114
Participants
Start Date
November 18, 2020
Primary Completion Date
October 26, 2023
Study Completion Date
July 30, 2025
AK104+anlotinib
Subjects receive AK104 10mg/kg intravenously (IV) every 2-week cycle plus anlotinib on Day 1-14 of every 3-week cycle (Q3W) until progression.
AK104+anlotinib
Subjects receive AK104 15mg/kg intravenously (IV) every 3-week cycle plus anlotinib on Day 1-14 of every 3-week cycle (Q3W) until progression.
AK104+anlotinib
Subjects receive AK104 10mg/kg Q3W plus anlotinib 1-14days of every 3-week cycle until progression.
Hunan cancer hospital, Changsha
Lead Sponsor
Akeso
INDUSTRY