Grant: Project Grant
McGill University
$902,700.00
Inositol Phosphates Analogs to Disarm the Intestinal Pathogen Clostridioides difficile
EF 2024-25
Résumé
Clostridioides difficile (or C. diff) is a bacterium that causes life-threatening intestinal infections and diarrhea. It is a common healthcare-associated infection, and one of the five 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 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 trials. 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.
Programme
Project Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
524165
Name
Castagner Bastien
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Pharmaceutical Sciences
Projecttitle
Inositol Phosphates Analogs to Disarm the Intestinal Pathogen Clostridioides difficile
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$902,700
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Anti-Virulence Approach; Antibacterial; Bacterial Toxin; C. Difficile Infection; Clostridioides Difficile; Drug Design; Inositol Phosphate; Structural Biology
Abstract
Clostridioides difficile (or C. diff) is a bacterium that causes life-threatening intestinal infections and diarrhea. It is a common healthcare-associated infection, and one of the five 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 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 trials. 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
202503
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Castagner, Bastien
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $902,700~ $0~