Grant: Project Grant
McGill University
$688,501.00
Small-Molecule Inducers of Toxin B Cleavage as a Therapeutic Approach Against Clostridioides difficile Infection
FY 2019-20
Summary
Clostridioides difficile (or C. diff) is a bacterium that causes life-threatening intestinal infections and diarrhea. It is the most common healthcare-associated infection, and one of the 5 pathogens considered an urgent threat by the U.S. Center for Disease Control and Prevention. Current antibiotic treatments for C. diff are plagued by high rates of disease relapse, creating a need for new treatment strategies. The bacterium produces and releases toxins in the digestive tract which are the primary cause of disease and exciting targets for a new therapy. At present there are no small molecule drugs that target the toxins, on the market or in clinical trial. We propose to develop innovative solutions to inactivate the toxins released by C. diff before they provoke disease. This strategy could provide much needed alternatives to antibiotics for the treatment of C. diff infection.
Department
Program
Project Grant
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
420606
Name
Castagner Bastien
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Pharmaceutical Sciences
Projecttitle
Small-Molecule Inducers of Toxin B Cleavage as a Therapeutic Approach Against Clostridioides difficile Infection
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$688,501
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Anti-Virulence Approach; Antibacterial; C. Difficile Infection; Clostridioides Difficile; Drug Design; Inositol Phosphate; Nosocomial Infection; Resistant Pathogen; Structural Biology
Abstract
Clostridioides difficile (or C. diff) is a bacterium that causes life-threatening intestinal infections and diarrhea. It is the most common healthcare-associated infection, and one of the 5 pathogens considered an urgent threat by the U.S. Center for Disease Control and Prevention. Current antibiotic treatments for C. diff are plagued by high rates of disease relapse, creating a need for new treatment strategies. The bacterium produces and releases toxins in the digestive tract which are the primary cause of disease and exciting targets for a new therapy. At present there are no small molecule drugs that target the toxins, on the market or in clinical trial. We propose to develop innovative solutions to inactivate the toxins released by C. diff before they provoke disease. This strategy could provide much needed alternatives to antibiotics for the treatment of C. diff infection.
Competitiondate
202003
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Castagner, Bastien
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $688,501~ $0~