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Phase 3 Completed N=71 Randomized Quadruple-blind Treatment

Efficacy of Alogliptin and With Pioglitazone in Patients With Type 2 Diabetes.

Source: ClinicalTrials.gov NCT00655863 ↗
Enrolled (actual)
71
Serious AEs
7.0%
Results posted
May 2013
Primary outcomePrimary: Change From Baseline in Postprandial Incremental Area Under the Curve for Total Triglycerides at Week 16. — -39.728; -346.957; -293.439 mg.h/dL — p=<0.001

Summary

The purpose of this study is to compare the efficacy of Alogliptin, once daily (QD), taken by itself and with pioglitazone on postprandial lipid measures in type 2 diabetes.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in Postprandial Incremental Area Under the Curve for Total Triglycerides at Week 16.
-39.728; -346.957; -293.439 <0.001 sig
SECONDARY
Change From Baseline in Postprandial Incremental Area Under the Curve for Total Triglycerides at Week 4.
-16.291; -288.490; -279.116
SECONDARY
Change From Baseline in Postprandial Incremental Area Under the Curve Changes for Lipid Parameters.
-9.488; -119.009; -98.758; 25.194; -130.459; -85.709
SECONDARY
Change From Baseline in Postprandial Incremental Area Under the Curve for Lipoprotein Parameters.
-0.020; -0.491; -0.312; -0.055; -0.654; -0.266
SECONDARY
Postprandial Changes Over Time From Baseline for Glucagon-like Peptide-1 (GLP-1)
0.52; -5.48; -4.88; 0.92; -2.93; -6.41
SECONDARY
Postprandial Changes Over Time From Baseline for Glucose
-5.957; -35.065; -65.905; -4.049; -24.721; -67.718
SECONDARY
Postprandial Changes Over Time From Baseline for Insulin
-5.047; -5.867; -18.287; 1.405; 3.161; -28.700
SECONDARY
Postprandial Changes Over Time From Baseline for Glucagon
7.222; -14.639; -17.704; 1.730; -17.015; -22.081
SECONDARY
Change From Baseline in Glycosylated Hemoglobin
-0.12; -0.55; -1.01; 0.38; -0.39; -0.95
SECONDARY
Change From Baseline in Fasting Plasma Glucose
-4.141; -20.669; -38.826; 4.864; -16.293; -38.242
SECONDARY
Change From Baseline in Postprandial C-Peptide
-0.106; -0.300; -1.199; 0.311; -0.011; -1.379
SECONDARY
Change From Baseline in Postprandial Proinsulin
-4.555; -13.024; -41.192; -0.208; -12.568; -56.478
SECONDARY
Change From Baseline in High-sensitive C-reactive Protein (Hs-CRP)
-1.514; 0.631; 0.155; 4.338; -0.402; -0.402
SECONDARY
Change From Baseline in Adiponectin
0.001; 0.000; 0.006; 0.000; 0.000; 0.007
SECONDARY
Change From Baseline in Anti-Vascular Cell Adhesion Molecule (VCAM)
-37.351; 2.392; 4.849; 5.067; -1.441; 13.665
SECONDARY
Change From Baseline in Anti-Intercellular Adhesion Molecule (ICAM)
-1.154; -0.294; -23.810; -2.495; -4.140; -16.556
SECONDARY
Change From Baseline in e-Selectin
1.041; 0.116; -6.437; 1.488; -1.671; -4.056
SECONDARY
Change From Baseline in Endothelial Function Through Pulse Wave Tonometry
-3.6; -4.7; -4.2; -1.6; 0.1; -1.3

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of type 2 diabetes
  • Females of childbearing potential who are sexually active must agree to use adequate contraception, and can neither be pregnant nor lactating from Screening throughout the duration of the study.
  • Either failed treatment with diet and exercise for 3 months prior to Screening or has been receiving a stable dose of metformin, sulfonylurea, nateglinide, or repaglinide for more than 3 months prior to Screening.
  • Inadequate glycemic control as defined by glycosylated hemoglobin concentration between 6.5 and 9.0%, inclusive.
  • Fasting plasma glucose less than 13.3 mmol per L.
  • Fasting serum triglyceride level of 1.7 to 5.0 mmol per L, inclusive.
  • Has not been receiving any lipid-lowering therapy within 3 months prior to Screening or on a stable statin and/or ezetimibe therapy (same drug and dose) for at least 3 months.
  • Body mass index greater than 23 kg/m2 and less than 45 kg/m2.
  • If has regular use of other, non-excluded medications, must be on a stable dose for at least 4 weeks prior to Screening. Use of as needed prescription medications and over-the-counter medications is allowed at the discretion of the investigator.
  • Is to be Apolipoprotein E 3/3 or Apolipoprotein E 3/4 phenotype positive prior to baseline.

Exclusion Criteria

  • History of type 1 diabetes.
  • History of drug abuse (defined as illicit drug use) or a history of alcohol abuse (defined as regular or daily consumption of more than 4 alcoholic drinks per day) within the past 2 years.
  • Diastolic blood pressure greater than 100 mm Hg or a systolic blood pressure of greater than 160 mm Hg.
  • History of cancer, other than basal cell carcinoma, that has not been in remission for at least 5 years prior to the first dose of study medication.
  • Hemoglobin less than 120 g per L for males and less than100 g per L for females.
  • Alanine transaminase level greater than 2.5 times the upper limit of normal, active liver disease, or jaundice.
  • Serum creatinine level greater than 133 μmol per L.
  • Fasting total cholesterol greater than 6.5 mmol per L.
  • New York Heart Association heart failure of any Class (I-IV) regardless of therapy.
  • History of coronary angioplasty, coronary stent placement, coronary bypass surgery, or myocardial infarction within 6 months prior to Screening.
  • History of acute metabolic diabetic complications.
  • History of any hemoglobinopathy that may affect determination of glycosylated hemoglobin.
  • History of infection with human immunodeficiency virus.
  • History of diabetic gastro paresis.
  • History of gastric bypass surgery.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00655863). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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