Clinical Trial

A Single-Arm, Multicenter, Exploratory Clinical Study of TACE Combined With Iparomlimab and Tuvonralimab Injection (QL1706) and Lenvatinib for Perioperative Treatment of Resectable Hepatocellular Carcinoma

Not Yet Recruiting Phase 2
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Summary
This is a single-arm, multicenter, exploratory clinical study evaluating the efficacy and safety of TACE combined with Iparomlimab and Tuvonralimab Injection (QL1706) and lenvatinib for perioperative treatment of resectable HCC (CNLC IIb-IIIa excluding Vp3/Vp4 or CNLC Ib-IIa with high-risk recurrence factors). Eligible subjects providing written informed consent will receive study treatment. The primary endpoint is MPR rate.
Trial Details
NCT Number NCT07131501
Lead Sponsor The First Affiliated Hospital with Nanjing Medical University
Conditions Hepatocellular Carcinoma, Immunotherapy, Preoperative, PD-1, CTLA-4
Enrollment 48 participants
Start Date 2025-08-11
Primary Completion 2026-09-30 (estimated)
Study Completion 2029-08-31 (estimated)
Updated on ClinicalTrials.gov 2025-08-20