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Clinical Trial Details

Trial ID: L6824
Source ID: NCT00763347
Associated Drug: Syr-619
Title: Efficacy and Safety Study of SYR-619 in Treating Subjects With Type 2 Diabetes Mellitus
Acronym:
Status: TERMINATED
Study Results: NO
Results:
Conditions: Diabetes Mellitus
Interventions: DRUG: SYR-619|DRUG: SYR-619|DRUG: SYR-619|DRUG: SYR-619|DRUG: Placebo|DRUG: Alogliptin
Outcome Measures: Primary: Change from baseline in glycosylated hemoglobin., Week 12 or Final Visit.. | Secondary: Change from baseline in glycosylated hemoglobin., Weeks 4, 8 and 12 or Final Visit.|Change from baseline in fasting plasma glucose., Weeks: 1, 2, 4, 8 and 12 or Final Visit.|Change from baseline in 1,5 anhydroglucitol., Weeks 2, 4, 8 and 12 or Final Visit.|Change from baseline in proinsulin., Weeks 4, 8 and 12 or Final Visit.|Change from baseline in insulin., Weeks 4, 8 and 12 or Final Visit.|Change from baseline in proinsulin/insulin ratio., Weeks 4, 8 and 12 or Final Visit.|Change from baseline in C-peptide., Weeks 4, 8 and 12 or Final Visit.|Homeostasis model assessment insulin resistance., Weeks 4, 8 and 12 or Final Visit.|Homeostasis model assessment beta-cell function., Weeks 4, 8 and 12 or Final Visit.|Incidence of marked hyperglycemia (fasting plasma glucose ≥200 mg/dL [≥11.10 mmol/L])., Weeks 1, 2, 4, 8 and 12 or Final Visit.|Incidence of rescue., Weeks 1, 2, 4, 8 and 12 or Final Visit.|Clinical response endpoint incidence of glycosylated hemoglobin ≤6.5%., Week 12 or Final Visit.|Clinical response endpoint incidence of glycosylated hemoglobin ≤7.0%., Week 12 or Final Visit.|Clinical response endpoint incidence of glycosylated hemoglobin improvement ≥1.0%., Week 12 or Final Visit.|Clinical response endpoint incidence of glycosylated hemoglobin improvement ≥1.5%., Week 12 or Final Visit.|Clinical response endpoint incidence of glycosylated hemoglobin improvement ≥2.0%., Week 12 or Final Visit.|Fasting lipids (triglycerides, total cholesterol, high-density lipoprotein and low-density lipoprotein cholesterol)., Weeks 4, 8, and 12 or Final Visit.|Postprandial area under the concentration-time curve and peak 2-hour values of plasma glucose, insulin and C-peptide during a 3-hour mixed-meal tolerance test in a subset of subjects., Week 12 or Final Visit.|Plasma concentration of SYR-619., Week 8.|Physical examination findings (including a clinical examination of skin and digits)., At All Visits|Vital sign measurements., At All Visits|Body temperature measurements., Week 12 or Final Visit.|12-lead electrocardiogram tracings., Week 12 or Final Visit.|Incidence of adverse events., At All Visits|Incidence of hypoglycemia (blood glucose <60 mg/dL [<3.33 mmol/L]) in the presence of symptoms or blood glucose <50 mg/dL [<2.78 mmol/L]) regardless of symptoms)., At All Visits|Clinical laboratory evaluations (hematology and serum chemistry)., At All Visits|Clinical laboratory evaluation (urinalysis)., Week 12 or Final Visit.
Sponsor/Collaborators: Sponsor: Takeda
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 82
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2006-11
Completion Date: 2007-02
Results First Posted:
Last Update Posted: 2012-05-21
Locations:
URL: https://clinicaltrials.gov/show/NCT00763347