35
Participants
Start Date
July 15, 2025
Primary Completion Date
March 1, 2027
Study Completion Date
September 1, 2027
QL1706 Plus Celecoxib Group
QL1706 (anti-PD-1/CTLA-4 bispecific antibody) will be administered at 5 mg/kg by intravenous infusion every 3 weeks. Celecoxib 200 mg will be taken orally twice daily starting on Day 1 of each 3-week treatment cycle. Treatment continues until disease progression, intolerable toxicity, or for a maximum of 2 years.
Peking University Cancer Hospital & Institute
OTHER