Drug intelligence / Profile preview

AZD3366

Development stage
Phase 1
Lead developer
AstraZeneca
Modality
Small Molecules, Recombinant Proteins and Enzymes
Administration
Intravenous
01

Overview

AZD3366 (also known as APT102) is a long-acting, engineered recombinant protein based on an optimized CD39L3 human apyrase. Developed using recombinant DNA technology in Chinese hamster ovary cells, it acts by hydrolyzing extracellular ATP and ADP to AMP, which is then converted to adenosine by endogenous CD73. This mechanism leads to inhibition of inflammation and thrombosis through broad attenuation of platelet activation at multiple P2 receptors (P2X1, P2Y1, P2Y12), providing more complete inhibition than current P2Y12 inhibitors like ticagrelor or clopidogrel. Preclinical studies have shown that AZD3366 reduces platelet aggregation and provides tissue protection in models of cardiovascular disease by limiting myocardial injury and reducing infarct size. It also demonstrates anti-inflammatory effects and may preserve vascular integrity with a lower risk of bleeding compared to standard antiplatelet therapies. The drug is being developed primarily for cardiovascular indications such as prevention of thrombosis and reduction of myocardial infarct size[1][3][5][7].

Brand names
Luminase
Other names
CD39L3 human apyrase (optimized recombinant form)
02

Targets

P2RX1 (Purinergic receptor P2X 1)P2RY1 (Purinergic Receptor P2Y1)P2Y (P2Y receptors)ENTPD3 (Ectonucleoside triphosphate diphosphohydrolase 3)

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