A Phase 1, First-in-human Study of Cabotamig (ARB202), Bispecific Antibody to CDH17 and CD3 in Advanced Gastrointestinal Malignancies

Arbele Pty Ltd3 sites in 2 countries33 target enrollmentStarted: May 30, 2022Last updated: March 19, 2026

Conditions

Interventions

Drugs

Trial Snapshot

Phase: Phase 1
Status: Completed
Sponsor: Arbele Pty Ltd
Enrollment: 33
Locations: 3
Primary Endpoint: Incidence and severity of adverse events

Study Overview Study Design Eligibility Criteria Arms & Interventions Outcomes Investigators Sites Records & Identifiers Similar Trials

Study Overview

Brief Summary

This study aims to find out:

The tolerability of Cabotamig (ARB202) in adults with advanced solid gastrointestinal tumors who failed the standard treatment. People can participate if their tumor has the CDH17 marker.
To find out how study drug is broken down in the body
To know the effects of the study drug on the tumor.

Study Design

Study Type: Interventional
Allocation: Non Randomized
Intervention Model: Sequential
Primary Purpose: Treatment
Masking: None

Eligibility Criteria

Ages: 18 Years to — (Adult, Older Adult)
Sex: All
Accepts Healthy Volunteers: No

Inclusion Criteria

•Histologically confirmed colorectal, pancreatic, gastric adenocarcinoma, primary liver cancer or metastatic liver disease, or cholangiocarcinoma that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective.
•Malignancies should possess with ≥10% expression of CDH17 confirmed by immunohistochemistry except for CRC patients. If the testing is based on fine-needle aspiration (FNA) biopsy, the patient will be considered eligible when tumor aspirate demonstrates detectable positive staining cells for CDH
•Eastern Cooperative Oncology Group (ECOG) performance status of ≤
•Life expectancy > 3 months.
•Measurable disease as defined by RECIST 1.1 criteria
•Blood coagulation parameters:
•PT INR ≤ 1.5X ULN
•PTT INR ≤1.2X ULN
•Patients must have adequate venous peripheral access for apheresis.
•Satisfactory organ and bone marrow function as defined by:
•absolute neutrophil count > 1,000/μL
•platelets >100,000/μL
•hemoglobin ≥9 g/dL
•serum ALT and AST ≤ 3X ULN or AST and ALT ≤5X ULN, if liver function abnormalities are thought to be from underlying malignancy
•total serum bilirubin ≤ 2X ULN
•Creatinine <1.5X ULN
•Stable amylase for 2 weeks

Exclusion Criteria

•Prior gene therapy or therapy with any murine monoclonal antibodies or any murine containing product.
•Concurrent treatment with any anticancer agent including chemotherapy, hormonal therapy or radiation therapy. Must be 5 X half-life or 6 weeks (whichever is shorter) post dosing of previous cancer therapies.
•History of allergy or hypersensitivity to murine proteins or study product excipients
•Females who are pregnant, trying to become pregnant, or breastfeeding.
•Diagnosis of HIV or chronic active viral hepatitis (HBV, HCV, HIV).
•Active infection requiring systemic treatment.
•Active brain, leptomeningeal, or paraspinal metastases, except for asymptomatic metastases and are stable on a steroid dose of ≤ 10mg/day of prednisone or its equivalent for at least 14 days prior to the start of study interventions.
•Impaired cardiac function (AHA NY Heart Association Grade II-IV) or clinically significant cardiac disease.
•Lack of recovery of prior CTCAE Grade 3 or above adverse events due to earlier therapies.
•Chronic use of corticosteroids in excess of >10mg daily of prednisone or equivalent within 4 weeks prior to alopecia.
•Concomitant use of complementary or alternative medication or therapy such as Chinese herbal medicine.
•History of Crohn's disease, inflammatory bowel disease, or ulcerative colitis within the past 5 years
•Abnormal bowel function which would make assessment of bowel permeability difficult to access
•Major trauma or major surgery within 4 weeks prior to first dose of study drug