Grant: Project Grant
University of Calgary
$2,796,075.00
A Phase I Feasibility and Safety Study of GCAR1, a Chimeric Antigen Receptor (CAR) T-cell Therapy for Patients with Relapsed/Refractory GPNMB-Expressing Solid Tumors
EF 2022-23
Résumé
CAR T-cell therapy is a promising new treatment that has been used successfully to treat and even cure refractory blood cancers. It involves taking functional T-cells from the patient, genetically modifying them to target the cancer cell, and then infusing them back into the patient to attack and clear the cancer by harnessing the patient's own immune system.
Scientists at the University of Calgary have been able to create a new CAR T-cell product that attacks different types of cancers in mouse models, including a rare type of sarcoma in adolescents and young adults, and other cancers such as breast and kidney cancers. We now want to take the next step to deliver this therapy directly to patients in a clinical trial.
The main goal of the proposed clinical trial is to deliver this CAR T therapy to patients, assess for safety (i.e. monitoring for complications related to treatment), and assess for anti-tumor activity. Ultimately, we hope that this treatment provides benefit for patients that receive this novel therapy. We are also going to be studying how these CAR T cells work, with additional research studies planned on samples obtained as part of this study.
There are a number of patients across Canada with tumors that express the same target for these CAR T cells. Our goal is to open this trial across multiple sites across Canada, providing a much needed therapy option for patients who would otherwise succumb to their disease. Through this work we will establish key collaborations, and if successful, this will lead to future projects with other novel CAR T products that we anticipate will be developed in the not-so-distant future.
We believe that CAR T therapy will continue to grow as a therapeutic option for patients with refractory malignancies and thus support for this in the early stages will result in significant impact to Canadians and others elsewhere in the future if proven successful.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
480122
Name
Shafey Mona
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Clinical
Prcname2
Cancer Biology & Therapeutics
Projecttitle
A Phase I Feasibility and Safety Study of GCAR1, a Chimeric Antigen Receptor (CAR) T-cell Therapy for Patients with Relapsed/Refractory GPNMB-Expressing Solid Tumors
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$2,796,075
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Alveolar Soft Part Sarcoma; Car T; Immunotherapy; Renal Cell Carcinoma; Sarcoma; Triple-Negative Breast Cancer
Abstract
CAR T-cell therapy is a promising new treatment that has been used successfully to treat and even cure refractory blood cancers. It involves taking functional T-cells from the patient, genetically modifying them to target the cancer cell, and then infusing them back into the patient to attack and clear the cancer by harnessing the patient's own immune system.
Scientists at the University of Calgary have been able to create a new CAR T-cell product that attacks different types of cancers in mouse models, including a rare type of sarcoma in adolescents and young adults, and other cancers such as breast and kidney cancers. We now want to take the next step to deliver this therapy directly to patients in a clinical trial.
The main goal of the proposed clinical trial is to deliver this CAR T therapy to patients, assess for safety (i.e. monitoring for complications related to treatment), and assess for anti-tumor activity. Ultimately, we hope that this treatment provides benefit for patients that receive this novel therapy. We are also going to be studying how these CAR T cells work, with additional research studies planned on samples obtained as part of this study.
There are a number of patients across Canada with tumors that express the same target for these CAR T cells. Our goal is to open this trial across multiple sites across Canada, providing a much needed therapy option for patients who would otherwise succumb to their disease. Through this work we will establish key collaborations, and if successful, this will lead to future projects with other novel CAR T products that we anticipate will be developed in the not-so-distant future.
We believe that CAR T therapy will continue to grow as a therapeutic option for patients with refractory malignancies and thus support for this in the early stages will result in significant impact to Canadians and others elsewhere in the future if proven successful.
Competitiondate
202303
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Shafey, Mona; Abdul Razak, Albiruni R; Hay, Kevin A; Henning, Jan-Willem; Kekre, Natasha; Mahoney, Douglas J; Morrissy, Sorana A; Noujaim, Jonathan; Simmons, Christine E
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $2,796,075~ $0~