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ticagrelor

Generic: TICAGRELOR·Brand: BRILINTA, Brilinta, TICAGRELOR

ticagrelor: sourced relationships with 2 companies · 3 clinical trials tracked · 2 FDA decisions.

ticagrelor evidence translation

What we can confirm

2 FDA records · 3 tracked trials

What it means

More than one company relationship is source-backed. Until you choose one, AI stays drug-only and does not guess ownership.

What to watch

Watch active trials and any change in FDA or trial status.
BioSniper AIPage evidence connected

Prepared research question

What is verified about ticagrelor, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence4 indications · 0 study sponsors

Related indications

Study sponsors

No additional listed-company sponsor is linked.

Dated Pipeline Records (2)
CompanyDated record stage
ASTRAZENECA PLC (AZN)
Reported 2011-07-20 · Current development: unknownSource
Untreated Follicular Lymphoma
Approved
DR REDDYS LABORATORIES LTD (RDY)
Reported 2024-10-29 · Current development: unknownSource
Approved
Clinical Trial Registry Records (3)

Dual Antithrombotic Therapy With Dabigatran and Ticagrelor in Patients With Acute Coronary Syndrome and Non-valvular Atrial Fibrillation Undergoing Percutaneous Coronary Intervention (ADONIS-PCI)

NCT04695106Registry updated 2026-06-16·Phase 4
Recruiting

Primary endpoint: Primary safety endpoint - first major or clinically relevant non-major bleeding event, as defined by the ISTH

InterventionalRandomizedopen1,194 targetStarted 2021-10Completion 2026-081 site · PolandMedical University of Gdansk

The Value of Screening for "High on Treatment Platelet Reactivity" in Patients Undergoing Lower Extremity Arterial Endovascular Interventions

NCT04007055Registry updated 2026-02-13·Phase 3
Terminated

Primary endpoint: Proportion of Participants With Primary Patency

InterventionalRandomizedopen31 targetStarted 2019-08Completion 2024-031 site · United StatesMarissa Jarosinski

Single-center, Double-blind (ACT-246475), Open-label (Clopidogrel, Prasugrel, and Ticagrelor), Placebo-controlled, Randomized, Two-way Crossover Study to Investigate the Pharmacodynamics, Safety, and Tolerability of a Single Oral Dose of Clopidogrel or, Prasugrel, or Ticagrelor When Administered After a Single Subcutaneous Dose of the P2Y12 Antagonist ACT-246475 in Healthy Male and Female Subjects

NCT03430661Registry updated 2025-07-03·Phase 1
Completed

Primary endpoint: Time-matched comparisons of IPA% (MPA) between treatments (i.e., Treatment A1 vs A2, Treatment B1 vs B2, and treatment C1 vs C2, treatments are defined below) following administration of ACT-246475 and its matching placebo.

InterventionalRandomizedtriple77 enrolledStarted 2018-01Completion 2019-051 site · United StatesViatris Innovation GmbH
FDA Decisions2 records
Approval(RDY)FDA ↗
ANDA208541UNKNOWNStandardOralTablet
Approval(AZN)FDA ↗
NDA022433Type 1 - New Molecular EntityStandardOralTablet

Frequently asked questions

Which companies have sourced relationships with ticagrelor?

ticagrelor has dated SEC/FDA relationship records for ASTRAZENECA PLC, DR REDDYS LABORATORIES LTD.

How many clinical trials involve ticagrelor?

BioSniper tracks 3 clinical trials involving ticagrelor.

What is ticagrelor's latest FDA decision?

The most recent tracked FDA decision for ticagrelor is Approval, dated October 29, 2024.