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LAROPIPRANT

FDA-approved withdrawn Small molecule Quality 24/100

Laropiprant is a marketed drug primarily indicated for dyslipidemia, with a key composition patent expiring in 2028. Its mechanism of action, blocking prostaglandin D2, differentiates it from competitors targeting similar pathways. The primary risk is the competitive landscape, including off-patent drugs like alprostadil and dinoprostone, as well as patent-protected options such as epoprostenol, iloprost, and selexipag.

At a glance

Generic nameLAROPIPRANT
Drug classlaropiprant
TargetProstaglandin D2 receptor
ModalitySmall molecule
Therapeutic areaMetabolic
PhaseFDA-approved

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: