IIIb randomized study of intermittent versus continuous androgen deprivation therapy using ELIGARD 22.5 mg 3-month depot in subjects with relapsing or locally advanced prostate cancer who a... | |||||||||||||
Medical condition: Histologically or cytologically confirmed adenocarcinoma of the prostate (PCa) meeting the following criteria: - Locally adv. (stage T3 or T4) PCa, N0 or N+, M0 with PSA >= 5 ng/ml, or - Relapsing ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) AT (Prematurely Ended) FI (Completed) SK (Completed) IE (Completed) HU (Completed) DE (Completed) ES (Completed) SE (Completed) GB (Completed) PT (Completed) BE (Completed) DK (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000899-15 | Sponsor Protocol Number: EORTC-1531-ROG | Start Date*: 2019-12-03 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer (EORTC) | |||||||||||||
Full Title: Radiotherapy and 6-month androgen deprivation therapy with or without apalutamide in Intermediate and Limited High Risk Localized Prostate Cancer: a phase III study | |||||||||||||
Medical condition: Intermediate and Limited High Risk Localized Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
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: 2005-004765-42 | Sponsor Protocol Number: CZOL446GGB12 including amd 1 | Start Date*: 2006-05-03 |
Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
Full Title: An Open label Randomised, multicentre study to evaluate the efficacy of two Zometa (Zoledronic acid) schedules on bone mineral density in prostrate cancer patients undergoing Androgen deprivation T... | ||
Medical condition: Decreased bone mineral density in prostate cancer patients being treated with ADT | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000314-38 | Sponsor Protocol Number: 1206-HNCG | Start Date*: 2014-07-28 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer (EORTC) | |||||||||||||
Full Title: A randomized phase II study to evaluate the efficacy and safety of chemotherapy (CT) vs androgen deprivation therapy (ADT) in patients with recurrent and/or metastatic, androgen receptor (AR) expre... | |||||||||||||
Medical condition: Salivary gland cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) NL (Completed) GB (GB - no longer in EU/EEA) HU (Completed) AT (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000512-17 | Sponsor Protocol Number: 20040138 | Start Date*: 2004-10-01 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-controlled Study to Evaluate AMG 162 in the Treatment of Bone Loss in Subjects Undergoing Androgen-Deprivation Therapy for Non-metastatic Prostate Cancer | |||||||||||||
Medical condition: Bone loss in pateints undergoing androgen-deprivation therapy (ADT) for non-metastatic prostate cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) HU (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001162-10 | Sponsor Protocol Number: EUOG2014-002 | Start Date*: 2015-05-06 | |||||||||||
Sponsor Name:European Uro- Oncology Group (EUOG) | |||||||||||||
Full Title: An Exploratory Phase 2, open-label, single-arm, efficacy and imaging Study of Oral Enzalutamide (MDV3100) Androgen Receptor (AR)-Directed Therapy in Hormono-Naïve patients with Metastatic Prostate ... | |||||||||||||
Medical condition: Patients with Metastatic Prostate Cancer who have never been treated with Androgen Deprivation Therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2015-002590-38 | Sponsor Protocol Number: 17777 | Start Date*: 2016-12-14 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled Phase III study of darolutamide (ODM-201) versus placebo in addition to standard androgen deprivation therapy and docetaxel in patients with metastati... | |||||||||||||
Medical condition: Metastatic hormone-sensitive prostate cancer (mHSPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SE (Completed) BE (Completed) ES (Completed) FI (Completed) DE (Completed) CZ (Completed) NL (Completed) PL (Completed) FR (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000076-37 | Sponsor Protocol Number: NL72585.091.20 | Start Date*: 2023-03-30 |
Sponsor Name:Radboud University Medical Center | ||
Full Title: Lutetium-177-PSMA in Oligo-metastatic Hormone Sensitive Prostate Cancer. | ||
Medical condition: Oligo-metastatic adenocarcinoma of the prostate. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: CY (Trial now transitioned) | ||
Trial results: (No results available) |
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