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Lescol (FLUVASTATIN)

Novartis · FDA-approved approved Small molecule Quality 65/100

Fluvastatin sodium inhibits HMG-CoA reductase, reducing cholesterol biosynthesis and increasing LDL receptor activity, lowering plasma cholesterol.

Lescol (Fluvastatin) is a small molecule HMG-CoA Reductase Inhibitor developed by Novartis, targeting the 3-hydroxy-3-methylglutaryl-coenzyme A reductase enzyme. It was FDA approved in 1993 for various indications including arteriosclerotic vascular disease, familial hypercholesterolemia, and hypercholesterolemia. Lescol is off-patent with multiple generic manufacturers available. It has a short half-life of 0.7 hours and 24% bioavailability. As a HMG-CoA Reductase Inhibitor, Lescol is used to lower cholesterol levels in the blood.

At a glance

Generic nameFLUVASTATIN
SponsorNovartis
Drug classHMG-CoA Reductase Inhibitor
TargetHMG-CoA reductase
ModalitySmall molecule
Therapeutic areaMetabolic
PhaseFDA-approved
First approval1993

Mechanism of action

Fluvastatin sodium works by blocking the enzyme HMG-CoA reductase, which is crucial for cholesterol production. This leads to less cholesterol being made in the liver, which then triggers the liver to take more cholesterol out of the bloodstream, ultimately reducing overall cholesterol levels.

Approved indications

Common side effects

Drug interactions

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results