- Trials with a EudraCT protocol (815)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
815 result(s) found for: prostate cancer OR breast cancer.
Displaying page 8 of 41.
| EudraCT Number: 2006-001657-94 | Sponsor Protocol Number: SPCG 13 | Start Date*: 2006-11-16 | |||||||||||
| Sponsor Name: [...] | |||||||||||||
| Full Title: Randomized adjuvant phase III trial of six cycles of docetaxel+hormonal treatment versus hormonal treatment in patients with intermediate or high-risk prostate cancer treated with radical radiothe... | |||||||||||||
| Medical condition: Intermediate or high-risk prostate cancer treated with radical radiotherapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FI (Completed) IE (Completed) SE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-001576-13 | Sponsor Protocol Number: FJ-228-0002 | Start Date*: 2005-05-17 | |||||||||||
| Sponsor Name:Gloucester Pharmaceuticals Inc. | |||||||||||||
| Full Title: An exploratory Phase II, multicenter, open-label trial evaluating the activity and tolerability of of FK228 in androgen independent metastatic prostate cancer patients with a rising PSA. | |||||||||||||
| Medical condition: Metastatic prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003007-38 | Sponsor Protocol Number: 56021927PCR3003 | Start Date*: 2016-01-11 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled Phase 3 Study of JNJ56021927 in Subjects with High-risk, Localized or Locally Advanced Prostate Cancer Receiving Treatment with Primary Radiation Therapy | |||||||||||||
| Medical condition: High- or very-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) SE (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) DE (Ongoing) BE (Trial now transitioned) NL (Completed) PL (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004639-35 | Sponsor Protocol Number: 2017/2601 | Start Date*: 2018-10-26 | ||||||||||||||||
| Sponsor Name:Gustave Roussy | ||||||||||||||||||
| Full Title: A Phase III trial of acetylsalicylic acid and atorvastatin in patients with castrate-resistant prostate cancer | ||||||||||||||||||
| Medical condition: castrate-resistant prostate cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-004818-34 | Sponsor Protocol Number: CTRIAL-IE-19-32 | Start Date*: 2021-04-23 | |||||||||||
| Sponsor Name:Cancer Trials Ireland | |||||||||||||
| Full Title: DASL-HiCaP: Darolutamide Augments Standard Therapy for Localised Very High-Risk Cancer of the Prostate (ANZUP1801). A randomised phase 3 double-blind, placebo-controlled trial of adding darolutamid... | |||||||||||||
| Medical condition: Clinically localised prostate cancer defined as very high risk, or with very high risk features. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002058-41 | Sponsor Protocol Number: DISFUNZIONE ERETTILE POST-RT | Start Date*: 2007-07-12 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
| Full Title: EFFICACY EVALUATION OF TADALAFIL 20 MG ON DEMAND VS TADALAFIL 5 MG DAILY AS TREATMENT MODALITY FOR ERECTILE DYSFUNCTION FOLLOWING RADICAL RADIOTHERAPY IN PROSTATIC CANCER | |||||||||||||
| Medical condition: Erectile dysfunction following radiotherapy for prostatic cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005595-33 | Sponsor Protocol Number: FE200486 CS21 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: An Open-label, Multi-Centre, Randomized, Parallel-group Study, Investigating the Efficacy and Safety of Degarelix One Month Dosing Regimens; 160 mg (40 mg/ml) and 80 mg (20mg/ml), in Comparison to ... | |||||||||||||
| Medical condition: Prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) CZ (Completed) GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005201-27 | Sponsor Protocol Number: D361EC00001 | Start Date*: 2022-06-27 | |||||||||||||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||
| Full Title: A Phase III Double-Blind, Randomised, Placebo-Controlled Study Assessing the Efficacy and Safety of Capivasertib + Docetaxel Versus Placebo + Docetaxel as Treatment for Patients with Metastatic Cas... | |||||||||||||||||||||||
| Medical condition: Metastatic Castration Resistant Prostate Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) GR (Trial now transitioned) BE (Trial now transitioned) PL (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2011-004103-20 | Sponsor Protocol Number: INO-VT-464-CL-001 | Start Date*: 2011-10-13 | |||||||||||
| Sponsor Name:Innocrin Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 1/2 Open-Label Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Seviteronel in Subjects with Castration-Resistant Prostate Cancer | |||||||||||||
| Medical condition: Castration-resistant prostate cancer (CRPC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-000080-42 | Sponsor Protocol Number: Keto1 | Start Date*: 2008-03-15 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
| Full Title: A Phase II study of Chetoconazolo in patients with Metastatic Hormone-Refractory Prostate Cancer. Pilot study | |||||||||||||
| Medical condition: Patients with advanced or metastatic hormone-refractory prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003720-32 | Sponsor Protocol Number: SPECTRE2015 | Start Date*: 2016-06-01 | |||||||||||
| Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
| Full Title: Combined Suppression Of Cholesterol Bioavailability And Androgen Deprivation Therapy To Treat Castration Resistant Prostate Cancer | |||||||||||||
| Medical condition: Castration Resistant Prostate Cancer | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-004295-37 | Sponsor Protocol Number: 1-2003 | Start Date*: 2005-08-26 |
| Sponsor Name:Finnish Uro-Oncological Group | ||
| Full Title: A phase III trial comparing docetaxel every third week to biweekly docetaxel monotherapy in metastatic hormone refractory prostate cancer patients. | ||
| Medical condition: Patients with metastatic hormone refractory prostate cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: SE (Completed) IE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004332-11 | Sponsor Protocol Number: P.64Cu.002.02 | Start Date*: 2018-03-28 | |||||||||||
| Sponsor Name:A.C.O.M. -ADVANCED CENTER ONCOLOGY MACERATA -S.R.L. | |||||||||||||
| Full Title: Use of 64CuCl2 PET/CT Imaging in the selection of patients with prostate cancer in biochemical relapse after prostatectomy, to be successfully treated with salvage radiotherapy on the prostatic bed | |||||||||||||
| Medical condition: cancer on the prostatic bed | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-000799-14 | Sponsor Protocol Number: 0080CA002 | Start Date*: 2015-01-16 | |||||||||||
| Sponsor Name:Novalon S. A. | |||||||||||||
| Full Title: Phase III, open-label, multi-center study to assess the pharmacodynamic (PD), pharmacokinetic (PK) and safety of Zoreline 10.8 mg goserelin subcutaneous implant (Novalon) in male patients with pros... | |||||||||||||
| Medical condition: Prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: BE (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000842-79 | Sponsor Protocol Number: IJB-PROS-PROSPERO-2016 | Start Date*: 2016-09-08 | ||||||||||||||||
| Sponsor Name:Institut Jules Bordet | ||||||||||||||||||
| Full Title: Prospective evaluation of 68Ga-PSMA PET-CT for Recurrence detection of Prostate Cancer and its impact on patient management The ProsPERo Trial | ||||||||||||||||||
| Medical condition: Males 18 years of age or older with histologically-proven prostate adenocarcinoma and biochemical relapse with rising PSA level after initial treatment with radical curative intent, not yet on pall... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-004321-86 | Sponsor Protocol Number: RN5609C00 | Start Date*: 2019-07-24 | ||||||||||||||||
| Sponsor Name:BioNTech SE | ||||||||||||||||||
| Full Title: First-in-human, dose titration and expansion trial to evaluate safety, immunogenicity and preliminary efficacy of W_pro1 (BNT112) monotherapy and in combination with cemiplimab in patients with pr... | ||||||||||||||||||
| Medical condition: Male adults with prostate cancer, both mCRPC (Arms 1A & 1B) and LPC (ARms 2&3) patients, will be treated with W_pro1 alone or in combination with cemiplimab. LPC patients will also receive neo-adju... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) HU (Prematurely Ended) DE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-015122-11 | Sponsor Protocol Number: GBG54 | Start Date*: 2012-08-27 | |||||||||||
| Sponsor Name:GBG Forschungs GmbH | |||||||||||||
| Full Title: A prospective, randomised multi-centre phase II study evaluating the adjuvant, neoadjuvant or palliative treatment with tamoxifen +/- GnRH analogue versus aromatase inhibitor + GnRH analogue in m... | |||||||||||||
| Medical condition: Breast Cancer in Male Patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004627-12 | Sponsor Protocol Number: CABASEM-SOGUG | Start Date*: 2011-12-22 | ||||||||||||||||
| Sponsor Name:SOGUG - Spanish Oncology Genitourinary Group | ||||||||||||||||||
| Full Title: Phase II Study of Weekly Cabazitaxel for Advanced Prostate Cancer in "Unfit" Hormone-Refractory Patients Previously Treated with Docetaxel. | ||||||||||||||||||
| Medical condition: Advanced Prostate Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-005611-46 | Sponsor Protocol Number: TAVT45C02 | Start Date*: 2021-06-21 | |||||||||||||||||||||
| Sponsor Name:Tavanta Therapeutics, Inc. | |||||||||||||||||||||||
| Full Title: Phase 3 study investigating the efficacy and safety of TAVT-45 (abiraterone acetate) Granules for Oral Suspension (a novel abiraterone acetate formulation) relative to a reference abiraterone aceta... | |||||||||||||||||||||||
| Medical condition: Metastatic Castrate Sensitive Prostate Cancer (mCSPC) and metastatic Castrate Resistant Prostate Cancer (mCRPC) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
| Trial protocol: FR (Completed) SE (Completed) HU (Completed) ES (Ongoing) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2020-005042-42 | Sponsor Protocol Number: CURF18PSM0001 | Start Date*: 2021-06-27 | |||||||||||||||||||||||||||||||
| Sponsor Name:CURIUM Austria GmbH | |||||||||||||||||||||||||||||||||
| Full Title: Prospective study of added value of florastamin (18F) PET/CT in localisation of clinically significant prostate cancer in patients with PI-RADS≤3 report of multi-parametric MRI, elevated serum PSA ... | |||||||||||||||||||||||||||||||||
| Medical condition: Prostate cancer suspected clinically and on the basis of elevated serum Prostate Specific Antigen (PSA) levels and PSA density and with result of multiparametric Magnetic Resonance Imaging (mpMRI) ... | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||||||||||||
| Trial protocol: AT (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
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