SBIR-STTR Award

Fluorogenic Assays for Factor Vlla and Tissue Factor
Award last edited on: 11/27/06

Sponsored Program
SBIR
Awarding Agency
NIH : NHLBI
Total Award Amount
$403,108
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Richard Jenny

Company Information

Haematologic Technologies Inc (AKA: Haematologic Technologies LLC)

57 River Road Unit 1021
Essex Junction, VT 05452
   (802) 878-1777
   hti@haemtech.com
   www.haemtech.com
Location: Single
Congr. District: 00
County: Chittenden

Phase I

Contract Number: 1R43HL073532-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2003
Phase I Amount
$74,217
Factor Vlla and Tissue Factor (TF) are essential proteins for the initiation of blood coagulation. Blood coagulation is initiated when cryptic TF becomes exposed on the surface of vascular cells where it can bind circulating factor Vlla. The factor Vlla/TF complex catalyzes the activation of certain blood zymogens that propagate the coagulation event. The amount of circulating factor Vlla has been shown to be a good indicator of hemostatic potential and for this reason is a potential risk indicator for the development of cardiovascular disease. In addition, over the past decade recombinant factor Vlla has become the drug of choice for treating hemophilia A and B patients who have developed inhibitors to factors VIII and IX respectively. Formation of the factor Vlla/TF complex is also the basis of specific coagulation assays. The Prothrombin time (PT assay) utilizes either natural or synthetic thromboplastin reagents to initiate coagulation in-vitro. Thus in addition to its in-vivo role, TF also has in-vitro applications. Furthermore, TF is not only present in the vasculature, but also in a numerous other tissues and cells including brain, lung, placenta, platelets, monocytes and tumor cells. In addition to its "normal" role in hemostasis, it is also known to be involved in the metastasis of tumor cells. The fact that TF and factor Vlla play such important roles both in-vivo and in-vitro, indicates that rapid and direct assays for these proteins could be of great utility. At the present time, reliable assays for factor Vlla and tissue factor that can be applied to simple as well as complex biological systems do not exist. The goal of this phase I proposal is to demonstrate the feasibility of developing fluorogenic-based assays that may be used to directly measure factor Vlla and TF in simple and complex biological systems. To accomplish this goal, the following specific aims are proposed: 1) To utilize aminonapthalene-based fluorogenic substrates for factor Vlla to develop basic assays that may be used to quantitate factor Vlla and TF in simple and well defined systems; b) to further develop the assay for tissue factor and demonstrate the ability to measure TF in more complex biological systems; and c) to further develop the assay for factor Vlla and demonstrate the ability to measure factor Vlla in more complex biological systems.

Thesaurus Terms:
blood coagulation test, coagulation factor VII, technology /technique development, thromboplastin blood coagulation, clotting factor, hemostasis, phosphatidylcholine, phosphatidylserine, plasma, thrombosis high throughput technology

Phase II

Contract Number: 2R44HL073532-02
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2005
(last award dollars: 2006)
Phase II Amount
$328,891

Factor VIla and tissue factor (TF) are essential proteins for the initiation of blood coagulation. Blood coagulation is initiated when cryptic TF becomes exposed on the surface of vascular cells where it can bind circulating factor VIla. The factor Vlla/TF complex catalyzes the activation of certain blood zymogens that propagate the coagulation event. The amount of circulating factor VIla has been shown to be a good indicator of hemostatic potential, and for this reason is a potential risk factor indicator for the development of cardiovascular disease. In addition, over the past decade recombinant factor VIla has become the drug of choice for treating hemophilia A and B patients who have developed inhibitors to factors VIII and IX respectively. Formation of the factor Vlla/TF complex is also the basis of specific coagulation assays. The prothrombin time (PT assay) utilizes either natural or synthetic thromboplastin reagents to initiate coagulation in-vitro. Thus in addition to its in-vivo role, TF also has in-vitro applications. Furthermore, TF is not only present in the vasculature, but also in numerous other tissues and cells including brain, lung, placenta, monocytes and tumor cells. In addition to its "normal" role in hemostasis, it is also known to be involved in the metastasis of tumor cells. The fact that factor VIla and TF play such important roles both in vivo and in vitro, indicates that rapid and direct assays for these proteins could be of great utility. At the present time, reliable assays for factor VIla and TF that can be applied to simple and well as complex biological samples do not exist. During the Phase-l project period we demonstrated the feasibility of developing sensitive fluorogenic assays that can directly measure functional factor VIla and TF in simple and complex biological systems. Phase-ll funding will be used to support the further development, refinement, optimization, validation and field-testing of these assays. It is anticipated that by the end of the Phase-ll project period these assays will be ready to market for research and pre-clinical applications