GCC19CART for Patients With Metastatic Colorectal Cancer

Program Status

Recruiting

Phase

Phase 1

Prior Immunotherapy Allowed

Yes

CRC-directed Trial

Yes

Drugs

GCC19CART

Tags

MSI-H/ MMRd, MSS/ MMRp

Comments

CAR-T cells therapy (GCC19CART) for CRC metastatic patients, with liver disease only who are not candidates for surgical resection.
Patients should have received standard of care chemotherapy.  Must have less than 5 liver lesions, with largest lesion less than 3 cm.

Location Location Status
United States
City of Hope Comprehensive Cancer Center
Duarte, California 91010
Recruiting
University of California San Francisco Medical Center
San Francisco, California 94143
Recruiting
University of Colorado Hospital - Anschutz Cancer Pavilion
Aurora, Colorado 80045
Recruiting
Dana-Farber Cancer Institute
Boston, Massachusetts 02215-5418
Recruiting
University of Michigan Comprehensive Cancer Center
Ann Arbor, Michigan 48109
Not yet recruiting
Baylor Scott & White Research Institute
Dallas, Texas 75204
Recruiting

Inclusion Criteria

Inclusion Criteria:

Adults > 18 years old
Clinical and histopathological diagnosis of metastatic colorectal cancer
Guanylate Cyclase (GCC) positive disease as determined by immunohistochemistry (IHC). Positivity on staining of archival tumor tissue is adequate.
Limited liver disease (less than 7 lesions with largest lesion less than 3 cm)
No surgical options with curative intent.
Received prior therapy with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy in the advanced or metastatic setting, an anti-vascular endothelial growth factor (anti-VEGF) biological therapy if not contraindicated, and if RAS wild-type an anti-epidermal growth factor receptor (anti-EGFR) therapy in a manner consistent with National Comprehensive Cancer Network (NCCN) guidelines. Treatment must have been discontinued for disease progression or intolerance to therapy.
Have at least one extracranial measurable target lesions according to the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 standard.

Exclusion Criteria

Exclusion Criteria:

Subjects with tumor lesion(s) in a location that may cause perforation of an organ or structure (such as the digestive track, urinary bladder, or blood vessel) with GCC19CART therapy.
No active infectious diseases or comorbid conditions that would interfere with safety or data quality.
Subjects with active infection requiring systemic therapy or causing fever (temperature > 38.1˚C) or subjects with unexplained fever (temperature > 38.1˚C) within 7 days prior to enrollment (leukapheresis) and reconfirmed prior to the day of investigational product administration.
Pregnant or breast-feeding women

Other protocol defined Inclusion/Exclusion criteria may apply

NCT ID

NCT05319314

Date Trial Added

2022-04-08

Updated Date

2023-06-05