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RECRUITING
NCT06478693
PHASE1

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

Sponsor: Myeloid Therapeutics

View on ClinicalTrials.gov

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.

Official title: 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

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

70

Start Date

2024-07-01

Completion Date

2028-05-31

Last Updated

2025-12-18

Healthy Volunteers

No

Interventions

DRUG

MT-303

MT-303

DRUG

MT-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