RecruitingNot applicableNCT07243691

Study on the Therapeutic Effect of Different Infusion Times of Tislelizumab on Postoperative High-risk Hepatocellular Carcinoma

Studying Adult hepatocellular carcinoma

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Key facts

Sponsor
Sir Run Run Shaw Hospital
Intervention
Tislelizumab: 200mg, intravenous infusion, Q3W(drug)
Enrollment
33 enrolled
Eligibility
18 years · All sexes
Timeline
20252027

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07243691 on ClinicalTrials.gov

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