- Trials with a EudraCT protocol (193)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
193 result(s) found for: Pioglitazone.
Displaying page 7 of 10.
EudraCT Number: 2012-004827-19 | Sponsor Protocol Number: NN9535-3626 | Start Date*: 2013-10-01 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Efficacy and safety of semaglutide once-weekly versus sitagliptin once-daily as add-on to metformin and/or TZD in subjects with type 2 diabetes | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) BG (Completed) PT (Completed) ES (Completed) HU (Completed) CZ (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000656-42 | Sponsor Protocol Number: 3102-006-10 | Start Date*: 2011-04-08 | |||||||||||
Sponsor Name:MSD Finland Oy | |||||||||||||
Full Title: A 66-Week Extension to: A Phase IIb, Randomized, Placebo-Controlled, Dose-Range Finding, Clinical Trial to Study the Safety and Efficacy of MK-3102 in Patients with Type 2 Diabetes Mellitus and Ina... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004625-25 | Sponsor Protocol Number: NN9068-4056 | Start Date*: 2014-08-29 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A clinical trial comparing efficacy and safety of insulin degludec/liraglutide (IDegLira) in subjects with type 2 diabetes mellitus using two different titration algorithms | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) AT (Completed) SK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001596-48 | Sponsor Protocol Number: NN9068-4229 | Start Date*: 2016-03-29 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A clinical trial comparing glycaemic control and safety of insulin degludec/liraglutide (IDegLira) versus insulin glargine (IGlar) as add-on therapy to SGLT2i in subjects with type 2 diabetes mellitus | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) FI (Completed) HU (Completed) ES (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001222-27 | Sponsor Protocol Number: EU-IIT-006 | Start Date*: 2007-11-06 | |||||||||||||||||||||
Sponsor Name:Imperial College London | |||||||||||||||||||||||
Full Title: The effect of Pioglitazone on vascular and ventricular function in people with type 2 diabetes PICCOLA | |||||||||||||||||||||||
Medical condition: Diabetes | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003843-36 | Sponsor Protocol Number: H8O-US-GWCO | Start Date*: 2008-09-19 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized Trial Comparing Exenatide with Placebo in Subjects with Type 2 Diabetes on Insulin Glargine With or Without Oral Antihyperglycemic Medications | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004112-13 | Sponsor Protocol Number: 33100 | Start Date*: 2009-06-26 | |||||||||||
Sponsor Name:Nottingham University | |||||||||||||
Full Title: PPAR-gamma: A noval therapeutic target for asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001283-22 | Sponsor Protocol Number: CL3-00780-150 | Start Date*: 2011-07-13 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier (I.R.I.S.) | |||||||||||||
Full Title: International follow-up study, after the investigational drug exposure in diabetic patients previously included in the REGULATE trial (benfluorex versus pioglitazone). | |||||||||||||
Medical condition: Type II diabetes The medical condition investigated in the REGULATE trial (CL3-00780-148) was type II diabetes. The applied CL3-00780-150 trial, REGULATE follow-up study, is thus performed in d... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003614-27 | Sponsor Protocol Number: GIA-DAP-16-005 | Start Date*: 2017-08-16 | |||||||||||
Sponsor Name:UNIVERSITÀ CATTOLICA DEL SACRO CUORE- POLICLINICO A. GEMELLI | |||||||||||||
Full Title: Study on the effect of dapagliflozin on myocardial insulin sensitivity and perfusion (DapaHeart) | |||||||||||||
Medical condition: TYPE 2 DIABETES | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000823-15 | Sponsor Protocol Number: DIASA3 | Start Date*: 2019-10-18 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Glucose metabolism in South Asian women with impaired glucose tolerance or impaired fasting glucose. DIAbetes in South Asians – DIASA 3 A 12-week intervention trial with oral antidiabetic medicati... | |||||||||||||
Medical condition: Pre-diabetes in women of South Asian ethnicity. Women of South Asian ethnicity with previous gestational diabetes, where pre-diabetes in the form of impaired glucose tolerance or impaired fasting ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000624-16 | Sponsor Protocol Number: LOEWE_B4 | Start Date*: 2011-11-28 | |||||||||||||||||||||
Sponsor Name:Justus Liebig Universität Gießen | |||||||||||||||||||||||
Full Title: Infertility and inflammatory urogenital diseases as a result of the metabolic syndrome Male infertility with infection and inflammation -MIBIE- | |||||||||||||||||||||||
Medical condition: infertility and inflammatory urogenital diseases as a result of the metabolic syndrome | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004227-19 | Sponsor Protocol Number: 3180A1-103-WW | Start Date*: 2006-02-08 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | ||
Full Title: A 4-WEEK RANDOMIZED, PARALLEL, DOUBLE-BLIND, PLACEBO-CONTROLLED MULTICENTER STUDY OF THE PRELIMINARY EFFICACY, SAFETY, AND PHARMACOKINETICS OF PPM-204 ADMINISTERED ORALLY TO TREATMENT-NAÏVE SUBJECT... | ||
Medical condition: Newly diagnosed Type 2 Diabetic Mellitus. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004216-70 | Sponsor Protocol Number: BM17864 | Start Date*: 2007-01-30 |
Sponsor Name:F.Hoffmann-La Roche Ltd. | ||
Full Title: A randomized, double-blind, parallel group, placebo-controlled (with open-label active comparator arm), dose-ranging study to determine the efficacy, safety, tolerability and pharmacokinetics of RO... | ||
Medical condition: Type 2 Diabetes Mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Prematurely Ended) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003897-87 | Sponsor Protocol Number: 3180A1-200-WW | Start Date*: 2007-06-19 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc., Clinical Research and Development | ||
Full Title: A 24-WEEK, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY OF THE SAFETY AND EFFICACY OF PPM-204 IN SUBJECTS WITH TYPE 2 DIABETES. | ||
Medical condition: Subjects with type 2 diabetes mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-006766-21 | Sponsor Protocol Number: MINI-SPIOMET | Start Date*: 2022-09-02 | |||||||||||
Sponsor Name:Hospital de Girona Dr. Josep Trueta | |||||||||||||
Full Title: Towards a treatment for accelerated maturation in girls testing spiomet in a randomised placebo controlled, multicentre study. | |||||||||||||
Medical condition: Girls with advanced puberty and accelerated bone maturation. Polycystic Ovary Syndrome (PCOS) | |||||||||||||
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Population Age: Children, Under 18 | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005771-10 | Sponsor Protocol Number: NN1250-3668 | Start Date*: 2009-08-07 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 26 week randomised, controlled, open label, multicentre, multinational, three-arm, treat to target trial comparing efficacy and safety of three different dosing regimens of either Soluble Insulin... | |||||||||||||
Medical condition: type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000750-13 | Sponsor Protocol Number: 1218.40 | Start Date*: 2008-06-30 |
Sponsor Name:Boehringer Ingelheim Finland Ky | ||
Full Title: A 78 week open label extension to trials assessing the safety and efficacy of BI 1356 (5 mg) as monotherapy or in combination with other antidiabetic medications in type 2 diabetic patients. | ||
Medical condition: Patients with type 2 Diabetes Mellitus. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) NL (Completed) SE (Completed) AT (Completed) SK (Completed) DE (Completed) ES (Completed) GB (Completed) CZ (Completed) BE (Completed) HU (Completed) IT (Completed) GR (Completed) PT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-012140-16 | Sponsor Protocol Number: 28431754DIA3008 | Start Date*: 2010-01-06 | ||||||||||||||||
Sponsor Name:Janssen-Cilag International NV | ||||||||||||||||||
Full Title: A Randomized, Multicenter, Double-Blind, Parallel, Placebo-Controlled Study of the Effects of JNJ 28431754 on Cardiovascular Outcomes in Adult Subjects With Type 2 Diabetes Mellitus | ||||||||||||||||||
Medical condition: Type 2 diabetes mellitus and history or high risk cardiovascular disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) HU (Completed) EE (Completed) CZ (Completed) SE (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004864-29 | Sponsor Protocol Number: F3Z-EW-IOPJ | Start Date*: 2008-02-13 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Prospective Randomized Trial to Compare Basal Bolus therapies that use either Insulin Lispro Protamine Suspension or Insulin Glargine together with Lispro Insulin in Patients with Type 2 Diabetes | |||||||||||||
Medical condition: Type II diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GR (Completed) GB (Completed) BE (Completed) SK (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005192-18 | Sponsor Protocol Number: A5351022 | Start Date*: 2007-03-15 | |||||||||||
Sponsor Name:Pfizer Ltd. | |||||||||||||
Full Title: A 1-YEAR, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED PHASE 3 STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CP-945,598 IN THE TREATMENT OF OVERWEIGHT, ORAL AGENT-TREATED SUBJECTS WITH TYPE 2 DIABET... | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) SK (Completed) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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