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standard-dose ticagrelor

First Affiliated Hospital of Harbin Medical University · FDA-approved active Small molecule Under review Quality 0/100

standard-dose ticagrelor is a P2Y12 receptor antagonist Small molecule drug developed by First Affiliated Hospital of Harbin Medical University. It is currently FDA-approved for Acute coronary syndrome (ACS) for reduction of cardiovascular death, myocardial infarction, and stent thrombosis, Secondary prevention of atherothrombotic events in patients with prior myocardial infarction.

Ticagrelor is a P2Y12 receptor antagonist that irreversibly blocks platelet activation and aggregation, reducing thrombotic events.

Ticagrelor is a small molecule that acts as a negative allosteric modulator of the P2Y purinoceptor 12, a type of purinergic receptor. It is used in standard-dose form for conditions such as coronary artery disease and coronary stenoses, typically in combination with aspirin.

At a glance

Generic namestandard-dose ticagrelor
SponsorFirst Affiliated Hospital of Harbin Medical University
Drug classP2Y12 receptor antagonist
TargetP2Y12
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Ticagrelor binds directly and reversibly to the P2Y12 adenosine diphosphate (ADP) receptor on platelets, preventing platelet activation and aggregation. Unlike clopidogrel, it does not require hepatic metabolism for activation and provides faster onset of action. This results in reduced platelet-mediated thrombosis and lower risk of cardiovascular events in acute coronary syndromes and other thrombotic conditions.

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 standard-dose ticagrelor

What is standard-dose ticagrelor?

standard-dose ticagrelor is a P2Y12 receptor antagonist drug developed by First Affiliated Hospital of Harbin Medical University, indicated for Acute coronary syndrome (ACS) for reduction of cardiovascular death, myocardial infarction, and stent thrombosis, Secondary prevention of atherothrombotic events in patients with prior myocardial infarction.

How does standard-dose ticagrelor work?

Ticagrelor is a P2Y12 receptor antagonist that irreversibly blocks platelet activation and aggregation, reducing thrombotic events.

What is standard-dose ticagrelor used for?

standard-dose ticagrelor is indicated for Acute coronary syndrome (ACS) for reduction of cardiovascular death, myocardial infarction, and stent thrombosis, Secondary prevention of atherothrombotic events in patients with prior myocardial infarction.

Who makes standard-dose ticagrelor?

standard-dose ticagrelor is developed and marketed by First Affiliated Hospital of Harbin Medical University (see full First Affiliated Hospital of Harbin Medical University pipeline at /company/first-affiliated-hospital-of-harbin-medical-university).

What drug class is standard-dose ticagrelor in?

standard-dose ticagrelor belongs to the P2Y12 receptor antagonist class. See all P2Y12 receptor antagonist drugs at /class/p2y12-receptor-antagonist.

What development phase is standard-dose ticagrelor in?

standard-dose ticagrelor is FDA-approved (marketed).

What are the side effects of standard-dose ticagrelor?

Common side effects of standard-dose ticagrelor include Bradycardia, Dyspnea, Bleeding (major and minor), Ventricular pauses.

What does standard-dose ticagrelor target?

standard-dose ticagrelor targets P2Y12 and is a P2Y12 receptor antagonist.

Related

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