Last reviewed · How we verify

Ticlid (TICLOPIDINE)

FDA-approved approved Small molecule

Ticlid (Ticlopidine) is a small molecule platelet aggregation inhibitor that targets the alpha-2B adrenergic receptor. Originally developed by, it was approved by the FDA in 1991 for indications including cerebrovascular occlusion, percutaneous coronary intervention, prevention of cerebral thrombosis, and subacute stent thrombosis prevention. Ticlid is now off-patent with 8 generic manufacturers. Key safety considerations include potential hematologic and gastrointestinal side effects. As a platelet aggregation inhibitor, Ticlid works by blocking the action of adenosine diphosphate (ADP) on platelets, thereby preventing platelet activation and aggregation.

At a glance

Generic nameTICLOPIDINE
TargetCytochrome P450 2B6, Bile salt export pump, Cytochrome P450 2A6
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1991

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
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results