Efficacy and Safety of Sorafenib in Previously Treated Advanced Hepatocellular Carcinoma: SOPT Study

PHASE2Enrolling by invitationINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

February 8, 2022

Primary Completion Date

October 31, 2024

Study Completion Date

December 31, 2025

Conditions
Advanced Hepatocellular Carcinoma
Interventions
DRUG

Sorafenib

Subjects will receive sorafenib 600mg orally daily. When dose reduction is necessary during the treatment of HCC, the sorafenib dose should be reduced to 400mg once daily. Escalation of sorafenib from a daily dose of 600mg to 800mg (400mg twice daily) is allowed if the subject who is tolerating the 600mg sorafenib dose level well. Treatment will continue until progression, unacceptable toxicity, withdrawal of consent, or study end, whichever occurs first.

Trial Locations (1)

Unknown

National Cancer Center, Korea, Seoul

All Listed Sponsors
lead

Bo Hyun Kim

OTHER_GOV