- Trials with a EudraCT protocol (92)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
92 result(s) found for: Insulin Dependent Diabetes AND Diabetes AND Sitagliptin.
Displaying page 1 of 5.
| 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: 2007-000019-27 | Sponsor Protocol Number: 0431-049 | Start Date*: 2007-03-14 | |||||||||||
| Sponsor Name:Merck & Co., Inc | |||||||||||||
| Full Title: A Multicenter, Double-Blind, Randomized Study to Evaluate the Safety and Efficacy of Sitagliptin Compared With Metformin in Patients With Type 2 Diabetes Mellitus With Inadequate Glycemic Control | |||||||||||||
| Medical condition: type II diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Completed) FI (Completed) IE (Completed) HU (Completed) DK (Completed) ES (Completed) GB (Completed) AT (Completed) GR (Completed) DE (Completed) EE (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006074-28 | Sponsor Protocol Number: 0893-015 | Start Date*: 2008-02-21 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
| Full Title: A Phase IIa, Multicenter, Double-Blind, Randomized, Active Comparator-Controlled Clinical Trial to Study the Efficacy and Safety of MK-0893 in Combination With Sitagliptin or in Combination With Me... | |||||||||||||
| Medical condition: Type II Diabetes Mellitus | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) ES (Completed) DK (Completed) DE (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-018318-62 | Sponsor Protocol Number: 0431-229 | Start Date*: 2010-06-01 | |||||||||||
| Sponsor Name:Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase III, Randomized, Clinical Trial to Evaluate the Safety and Efficacy of the Addition of Sitagliptin in Patients With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control on a Sulfon... | |||||||||||||
| Medical condition: Diabetes Mellitus type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001752-10 | Sponsor Protocol Number: TAK-875_302 | Start Date*: 2012-10-30 | |||||||||||||||||||||||||||||||
| Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd. | |||||||||||||||||||||||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of TAK-875 25 mg and 50 mg Compared to Placebo and Sitagliptin 100 mg When... | |||||||||||||||||||||||||||||||||
| Medical condition: Type 2 diabetes mellitus (T2DM) | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) BG (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2006-005051-15 | Sponsor Protocol Number: 0431-051 | Start Date*: 2007-01-15 | |||||||||||
| Sponsor Name:Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase III, Multicenter, Randomized, Double-Blind Clinical Trial to Study the Safety and Efficacy of the Addition of Sitagliptin (MK-0431) to Patients with Type 2 Diabetes Mellitus Who Have Inade... | |||||||||||||
| Medical condition: type II Diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) IE (Completed) DK (Completed) FI (Completed) BE (Completed) FR (Completed) PT (Completed) AT (Prematurely Ended) IT (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012776-27 | Sponsor Protocol Number: DSSita-02 | Start Date*: 2009-09-16 | ||||||||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | ||||||||||||||||||
| Full Title: The effect of sitagliptin on myocardial performance in patients with type 2 diabetes and coronary artery disease. | ||||||||||||||||||
| Medical condition: Coronary artery disease | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-004916-12 | Sponsor Protocol Number: D1690C00007 | Start Date*: 2008-11-11 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A 24-Week, International, Multi-centre, Randomised, Parallel-group, Double-blind, Active-controlled, Phase III study to Evaluate the Efficacy and Safety of Dapagliflozin in Combination with Metform... | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) DE (Prematurely Ended) AT (Prematurely Ended) CZ (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-001050-40 | Sponsor Protocol Number: NN304-3511 | Start Date*: 2008-10-29 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: A 26 week randomised, open labelled, parallel group, multi-national, treat-to-target trial comparing efficacy and safety of insulin detemir once daily in combination with sitagliptin and metformin ... | |||||||||||||
| Medical condition: type 2 diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) HU (Completed) SK (Completed) FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003731-22 | Sponsor Protocol Number: MK-0431A-296 | Start Date*: 2020-09-03 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Study to Assess the Pharmacokinetics and Ability for Pediatric Patients with Type 2 Diabetes to Swallow MK-0431A XR Tablets | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-003529-26 | Sponsor Protocol Number: 0431-073 | Start Date*: 2008-01-18 | |||||||||||
| Sponsor Name:Merck & Co., Inc. | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind Study to Evaluate the Efficacy and Safety of Sitagliptin Versus Glipizide in Patients With Type 2 Diabetes Mellitus and End-Stage Renal Disease Who Are on Di... | |||||||||||||
| Medical condition: Type II Diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003640-11 | Sponsor Protocol Number: MK0431C-102 | Start Date*: 2008-10-30 | |||||||||||
| Sponsor Name:MERCK & CO., INC. | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind Study of the Co-Administration of Sitagliptin and Pioglitazone in Patients With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control. | |||||||||||||
| Medical condition: Patients With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) SI (Completed) AT (Completed) LT (Completed) EE (Completed) LV (Completed) GR (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2011-000518-21 | Sponsor Protocol Number: CLMF237ADE02 | Start Date*: 2011-06-20 | |||||||||||
| Sponsor Name:Novartis Pharma GmbH | |||||||||||||
| Full Title: Cross-over study to assess the difference in fasting plasma glucose (FPG) between vildagliptin (Galvus®/Eucreas®) and sitagliptin (Januvia®/Janumet®) after two weeks (FPG-VISIT) | |||||||||||||
| Medical condition: Diabetes mellitus type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-007334-22 | Sponsor Protocol Number: EFC10780 | Start Date*: 2009-11-02 | |||||||||||
| Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
| Full Title: A randomized, double-blind, double-dummy, 2-arm parallel-group, multicenter 24-week study comparing the efficacy and safety of AVE0010 to sitagliptin as add-on to metformin in obese type 2 diabetic... | |||||||||||||
| Medical condition: Type II Diabetes | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001392-37 | Sponsor Protocol Number: 0431-053 | Start Date*: 2006-07-21 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme GesmbH | |||||||||||||
| Full Title: A Multicenter, Double-Blind, Randomized Study to Evaluate the Safety and Efficacy of the Addition of Sitagliptin to Patients With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control on Me... | |||||||||||||
| Medical condition: type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003600-20 | Sponsor Protocol Number: MK-0431E-211 | Start Date*: 2012-08-02 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase III Randomized Clinical Trial to Study the Efficacy and Safety of the Co-Administration of Sitagliptin and Atorvastatin in Patients with Type 2 Diabetes Mellitus with Inadequate Glycemic Co... | |||||||||||||
| Medical condition: Type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) HU (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004930-33 | Sponsor Protocol Number: BIASP-3963 | Start Date*: 2012-04-02 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: A 24 week randomised, open label, 3 parallel-group comparison of once and twice daily biphasic insulin aspart (BIAsp) 30 plus sitagliptin and twice daily BIAsp 30, all in combination with metfor... | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007805-58 | Sponsor Protocol Number: KP-MSD-01-08 | Start Date*: 2009-11-16 | ||||||||||||||||||||||||||
| Sponsor Name:Med. Klinik II, Grosshadern, Klinikum der Universität München | ||||||||||||||||||||||||||||
| Full Title: The effect of sitagliptin on postprandial lipoprotein metabolism in patients with diabetes mellitus type 2 | ||||||||||||||||||||||||||||
| Medical condition: Diabetes mellitus type 2 | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2011-004622-96 | Sponsor Protocol Number: 0431-260 | Start Date*: 2011-12-23 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. (hereafter referred to as | |||||||||||||
| Full Title: A Phase III, Multicenter, Randomized, Double-Blind, Placebo- Controlled Clinical Trial to Study the Safety and Insulin-Sparing Efficacy of the Addition of Sitagliptin in Patients With Type 2 Diabet... | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DE (Completed) IE (Completed) LT (Completed) DK (Completed) HU (Completed) BE (Completed) GB (Completed) IT (Completed) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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