148
Participants
Start Date
October 20, 2021
Primary Completion Date
December 31, 2023
Study Completion Date
December 31, 2023
GFH018
Subjects are planned to be dosed in oral GFH018 tablets twice daily for a continuous 14 days in a 28 days cycle (7days on 7days off may be tested based on available data from phase I dose escalation study of single agent). the starting dose of GFH018 will be derived from the maximum safe dose explored in rom phase I dose escalation study of single agent.
Toripalimab
Subjects are planned to be dosed at 3 mg/kg Toripalimab as an intravenous infusion once every 2 weeks.
Linear Clinical Research Ltd, Perth
Sun Yat-sen university cancer center, Guangzhou
Shang hai east hospital, Shanghai
Genfleet Therapeutics (Shanghai) Inc.
INDUSTRY