A Study of BLYG8824A in Participants With Locally Advanced or Metastatic Colorectal Cancer

  • STATUS
    Recruiting
  • End date
    Jan 2, 2026
  • participants needed
    60
  • sponsor
    Genentech, Inc.
Updated on 19 February 2024
measurable disease
solid tumour
monoclonal antibodies
oxaliplatin
irinotecan
PCR test
combination therapy
fluoropyrimidine
metastatic colorectal cancer
antibody therapy
colorectal cancer
EGFR

Summary

This study will evaluate the safety, tolerability, and pharmacokinetics of BLYG8824A and will make a preliminary assessment of the anti-tumor activity of BLYG8824A in patients with locally advanced or metastatic colorectal cancer.

Details
Condition Colorectal Cancer, Colorectal Cancer, Rectal disorder
Age 18-100 years
Treatment BLYG8824A
Clinical Study IdentifierNCT04468607
SponsorGenentech, Inc.
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

ECOG performance status of 0 or 1
Life expectancy of at least 12 weeks
Histologically or cytologically documented invasive CRC: incurable, unresectable, locally advanced or metastatic CRC previously treated with multimodality therapy or mCRC
Locally advanced or metastatic CRC that has relapsed or is refractory to established therapies
Prior disease progression (or intolerance) following oxaliplatin, irinotecan, fluoropyrimidines, and anti-EGFR monoclonal antibodies
An archival tissue specimen or fresh baseline biopsy (when archival is not available) is required for enrollment into the study
Measurable disease, according to the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. Non-measurable evaluable disease is acceptable for dose-escalation
Adequate hematologic and end organ function
Acute, clinically significant treatment-related toxicity from prior therapy resolved to Grade 1 prior to study entry
Expansion Cohort-Specific Inclusion Criteria
MSS or MSI-L disease as determined by polymerase chain reaction (PCR) and/or IHC
Measurable disease by RECIST v1.1 with at least one measurable target lesion in the expansion cohort
Progression must have occurred during or after most recent treatment for locally advanced or metastatic colorectal cancer

Exclusion Criteria

Pregnant or breastfeeding, or intending to become pregnant during the study or within 4 months after the final dose of BLYG8824A
Significant cardiopulmonary dysfunction
Known clinically significant liver disease
Positive serologic or PCR test results for acute or chronic HBV infection
Acute or chronic HCV infection
HIV seropositivity
Poorly controlled Type 2 diabetes mellitus
Current treatment with medications that are well known to prolong the QT interval
Primary CNS malignancy, untreated CNS metastases, or active CNS metastases
Leptomeningeal disease
Spinal cord compression that has not been definitively treated with surgery and/or radiation
History of autoimmune disease
Prior allogeneic stem cell or solid organ transplantation
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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