Drug

Ticagrelor

As of the edition of 20 October 2026, Ticagrelor is a small molecule: marketed, first approved in 2010 (EU); acts on P2RY12.

Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.

The drug

Status
Marketed; latest approval 2025
Kind
Small molecule
Brand name
Brilinta
First approved
3 December 2010 (EU)
Approvals on record
10 in 7 regions
Holder of the most recent approval
Pharos Pharmaceutical Oriented Services Ltd.; 3 holders in all
Withdrawn from market
27 March 2013 (in some regions)
Registered trials
302, 25 stopped early
Disease areas
Heart and blood vessels; Nervous system; Nutrition and metabolism; Hormones; Pregnancy and women's health; Urinary and reproductive

US protection

No US approval on record.

With no US approval on record there are no listed US patents or exclusivities.

This is the US only.

Companies that need a new molecule because of this drug

1 company on route B because of this drug.

Companies on route B for this drug

In the product

1 company is on route B because of Ticagrelor.

Target

GeneProteinUniProt
P2RY12P2Y purinoceptor 12Q9H244

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated532791
Phase 1272610
Phase 2251902
Phase 36838911
Phase 4129741411
All trials302

Who has held its approvals

CompanyRoleYears
AstraZenecaApplicant and Lead sponsor of trials2006 to now