A Study of Anti-PD-1/CTLA-4 Bispecific AK104 Plus Lenvatinib in First-line Advanced Hepatocellular Carcinoma

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

59

Participants

Timeline

Start Date

July 7, 2020

Primary Completion Date

November 20, 2023

Study Completion Date

November 20, 2023

Conditions
Hepatocellular Carcinoma
Interventions
BIOLOGICAL

AK104

Subjects will receive AK104 and lenvatinib until disease progression or for a maximum of 24 months

DRUG

Lenvatinib

Subjects will receive AK104 and lenvatinib until disease progression for a maximum of 24 months

Trial Locations (1)

Unknown

Chinese PLA General Hospital, Beijing

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Akeso Pharmaceuticals, Inc.

OTHER

lead

Akeso

INDUSTRY