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A Study of MT-303 in Adults With Advanced or Metastatic GPC3-Expressing Cancers, Including HCC
Sponsor: Myeloid Therapeutics
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
Conditions
Interventions
MT-303
MT-303
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