ER Niacin/Laropiprant Impact on Cardiovascular Markers and Atheroprogression in HIV-infected Individuals on cART (NILACH)

Calmy Alexandra

Status and phase

Terminated

Phase 4

Conditions

HIV

Atherosclerosis

Treatments

Drug: niacin/laropiprant

Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT01683656

NILACH 2012DR4097

Details and patient eligibility

About

HIV-infected patients are at increased risk for cardiovascular disease. Large investigations support an inverse correlation between HDL-C levels and coronary heart disease. Therefore a treatment lowering HDL-C such as niacin could reduce the risk of atheroprogression not only through its benefit in terms of lipid profile, but also by reducing atherosclerotic inflammation.

The study aims at showing that a therapy targeting HDL-C increase in HIV-infected patients on suppressive cART has the potential for reducing subclinical atherosclerotic inflammation associated with HIV itself in HIV-individuals on cART.

NILACH is a randomised, multicenter, double blind, placebo controlled, 48 weeks trial to test the effect of the newly marketed niacin/laropiprant on carotid intima-media thickness (IMT) in 90 subjects.

Regimen 1: ER niacin/laropiprant 1g/20 mg for the first 4 weeks and 2g/40mg from week 5 to the end of the study (the titration aims to reduce adverse reactions)
Regimen 2: ER niacin/laropiprant placebo p.m.

The primary end point is the change in mean common carotid intima-media thickness from baseline and 48 weeks, compared between the niacin/laropiprant group and the placebo group.

The proposed in vivo experiments should provide insights on the potential benefits of niacin treatment of cardiovascular disease in HIV patients. In addition, we will be able to further clarify the role of systemic inflammatory mediators in the development of early atherosclerosis of HIV-infected patients on antiretroviral therapy. Detection and treatment of non-infectious co-morbidities such as cardiovascular diseases have become essential for HIV-infected individuals exposed to lifelong antiretroviral therapy and go beyond mere management of opportunistic infections or virologic suppression.

Enrollment

4 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Adult patients > 40 years;
Women of childbearing potential must use two reliable contraceptive methods during the entire trial, from day 1 to one month after the end of the trial.
Signing the study consent form;
Stable cART since at least 3 months (ie no recent drug change);
HIV-RNA below 100 copies for at least 6 months;
HDL-cholesterol <1.29 mmol/l for men; <1.42 mmol/l for women

Exclusion criteria

Pregnancy or lactation;
Congestive Heart Failure;
Malignant Hypertension;
Acute or chronic coronary artery diseases;
Any known cardiac arrhythmias;
Diabetes;
Concomitant cancer, rheumatologic disease or inflammatory bowel diseases;
Concomitant renal or hepatic disease:
- Creatinine above 150 micromol/L
- Transaminases above 5 times upper normal limit
- Prothrombin time (Quick) value below 50%;
Prior intolerance to niacin therapy (reported in a medical report);
Cyclosporine, anti-inflammatory drugs (other than aspirin) or cytokine therapy in concomitant intake;
Abnormal thyroid function;
Excessive consumption of alcohol;
Known severe lactose intolerance.