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Niacin/ Laropiprant

Ludwig-Maximilians - University of Munich · FDA-approved active Small molecule

Niacin reduces triglycerides and LDL cholesterol while raising HDL cholesterol; laropiprant is a prostaglandin D2 receptor antagonist that reduces niacin-induced flushing.

Niacin reduces triglycerides and LDL cholesterol while raising HDL cholesterol; laropiprant is a prostaglandin D2 receptor antagonist that reduces niacin-induced flushing. Used for Dyslipidemia (elevated triglycerides and/or low HDL cholesterol) in patients at risk for cardiovascular disease.

At a glance

Generic nameNiacin/ Laropiprant
Also known asTredaptive, EU/1/08/459/001
SponsorLudwig-Maximilians - University of Munich
Drug classLipid-modifying agent; prostaglandin D2 receptor antagonist
TargetDGAT2 (niacin); DP1 prostaglandin receptor (laropiprant)
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Niacin (vitamin B3) works as a lipid-modifying agent by inhibiting hepatic diacylglycerol acyltransferase-2 (DGAT2) and affecting lipoprotein metabolism. Laropiprant blocks the DP1 prostaglandin receptor, which mediates the vasodilatory flushing response that commonly limits niacin tolerability. The combination allows higher niacin doses to be used with improved tolerability.

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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