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Grant: Proof of Principle Program - Phase II

Research Institute of the McGill University Health Centre

$299,934.00

An IGF-Trap for the treatment of breast cancer: consolidation of the pre-clinical profile and commercialization.

EF 2014-15

Résumé
We engineered a recombinant protein that can trap a growth factor (the insulin like growth factor, IGF-I) that is essential for the growth of breast cancer cells. When tested in an animal model of triple negative breast cancer, the IGF-Trap blocked tumor growth and metastasis. In the present application, we propose to further characterize the biological activities of the IGF-Trap, particularly its distribution in different organ sites and its ability to reduce the bioactivity of blood IGF-I in vivo. We also seek to identify which breast cancer subtypes are most sensitive to this candidate drug. Together the data should accelerate commercialization and the transition of the IGF-Trap into the clinic.
Programme
Proof of Principle Program - Phase II
Emplacement
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
325291
Name
Brodt Pnina
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
AmorChem (Montreal, QC)
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Proof of Principle
Projecttitle
An IGF-Trap for the treatment of breast cancer: consolidation of the pre-clinical profile and commercialization.
Programtype2
Operating Grants
Orgnameinp2
Research Institute of the McGill University Health Centre
Cihramount2
$299,934
Cihrequipment2
$0
Programname2
Proof of Principle Program - Phase II
Keyworddelim
Breast Cancer; Commercialization; Igf; Igf-Trap
Abstract
We engineered a recombinant protein that can trap a growth factor (the insulin like growth factor, IGF-I) that is essential for the growth of breast cancer cells. When tested in an animal model of triple negative breast cancer, the IGF-Trap blocked tumor growth and metastasis. In the present application, we propose to further characterize the biological activities of the IGF-Trap, particularly its distribution in different organ sites and its ability to reduce the bioactivity of blood IGF-I in vivo. We also seek to identify which breast cancer subtypes are most sensitive to this candidate drug. Together the data should accelerate commercialization and the transition of the IGF-Trap into the clinic.
Competitiondate
201502
Approvedterm2
1 yr 0 mth
Pinamesdelim
Brodt, Pnina
Approvedterm
1 an 0 mois
Cihrcontribution2
Knowledge Translation Branch~ $299,934~ $0~