RecruitingPhase 1NCT07160335

A Phase I Clinical Study to Evaluate the PK Profile, Efficacy, Safety and Immunogenicity of HLX17 vs. Keytruda® in Multiple Resected Solid Tumors

Studying Small cell lung cancer

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Shanghai Henlius Biotech
Intervention
HLX17(drug)
Enrollment
174 enrolled
Eligibility
18-70 years · All sexes
Timeline
20252028

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 NCT07160335 on ClinicalTrials.gov

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