- Trials with a EudraCT protocol (189)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
189 result(s) found for: Prostate specific antigen test.
Displaying page 9 of 10.
EudraCT Number: 2019-001745-40 | Sponsor Protocol Number: MK-7339-007 | Start Date*: 2019-11-24 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: A Phase 2 Study of Olaparib in Combination with Pembrolizumab in Participants with Previously Treated, Homologous Recombination Repair Mutation (HRRm) and/or Homologous Recombination Deficiency (HR... | |||||||||||||
Medical condition: HRRm and/or HRD-positive cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) FR (Trial now transitioned) DE (Trial now transitioned) ES (Restarted) LV (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001539-30 | Sponsor Protocol Number: C21013 | Start Date*: 2012-09-27 | |||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Study in Japan and Ex-Japan to Characterize the Pharmacokinetic and Pharmacodynamic Response to Orteronel (TAK-700) in Chemotherapy-Naïve Patients with Castration-Resistant Prostate Cancer | |||||||||||||
Medical condition: progressive castration-resistant prostate cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IE (Completed) GR (Completed) GB (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003555-38 | Sponsor Protocol Number: CP-MGC018-01 | Start Date*: 2019-08-05 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:MacroGenics, Inc. | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2, First-in-Human, Open-Label, Dose-Escalation Study of MGC018 (Anti–B7-H3 Antibody Drug Conjugate) Alone and in Combination with MGA012 (Anti–PD-1 Antibody) in Patients with Advanced Sol... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Advanced Solid Tumors | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: PL (Completed) ES (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003025-18 | Sponsor Protocol Number: VAPER | Start Date*: 2015-05-08 |
Sponsor Name:King's College London [...] | ||
Full Title: In Vivo Generation of Optimal Tumour Antigen-specific Anticancer Immune Responses, by Vaccination with Human Telomerase Reverse Transcriptase (hTERT) Peptides, in Combination with Specific Adjuvant... | ||
Medical condition: Advanced malignancies | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003135-30 | Sponsor Protocol Number: URO-901-3005 | Start Date*: 2019-12-12 | |||||||||||
Sponsor Name:Urovant Sciences GmbH | |||||||||||||
Full Title: A Phase 3 Double-Blind, Randomized, Placebo-Controlled, Multi-Center Study to Evaluate the Efficacy, Safety and Tolerability of Vibegron in Men with Overactive Bladder (OAB) Symptoms on Pharmacolog... | |||||||||||||
Medical condition: Overactive Bladder (OAB) in men with Benign Prostatic Hyperplasia (BPH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: LT (Completed) ES (Ongoing) HU (Completed) PT (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005774-25 | Sponsor Protocol Number: SC104 | Start Date*: 2024-09-06 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:SOTIO Biotech AG | ||||||||||||||||||||||||||||||||||||||
Full Title: A phase 2, open-label, single-arm, multicenter study of SOT101 in combination with pembrolizumab to evaluate the efficacy and safety in patients with selected advanced/refractory solid tumors | ||||||||||||||||||||||||||||||||||||||
Medical condition: advanced/refractory solid tumors | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) ES (Temporarily Halted) CZ (Prematurely Ended) BE (Completed) IT (Prematurely Ended) HU (Completed) PL (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001358-24 | Sponsor Protocol Number: B9991040 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||||||||||||
Full Title: A Phase 1b/2 Study to Evaluate Safety and Clinical Activity of Avelumab in Combination with Bempegaldesleukin (NKTR-214) with or without Talazoparib or Enzalutamide in Participants with Locally Adv... | |||||||||||||||||||||||
Medical condition: Locally recurrent (not amenable for curative intent) or metastatic squamous cell carcinoma of the of the oral cavity, oropharynx, hypopharynx, or larynx; metastatic castration-resistant prostate... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) IT (Prematurely Ended) ES (Prematurely Ended) BE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000285-10 | Sponsor Protocol Number: CCS1477-01 | Start Date*: 2021-06-08 |
Sponsor Name:CellCentric Ltd | ||
Full Title: An open-label Phase I/IIa study to evaluate the safety and efficacy of CCS1477 as monotherapy and in combination, in patients with advanced solid/metastatic tumours. | ||
Medical condition: Metastatic Castrate Resistant Prostate Cancer (mCRPC) and other advanced cancers with solid tumours. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004036-36 | Sponsor Protocol Number: 178-MA-1008 | Start Date*: 2016-07-18 | |||||||||||
Sponsor Name:Astellas Pharma Global development, Inc | |||||||||||||
Full Title: A Phase 4, Double-Blind, Randomized, Placebo-controlled, Multi- Center Study to Evaluate the Efficacy, Safety, and Tolerability of Mirabegron in Men with Overactive Bladder (OAB) Symptoms While ... | |||||||||||||
Medical condition: Over active bladder (OAB) in men with Lower Urinary Tract Symptoms (LUTS) due to Benign Prostatic Hyperplasia (BPH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) PL (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000345-39 | Sponsor Protocol Number: B9991032 | Start Date*: 2019-02-19 | ||||||||||||||||
Sponsor Name:Pfizer Inc. | ||||||||||||||||||
Full Title: A Phase 2 Study to Evaluate Safety and Anti-tumor Activity of Avelumab in Combination with Talazoparib In Patients with BRCA or ATM Mutant Tumors | ||||||||||||||||||
Medical condition: locally advanced (primary or recurrent) or metastatic solid tumors with a pathogenic or likely pathogenic germline or loss-of-function somatic BRCA1, or BRCA2, or ATM gene defect | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) FR (Completed) BE (Completed) DK (Completed) ES (Ongoing) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003847-22 | Sponsor Protocol Number: ICORG11-04 | Start Date*: 2012-02-02 | |||||||||||
Sponsor Name:ICORG | |||||||||||||
Full Title: ECOG 2809: Phase II, Randomized Study of MK-2206 - Bicalutamide Combination in Patients With Rising PSA at High-Risk of Progression After Primary Therapy | |||||||||||||
Medical condition: Patients with Rising PSA at high risk of Prostate cancer progression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004486-86 | Sponsor Protocol Number: SRA737-01 | Start Date*: 2016-04-25 | |||||||||||
Sponsor Name:Sierra Oncology, Inc. | |||||||||||||
Full Title: A Phase 1/2 Trial of SRA737 (a Chk1 Inhibitor) Administered Orally in Subjects with Advanced Cancer | |||||||||||||
Medical condition: Patients with histologically or cytologically proven advanced solid tumours, refractory to conventional treatment, or for which no conventional therapy is considered appropriate by the Investigator. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011498-34 | Sponsor Protocol Number: TAS 2009 | Start Date*: 2009-10-22 | ||||||||||||||||
Sponsor Name:Ergomed Clinical Research Limited | ||||||||||||||||||
Full Title: An Open-Label, Multi-Center Phase I/II Dose Escalation Study to Investigate the Safety and Tolerability of Multiple Doses of Oral Tasidotin HCL in Patients with Advanced Solid Tumors (part A), and ... | ||||||||||||||||||
Medical condition: Solid tumours and metastatic melanoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004881-85 | Sponsor Protocol Number: PSMA-POLM | Start Date*: 2020-12-02 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SANT'ANDREA | |||||||||||||
Full Title: PET-CT with 68Ga-PSMA as a marker of neoangiogenesis in lung adenocarcinoma | |||||||||||||
Medical condition: Lung adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006277-24 | Sponsor Protocol Number: EFC6145 | Start Date*: 2008-04-10 | |||||||||||
Sponsor Name:sanofi-aventis recherche et développement | |||||||||||||
Full Title: A RANDOMIZED DOUBLE-BLIND PLACEBO-CONTROLLED PARALLEL GROUP STUDY OF THE EFFICACY AND SAFETY OF 4 ADMINISTRATIONS OF XRP0038/NV1FGF 4mg AT 2–WEEK INTERVALS ON AMPUTATION OR ANY DEATH IN CRITICAL LI... | |||||||||||||
Medical condition: Critical Limb Ischemia with skin lesions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) HU (Completed) GB (Completed) CZ (Completed) GR (Completed) ES (Completed) AT (Completed) FI (Completed) SE (Completed) FR (Completed) EE (Completed) IT (Completed) DK (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004332-36 | Sponsor Protocol Number: DTX-SPL8783-002 | Start Date*: 2020-02-01 | |||||||||||
Sponsor Name:Starpharma Pty Ltd | |||||||||||||
Full Title: A Phase 1/2 Modular, Multi-Arm Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of DTX-SPL8783 (DEP docetaxel/DEP-DTX) in Combination with Anti-Cancer Treatments, in Patients wit... | |||||||||||||
Medical condition: Advanced malignant solid tumours | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001958-27 | Sponsor Protocol Number: H6D-MC-LVHG | Start Date*: 2006-07-13 |
Sponsor Name:Lilly ICOS LLC | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Design, 5-Group, Multinational Study to Evaluate the Efficacy, Dose Response, and Safety of Tadalafil Once-a-Day Dosing for 12 Weeks in Men ... | ||
Medical condition: Primary treatment of the signs and symptoms of benign prostatic hyperplasia in men (also referred to as BPH-LUTS [lower urinary tract symptoms]). BPH-LUTS include urinary frequency, urgency, interm... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Completed) DE (Completed) ES (Completed) GR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002172-42 | Sponsor Protocol Number: Bay 38-9456/11336 | Start Date*: 2005-02-09 | |||||||||||
Sponsor Name:Bayer Oy | |||||||||||||
Full Title: A randomized, double-blind, double-dummy, multi-center, parallel group study to compare the tolerability and efficacy of once daily vardenafil versus vardenafil PRN versus placebo in men immediatel... | |||||||||||||
Medical condition: Erektiohäiriö | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) DE (Completed) AT (Completed) GB (Completed) IT (Completed) ES (Completed) | |||||||||||||
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: 2012-002552-16 | Sponsor Protocol Number: RRK4368 | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:University Hospitals Birmingham NHS Foundation Trust | |||||||||||||
Full Title: Cabazitaxel in platinum pre-treated patients with locally advanced or metastatic transitional cell carcinoma who developed disease progression within 12 months of platinum based chemotherapy. | |||||||||||||
Medical condition: Transitional cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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