- Trials with a EudraCT protocol (193)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
193 result(s) found for: Pioglitazone.
Displaying page 4 of 10.
EudraCT Number: 2007-001771-11 | Sponsor Protocol Number: 0431-061 | Start Date*: 2007-07-02 | |||||||||||
Sponsor Name:MERCK SHARP DOHME | |||||||||||||
Full Title: A Phase I Double-Blind, Randomized, Placebo-Controlled Clinical Trial to Study the Safety, Efficacy, and Mechanism of Action of Sitagliptin and Pioglitazone in Patients With Type 2 Diabetes Mell... | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002611-29 | Sponsor Protocol Number: MEL001 | Start Date*: 2012-04-04 |
Sponsor Name:Freistaat Bayern | ||
Full Title: A prospective phase I and consecutive phase II, twoarm, randomized multi-center trial of temsirolimus in combination with pioglitazone, etoricoxib and metronomic low-dose trofosfamide versus dacarb... | ||
Medical condition: metastatic melanoma or metastatic uveal carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005626-29 | Sponsor Protocol Number: IRFMN-SARCO-7953 | Start Date*: 2021-05-05 | ||||||||||||||||||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | ||||||||||||||||||||||||||||
Full Title: A phase II study on trabectedin in combination with PPARg agonist pioglitazone in patients with round cell myxoid liposarcomas or dedifferentiated G1 and G2 liposarcomas with stable disease after a... | ||||||||||||||||||||||||||||
Medical condition: Patients with myxoid/round cell liposarcoma treated with at least 4 cycle of T alone with a stable disease at the last tumor evaluation | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003840-22 | Sponsor Protocol Number: D6160C00048 | Start Date*: 2005-06-10 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Double-blind, Multi-centre, Active-Controlled (15, 30, and 45mg Pioglitazone) Long-Term Extension Study to Evaluate the Safety and Tolerability of Oral Tesaglitazar (0.5 and 1 mg) in Patients wit... | |||||||||||||
Medical condition: Type II Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002090-47 | Sponsor Protocol Number: 0533-005 | Start Date*: 2006-07-07 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: An Efficacy and Tolerability Study of MK-0533 in Patients with Type II Diabetes Mellitus Who Have Inadequate Glycemic Control. | |||||||||||||
Medical condition: Type II Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) HU (Prematurely Ended) DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004137-42 | Sponsor Protocol Number: 0431-066 | Start Date*: 2007-10-28 | |||||||||||
Sponsor Name:Merck Sharp & Dohme GmbH | |||||||||||||
Full Title: A Phase III Randomized, Active-Comparator (Pioglitazone) Controlled Clinical Trial to Study the Efficacy and Safety of MK-0431A (A Fixed-Dose Combination Tablet of Sitagliptin and Metformin) in Pat... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) IE (Completed) HU (Completed) SE (Completed) SI (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005768-15 | Sponsor Protocol Number: NN5401-3592 | Start Date*: 2009-06-23 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 26-week, randomised, open-labelled, two-arm, parallel-group, treat-to-target trial comparing efficacy and safety of soluble insulin analogue combination (SIAC) twice daily (BID) with biphasic ins... | |||||||||||||
Medical condition: type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001463-29 | Sponsor Protocol Number: KG2110375 | Start Date*: 2007-08-14 | |||||||||||
Sponsor Name:GlaxoSmithKline R&D Ltd | |||||||||||||
Full Title: A Once-Daily Dose-Ranging Study of GSK189075 Versus Placebo In The Treatment of Type 2 Diabetes Mellitus in Treatment-Naïve Subjects | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LT (Completed) GR (Completed) DE (Completed) HU (Prematurely Ended) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005492-17 | Sponsor Protocol Number: 01-06-TL-322OPI-002 | Start Date*: 2007-01-19 | |||||||||||
Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd., | |||||||||||||
Full Title: A Multicenter, Double-Blind Study to Determine the Efficacy and Safety of SYR-322 plus Pioglitazone HCl (Actos), SYR-322 Alone or Pioglitazone HCl Alone in Subjects with Type 2 Diabetes | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LV (Completed) SK (Completed) EE (Completed) LT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000311-26 | Sponsor Protocol Number: 0431-019 | Start Date*: 2004-07-21 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of the Addition of MK-0431 to Patients with Type 2 Diabetes Mellitus who Have Inadequate Glycemic Control on Piogli... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LT (Completed) AT (Completed) IT (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000218-19 | Sponsor Protocol Number: CSTI571BDE59 | Start Date*: 2008-05-21 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A single stage phase II, multi-centre, open label study of Glivec in combination with pioglitazone, etoricoxib, dexamethasone and low-dose treosulfane for anti-inflammatory and angiostatic treatmen... | |||||||||||||
Medical condition: prostrate carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005884-92 | Sponsor Protocol Number: EFC6017 | Start Date*: 2009-03-30 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, 2-arm parallel-group, multicenter study with a 24-week main treatment period and an extension assessing the efficacy and safety of AVE0010 on top of ... | |||||||||||||
Medical condition: Type II diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) FR (Completed) DE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004100-35 | Sponsor Protocol Number: FSJD-PIOSPIMET-2012 | Start Date*: 2012-12-20 |
Sponsor Name:Fundació per la Recerca i la Docència Sant Joan de Déu | ||
Full Title: A prospective, open-label, randomized, two-armed clinical trial to evaluate the efficacy and safety of a combination of ethinyl-estradiol and levonorgestrel versus a low-dose combination of pioglit... | ||
Medical condition: Ovarian hyperandrogenism | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005092-24 | Sponsor Protocol Number: FSJD-PIOSPIMET-2015 | Start Date*: 2016-01-22 |
Sponsor Name:FUNDACIÓ SANT JOAN DE DÉU | ||
Full Title: A prospective, open-label, randomized, two-armed clinical trial to evaluate the efficacy and safety of a combination of ethinyl-estradiol and levonorgestrel versus a low-dose combination of pioglit... | ||
Medical condition: ovarian hyperandrogenism with hyperinsulinaemia | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001982-41 | Sponsor Protocol Number: RAE04 | Start Date*: 2006-10-03 | |||||||||||
Sponsor Name:Bradford Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: An evaluation of the safety and effectiveness of combination therapy using the thiazolidinedione pioglitazone alongside insulin in type 2 diabetes mellitus. | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001473-24 | Sponsor Protocol Number: F3Z-MC-IOQL | Start Date*: 2014-02-05 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: An Individualized treatMent aPproach for oldER patIents: A randomized, controlled stUdy in type 2 diabetes Mellitus | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011106-42 | Sponsor Protocol Number: 2008MZ09B | Start Date*: 2009-06-25 |
Sponsor Name:Institute for Clinical and Experimental Medicine | ||
Full Title: Aditive effects of omega-3 polyunsaturated fatty acids and pioglitazone in the treatment of type 2 diabetes mellitus | ||
Medical condition: The project deals with hummoral and metabolic aspects of insulin resistance (IR), which is assumed to be the basic metabolic disorder which leads to the development of type 2 diabetes mellitus (T2D... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002456-41 | Sponsor Protocol Number: 1218.15 | Start Date*: 2008-05-13 | |||||||||||
Sponsor Name:Boehringer-Ingelheim Ellas AE | |||||||||||||
Full Title: A randomised, double-blind, placebo controlled, parallel group 24 week study to assess the efficacy and safety of BI 1356 (5 mg) in combination with 30 mg pioglitazone (both administered orally onc... | |||||||||||||
Medical condition: Patients with type 2 Diabetes Mellitus with insufficient glycaemic control. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) HU (Completed) PT (Completed) AT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004790-18 | Sponsor Protocol Number: 2008DM05 | Start Date*: 2008-10-21 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Response to Oral Agents in Diabetes (ROAD) Pilot Study | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006744-21 | Sponsor Protocol Number: DE-PIO-029 | Start Date*: 2008-04-28 | |||||||||||
Sponsor Name:Takeda Pharma GmbH | |||||||||||||
Full Title: Comparison of the Effects of Pioglitazone vs. Placebo when given in addition to Standard Insulin Treatment in Patients with Type 2 Diabetes Mellitus and Renal Failure – The PIOren Study | |||||||||||||
Medical condition: The study population will consist of insufficiently controlled patients with type 2 diabetes with renal failure requiring dialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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