drugset / Trial / NCT06478693

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

NCT06478693

Phase 1 Recruiting 70 enrolled Myeloid Therapeutics CREATE Medicines · collab
Non-randomizedSequentialOpen-labelTreatment

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.

Timeline

Start
2024-07-01
Primary completion
2027-12-31
Completion
2028-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject MT-303 Unknown Intravenous
Background Atezolizumab Monoclonal antibody Intravenous
Background Bevacizumab Monoclonal antibody Intravenous