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Cilostazol + Probucol group

Otsuka Beijing Research Institute · FDA-approved active Small molecule

This combination drug inhibits platelet aggregation and reduces cholesterol oxidation to improve blood flow and reduce cardiovascular events.

This combination drug inhibits platelet aggregation and reduces cholesterol oxidation to improve blood flow and reduce cardiovascular events. Used for Intermittent claudication and peripheral arterial disease, Atherosclerotic cardiovascular disease prevention.

At a glance

Generic nameCilostazol + Probucol group
Also known asPletaal and Changtai
SponsorOtsuka Beijing Research Institute
Drug classAntiplatelet agent + Antioxidant lipid-lowering agent
TargetPhosphodiesterase-3 (cilostazol); LDL oxidation pathway (probucol)
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Cilostazol is a phosphodiesterase-3 inhibitor that increases cAMP in platelets and vascular smooth muscle, promoting vasodilation and inhibiting platelet aggregation. Probucol is a lipophilic antioxidant that reduces LDL cholesterol oxidation and has antiatherosclerotic properties. Together, they work synergistically to improve peripheral circulation and reduce thrombotic 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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