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A Phase II Clinical Study to Evaluate HLX43 in Patients With Locally Advanced or Metastatic HCC Failed or Intolerance to Standard Therapy

StatusRecruiting
PhasePhase 2
Started2025-03-03
View on ClinicalTrials.gov ↗

Amendment history

2025-03-05
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Start dateestimated 2025-02-15→confirmed 2025-03-03
Study sites0→1
2024-12-16
minor
Original filing
The study is being conducted to to explore the reasonable dosage and evaluate the efficacy, safety and tolerability of HLX43 (Anti-PD-L1 ADC) in Patients with Locally Advanced or Metastatic Hepatocellular Carcinoma (HCC) Failed or Intolerance to Standard Therapy
Trial Details
NCT Number NCT06742892
Lead Sponsor Shanghai Henlius Biotech
Conditions Carcinoma, Hepatocellular
Enrollment 90 participants
Start Date 2025-03-03
Primary Completion 2026-10-31 (estimated)
Study Completion 2027-06-05 (estimated)
Updated on ClinicalTrials.gov 2025-03-10