- Trials with a EudraCT protocol (50)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
50 result(s) found for: Nilutamide.
Displaying page 1 of 3.
EudraCT Number: 2004-000299-15 | Sponsor Protocol Number: BC1-03 | Start Date*: 2004-11-03 |
Sponsor Name:Algeta AS | ||
Full Title: A double-blind, dose-response, phase II, multicentre study of radium-223 (Alpharadin TM ) for the palliation of painful bone metastases in hormone refractory prostate cancer patients | ||
Medical condition: The target population is patients suffering from bone pain due to skeletal metastasis secondary to prostate cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Completed) GB (Completed) | ||
Trial results: View results |
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: 2005-006018-16 | Sponsor Protocol Number: | Start Date*: 2006-02-27 |
Sponsor Name:Royal Marsden Hospital | ||
Full Title: A Randomised Phase III Trial Of Low Dose DailyDexamethasone Versus Intermittent Dexamethasone Versus Prednisolone In Hormone Refractory Prostate Cancer | ||
Medical condition: Hormone refractory prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002149-36 | Sponsor Protocol Number: G-202-002 | Start Date*: 2012-12-10 | |||||||||||
Sponsor Name:GenSpera, Inc. | |||||||||||||
Full Title: An Open-Label, Single-Arm, Phase 2 Study of G-202 in Patients with Chemotherapy-Naïve Metastatic Castrate-Resistant Prostate Cancer | |||||||||||||
Medical condition: chemotherapy-naïve metastatic castrate-resistant prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001984-22 | Sponsor Protocol Number: GETUG 15/0403 | Start Date*: 2007-02-19 | |||||||||||
Sponsor Name:Fédération Nationale des Centres de Lutte Contre le Cancer | |||||||||||||
Full Title: Essai randomisé de phase III comparant l’association traitement hormonal + docétaxel au traitement hormonal seul dans les cancers de la prostate métastatiques | |||||||||||||
Medical condition: L’utilisation précoce dans une situation d’androgènosensibilité d’une chimiothérapie active laisse envisager une meilleure efficacité à un stade plus précoce du cancer de la prostate métastatique, ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004756-20 | Sponsor Protocol Number: EFC6546 | Start Date*: 2007-09-19 |
Sponsor Name:sanofi-aventis recherche & développement | ||
Full Title: A Multicenter, Randomized, Double-Blind Study Comparing the Efficacy and Safety of Aflibercept Versus Placebo Administered Every 3 Weeks in Patients Treated with Docetaxel / Prednisone for Metastat... | ||
Medical condition: Patients with metastatic androgen-independent prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: FR (Completed) SE (Completed) CZ (Completed) PT (Completed) ES (Completed) DK (Completed) HU (Completed) EE (Completed) BE (Completed) NL (Completed) IT (Completed) DE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005364-65 | Sponsor Protocol Number: | Start Date*: 2007-06-27 |
Sponsor Name:AUO | ||
Full Title: Intermittent Treatment with Taxotere and Prednisone in patients with asymptomatic, hormone-refractory prostate cancer: A Multicenter Phase II Trial | ||
Medical condition: asymptomatic hormone-refractory prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005249-21 | Sponsor Protocol Number: 1239.3 | Start Date*: 2006-02-16 |
Sponsor Name:Boehringer Ingelheim Ltd. | ||
Full Title: A multi-centre 3-arm randomized phase II trial of BIBF 1120 versus BIBW 2992 versus sequential administration of BIBF 1120 and BIBW 2992 in patients with hormone-resistant prostate cancer | ||
Medical condition: Chemo-naive hormone refractory prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001166-13 | Sponsor Protocol Number: COU-AA-001 | Start Date*: 2005-09-21 | |||||||||||
Sponsor Name:Cougar Biotechnology, Inc | |||||||||||||
Full Title: A Phase I/II Open Label Study of the 17α-hydroxylase/ C17,20 lyase inhibitor, Abiraterone acetate, in Patients with Prostate Cancer who have failed hormone therapy | |||||||||||||
Medical condition: Hormone refractory prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005255-18 | Sponsor Protocol Number: 1216.19 | Start Date*: 2006-07-03 |
Sponsor Name:Boehringer Ingelheim UK Ltd | ||
Full Title: A single arm phase II study to investigate the efficacy, safety and pharmacokinetics of a single dose of 200 mg of i.v. BI 2536, administered once every 3 weeks in patients with advanced metastatic... | ||
Medical condition: Advanced Metastatic Hormone Refractory Prostate Cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002370-64 | Sponsor Protocol Number: AUPSG 01/07 | Start Date*: 2007-06-11 | |||||||||||
Sponsor Name:Austrian Prostate Study Group (AUPSG) | |||||||||||||
Full Title: Multi-center, randomized, double-blind phase II study of sorafenib or placebo with best supportive care after failure of deocetaxol in metastatic hormone-refractory prostate cancer | |||||||||||||
Medical condition: metastatic hormone-refractory prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004545-15 | Sponsor Protocol Number: MLAM 2007/01 | Start Date*: 2008-06-10 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: The Split Dose Study: Split dose Rhenium-188-HEDP regimen in hormone refractory prostate cancer patients with bone metastases; a phase I toxicity study and phase II efficacy study. | ||
Medical condition: Hormone refractory prostate cancer with painful bone metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-004322-24 | Sponsor Protocol Number: ARN-509-003 | Start Date*: 2013-08-27 | |||||||||||
Sponsor Name:Aragon Pharmaceuticals, Inc | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase III Study of ARN-509 in Men with Non-Metastatic (M0) Castration-Resistant Prostate Cancer | |||||||||||||
Medical condition: Castration-Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: AT (Trial now transitioned) FI (Completed) SE (Completed) NL (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) NO (Completed) DE (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) FR (Trial now transitioned) DK (Trial now transitioned) HU (Completed) CZ (Trial now transitioned) SK (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004429-17 | Sponsor Protocol Number: CO39303 | Start Date*: 2018-09-19 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE III, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER TRIAL TESTING IPATASERTIB PLUS ABIRATERONE PLUS PREDNISONE/PREDNISOLONE, RELATIVE TO PLACEBO PLUS ABIRATERONE PLUS PREDNISONE/... | |||||||||||||
Medical condition: Metastatic Castrate-Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NO (Completed) PT (Completed) DE (Completed) DK (Completed) HU (Completed) GB (GB - no longer in EU/EEA) AT (Completed) IE (Completed) BE (Completed) ES (Ongoing) GR (Completed) PL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005766-39 | Sponsor Protocol Number: C1034T08 | Start Date*: 2007-04-03 | |||||||||||
Sponsor Name:Centocor B.V. | |||||||||||||
Full Title: A Randomized, Double-blind, Multicenter, Phase 2 Study of a Human Monoclonal Antibody to Human aV Integrins (CNTO 95) in Combination With Docetaxel and Prednisone for the First-Line Treatment of Su... | |||||||||||||
Medical condition: Hormone refractory prostate cancer (HRPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) AT (Prematurely Ended) DE (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004117-40 | Sponsor Protocol Number: MK-3475-641 | Start Date*: 2020-03-05 | ||||||||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Double-blind Trial of Pembrolizumab (MK-3475) Plus Enzalutamide Versus Placebo Plus Enzalutamide in Participants With Metastatic Castration-Resistant Prostate Cancer (mCRPC) ... | ||||||||||||||||||
Medical condition: Metastatic Castration-Resistant Prostate Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) AT (Trial now transitioned) GB (GB - no longer in EU/EEA) PL (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) IE (Trial now transitioned) IT (Trial now transitioned) CZ (Ongoing) HU (Trial now transitioned) BG (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002312-41 | Sponsor Protocol Number: MK-3475-365 | Start Date*: 2016-10-22 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc | |||||||||||||
Full Title: Phase Ib/II Trial of Pembrolizumab (MK-3475) Combination Therapies in Metastatic Castration-Resistant Prostate Cancer (mCRPC) (KEYNOTE-365) | |||||||||||||
Medical condition: Metastatic Castration-Resistant Prostate Cancer (mCRPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Temporarily Halted) DE (Trial now transitioned) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) SE (Trial now transitioned) DK (Trial now transitioned) IE (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) NL (Ongoing) AT (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005465-36 | Sponsor Protocol Number: 62202-761 | Start Date*: 2009-04-29 | |||||||||||
Sponsor Name:Meletios Athanasios Dimopoulos | |||||||||||||
Full Title: Pilot study of the significance of PTEN expression in patients with hormone refractory prostate cancer (HRPC) treated with Cetuximab as monotherapy for 8 weeks, followed by Docetaxel plus Cetuximab | |||||||||||||
Medical condition: Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003192-28 | Sponsor Protocol Number: SOG-MIE-2014-04 | Start Date*: 2015-01-02 | |||||||||||
Sponsor Name:SOGUG | |||||||||||||
Full Title: Phase II multicenter study to analyze the predictive value of fusion gene TMPRSS2-ETS in response to enzalutamide in patients with metastatic CRPC no previously treated with chemotherapy | |||||||||||||
Medical condition: Metastatic castration-resistant prostate cancer no previously treated with chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001933-16 | Sponsor Protocol Number: 26866138PCR2002 | Start Date*: 2007-03-13 |
Sponsor Name:Christos N. Papandreou | ||
Full Title: "A Phase II, Open-Label study of Velcade(Bortezomib)for patients with Androgen-Independent Prostate Carcinoma who progressed on or after prior chemotherapy" | ||
Medical condition: Treatment of patients with Androgen-Independent Prostate Carcinoma who progressed on or after prior chemotherapy. | ||
Disease: | ||
Population Age: | Gender: Male | |
Trial protocol: GR (Ongoing) | ||
Trial results: (No results available) |
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