Drug intelligence / Profile preview

unfractionated heparin + eptifibatide

Development stage
Unknown
Lead developer
Millennium Pharmaceuticals
Modality
Peptides, Small Molecules
Administration
Intravenous
01

Overview

**unfractionated heparin + eptifibatide** is a combination of two intravenous antithrombotic agents used primarily in the management of acute coronary syndromes (ACS), especially non-ST-segment elevation ACS and during percutaneous coronary intervention (PCI). Unfractionated heparin is a glycosaminoglycan anticoagulant that enhances the inhibition of thrombin and factor Xa by antithrombin III, reducing the formation of fibrin clots. Eptifibatide is a synthetic cyclic heptapeptide belonging to the glycoprotein IIb/IIIa inhibitor class ("arginine-glycine-aspartate-mimetics"), which reversibly inhibits platelet aggregation by preventing the binding of fibrinogen, von Willebrand factor, and other adhesive ligands to the GP IIb/IIIa receptor on platelets[2][4][8][6]. The combination targets complementary mechanisms of thrombus formation: heparin targets the coagulation cascade, while eptifibatide inhibits platelet aggregation, thereby synergistically reducing the risk of ischemic adverse effects in ACS[1]. This therapy is intended for use in hospitalized patients, often alongside aspirin. Developers and manufacturers for each drug are listed separately below.

Other names
unfractionated heparin + eptifibatide
02

Targets

F10 (Factor Xa)GPIIb/IIIa (Integrin alpha-IIb/beta-3)ATIII (Antithrombin III)F2 (Thrombin)

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