- 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 2 of 41.
| 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: 2011-002114-36 | Sponsor Protocol Number: 20110113 | Start Date*: 2011-10-04 | |||||||||||||||||||||
| Sponsor Name:Amgen Inc | |||||||||||||||||||||||
| Full Title: Open-Label Access Protocol of Denosumab for Subjects with Advanced Cancer | |||||||||||||||||||||||
| Medical condition: Bone Metastases in Subjects with Advanced Breast Cancer and Bone Metastases in Men with Hormone-Refractory Prostate Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) AT (Completed) FR (Completed) ES (Completed) PL (Completed) BE (Completed) LV (Completed) LT (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2013-004405-30 | Sponsor Protocol Number: ARN-AR18-CT-102 | Start Date*: 2014-02-12 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Arno Therapeutics Inc | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 1 Study of Onapristone in Patients with Advanced Castration-resistant Prostate Cancer | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Advanced Castration-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: 2014-001189-87 | Sponsor Protocol Number: SAKK96/12 | Start Date*: 2017-07-18 | ||||||||||||||||
| Sponsor Name:Swiss Group for Clinical Cancer Research | ||||||||||||||||||
| Full Title: Prevention of Symptomatic Skeletal Events with Denosumab Administered every 4 Weeks versus every 12 Weeks - A Non-Inferiority Phase III trial | ||||||||||||||||||
| Medical condition: Bone metastases from castration resistant prostate cancer or from breast cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-002975-16 | Sponsor Protocol Number: ABX-CT-301 | Start Date*: 2018-10-31 | |||||||||||||||||||||
| Sponsor Name:ABX GmbH | |||||||||||||||||||||||
| Full Title: Phase III study of F-18-PSMA-1007 vs F-18-Fluorocholine PET to compare the detection rate of prostate cancer lesions in patients with biochemical recurrence after previous definitive treatment for ... | |||||||||||||||||||||||
| Medical condition: Suspicion of prostate cancer recurrence after previous definitive treatment, based on American Society for Radiation Oncology (ASTRO) criteria of 3 consecutive PSA rises and/or ASTRO/Phoenix criter... | |||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male | ||||||||||||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2020-005754-23 | Sponsor Protocol Number: ASSTBS-FRADIO-SPA-2020 | Start Date*: 2021-04-06 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Stereotactic body radiation therapy on Prostate with or without Androgen deprivation therapy, a phase III randomized controlled trial (SPA Trial) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: prostate acinar adenocarcinoma | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-001192-39 | Sponsor Protocol Number: P11-1 | Start Date*: 2012-01-26 | |||||||||||||||||||||||||||||||
| Sponsor Name:Dendreon Corporation | |||||||||||||||||||||||||||||||||
| Full Title: AN OPEN-LABEL STUDY OF SIPULEUCEL-T IN EUROPEAN MEN WITH METASTATIC, CASTRATE RESISTANT PROSTATE CANCER | |||||||||||||||||||||||||||||||||
| Medical condition: metastatic castrate resistant prostate cancer | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||||||||||||
| Trial protocol: AT (Completed) GB (Completed) NL (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2010-021434-55 | Sponsor Protocol Number: FE 200486 CS35A | Start Date*: 2010-11-11 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: An Open-label, Multi-Centre, Extension Trial, Evaluating the Long-Term Progression-Free Survival of Degarelix or Goserelin Three-Month Dosing Regimens in Patients with Prostate Cancer Requiring And... | |||||||||||||
| Medical condition: Prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: HU (Prematurely Ended) GB (Prematurely Ended) FI (Prematurely Ended) NL (Prematurely Ended) CZ (Completed) BE (Completed) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012405-18 | Sponsor Protocol Number: 09/0221 | Start Date*: 2010-02-15 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: Single site, phase II, double blind, randomised, placebo controlled study of the effect of dutasteride (Avodart)0.5 mg on the volume and characteristics of prostate cancer, as assessed by multifunc... | |||||||||||||
| Medical condition: Low risk prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: Removed from public view | |||||||||||||
| EudraCT Number: 2016-003740-36 | Sponsor Protocol Number: ICNAS-P01/2016 | Start Date*: 2019-03-11 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:ICNAS Produção Lda. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Comparative study of 68Ga-PSMA-11 PET and 18F-Fluorocholine PET in the detection of Recurrence in Prostate Cancer Patients after Radical Treatment | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Prostate Cancer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: PT (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-005438-20 | Sponsor Protocol Number: ESTO1 | Start Date*: 2012-05-22 | |||||||||||
| Sponsor Name:University of Tampere | |||||||||||||
| Full Title: Effects of short-term atorvastatin treatment on prostate cancer - a pre-surgical pilot trial | |||||||||||||
| Medical condition: Prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-003785-77 | Sponsor Protocol Number: 59244 | Start Date*: 2017-03-16 |
| Sponsor Name: | ||
| Full Title: Microdosing as a tool to individualize docetaxel dosing: development of a limited sampling model | ||
| Medical condition: Patients with breast-, prostate or non-small cell lung cancer (NSCLC), who are eligible for treatment with docetaxel. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-006055-39 | Sponsor Protocol Number: FE200486 CS26 | Start Date*: 2008-01-30 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: An Open-Label, Multi-Centre, Randomised Parallel-Group Study, Investigating Efficacy and Safety of Different Degarelix Three-Month Dosing Regimens in Patients with Prostate Cancer Requiring Androge... | |||||||||||||
| Medical condition: Prostate Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: HU (Completed) FI (Prematurely Ended) CZ (Prematurely Ended) BE (Completed) SE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021900-93 | Sponsor Protocol Number: CLIN1001 PCM301 | Start Date*: 2010-12-14 | |||||||||||
| Sponsor Name:STEBA BIOTECH SA | |||||||||||||
| Full Title: A European randomised Phase 3 study to assess the efficacy and safety of TOOKAD® Soluble for low risk localised prostate cancer compared to Active Surveillance | |||||||||||||
| Medical condition: Low-risk prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Completed) GB (Completed) DE (Completed) NL (Completed) BE (Completed) SE (Completed) FI (Completed) DK (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-006913-34 | Sponsor Protocol Number: FE200486 CS21A | Start Date*: 2007-03-23 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: An Open-Label, Multi-Centre, Extension Study, Evaluating the Long-Term Safety and Tolerability of Degarelix One-Month Dosing Regimen in Patients with Prostate Cancer Requiring Androgen Ablation The... | |||||||||||||
| Medical condition: Patients with histologically proven prostate cancer of all stages in whom endocrine treatment is indicated. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: HU (Completed) NL (Completed) DE (Completed) CZ (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021501-20 | Sponsor Protocol Number: 2010-021501-20 | Start Date*: 2010-06-22 | |||||||||||
| Sponsor Name:ISTITUTO NEUROLOGICO MEDITERRANEO NEUROMED | |||||||||||||
| Full Title: study for evaluation of 18F-choline PET/CT efficacy in patients with prostate carcinoma. | |||||||||||||
| Medical condition: patient with prostate carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-003814-40 | Sponsor Protocol Number: FE200486 CS12A | Start Date*: 2005-02-01 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: An open-label, multi-centre, extension study evaluation the long-term safety and tolerability of Degarelix one-month depots in patients with prostate cancer | |||||||||||||
| Medical condition: Prostate Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004572-13 | Sponsor Protocol Number: ARD-0301-010 | Start Date*: 2006-11-06 | |||||||||||
| Sponsor Name:Ardana Bioscience Ltd | |||||||||||||
| Full Title: A Phase II multi-centre, randomized, open-label study investigating the pharmacokinetics, pharmacodynamics, efficacy and safety of two loading dose regimens of a new GnRH antagonist, Teverelix, lon... | |||||||||||||
| Medical condition: Locally advanced and/or metatstatic prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: LT (Completed) LV (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000423-12 | Sponsor Protocol Number: CP506-001 | Start Date*: 2022-12-13 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Maastricht University | ||||||||||||||||||||||||||||||||||||||
| Full Title: A modular, first time in human, open label, multiple dose, accelerated escalation with cohort expansion study of the safety and pharmacokinetics of intravenous infusion of CP-506, a tumor agnostic ... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Tumour Agnostic treatment. ● Module differentiation: – Module 1 - monotherapy – solid tumour patients with cancer types that are enriched for HRD/FAD defects – Module 2 – combination with Carboplat... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2022-002571-11 | Sponsor Protocol Number: ENHANCE | Start Date*: 2022-11-25 | |||||||||||
| Sponsor Name:Institut Mutualiste Montsouris | |||||||||||||
| Full Title: EvaluatioN of High-Intensity Focused Ultrasound (HIFU) Hemi-ablation and short-term AndrogeN deprivation therapy Combination to Enhance prostate control for intermediate risk localized prostate can... | |||||||||||||
| Medical condition: Intermediate risk localized prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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