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Slo-Niacin, atorvastatin

University of Washington · FDA-approved active Small molecule

Slo-Niacin (niacin) reduces triglycerides and raises HDL cholesterol, while atorvastatin inhibits HMG-CoA reductase to lower LDL cholesterol and overall cardiovascular risk.

Slo-Niacin (niacin) reduces triglycerides and raises HDL cholesterol, while atorvastatin inhibits HMG-CoA reductase to lower LDL cholesterol and overall cardiovascular risk. Used for Dyslipidemia and hypercholesterolemia, Cardiovascular disease prevention.

At a glance

Generic nameSlo-Niacin, atorvastatin
Also known asLipitor (R) (Atorvastatin), Slo-Niacin (R) (time-release niacin
SponsorUniversity of Washington
Drug classNiacin derivative and HMG-CoA reductase inhibitor (statin combination)
TargetNicotinic acid receptor (GPR109A) and HMG-CoA reductase
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Niacin is a B vitamin that decreases hepatic VLDL production and increases HDL cholesterol through nicotinic acid receptor signaling. Atorvastatin is a statin that competitively inhibits HMG-CoA reductase, the rate-limiting enzyme in cholesterol synthesis, thereby reducing LDL cholesterol levels. Together, this combination addresses multiple lipid abnormalities to reduce atherosclerotic cardiovascular disease risk.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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