Overview

A Study to Evaluate of PM8002 Combined With PM1009 in Patients With First-line HCC

Status:
NOT_YET_RECRUITING
Trial end date:
2027-12-01
Target enrollment:
Participant gender:
Summary
This study to evaluate the preliminary efficacy, safety and pharmacokinetics of PM8002 combined with PM1009 in Patients with first-line Hepatocellular Carcinoma.
Phase:
PHASE1
Details
Lead Sponsor:
Biotheus Inc.
Treatments:
atezolizumab
Bevacizumab