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

Inclusion Criteria6

  • Aged 18 years or older
  • Histological diagnosis of advanced/recurrent or metastatic and/or unresectable HCC. \[Note: participants with other tumor types expressing GPC3 may be eligible for Module 1 pending a discussion with the Medical Monitor. Only participants with HCC are eligible for Module 2.
  • Measurable lesion per RECIST 1.1 criteria
  • Eastern Cooperative Oncology Group (ECOG) performance status grade of 0 or 1
  • Child-Pugh score: Class A
  • Adequate organ function

Exclusion Criteria12

  • Known active CNS metastasis and/or carcinomatous meningitis.
  • Any acute illness including active infection
  • History of liver transplantation or on waiting list
  • Participants with untreated or incompletely treated varices with bleeding or high risk for bleeding
  • Uncontrolled pleural effusion, pericardial effusion, or ascites
  • History of symptomatic congestive heart failure
  • History of chronic or recurrent (within the last year) severe autoimmune or immune mediated disease requiring steroids or other immune-suppressive treatments.
  • Known fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma and HCC.
  • Significant cardiovascular disease
  • History of severe hypersensitivity to atezolizumab and/or bevacizumab.
  • History of idiopathic pulmonary fibrosis
  • Prior history of hypertensive crisis or hypertensive encephalopathy.

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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