RecruitingPhase 1NCT07176650

Phase I Clinical Study To Evaluate Pharmacokinetic Profile, Safety, Efficacy and Immunogenicity Of Ipilimumab Biosimilar HLX13 Vs. YERVOY® (US-Sourced YERVOY®) As A First-Line Treatment For Patients With Unresectable Hepatocellular Carcinoma

Studying Adult hepatocellular carcinoma

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Shanghai Henlius Biotech
Intervention
HLX13(drug)
Enrollment
246 enrolled
Eligibility
18-65 years · All sexes
Timeline
20252026

Study locations (30)

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 NCT07176650 on ClinicalTrials.gov

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