59
Participants
Start Date
June 14, 2025
Primary Completion Date
April 30, 2026
Study Completion Date
April 30, 2029
QL1706
Eligible participants will receive QL1706 at 5.0 mg/kg intravenously every 3 weeks, lenvatinib at 8 mg orally once daily every 3 weeks, oxaliplatin at 85 mg/m², and gemcitabine at 1000 mg/m² (on days 1 and 8 of each cycle) for up to 8 cycles. Then, they will continue with QL1706 and lenvatinib until clinical progression, imaging progression per RECIST 1.1, unacceptable toxicity, withdrawal of consent, or other discontinuation criteria are met.
RECRUITING
the Third Affiliated Hospital of Naval Medical University, Shanghai
Eastern Hepatobiliary Surgery Hospital
OTHER