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Clinical Trial Summary

This is a phase 2,open-label, multi-center study to evaluate the efficacy, safety, pharmacokinetics (PK) and immunogenicity of HS-20093 as a monotherapy in patients with small cell lung cancer(SCLC).


Clinical Trial Description

Intravenous (IV) administration of HS-20093 Q3W; Participants will continue treatment until the end of the study in the absence of unacceptable toxicities and disease progression. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06052423
Study type Interventional
Source Hansoh BioMedical R&D Company
Contact
Status Withdrawn
Phase Phase 2
Start date November 30, 2024
Completion date June 30, 2027