Drug intelligence / Profile preview

aspirin + cilostazol

Development stage
Unknown
Lead developer
Bayer
Modality
Small Molecules
Administration
Oral
01

Overview

Aspirin + cilostazol is a fixed-dose combination of two antiplatelet agents used primarily for secondary prevention of ischemic stroke, especially in patients with noncardioembolic stroke. Aspirin acts as an irreversible inhibitor of cyclooxygenase-1 (COX-1), thereby inhibiting thromboxane A2 formation and reducing platelet aggregation. Cilostazol is a selective phosphodiesterase 3 (PDE3) inhibitor that increases intracellular cAMP in platelets and blood vessels, leading to inhibition of platelet aggregation and vasodilation. Clinical trials have shown that dual antiplatelet therapy with aspirin plus cilostazol reduces the risk of recurrent ischemic stroke more effectively than monotherapy, without significantly increasing the risk of severe or life-threatening bleeding. This combination may also slow progression of intracranial artery stenosis compared to aspirin alone[1][2][3][4].

Other names
cilostazol + aspirin
02

Targets

PGHS-1 (Prostaglandin G/H Synthase 1)PDE3A (Phosphodiesterase 3A)

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