- Trials with a EudraCT protocol (292)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
292 result(s) found for: Bladder tumor.
Displaying page 2 of 15.
EudraCT Number: 2013-005274-22 | Sponsor Protocol Number: 1408P1921 | Start Date*: 2014-07-30 | |||||||||||
Sponsor Name:Shionogi & Co., Ltd | |||||||||||||
Full Title: A multicenter, open-label, phase 2 study of S-588410 as maintenance monotherapy after first-line platinum-containing chemotherapy in patients with advanced and/or metastatic bladder cancer | |||||||||||||
Medical condition: Advanced and/or metastatic bladder cancer, which is under control according to first-line chemotherapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002267-33 | Sponsor Protocol Number: OCTO-089 | Start Date*: 2017-06-13 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: A parallel group phase I/II marker lesion study to assess the safety, tolerability and efficacy of intravenous or intravesical pembrolizumab in intermediate risk recurrent non-muscle invasive bladd... | |||||||||||||
Medical condition: Intermediate risk recurrent non-muscle invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004026-17 | Sponsor Protocol Number: MK-3475-057 | Start Date*: 2016-01-13 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: A Phase II Clinical Trial to Study the Efficacy and Safety of Pembrolizumab (MK-3475) and Pembrolizumab in Combination with Other Investigational Agents in Subjects with High Risk Non-muscle Invasi... | |||||||||||||
Medical condition: Non-Muscle Invasive Bladder Cancer (NMIBC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) FI (Trial now transitioned) GB (GB - no longer in EU/EEA) NL (Trial now transitioned) GR (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000782-35 | Sponsor Protocol Number: 28-02 (ZKS000429) | Start Date*: 2009-01-21 | |||||||||||
Sponsor Name:Verein fuer Krebsfoschung (Society for Cancer Research) | |||||||||||||
Full Title: Dose-escalating study to determine the maximum tolerated dose (MTD) of the mistletoe extract WEME 200 mg for intravesical instillation in patients with completely resected (R0) superficial bladder ... | |||||||||||||
Medical condition: Patients after transurethral R0-resection (TUR) of a histologically confirmed superficial bladder carcinoma (pTa low grade [multilocular or recurrence], pT1 low grade); re-resections included. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003541-11 | Sponsor Protocol Number: BL006 | Start Date*: 2021-04-15 | |||||||||||
Sponsor Name:UroGen Pharma Ltd. | |||||||||||||
Full Title: A Randomized, Controlled, Open-label Study of the Efficacy, Durability, and Safety of UGN-102 With or Without TURBT in Patients with Low Grade Intermediate Risk Non-Muscle Invasive Bladder Cancer (... | |||||||||||||
Medical condition: Non-Muscle Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) BG (Completed) LV (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004311-12 | Sponsor Protocol Number: RUTIVAC-1 | Start Date*: 2017-02-14 | |||||||||||
Sponsor Name:ARCHIVEL FARMA, S.L. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED PHASE II TRIAL TO EVALUATE THE IMMUNOMODULATORY EFFECT OF RUTI® IN INDIVIDUALS WITH HIGH-RISK NON-MUSCLE-INVASIVE BLADDER CANCER (NMIBC) TREATED WITH ... | |||||||||||||
Medical condition: High-Risk Non-Muscle-Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001943-23 | Sponsor Protocol Number: EFC6668 | Start Date*: 2007-12-17 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche et Développement | |||||||||||||
Full Title: Randomized Study of LAROTAXEL + Cisplatin (LC) vs. Gemcitabine + Cisplatin (GC) in the First Line Treatment of Locally Advanced/Metastatic Urothelial Tract or Bladder Cancer | |||||||||||||
Medical condition: Locally Advanced/Metastatic Urothelial Tract or Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Prematurely Ended) ES (Completed) SE (Prematurely Ended) FR (Completed) BE (Completed) IT (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001321-14 | Sponsor Protocol Number: INCB54828-201 | Start Date*: 2017-01-12 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 2, Open-Label, Single-Agent, Multicenter Study to Evaluate the Efficacy and Safety of INCB054828 in Subjects With Metastatic or Surgically Unresectable Urothelial Carcinoma Harboring FGF/FG... | |||||||||||||
Medical condition: Subjects with metastatic or surgically unresectable urothelial cancer (may include primary site from ureters, upper tract, renal pelvis, and bladder) with an FGF/FGFR alteration, who failed at leas... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) FR (Completed) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000081-33 | Sponsor Protocol Number: JaNEO-001 | Start Date*: 2016-05-04 | |||||||||||||||||||||
Sponsor Name:Ligartis GmbH | |||||||||||||||||||||||
Full Title: Phase Ib/II study assessing the neo-adjuvant combination therapy of vinflunine with cisplatin followed by radical cystectomy in patients with muscle-invasive bladder cancer | |||||||||||||||||||||||
Medical condition: Patients with muscle-invasive bladder cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001811-59 | Sponsor Protocol Number: D933RC00001 | Start Date*: 2019-02-26 | ||||||||||||||||
Sponsor Name:AstraZeneca AB | ||||||||||||||||||
Full Title: A Phase III, Randomized, Open-Label, Multi-Center, Global Study to Determine the Efficacy and Safety of Durvalumab in Combination with Gemcitabine+Cisplatin for Neoadjuvant Treatment Followed by Du... | ||||||||||||||||||
Medical condition: Patients with histologically or cytologically documented muscle-invasive transitional cell carcinoma (TCC) of the bladder | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001189-98 | Sponsor Protocol Number: NICSA | Start Date*: 2017-08-28 | |||||||||||
Sponsor Name:Aarhus Universitet | |||||||||||||
Full Title: Neoadjuvant short-term Intensive Chemoresection versus Standard Adjuvant intravesical instillations in NMIBC - A study on effect and tolerability of neoadjuvant short-term intensive chemoresection... | |||||||||||||
Medical condition: Patients with recurrent non-muscle invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003112-27 | Sponsor Protocol Number: NORTH-REG-3 | Start Date*: 2020-09-14 | |||||||||||
Sponsor Name:Aarhus University [...] | |||||||||||||
Full Title: Nordic Urothelial Cancer Research Group Study on Reduced BCG Dwell-Time in High Risk NMIBC Short title: NORTH-REG Dwell-Time Study | |||||||||||||
Medical condition: Reduced BCG dwell time in patients who are diagnosed with high risk non-muscle-invasive- bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000557-36 | Sponsor Protocol Number: UC-Aurora_INT01 | Start Date*: 2014-08-21 | |||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei tumori | |||||||||||||
Full Title: A Phase 2 study of the Aurora kinase A inhibitor Alisertib (MLN8237) in patients with relapsed or refractory transitional-cell carcinoma of the bladder and urothelial tract | |||||||||||||
Medical condition: Advanced urotelial cancer of the bladder, urethra, or the upper urinary tract who are resistant to platinum based therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012274-13 | Sponsor Protocol Number: R39-09-01 | Start Date*: 2009-09-17 | |||||||||||
Sponsor Name:FIDIA | |||||||||||||
Full Title: ONCOFID-P (Paclitaxel-hyaluronic acid) in the intravesical therapy of patients with non-muscle invasive cancer of the bladder. A phase II marker lesion study | |||||||||||||
Medical condition: Patients affected by multiple recurrent Ta G1-G2 papillary cancer of the bladder. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005427-10 | Sponsor Protocol Number: 1200.261 | Start Date*: 2016-04-29 | |||||||||||
Sponsor Name:Boehringer Ingelheim España, S.A. | |||||||||||||
Full Title: Phase II open label single arm exploratory trial of oral afatinib monotherapy following platinum failure for patients with advanced/metastatic urothelial tract carcinoma with ERBB receptor deregula... | |||||||||||||
Medical condition: patients with advanced/metastatic urothelial tract carcinoma with ERBB receptor deregulation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005948-29 | Sponsor Protocol Number: BL011 | Start Date*: 2022-03-09 | |||||||||||
Sponsor Name:UroGen Pharma Ltd. | |||||||||||||
Full Title: A Phase 3, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of UGN-102 as Primary Chemoablative Therapy in Patients with Low Grade (LG) Non-Muscle-Invasive Bladder Cancer (NMIBC) a... | |||||||||||||
Medical condition: Non-Muscle Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Trial now transitioned) LV (Trial now transitioned) AT (Trial now transitioned) LT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001883-48 | Sponsor Protocol Number: D933SC00001 | Start Date*: 2018-11-28 | |||||||||||
Sponsor Name:Astrazeneca AB | |||||||||||||
Full Title: Phase III, Randomized, Open-Label, Controlled, Multi-Center, Global Study of First-Line Durvalumab in Combination with Standard of Care Chemotherapy and Durvalumab in Combination with Tremelimumab ... | |||||||||||||
Medical condition: Patients with Unresectable Locally Advanced or Metastatic Urothelial Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011049-15 | Sponsor Protocol Number: IB 2009–08 | Start Date*: 2009-06-29 | |||||||||||
Sponsor Name:Institut Bergonié - Département d’Oncologie Médicale | |||||||||||||
Full Title: Evaluation de l’efficacité du temsirolimus chez des patients récidivant d’un cancer de la vessie après une première ligne de chimiothérapie. Essai clinique de phase II multicentrique. | |||||||||||||
Medical condition: Cancer de la vessie récidivant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019181-91 | Sponsor Protocol Number: EAURF2008-01 | Start Date*: 2013-05-24 | |||||||||||
Sponsor Name:EAU Foundation for Urological Research | |||||||||||||
Full Title: Treatment of High Grade Non-Muscle Invasive Urothelial Carcinoma of the Bladder by Standard Number and Dose of Intravesical BCG Instillations Versus Reduced Number of Intravesical Instillations wi... | |||||||||||||
Medical condition: Non muscle invasive bladder cancer after transurethral resection of the Bladder Tumor (TURT). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Prematurely Ended) BE (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003625-17 | Sponsor Protocol Number: CA209-275 | Start Date*: 2015-01-27 | |||||||||||||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||||||||||||
Full Title: A phase II single arm clinical trial of nivolumab (BMS-936558) in subjects with metastatic or unresectable urothelial cancer who have progressed or recurred following treatment with a platinum agen... | |||||||||||||||||||||||||||||||||
Medical condition: metastatic or unresectable urothelial cancer | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) BE (Completed) SE (Completed) CZ (Completed) FI (Completed) PL (Completed) IT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
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