50
Participants
Start Date
February 8, 2022
Primary Completion Date
October 31, 2024
Study Completion Date
December 31, 2025
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.
National Cancer Center, Korea, Seoul
Bo Hyun Kim
OTHER_GOV