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Cilostazol+Probucol

Otsuka Beijing Research Institute · FDA-approved active Small molecule Under review Quality 0/100

Cilostazol+Probucol is a Antiplatelet agent + Antioxidant lipid-lowering agent Small molecule drug developed by Otsuka Beijing Research Institute. It is currently FDA-approved for Intermittent claudication and peripheral arterial disease, Secondary prevention of atherosclerotic cardiovascular disease. Also known as: Pletaal and Changtai.

Cilostazol inhibits phosphodiesterase-3 to increase cAMP and promote vasodilation and antiplatelet effects, while probucol acts as an antioxidant to reduce lipid peroxidation and improve lipid profiles.

Cilostazol is a small molecule phosphodiesterase 3A inhibitor used in clinical trials for various conditions, including brain ischemia, intracranial hemorrhages, hyperlipidemias, type 2 diabetes mellitus, and arteriosclerosis obliterans. Probucol is also being studied in clinical trials for these conditions, although its exact mechanism of action is not specified in the provided information.

At a glance

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

Mechanism of action

Cilostazol is a phosphodiesterase-3 inhibitor that increases intracellular cAMP levels, leading to vasodilation, inhibition of platelet aggregation, and improved blood flow. Probucol is a lipophilic antioxidant that reduces oxidative stress and LDL cholesterol oxidation. The combination targets both platelet dysfunction and lipid-mediated atherosclerosis in cardiovascular disease.

Approved indications

Common side effects

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

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Frequently asked questions about Cilostazol+Probucol

What is Cilostazol+Probucol?

Cilostazol+Probucol is a Antiplatelet agent + Antioxidant lipid-lowering agent drug developed by Otsuka Beijing Research Institute, indicated for Intermittent claudication and peripheral arterial disease, Secondary prevention of atherosclerotic cardiovascular disease.

How does Cilostazol+Probucol work?

Cilostazol inhibits phosphodiesterase-3 to increase cAMP and promote vasodilation and antiplatelet effects, while probucol acts as an antioxidant to reduce lipid peroxidation and improve lipid profiles.

What is Cilostazol+Probucol used for?

Cilostazol+Probucol is indicated for Intermittent claudication and peripheral arterial disease, Secondary prevention of atherosclerotic cardiovascular disease.

Who makes Cilostazol+Probucol?

Cilostazol+Probucol is developed and marketed by Otsuka Beijing Research Institute (see full Otsuka Beijing Research Institute pipeline at /company/otsuka-beijing-research-institute).

Is Cilostazol+Probucol also known as anything else?

Cilostazol+Probucol is also known as Pletaal and Changtai.

What drug class is Cilostazol+Probucol in?

Cilostazol+Probucol belongs to the Antiplatelet agent + Antioxidant lipid-lowering agent class. See all Antiplatelet agent + Antioxidant lipid-lowering agent drugs at /class/antiplatelet-agent-antioxidant-lipid-lowering-agent.

What development phase is Cilostazol+Probucol in?

Cilostazol+Probucol is FDA-approved (marketed).

What are the side effects of Cilostazol+Probucol?

Common side effects of Cilostazol+Probucol include Headache, Diarrhea, Palpitations, Dizziness.

What does Cilostazol+Probucol target?

Cilostazol+Probucol targets Phosphodiesterase-3 (cilostazol); Antioxidant mechanism (probucol) and is a Antiplatelet agent + Antioxidant lipid-lowering agent.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing