- Trials with a EudraCT protocol (104)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
104 result(s) found for: Gleason score.
Displaying page 1 of 6.
EudraCT Number: 2017-000490-36 | Sponsor Protocol Number: CHUBX2016/38 | Start Date*: 2018-02-19 | ||||||||||||||||
Sponsor Name:CHU de Bordeaux | ||||||||||||||||||
Full Title: Etude monocentrique, exploratoire, comparant la TEP/TDM au 68Ga-RM2 à la TEP/TDM au 68Ga-PSMA-617 chez des patients atteints de cancers de la prostate de différents risques métastatiques, candidats... | ||||||||||||||||||
Medical condition: Prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002355-40 | Sponsor Protocol Number: SPCG 12 | Start Date*: 2005-08-23 |
Sponsor Name:Scandinavian prostate cancer group | ||
Full Title: An open randomized phase III trial of six cycles of docetaxel versus surveillance after radical prostatectomy in prostate cancer patients with high grade pT3 or margin positive pT2 | ||
Medical condition: Men, 18-70 years old, who have had radical prostatectomy due to prostate cancer and with a high grade pT3 or margin positive pT2 tumour may be candidates for the study. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Ongoing) FI (Completed) DK (Completed) IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004694-41 | Sponsor Protocol Number: PRX302-2-08 | Start Date*: 2017-02-03 | |||||||||||
Sponsor Name:Sophiris Bio Corp. 1258 Prospect Street La Jolla, CA 92037 USA | |||||||||||||
Full Title: A Multi-Centre, Open Label, Phase IIb Study, Evaluating the Safety, Tolerability and Efficacy of Targeted Intraprostatic Administration of PRX302 to Treat Men with Histologically Proven, Clinically... | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004874-96 | Sponsor Protocol Number: HL/IDP/PTS/001 | Start Date*: 2005-08-17 |
Sponsor Name:Newcastle Upon Tyne Hospitals NHS Trust | ||
Full Title: Protocol: HL/IDP/PTS/001 Tumour Profiling In An Open-Labelled, 2-Arm Study Investigating The Tolerability And Efficacy Of Taxotere In Patients With High Risk Prostate Cancer | ||
Medical condition: Prostate Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002511-99 | Sponsor Protocol Number: IOV-PR-CH-PET-1-2013 | Start Date*: 2013-11-25 | |||||||||||
Sponsor Name:ISTITUTO ONCOLOGICO VENETO | |||||||||||||
Full Title: Role of PET/ CT with 18F-fluorocholine in the staging of patients with intermediate/high risk prostate cancer. Phase III, randomized, open-label clinical trial | |||||||||||||
Medical condition: Histologically proven prostate cancer with Gleason score =7 and PSA>=10ng/ml or Gleason score >=8 and any PSA level or cT2-T3 and any PSA level or any Gleason score and PSA>=20ng/ml and indication ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2006-002772-17 | Sponsor Protocol Number: 22043-30041 | Start Date*: 2009-06-22 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Immediate or early salvage post-operative external radiotherapy combined with concomitant and adjuvant hormonal treatment versus immediate or early salvage post-operative external radiotherapy alon... | |||||||||||||
Medical condition: Prostatic carcinoma with pathological stage pT3a-b R0-1 N0M0 / pT2R1 N0M0, Gleason score 5-10 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Prematurely Ended) BE (Prematurely Ended) FR (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000478-42 | Sponsor Protocol Number: 008285QM | Start Date*: 2013-02-18 |
Sponsor Name:Queen Mary, University of London | ||
Full Title: NEPTUNE: A Randomised Phase II Study of Neoadjuvant TAK-700 and Leuprorelin Acetate versus Surgery Alone in Intermediate and High Risk Clinically Localized Prostate Cancer | ||
Medical condition: High or Intermediate Risk, Untreated, Clinically Localised Prostate Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-002371-33 | Sponsor Protocol Number: FS05-01 | Start Date*: 2006-01-02 |
Sponsor Name:Urologische Partnerschaft | ||
Full Title: Finasterid-unterstützte Diagnostik des Prostatakarzinoms bei Patienten mit BPH | ||
Medical condition: Adenoma of the prostate, elevated serum-PSA value | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002276-37 | Sponsor Protocol Number: AK-2017-PC-1 | Start Date*: 2017-08-25 | |||||||||||
Sponsor Name:Rigshospitalet, Department of Clinical Physiology, Nuclear Medicine & PET | |||||||||||||
Full Title: Phase II trial: uPAR-PET/MR in patients with newly diagnosed prostate cancer; non-invasive characterization of tumor aggressiveness | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003165-15 | Sponsor Protocol Number: FACBC-STAGING-2014 | Start Date*: 2014-12-02 | |||||||||||
Sponsor Name:AOU di Bologna Policlinico S.Orsola-Malpighi | |||||||||||||
Full Title: 18F-FACBC PET/CT FOR STAGING HIGH RISK PROSTATE CANCER | |||||||||||||
Medical condition: Patients affected by moderate to high risk primary prostate cancer who are scheduled for surgery with a planned, elective lymph node dissection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2014-001784-13 | Sponsor Protocol Number: ISRCTN91422391 | Start Date*: 2014-12-29 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: PROVENT: A randomised, double blind, placebo controlled feasibility study to examine the clinical effectiveness of aspirin and/or Vitamin D3 to prevent disease progression in men on active surveill... | |||||||||||||
Medical condition: Prostate cancer disease progression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022037-29 | Sponsor Protocol Number: AFU-GETUG 20/0310 | Start Date*: 2011-01-31 | |||||||||||
Sponsor Name:FNCLCC (Fédération Nationale des Centres de Lutte Contre le Cancer) | |||||||||||||
Full Title: Phase III randomised trial to evaluate the benefit of adjuvant hormonal treatment with leuprorelin acetate (Eligard® 45 mg) for 24 months after radical prostatectomy in patients with high risk of r... | |||||||||||||
Medical condition: PROSTATIC ADENOCARCINOMA WITH HIGH RISK OF RECURRENCE. | |||||||||||||
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Population Age: | Gender: Male | ||||||||||||
Trial protocol: FR (Trial now transitioned) SK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001920-36 | Sponsor Protocol Number: NIMAO/2018-01/JF-01 | Start Date*: 2020-12-03 | |||||||||||
Sponsor Name:CHU de NIMES | |||||||||||||
Full Title: Phase II a study to evaluate the safety, tolerability, distribution and dose effect of neoadjuvant doxorubicin arterial embolization in patients with prostate cancer at high risk of recurrence befo... | |||||||||||||
Medical condition: patients with high-risk prostate cancer with a Gleason score of 9-10 on biopsy,multimodal treatment radical prostatectomy validated in CPR, managed in Hospital of Nîmes. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014446-28 | Sponsor Protocol Number: JANUS | Start Date*: 2009-12-03 | |||||||||||
Sponsor Name:UNIVERSITA` CAMPUS BIOMEDICO | |||||||||||||
Full Title: A PHASE II TRANSLATIONAL STUDY INVESTIGATING THE BIOLOGICAL EFFECTS OF THE ZOLEDRONIC ACID AS NEOADJUVANT THERAPY ON INVASIVE PROSTATE CANCER | |||||||||||||
Medical condition: invasive prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018770-20 | Sponsor Protocol Number: DC-005 | Start Date*: 2010-05-21 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Phase I/II trial of vaccine therapy in curative resected prostate cancer patients using autologous dendritic cells loaded with mRNA from primary prostate cancer tissue, hTERT and surviving. | ||
Medical condition: Prostatic cancer patients who have received curative surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
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: 2014-000476-26 | Sponsor Protocol Number: N14DAR | Start Date*: 2020-07-13 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Netherlands Cancer Institute | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Dynamics of Androgen Receptor genomics and transcriptomics after neoadjuvant androgen ablation (DARANA) | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Prostate cancer | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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