RecruitingPhase 1NCT06478693

A Study of MT-303 in Adults With Advanced or Metastatic GPC3-Expressing Cancers, Including HCC

A Phase 1, Open-Label, First-in-Human, Dose Escalation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of MT-303 in Adults With Advanced or Metastatic GPC3-Expressing Cancers, Including Hepatocellular Carcinoma


Sponsor

Myeloid Therapeutics

Enrollment

70 participants

Start Date

Jul 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This is a multicenter, open-label, Phase 1, first-in-human, dose-escalation study designed to assess the safety, tolerability and define the RP2D of MT-303 alone (Module 1) and in combination with Atezo/Bev (Module 2) in participants with advanced hepatocellular carcinoma expressing GPC3.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests MT-303, an experimental antibody therapy, in patients with advanced hepatocellular carcinoma (liver cancer) or other cancers that express a protein called GPC3, which is found on the surface of certain cancer cells. **You may be eligible if...** - You are 18 or older - You have confirmed advanced, recurrent, or metastatic liver cancer (HCC) or another GPC3-expressing cancer type - Your liver function is adequate (Child-Pugh Class A) - Your overall health is adequate (ECOG 0 or 1) **You may NOT be eligible if...** - You have active infection, including untreated hepatitis - Your cancer has spread to the brain or the membranes around it - You have had a liver transplant or are on the transplant waiting list - You have uncontrolled variceal bleeding 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

DRUGMT-303

MT-303

DRUGMT-303 +Atezolizumab + Bevacizumab

MT-303 in combination with Atezo/Bev


Locations(9)

St Vincent's Hospital

Sydney, New South Wales, Australia

Integrated Clinical Oncology Network (ICON) Pty Ltd

Woolloongabba, Queensland, Australia

The Alfred Hospital

Melbourne, Victoria, Australia

Linear Clinical Research

Murdoch, Western Australia, Australia

Pusan National Univesity Hospital

Busan, South Korea

Cha University Bundang Medical Center

Gyeonggi-do, South Korea

Seoul National University Hospital

Seoul, South Korea

National Taiwan University Hospital

Taipei, Taiwan

Taipei Tzu Chi Hospital

Taipei, Taiwan

View Full Details on ClinicalTrials.gov

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NCT06478693


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