Effectiveness of Sitagliptin for HIV Insulin Resistance and Inflammation

Completed · Phase 3 · Has a placebo group

Conditions studied: Inflammation, Macrophage Infiltration, Cardiovascular Disease

In brief

People living with human immunodeficiency virus infection (HIV) have 2-4fold greater risk for developing diabetes and heart disease than the general population. They need safe and effective treatments that reduce the risk for developing diabetes and heart disease, and improve their quality of life. This project will explore whether a new anti-diabetes medication (Januvia) with a novel mechanism of action reduces inflammation, and improves blood vessel function in HIV infected men and women with several risk factors for developing cardiovascular disease.

Key facts

Study ID

NCT01552694

Run by

Washington University School of Medicine

People needed

38

Starts

2012-10-01

Expected to finish

2014-12-01

Last updated by the study team

2018-05-08

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18-65 yr old HIV infected men and women.
• Stable (at least the past 6 months) on combined antiretroviral therapy (cART).
• Stable immune (> 300 CD4+ T-cells/µL) and virologic (< 50 copies HIV RNA/mL) status.
• Insulin resistant/impaired glucose tolerance (fasting glucose 100-125mg/dL, or 2-hr glucose 140-200mg/dL or fasting HOMA-IR= 2.5-6.0).
• Waist circumference > 102 cm (men), > 88 cm (women).
• BMI > 20 kg/m2.
• Fasting hypertriglyceridemia > 150 mg/dL.
• Low HDL-cholesterol (< 40 mg/dL in men or < 50 mg/dL in women).
• Platelet count > 30,000/mm3.
• Absolute neutrophil count > 750/mm3.
• Transaminases < 2.5x the upper limit of normal.
• Long-term non-progressors (not taking anti-HIV medications) are not eligible.

You may not qualify if…

• Diabetes (T2DM, IDDM or diabetic ketoacidosis) or taking any glucose-lowering medication (e.g., insulin, TZDs, metformin, sulfonylurea).
• Any agent that might artifactually alter glycemic control (e.g., glucocorticoids, megace, rhGH, GH-secretagogue, testosterone derivatives, creatine monohydrate, chromium picolinate, AA/protein supplements, medium- or long-chain fatty acids) during 6 months prior to or during enrollment.
• History of serious CV disease. NYHA Functional Class III or IV (e.g., recent MI, unstable angina, edema, CHF, CAD, CABG, stroke, resting hypertension > 160/95 mmHg), irregular heart rhythm, resting ST-segment depression > 1mm). Treatment with medications for CV condition (e.g., α- or ß-blockers). Some BP-lowering medications (Ca++channel blocker, diuretic, or ACE inhibitor) are permitted.
• Moderate to severe renal insufficiency. Serum creatinine > 1.7 mg/dL (men) > 1.5 mg/dL (women).
• Plan or anticipate a change in anti-HIV medications during the study.
• Lipid-lowering medications are permitted (fibrate or statin or niacin), but must be stable on that agent for at least 6 months prior to enrollment. Lipid-lowering agents cannot be started during the treatment period.
• Chronic hepatitis B (HBV-surface antigen positive). Active hepatitis C (detectable Hep C RNA).
• Positive urine drug test for opiates, methamphetamine, heroin, cocaine. Active substance abuse that the MD-scientist believes may compromise safety, compliance, interfere with study drug or data interpretation.
• Hematocrit < 34% in men or < 25% in women with symptoms (fatigue, "tired-legs", shortness of breath). Hemoglobin < 10 gm/dL with symptoms.
• Pregnant or nursing mothers. Women must agree to use an acceptable form of birth control during the study. If using birth control pills-must be stable on this medication for at least 6 months prior to enrollment.
• Active malignancy or treatment with chemotherapeutic agents or radiation therapy or any cytokine or anti-cytokine therapy during 6 months prior to enrollment.
• History of pancreatitis
• > 10% unintentional weight loss during the 6 months prior to enrollment.
• Reduced cognitive function/unable to provide voluntary informed consent. Prisoners are excluded.
• Blinded investigational drugs for 3 months prior to enrollment that will not be unblinded before enrollment.
• Nausea, vomiting, diarrhea (> 4 loose stools/day) that are unresponsive to treatment.

Where it is running

• Washington University School of Medicine — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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