- Trials with a EudraCT protocol (122)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
122 result(s) found for: Urine Cytology.
Displaying page 1 of 7.
EudraCT Number: 2016-004269-14 | Sponsor Protocol Number: HP002-001 | Start Date*: 2018-05-07 |
Sponsor Name:Hamlet Pharma AB | ||
Full Title: A Randomized Placebo controlled Phase I/II Study Evaluating the Safety and Efficacy of Alpha1H in adult patients with non-muscle invasive bladder cancer awaiting transurethral surgery | ||
Medical condition: Non-muscle invasive bladder cancer awaiting transurethral surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001791-36 | Sponsor Protocol Number: 310781 | Start Date*: 2008-01-24 |
Sponsor Name:Bayer Schering Pharma AG | ||
Full Title: A double-blind, randomized, placebo and active controlled, multicenter study to investigate efficacy and safety after oral administration of 2 and 3 mg ZK 283197, 1 mg 17ß-estradiol and placebo onc... | ||
Medical condition: Vasomotor symptoms (hot flushes) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DE (Completed) NL (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000138-37 | Sponsor Protocol Number: PERISCOPE | Start Date*: 2013-09-25 | ||||||||||||||||
Sponsor Name:NKI-AvL | ||||||||||||||||||
Full Title: Treatment of PERItoneal dissemination in Stomach Cancer patients with cytOreductive surgery and hyperthermic intraPEritoneal chemotherapy | ||||||||||||||||||
Medical condition: Gastric cancer with peritoneal carcinomatosis or positive peritoneal cytology. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001028-32 | Sponsor Protocol Number: CIVI/2018/NH-01 | Start Date*: 2020-09-09 | |||||||||||
Sponsor Name:CHU DE NIMES | |||||||||||||
Full Title: Safety and Efficacy of Neoadjuvant immunotherapy with Durvalumab (MEDI 4736) in combination with neoadjuvant chemotherapy (Gemcitabin/Cisplatin or Gemcitabin/Carboplatin) in patients with operable,... | |||||||||||||
Medical condition: The patient has a histologically-confirmed (ureteroscopic biopsy) or cytologically(urine cytology)-confirmed diagnosis of high-grade urothelial carcinoma of the renal pelvis or ureter. Presence of ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002760-16 | Sponsor Protocol Number: 04/QO603/42 HEXVIX | Start Date*: 2005-01-12 | |||||||||||
Sponsor Name:Guy's and St Thomas' NHS Foundation Trust | |||||||||||||
Full Title: A randomised Study of “bluelight” hexyl amino levulinic acid (HAL) photodynamic assisted resection of bladder tumours versus conventional “white light” transurethral resection of newly diagnosed bl... | |||||||||||||
Medical condition: Superficial Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000059-38 | Sponsor Protocol Number: 21810 | Start Date*: 2021-11-17 | |||||||||||
Sponsor Name:Bayer Consumer Care AG | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled multicenter study to investigate efficacy and safety of elinzanetant for the treatment of vasomotor symptoms over 52 weeks in postmenopausal women. | |||||||||||||
Medical condition: Vasomotor symptoms associated with menopause | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) FI (Completed) DK (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001888-40 | Sponsor Protocol Number: DEP NHL-P 001.A | Start Date*: 2006-07-24 | |||||||||||
Sponsor Name:Mundipharma Research Ltd. | |||||||||||||
Full Title: A phase II prospective non-comparative multicenter clinical trial to determine the efficacy and safety of intrathecal liposomal cytarabine (DepoCyte®) in preventing CNS-relapse in patients with agg... | |||||||||||||
Medical condition: Prophylaxis of CNS relapse in adult patients with aggressive Non-Hodgkin-Lymphomas at risk for CNS metastasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003159-44 | Sponsor Protocol Number: SOGUG-2017-A-IEC(VEJ)-1 | Start Date*: 2018-09-27 | |||||||||||
Sponsor Name:Spanish Oncology Genitourinary Group | |||||||||||||
Full Title: Phase II trial of durvalumab (Medi4736) plus tremelimumab with concurrent radiotherapy in patients with localized muscle invasive bladder cancer treated with a selective bladder preservation approach | |||||||||||||
Medical condition: Localized muscle invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004855-34 | Sponsor Protocol Number: 21652 | Start Date*: 2021-11-25 | |||||||||||
Sponsor Name:Bayer Consumer Care AG | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled multicenter study to investigate efficacy and safety of elinzanetant for the treatment of vasomotor symptoms over 26 weeks in postmenopausal women | |||||||||||||
Medical condition: Vasomotor symptoms associated with menopause | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) NO (Completed) PT (Completed) SK (Completed) PL (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004908-33 | Sponsor Protocol Number: 21651 | Start Date*: 2021-10-18 | |||||||||||
Sponsor Name:Bayer Consumer Care AG | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled multicenter study to investigate efficacy and safety of elinzanetant for the treatment of vasomotor symptoms over 26 weeks in postmenopausal women | |||||||||||||
Medical condition: Vasomotor symptoms associated with menopause | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) IT (Completed) HU (Completed) NL (Completed) GR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021718-41 | Sponsor Protocol Number: 214868-004-03 | Start Date*: 2011-03-03 | |||||||||||
Sponsor Name:Allergan Ltd | |||||||||||||
Full Title: A Pilot, Multicenter, Double-blind, Placebo-controlled, Dose-escalation Study of the Safety and Efficacy of AGN-214868 in Patients with Idiopathic Overactive Bladder and Urinary Incontinence | |||||||||||||
Medical condition: To evaluate the safety and efficacy of AGN-214868 compared with placebo in the treatment of patients with idiopathic overactive bladder (IOAB) and urinary incontinence. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003751-42 | Sponsor Protocol Number: ICH-013-UroNEOadI | Start Date*: 2022-01-25 | |||||||||||
Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: Randomized phase III clinical trial of Neo-Adjuvant Intravesical mitomycin C (MMC) treatment in patients with primary treatment-naïve vesical neoplasms. | |||||||||||||
Medical condition: Patients with primary treatment-naïve vesical neoplasms. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017396-19 | Sponsor Protocol Number: CA184104 | Start Date*: 2011-04-12 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: Randomized, Multicenter, Double-Blind, Phase 3 Trial Comparing the Efficacy of Ipilimumab in Addition to Paclitaxel and Carboplatin versus Placebo in Addition to Paclitaxel and Carboplatin in Subje... | ||||||||||||||||||
Medical condition: Stage IV/Recurrent Non-Small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) SE (Completed) DE (Completed) BE (Completed) GB (Completed) AT (Completed) NL (Completed) DK (Completed) CZ (Completed) PT (Completed) IE (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-000173-21 | Sponsor Protocol Number: (no code number allocated) | Start Date*: 2005-11-28 |
Sponsor Name:Dieter Hoelzer, MD,PhD | ||
Full Title: A PHASE II CLINICAL STUDY TO DETERMINE THE EFFICACY AND SAFETY OF DEPOCYTE® (CYTARABINE LIPOSOME INJECTION) FOR THE TREATMENT OF CNS RELAPSE IN ADULT PATIENTS WITH ACUTE LYMPHOBLASTIC LEUKEMIA OR H... | ||
Medical condition: Acute lymphoblastic leukaemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000135-31 | Sponsor Protocol Number: TABENETOC | Start Date*: 2022-01-12 |
Sponsor Name:Region Östergötland | ||
Full Title: The Effect of tinzaparin on Biomarkers in FIGO Stage III-IV Ovarian Cancer Patients Undergoing Neoadjuvant Chemotherapy – A randomized pilot study | ||
Medical condition: Epithelial ovarian cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000850-48 | Sponsor Protocol Number: CA184-156 | Start Date*: 2012-06-15 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: Randomized, Multicenter, Double-Blind, Phase 3 Trial Comparing the Efficacy of Ipilimumab plus Etoposide/Platinum versus Etoposide/Platinum in Subjects with Newly Diagnosed Extensive-Stage Disease ... | |||||||||||||
Medical condition: Extensive Stage Disease Small Cell Lung Cancer (ED-SCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FI (Completed) IT (Completed) SE (Completed) DE (Completed) CZ (Completed) AT (Completed) GB (Completed) PT (Completed) HU (Completed) ES (Completed) NL (Completed) IE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001236-28 | Sponsor Protocol Number: R39_21_01 | Start Date*: 2022-11-22 | |||||||||||
Sponsor Name:Fidia Farmaceutici S.p.A. | |||||||||||||
Full Title: A phase III, single-arm study to evaluate the efficacy and safety of ONCOFID-P-B (paclitaxel-hyaluronic acid conjugate) administered intravesically to patients with BCG-unresponsive Carcinoma in Si... | |||||||||||||
Medical condition: BCG-unresponsive Carcinoma in Situ of the bladder with or without Ta-T1 papillary disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004743-22 | Sponsor Protocol Number: FFR30006 | Start Date*: Information not available in EudraCT |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy and Safety of Once-Daily, Intranasal Administration of GW685698X Aqueous Nasal Spray 100mc... | ||
Medical condition: Vasomotor/Idiopathic Rhinitis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) CZ (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004744-43 | Sponsor Protocol Number: FFR30007 | Start Date*: Information not available in EudraCT |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy and Safety of Once-Daily, Intranasal Administration of GW685698X Aqueous Nasal Spray 100mc... | ||
Medical condition: Vasomotor/Idiopathic Rhinitis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) CZ (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004206-25 | Sponsor Protocol Number: 1839IL/0711 | Start Date*: 2005-03-02 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A PHASE II MULTICENTRE RANDOMISED, PARALLEL GROUP, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF ZD1839 (IRESSA TM) (250MG TABLET) PLUS BEST SUPPORTIVE CARE (BSC) VERSUS PLACEBO PLUS BSC IN CHEMOTHERAP... | ||
Medical condition: Non-Small Cell Lung Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) CZ (Completed) | ||
Trial results: View results |
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