GCC19CART for Patients With Metastatic Colorectal Cancer

Last updated: June 2, 2023
Sponsor: Innovative Cellular Therapeutics Inc.
Overall Status: Active - Recruiting

Phase

1

Condition

Colon Cancer; Rectal Cancer

Colon Cancer

Colorectal Cancer

Treatment

GCC19CART

Clinical Study ID

NCT05319314
ICT-GCC19CART-US-001
  • Ages > 18
  • All Genders

Study Summary

Study ICT-GCC19CART-US-001 (CARAPIA-1) is a Phase 1 study evaluating the safety, tolerability, clinical activity, pharmacokinetics and pharmacodynamics of GCC19CART in subjects with relapsed or refractory metastatic colorectal cancer.

Eligibility Criteria

Inclusion

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-basedchemotherapy in the advanced or metastatic setting, an anti-vascular endothelialgrowth factor (anti-VEGF) biological therapy if not contraindicated, and if RASwild-type an anti-epidermal growth factor receptor (anti-EGFR) therapy in a mannerconsistent with National Comprehensive Cancer Network (NCCN) guidelines. Treatmentmust have been discontinued for disease progression or intolerance to therapy.
  • Have at least one extracranial measurable target lesions according to the ResponseEvaluation Criteria in Solid Tumors (RECIST) 1.1 standard.

Exclusion

Exclusion Criteria:

  • Subjects with tumor lesion(s) in a location that may cause perforation of an organ orstructure (such as the digestive track, urinary bladder, or blood vessel) withGCC19CART therapy.
  • No active infectious diseases or comorbid conditions that would interfere with safetyor 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 ofinvestigational product administration.
  • Pregnant or breast-feeding women Other protocol defined Inclusion/Exclusion criteria may apply

Study Design

Total Participants: 30
Treatment Group(s): 1
Primary Treatment: GCC19CART
Phase: 1
Study Start date:
August 01, 2022
Estimated Completion Date:
October 31, 2024

Connect with a study center

  • City of Hope Comprehensive Cancer Center

    Duarte, California 91010
    United States

    Active - Recruiting

  • University of California San Francisco Medical Center

    San Francisco, California 94143
    United States

    Active - Recruiting

  • University of Colorado Hospital - Anschutz Cancer Pavilion

    Aurora, Colorado 80045
    United States

    Active - Recruiting

  • University of Florida

    Gainesville, Florida 32610
    United States

    Site Not Available

  • Dana-Farber Cancer Institute

    Boston, Massachusetts 02215-5418
    United States

    Active - Recruiting

  • University of Michigan Comprehensive Cancer Center

    Ann Arbor, Michigan 48109
    United States

    Site Not Available

  • Baylor Scott & White Research Institute

    Dallas, Texas 75204
    United States

    Active - Recruiting

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