Last reviewed · How we verify

Kengreal (CANGRELOR)

Chiesi · FDA-approved approved Small molecule Quality 66/100

Kengreal blocks the action of ADP on platelets, preventing platelet activation and aggregation.

Kengreal (Cangrelor) is a P2Y12 platelet inhibitor, a small molecule drug developed by Medicines Co and currently owned by Chiesi. It targets the P2Y12 purinoceptor, a receptor on platelets that plays a key role in blood clotting. Kengreal is FDA-approved for use in percutaneous coronary intervention (PCI) and works by blocking the action of adenosine diphosphate (ADP) on platelets, thereby preventing platelet activation and aggregation. As of 2023, Kengreal is still patented, but generic manufacturers are available. Key safety considerations include bleeding risks and potential interactions with other medications.

At a glance

Generic nameCANGRELOR
SponsorChiesi
Drug classP2Y12 Platelet Inhibitor [EPC]
TargetP2Y purinoceptor 12
ModalitySmall molecule
Therapeutic areaMetabolic
PhaseFDA-approved
First approval2015
Annual revenue200

Mechanism of action

Cangrelor is direct P2Y12 platelet receptor inhibitor that blocks ADP-induced platelet activation and aggregation. Cangrelor binds selectively and reversibly to the P2Y12 receptor to prevent further signaling and platelet activation.

Approved indications

Common side effects

Key clinical trials

Patents

PatentExpiryType

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
FDA Orange BookPatents + exclusivity
SEC EDGARRevenue + earnings

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: