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A Study to Evaluate of PM8002 Combined With PM1009 in Patients With First-line HCC
Sponsor: Biotheus Inc.
Summary
This study to evaluate the preliminary efficacy, safety and pharmacokinetics of PM8002 combined with PM1009 in Patients with first-line Hepatocellular Carcinoma.
Official title: A Phase Ib/II Clinical Trial to Evaluate the Preliminary Efficacy, Safety and Pharmacokinetics of PM8002 Injection Combined With PM1009 Injection in Patients With Locally Advanced or Metastatic Hepatocellular Carcinoma
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
140
Start Date
2024-12
Completion Date
2027-12
Last Updated
2024-12-16
Healthy Volunteers
No
Conditions
Interventions
PM8002
PM8002 via IV infusion, Q3W
PM1009
PM8002 via IV infusion, Q3W
atezolizumab
atezolizumab,1200mg, via IV infusion, Q3W
bevacizumab
bevacizumab,15mg/kg, via IV infusion, Q3W