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Clinical Trial Details

Trial ID: L1979
Source ID: NCT00432276
Associated Drug: Alogliptin
Title: Efficacy of Alogliptin and Pioglitazone in Subjects With Type 2 Diabetes Mellitus
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT00432276/results
Conditions: Diabetes Mellitus
Interventions: DRUG: Alogliptin|DRUG: Pioglitazone|DRUG: Metformin|DRUG: Placebo
Outcome Measures: Primary: Change From Baseline in Glycosylated Hemoglobin (HbA1c), The change from Baseline to Week 26 and Week 52 in HbA1c (the concentration of glucose bound to hemoglobin as a percent of the absolute maximum that can be bound)., Baseline and Weeks 26 and 52. | Secondary: Change From Baseline in HbA1c Over Time, The change from Baseline in HbA1c (the concentration of glucose bound to hemoglobin as a percent of the absolute maximum that can be bound) during the study. Least Squares Means were from an Analysis of Covariance (ANCOVA) model with treatment, study schedule, and geographic region as class variables, and baseline metformin dose and baseline HbA1c as covariates., Baseline and Weeks 4, 8, 12, 16, 20, 34 and 42.|Percentage of Participants With Glycosylated Hemoglobin ≤ 6.5%, Clinical response at Weeks 26 and 52 was assessed by the percentage of participants with HbA1c less than or equal to 6.5%., Weeks 26 and 52.|Percentage of Participants With Glycosylated Hemoglobin ≤ 7.0%, Clinical response at Weeks 26 and 52 was assessed by the percentage of participants with HbA1c less than or equal to 7%., Weeks 26 and 52.|Percentage of Participants With Glycosylated Hemoglobin ≤ 7.5%, Clinical response at Weeks 26 and 52 was assessed by the percentage of participants with HbA1c less than or equal to 7.5%., Weeks 26 and 52.|Percentage of Participants With a Decrease in Glycosylated Hemoglobin ≥ 0.5%, Clinical response at Weeks 26 and 52 was assessed by the percentage of participants with a decrease from Baseline in HbA1c of greater than or equal to 0.5%., Weeks 26 and 52.|Percentage of Participants With a Decrease in Glycosylated Hemoglobin ≥ 1.0%, Clinical response at Weeks 26 and 52 was assessed by the percentage of participants with a decrease from Baseline in HbA1c of greater than or equal to 1.0%., Weeks 26 and 52.|Percentage of Participants With a Decrease in Glycosylated Hemoglobin ≥ 1.5%, Clinical response at Weeks 26 and 52 was assessed by the percentage of participants with a decrease from Baseline in HbA1c of greater than or equal to 1.5%., Weeks 26 and 52.|Percentage of Participants With a Decrease in Glycosylated Hemoglobin ≥ 2.0%, Clinical response at Weeks 26 and 52 was assessed by the percentage of participants with a decrease from Baseline in HbA1c of greater than or equal to 2.0%., Weeks 26 and 52.|Change From Baseline in Fasting Plasma Glucose, The change from Baseline in fasting plasma glucose (FPG) was assessed at Weeks 2, 4, 8, 12, 16, 20, 26, 34, 42 and 52. Least Squares Means were from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline FPG as covariates., Baseline and Weeks 2, 4, 8, 12, 16, 20, 26, 34, 42 and 52.|Percentage of Participants With Marked Hyperglycemia, Marked Hyperglycemia is defined as fasting plasma glucose greater than or equal to 200 mg/dL (11.10 mmol/L)., Baseline to Week 52|Percentage of Participants Meeting Hyperglycemic Rescue Criteria, Rescue was defined as meeting 1 of the following criteria, confirmed by a 2nd sample drawn within 7 days after the first sample and analyzed by the central laboratory: 1. After more than 2 weeks of treatment but prior to the Week 4 Visit: A single fasting plasma glucose (FPG) ≥275 mg/dL; 2. From the Week 4 Visit but prior to the Week 8 Visit: A single FPG ≥250 mg/dL; 3. From the Week 8 Visit but prior to the Week 12 Visit: A single FPG ≥225 mg/dL; 4. From the Week 12 Visit through the End-of-Treatment Visit: HbA1c ≥8.5% AND ≤0.5% reduction in HbA1c as compared with the baseline HbA1c., Baseline to Week 52|Change From Baseline in Fasting Proinsulin, Proinsulin is a precursor to insulin, and was measured as an indicator of pancreatic function. The change from Baseline in fasting proinsulin was assessed at Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52. Least Squares Means were from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline fasting proinsulin as covariates., Baseline and Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52.|Change From Baseline in Fasting Insulin, The change from Baseline in fasting insulin was assessed at Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52. Least Squares Means were from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline fasting insulin as covariates., Baseline and Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52.|Change From Baseline in Proinsulin/Insulin Ratio, The ratio of proinsulin to insulin was calculated as proinsulin (pmol/L) / insulin (μIU/mL) at weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52 relative to the Baseline value. Least squares means were from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline fasting proinsulin/insulin ratio as covariates., Baseline and Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52.|Change From Baseline in C-peptide, C-peptide is a byproduct created when the hormone insulin is produced and is measured by a blood test. Change from Baseline was assessed at Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline fasting C-peptide as covariates., Baseline and Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52.|Change From Baseline in Calculated HOMA Insulin Resistance, The Homeostasis Model Assessment of insulin resistance (HOMA IR) measures insulin resistance based on fasting glucose and insulin measurements: HOMA IR = fasting plasma insulin (µIU/mL) \* fasting plasma glucose (mmol/L) / 22.5 A higher number indicates a greater degree of insulin resistance. The change from Baseline in HOMA IR was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline HOMA insulin resistance as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Calculated HOMA Beta-cell Function, The Homeostasis Model Assessment (HOMA) estimates steady state beta cell function (%B) as a percentage of a normal reference population. HOMA %B = 20 \* insulin (µIU/mL) / fasting plasma glucose (mmol/L) - 3.5 The change from Baseline in the homeostasis model assessment of beta cell function was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline HOMA beta cell function as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Body Weight, Change from Baseline in body weight was assessed at Weeks 4, 8, 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline body weight as covariates., Baseline and Weeks 4, 8, 12, 26, 42 and 52.|Change From Baseline in Total Cholesterol, Change from Baseline in total cholesterol was assessed at Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline total cholesterol as covariates., Baseline and Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52.|Change From Baseline in High-Density Lipoprotein Cholesterol, Change from Baseline in high-density lipoprotein cholesterol (HDL-C) was assessed at Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline HDL cholesterol as covariates., Baseline and Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52.|Change From Baseline in Low-Density Lipoprotein Cholesterol, Change from Baseline in low-density lipoprotein cholesterol (LDL-C) was assessed at Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline LDL cholesterol as covariates., Baseline and Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52.|Change From Baseline in Triglycerides, Change from Baseline in triglycerides was assessed at Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline triglycerides as covariates., Baseline and Weeks 4, 8, 12, 16, 20, 26, 34, 42 and 52.|Change From Baseline in Free Fatty Acids, Change from Baseline in free fatty acids was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline free fatty acids as covariates., Baseline and Weeks 12, 26, 42, and 52.|Change From Baseline in Apolipoprotein A1, Change from Baseline in Apolipoprotein A1 was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline apolipoprotein A1 as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Apolipoprotein A2, Change from Baseline in Apolipoprotein A2 was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline apolipoprotein A2 as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Apolipoprotein B, Change from Baseline in Apolipoprotein B was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline apolipoprotein B as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Apolipoprotein C-III, Change from Baseline in Apolipoprotein C-III was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline apolipoprotein C-III as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Plasminogen Activator Inhibitor-1, Change from Baseline in plasminogen activator inhibitor-1 (PAI-1) was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline PAI-1 as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in High-sensitivity C-Reactive Protein, Change from Baseline in high-sensitivity C-Reactive Protein (hsCRP) was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline hsCRP as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Adiponectin, Change from Baseline in adiponectin was assessed at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline adiponectin as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Nuclear Magnetic Resonance Lipid Fractionation Total Triglycerides, Nuclear Magnetic Resonance (NMR) lipid fractionation was used to assess the change from Baseline in total triglyceride levels at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline NMR triglycerides as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Very Low Density Lipoprotein (VLDL) / Chylomicron Particles, The change from Baseline in levels of total VLDL/chylomicron particles and large VLDL/chylomicron particles was assessed by NMR lipid fractionation at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline VLDL/chylomicron particles as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in VLDL / Chylomicron Triglycerides, The change from Baseline in levels of VLDL/chylomicron triglycerides was assessed by NMR lipid fractionation at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline VLDL/chylomicron triglycerides as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in VLDL Particles, The change from Baseline in levels of medium VLDL particles and small VLDL particles was assessed by NMR fractionation at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline VLDL particles as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Mean VLDL Particle Size, Change from Baseline in mean VLDL particle size was assessed by NMR lipid fractionation at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline mean VLDL particle size as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Intermediate Density Lipoprotein (IDL) Particles, The change from Baseline in levels of IDL particles was assessed by NMR lipid fractionation at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline IDL particles as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Low Density Lipoprotein (LDL) Particles, The change from Baseline in levels of total, large, medium-small, total small and very small LDL particles was assessed by NMR fractionation at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline LDL particles as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Mean LDL Particle Size, Change from Baseline in mean LDL particle size was assessed by NMR lipid fractionation at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline mean LDL particle size as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in High Density Lipoprotein (HDL) Particles, The change from Baseline in levels of total, large, medium and small HDL particles was assessed by NMR fractionation at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline HDL particles as covariates., Baseline and Weeks 12, 26, 42 and 52.|Change From Baseline in Mean HDL Particle Size, Change from Baseline in mean HDL particle size was assessed by NMR lipid fractionation at Weeks 12, 26, 42 and 52. Least squares means are from an ANCOVA model with treatment, study schedule and geographic region as class variables, and baseline metformin dose and baseline mean HDL particle size as covariates., Baseline and Weeks 12, 26, 42 and 52.
Sponsor/Collaborators: Sponsor: Takeda
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE3
Enrollment: 803
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2007-01
Completion Date: 2009-06
Results First Posted: 2013-04-04
Last Update Posted: 2013-04-04
Locations: Birmingham, Alabama, United States|Huntsville, Alabama, United States|Lake Havasu City, Arizona, United States|Little Rock, Arkansas, United States|Foothill Ranch, California, United States|Los Alamitos, California, United States|Los Angeles, California, United States|Pismo Beach, California, United States|San Diego, California, United States|Golden, Colorado, United States|Clearwater, Florida, United States|Hialeah, Florida, United States|Lakeland, Florida, United States|Marianna, Florida, United States|Miami, Florida, United States|North Miami Beach, Florida, United States|Pembroke Pines, Florida, United States|Sebastian, Florida, United States|South Miami, Florida, United States|Tampa, Florida, United States|Winter Park, Florida, United States|Blue Ridge, Georgia, United States|Conyers, Georgia, United States|Decatur, Georgia, United States|Duluth, Georgia, United States|Dunwoody, Georgia, United States|Warner Robins, Georgia, United States|Boise, Idaho, United States|Coeur D'Alene, Idaho, United States|Burr Ridge, Illinois, United States|Chicago, Illinois, United States|Melrose Park, Illinois, United States|Naperville, Illinois, United States|O'Fallon, Illinois, United States|Bloomington, Indiana, United States|Mishawaka, Indiana, United States|Overland Park, Kansas, United States|Marrero, Louisiana, United States|Elkton, Maryland, United States|Rockville, Maryland, United States|Towson, Maryland, United States|Marlborough, Massachusetts, United States|Bay City, Michigan, United States|St. Clair Shores, Michigan, United States|McCook, Nebraska, United States|Las Vegas, Nevada, United States|Blackwood, New Jersey, United States|Trenton, New Jersey, United States|West Caldwell, New Jersey, United States|Asheboro, North Carolina, United States|Charlotte, North Carolina, United States|Mooresville, North Carolina, United States|Shelby, North Carolina, United States|Sparta, North Carolina, United States|Bismarck, North Dakota, United States|Orrville, Ohio, United States|Norman, Oklahoma, United States|Ashland, Oregon, United States|Aliquippa, Pennsylvania, United States|Altoona, Pennsylvania, United States|Dawningtown, Pennsylvania, United States|Fleetwood, Pennsylvania, United States|Kingston, Pennsylvania, United States|Norristown, Pennsylvania, United States|Pittsburgh, Pennsylvania, United States|Tipton, Pennsylvania, United States|Florence, South Carolina, United States|Taylors, South Carolina, United States|Williamston, South Carolina, United States|Watertown, South Dakota, United States|Kingsport, Tennessee, United States|Milan, Tennessee, United States|Nashville, Tennessee, United States|Arlington, Texas, United States|Austin, Texas, United States|Colleyville, Texas, United States|El Paso, Texas, United States|Garland, Texas, United States|Houston, Texas, United States|Hurst, Texas, United States|San Antonio, Texas, United States|Seguin, Texas, United States|Hampton, Virginia, United States|Norfolk, Virginia, United States|Richmond, Virginia, United States|Virginia Beach, Virginia, United States
URL: https://clinicaltrials.gov/show/NCT00432276