Grant: Proof of Principle Program Phase I - Drug Development
University of Alberta
$150,000.00
Novel Inhibitors of Viral Infectivity
FY 2009-10
Summary
We have discovered novel inhibitors of viral infection, which have potential uses as therapeutic or prophylactic drugs against a variety of human pathogenic viruses. These novel drugs act on novel targets through also novel mechanisms. We have identified HCV as a priority target. There is only one treatment clinically approved for HCV, which has major side effects and is only 50% effective against the most predominant HCV genotype in North America, genotype 1. We have solid in vitro evidence of activity of our lead compound against HCV and preliminary evidence of activity in animal models of HCV infection. We have solid evidence of minimal, if any, toxicity in animal models. We will now fully characterize the clinical potential of these drugs by performing extensive efficacy and toxicity studies.
Department
Program
Proof of Principle Program Phase I - Drug Development
Recipient
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
188107
Name
Schang Luis M
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Proof of Principle
Projecttitle
Novel Inhibitors of Viral Infectivity
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
Proof of Principle Program Phase I - Drug Development
Keyworddelim
Antiviral; Enveloped; Fusion Inhibitors; Hcv; Potency; Pre-Clinical Testing; Virus
Abstract
We have discovered novel inhibitors of viral infection, which have potential uses as therapeutic or prophylactic drugs against a variety of human pathogenic viruses. These novel drugs act on novel targets through also novel mechanisms. We have identified HCV as a priority target. There is only one treatment clinically approved for HCV, which has major side effects and is only 50% effective against the most predominant HCV genotype in North America, genotype 1. We have solid in vitro evidence of activity of our lead compound against HCV and preliminary evidence of activity in animal models of HCV infection. We have solid evidence of minimal, if any, toxicity in animal models. We will now fully characterize the clinical potential of these drugs by performing extensive efficacy and toxicity studies.
Competitiondate
200904
Approvedterm2
1 yr 0 mth
Pinamesdelim
Schang, Luis M
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $150,000~ $0~