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Grant: Travel Awards - Institute Community Support

Direct Payment

$600.00

Development of a mutant human coagulation protein as a novel antidote for new direct factor Xa anticoagulant drugs, and as a tool for investigating the activity and regulation of intrinsic and extrinsic tenase, key enzyme complexes in blood coagulation.

EF 2012-13

Résumé
Heart attacks and strokes, the number one cause of death and disability in Canada, are often caused by defective blood clotting in the human body. This research project aims to translate discoveries made on the scientific bench to the bedside by figuring out the way blood clots are controlled in the body in order to develop a way to counteract the clotting system. In the past several years, numerous new anti-clotting drugs have entered the market worldwide for the treatment of strokes that target the blood clotting system. Unfortunately, given the biological nature of these new agents, readily accessible and effective antidotes and unavailable. This creates a major barrier to the widespread use of these easy to administer lifesaving drugs because for some patients, these drugs can cause life-threatening bleeding. These at-risk patients would need an antidote to quickly reverse their anticoagulation. Our laboratory has engineered a new molecule for which we have pilot data on a novel way to use this molecule to measure the action of the critical parts of the blood clotting system called tenase and prothrombinase. Because this part of the system is also the target for these new drugs, a clearer understanding of how they work aid in the development of an effective antidote for the new anti-clotting agents. Because our molecule also directly targets the tenase and prothrombinase systems, this new molecule or versions of it also has the potential to become a new anti-clotting therapy for the treatment of heart attacks and stroke.
Programme
Travel Awards - Institute Community Support
Bénéficiaire
Emplacement
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
278235
Name
Yeh Calvin H
Region
Ontario
Country
Canada
Orgtype
Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Institute of Circulatory and Respiratory Health
Projecttitle
Development of a mutant human coagulation protein as a novel antidote for new direct factor Xa anticoagulant drugs, and as a tool for investigating the activity and regulation of intrinsic and extrinsic tenase, key enzyme complexes in blood coagulation.
Programtype2
Undefined
Orgnameinp2
Direct Payment
Cihramount2
$600
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Anticoagulation; Antithrombin; Coagulation; Enzyme Kinetics; Factor Xa; Fondaparinux; Hemophilia; Heparin; Ics Travel Awards; Thrombin
Abstract
Heart attacks and strokes, the number one cause of death and disability in Canada, are often caused by defective blood clotting in the human body. This research project aims to translate discoveries made on the scientific bench to the bedside by figuring out the way blood clots are controlled in the body in order to develop a way to counteract the clotting system. In the past several years, numerous new anti-clotting drugs have entered the market worldwide for the treatment of strokes that target the blood clotting system. Unfortunately, given the biological nature of these new agents, readily accessible and effective antidotes and unavailable. This creates a major barrier to the widespread use of these easy to administer lifesaving drugs because for some patients, these drugs can cause life-threatening bleeding. These at-risk patients would need an antidote to quickly reverse their anticoagulation. Our laboratory has engineered a new molecule for which we have pilot data on a novel way to use this molecule to measure the action of the critical parts of the blood clotting system called tenase and prothrombinase. Because this part of the system is also the target for these new drugs, a clearer understanding of how they work aid in the development of an effective antidote for the new anti-clotting agents. Because our molecule also directly targets the tenase and prothrombinase systems, this new molecule or versions of it also has the potential to become a new anti-clotting therapy for the treatment of heart attacks and stroke.
Competitiondate
201301
Approvedterm2
0 yr 3 mths
Pinamesdelim
Yeh, Calvin H
Approvedterm
0 an 3 mois
Cihrcontribution2
Inst of Circ &Respiratory Hlth~ $600~ $0~