This is a prospective, open label, multi-center, interventional study to assess the safety and efficacy of Druvalumab plus Tremelimumab as first-line treatment in Chinese patients with unresectable hepatocellular carcinoma.
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≥Grade 3 Adverse Events and Adverse Events of Special Interest of Cohort 1
Timeframe: From the time of signature of informed consent, throughout the treatment period, and up to the follow-up period, assessed up to 29 months
AstraZeneca Clinical Study Information Center