Drug intelligence / Profile preview

cilostazol + prednisolone

Development stage
Unknown
Lead developer
Otsuka Holdings
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules
Administration
Oral, Intravenous, Intramuscular, Ophthalmic, Topical, Rectal, Intraarticular
01

Overview

Cilostazol + prednisolone is a combination of two pharmaceutical agents, each with distinct mechanisms and clinical uses. Cilostazol is an antiplatelet agent and vasodilator, primarily used for the symptomatic relief of intermittent claudication in patients with peripheral arterial disease. It works by inhibiting phosphodiesterase III, leading to increased cyclic AMP in platelets and blood vessels, which inhibits platelet aggregation and promotes vasodilation[1][3][8]. Prednisolone is a synthetic glucocorticoid corticosteroid used for its potent anti-inflammatory and immunosuppressive effects across a wide range of conditions including allergic reactions, autoimmune diseases, asthma, arthritis, inflammatory bowel disease, and more[4][7]. It acts as an agonist at the glucocorticoid receptor to modulate gene expression that suppresses inflammation[4][7]. The combination may be considered when both antiplatelet/vasodilatory effects (from cilostazol) and anti-inflammatory/immunosuppressive actions (from prednisolone) are desired; however, there are no widely recognized fixed-dose combination products or unique brand names for this pairing.

02

Targets

GR (Glucocorticoid receptor)PDE3A (Phosphodiesterase 3A)

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