RecruitingPhase 1NCT05411133

Treatment of Cabotamig (ARB202) in Advanced Gastrointestinal Cancer Patients

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


Sponsor

Arbele Pty Ltd

Enrollment

68 participants

Start Date

May 30, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to find out: 1. 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. 2. To find out how study drug is broken down in the body 3. To know the effects of the study drug on the tumor.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new drug called cabotamig (ARB202) for people with advanced gastrointestinal cancers including colorectal, pancreatic, gastric, liver, or bile duct cancers. The drug targets a protein called CDH17, which is found on many gastrointestinal cancer cells. **You may be eligible if...** - You have been diagnosed with colorectal, pancreatic, gastric, primary liver, or bile duct cancer (cholangiocarcinoma) that has spread or cannot be removed - Standard treatments have failed or no longer work - Your tumor has been tested and expresses the CDH17 protein (except for colorectal cancer patients who may not need this test) **You may NOT be eligible if...** - Your tumor does not express CDH17 (for most cancer types) - You have not tried standard treatments first - You have serious organ dysfunction or other conditions that make the treatment unsafe Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGCabotamig (ARB202)

Cabotamig (ARB202), Atezolizumab


Locations(3)

Southern Oncology Clinical Research Unit

Adelaide, Australia

St George Private Hospital

Sydney, Australia

Queen Mary Hospital

Hong Kong, Hong Kong

View Full Details on ClinicalTrials.gov

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NCT05411133


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