- Trials with a EudraCT protocol (473)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
473 result(s) found for: Bladder disease.
Displaying page 6 of 24.
EudraCT Number: 2004-000476-13 | Sponsor Protocol Number: SP738 | Start Date*: 2004-08-10 |
Sponsor Name:Schwarz Biosciences GmbH | ||
Full Title: LONG-TERM OPEN-LABEL EXTENSION TRIAL FOR SUBJECTS COMPLETING THE PHASE 3 TRIAL OF FESOTERODINE (SP583) FOR THE TREATMENT OF OVERACTIVE BLADDER SYNDROME | ||
Medical condition: overactive bladder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002424-41 | Sponsor Protocol Number: OGX-427-02 | Start Date*: 2011-11-22 | |||||||||||
Sponsor Name:OncoGenex Technologies, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind Phase 2 Study Comparing Gemcitabine and Cisplatin in Combination with OGX-427 or Placebo in Patients With Advanced Transitional Cell Carcinoma | |||||||||||||
Medical condition: Metastatic or locally inoperable, advanced (T4b, N2, N3 or M1) transitional cell carcinoma (TCC) of the urinary tract (bladder, urethra, ureter and renal pelvis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004743-37 | Sponsor Protocol Number: GCT1015-03 | Start Date*: 2017-03-28 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Genmab A/S | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A multi-center, open-label trial investigating the efficacy and safety of continued treatment with tisotumab vedotin in patients with solid tumors known to express tissue factor | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Cancer of the ovary, cervix, endometrium, bladder, prostate (castrationresistant prostate cancer [CRPC]), esophagus, lung (non-small cell lung cancer [NSCLC]), and Squamous cell carcinoma of the he... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) GB (Completed) SE (Completed) HU (Completed) DK (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001120-29 | Sponsor Protocol Number: GEN702 | Start Date*: 2016-09-30 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Genmab A/S | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Dose-escalating and cohort expansion safety trial of tissue factor specific antibody drug conjugate tisotumab vedotin (HuMax®-TF-ADC) in patients with locally advanced and/or metastatic solid tumor... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Cancer of the ovary, cervix, endometrium, bladder, prostate (castration-resistant prostate cancer [CRPC]), esophagus or lung (non-small cell lung cancer [NSCLC]) | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) DK (Completed) BE (Completed) HU (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001112-35 | Sponsor Protocol Number: 010463QM | Start Date*: 2015-11-09 | |||||||||||||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||||||||||||
Full Title: A phase II study investigating preoperative MPDL3280A in operable transitional cell carcinoma of the bladder | |||||||||||||||||||||||
Medical condition: T2T4N0M0 transitional cell carcinoma of the bladder | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Prematurely Ended) FR (Completed) NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000957-30 | Sponsor Protocol Number: 191622-117 | Start Date*: 2012-08-28 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: BOTOX® for the Treatment of Urinary Incontinence due to Neurogenic Detrusor Overactivity in Patients with Multiple Sclerosis | |||||||||||||
Medical condition: Urinary incontinence due to neurogenic detrusor overactivity (NDO) resulting from multiple sclerosis (MS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) PT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000507-44 | Sponsor Protocol Number: D-FR-52120-223 | Start Date*: 2016-06-29 | |||||||||||
Sponsor Name:Ipsen Innovation | |||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, DOUBLE BLIND, PARALLEL GROUP, PLACEBO CONTROLLED STUDY TO ASSESS THE EFFICACY AND SAFETY OF ONE OR MORE INTRADETRUSOR TREATMENTS OF 600 OR 800 UNITS OF DYSPORT... | |||||||||||||
Medical condition: Urinary incontinence caused by neurogenic detrusor overactivity due to either spinal cord injury or multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Completed) FR (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001527-39 | Sponsor Protocol Number: SGN22E-002 | Start Date*: 2021-02-16 | ||||||||||||||||||||||||||
Sponsor Name:Seagen Inc. | ||||||||||||||||||||||||||||
Full Title: A study of enfortumab vedotin (ASG-22CE) as monotherapy or in combination with other anticancer therapies for the treatment of urothelial cancer | ||||||||||||||||||||||||||||
Medical condition: Urothelial cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003344-21 | Sponsor Protocol Number: 7465-CL-0301 | Start Date*: 2019-05-27 | |||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. (APGD) | |||||||||||||
Full Title: An Open-Label, Randomized Phase 3 Study to Evaluate Enfortumab Vedotin vs Chemotherapy in Subjects with Previously Treated Locally Advanced or Metastatic Urothelial Cancer (EV-301) | |||||||||||||
Medical condition: Locally advanced or metastatic urothelial cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) BE (Completed) AT (Completed) DK (Completed) GB (GB - no longer in EU/EEA) NL (Completed) PT (Trial now transitioned) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020601-32 | Sponsor Protocol Number: 178-CL-100 | Start Date*: 2011-03-23 | |||||||||||
Sponsor Name:Astellas Pharma Europe BV | |||||||||||||
Full Title: A Randomized, Double-Blind, Factorial, Parallel-Group, Active and Placebo-Controlled, Multicenter Dose-Ranging Study to Evaluate the Efficacy, Safety and Tolerability of Six Dose Combinations of So... | |||||||||||||
Medical condition: Overactive Bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) SE (Completed) FI (Completed) HU (Completed) CZ (Completed) DK (Completed) SK (Completed) PT (Completed) NO (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002206-20 | Sponsor Protocol Number: MK-3475-052 | Start Date*: 2014-12-22 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase II Clinical Trial of Pembrolizumab (MK-3475) in Subjects with Advanced/Unresectable or Metastatic Urothelial Cancer | |||||||||||||
Medical condition: advanced/unresectable (inoperable) or metastatic urothelial cancer of the renal pelvis, ureter, bladder, or urethra. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DK (Completed) IT (Completed) IE (Completed) GB (GB - no longer in EU/EEA) HU (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015119-42 | Sponsor Protocol Number: GMIHO-007/2008_AG48 | Start Date*: 2010-05-12 | ||||||||||||||||||||||||||
Sponsor Name:GMIHO Gesellschaft für Medizinische Innovation - Hämatologie und Onkologie mbH | ||||||||||||||||||||||||||||
Full Title: An open-label, randomised, multicentre, phase II study to evaluate the efficacy of chemotherapy with gemcitabine and cisplatin in combination with the EGF receptor antibody panitumumab (GemCisP) ve... | ||||||||||||||||||||||||||||
Medical condition: Locally advanced/metastatic urothelial carcinoma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000205-24 | Sponsor Protocol Number: G1T28-209 | Start Date*: 2021-10-28 | ||||||||||||||||
Sponsor Name:G1 Therapeutics, Inc. | ||||||||||||||||||
Full Title: A Phase 2, Randomized, Open-Label Study of Trilaciclib Administered with First-Line Platinum-Based Chemotherapy and Avelumab Maintenance Therapy in Patients with Untreated, Locally Advanced or Meta... | ||||||||||||||||||
Medical condition: Untreated, Locally Advanced or Metastatic Urothelial Carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) HU (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003471-30 | Sponsor Protocol Number: D-FR-52120-222 | Start Date*: 2016-09-26 | |||||||||||
Sponsor Name:Ipsen Innovation | |||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, DOUBLE BLIND, PARALLEL GROUP, PLACEBO CONTROLLED STUDY TO ASSESS THE EFFICACY AND SAFETY OF ONE OR MORE INTRADETRUSOR TREATMENTS OF 600 OR 800 UNITS OF DYSPORT... | |||||||||||||
Medical condition: Urinary incontinence (UI) caused by neurogenic detrusor overactivity due to either spinal cord injury or multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) PT (Completed) CZ (Completed) IT (Completed) NL (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006299-39 | Sponsor Protocol Number: 191622-082-01 | Start Date*: 2008-04-23 | |||||||||||
Sponsor Name:Allergan | |||||||||||||
Full Title: A Placebo-Controlled, Randomized, Safety and Efficacy Study of BOTOX® (Botulinum Toxin Type A) Purified Neurotoxin Complex in Patients with Neurogenic Detrusor Overactivity and Neurological Respira... | |||||||||||||
Medical condition: Patients with urinary incontinence due to neurogenic detrusor overactivity as a result of spinal cord injury or multiple sclerosis who have not been adequately managed with anticholinergic therapy ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001744-62 | Sponsor Protocol Number: 2018/2727 | Start Date*: 2018-11-28 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Gustave Roussy | ||||||||||||||||||||||||||||||||||||||
Full Title: A multicenter, open label, phase II basket trial exploring the efficacy and safety of the combination of rucaparib (PARP inhibitor) and atezolizumab (anti-PD-L1 antibody) in patients with DNA repai... | ||||||||||||||||||||||||||||||||||||||
Medical condition: •Molecularly selected cohorts that harbor DNA repair deficiency: –Non-Small Cell Lung Cancer –Urothelial Bladder Cancer –Metastatic Castration Resistant Prostate Cancer –Others: any histology, exce... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003520-37 | Sponsor Protocol Number: RG_18-220 | Start Date*: 2020-02-07 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: A multi-stage randomised trial of durvalumab (Medi4736) with chemoradiotherapy with 5-fluorouracil and mitomycin C in patients with muscle-invasive bladder cancer | |||||||||||||
Medical condition: Muscle invasive bladder cancer | |||||||||||||
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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: 2022-002265-15 | Sponsor Protocol Number: BO44157 | Start Date*: 2023-03-27 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE II, RANDOMIZED, MULTICENTER, OPEN LABEL, CONTROLLED STUDY OF RO7247669 ALONE OR IN COMBINATION WITH TIRAGOLUMAB VERSUS ATEZOLIZUMAB IN PATIENTS WITH PREVIOUSLY UNTREATED LOCALLY ADVANCED OR... | |||||||||||||
Medical condition: Previously Untreated Locally Advanced or Metastatic Urothelial Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) GR (Trial now transitioned) DK (Trial now transitioned) IT (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002311-34 | Sponsor Protocol Number: MK-3475-672(INCB24360-ECHO-307) | Start Date*: 2017-12-12 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 3 Randomized, Double-blind Trial of Pembrolizumab (MK-3475) in Combination with Epacadostat (INCB024360) or Placebo in Participants with Cisplatin-ineligible Urothelial Carcinoma (KEYNOTE-6... | |||||||||||||
Medical condition: Bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Temporarily Halted) NL (Completed) GB (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004898-30 | Sponsor Protocol Number: 191622-121 | Start Date*: 2013-07-18 | |||||||||||
Sponsor Name:Allergan Ltd | |||||||||||||
Full Title: Long-term Extension Study of BOTOX® in the Treatment of Urinary Incontinence Due to Neurogenic Detrusor Overactivity in Patients 5 to 17 Years of Age | |||||||||||||
Medical condition: Urinary Incontinence due to Neurogenic Detrusor Overactivity | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) AT (Completed) IT (Completed) DE (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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