Optimizing human apyrase to treat arterial thrombosis and limit reperfusion injury without increasing bleeding risk

Author:

Moeckel Douglas1,Jeong Soon Soeg2,Sun Xiaofeng3,Broekman M. Johan45,Nguyen Annie1,Drosopoulos Joan H. F.45,Marcus Aaron J.45,Robson Simon C.3,Chen Ridong2,Abendschein Dana1

Affiliation:

1. Center for Cardiovascular Research, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.

2. APT Therapeutics Inc., 4041 Forest Park Avenue, St. Louis, MO 63108, USA.

3. Division of Gastroenterology/Hepatology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA.

4. Thrombosis Research Laboratory, Research Service, Veterans Affairs New York Harbor Healthcare System, New York, NY 10010, USA.

5. Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY 10021, USA.

Abstract

APT102, an optimized human apyrase designed for treatment of myocardial infarction, improves recanalization of occluded arteries and decreases heart muscle damage, without an increased bleeding risk.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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