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Ticagrelor monotherapy

Yonsei University · FDA-approved active Small molecule ✓ Verified May 2026 Quality 5/100

Ticagrelor monotherapy is a Small molecule drug developed by Yonsei University. It is currently FDA-approved. Also known as: Brilinta®, Brilinta, Study group.

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 the treatment of conditions such as coronary artery disease, CABG, and thrombosis, often in combination with other antiplatelet therapies like aspirin and clopidogrel.

At a glance

Generic nameTicagrelor monotherapy
Also known asBrilinta®, Brilinta, Study group
SponsorYonsei University
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

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 Ticagrelor monotherapy

What is Ticagrelor monotherapy?

Ticagrelor monotherapy is a Small molecule drug developed by Yonsei University.

Who makes Ticagrelor monotherapy?

Ticagrelor monotherapy is developed and marketed by Yonsei University (see full Yonsei University pipeline at /company/yonsei-university).

Is Ticagrelor monotherapy also known as anything else?

Ticagrelor monotherapy is also known as Brilinta®, Brilinta, Study group.

What development phase is Ticagrelor monotherapy in?

Ticagrelor monotherapy is FDA-approved (marketed).

Related

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