406
Participants
Start Date
September 30, 2024
Primary Completion Date
November 30, 2027
Study Completion Date
January 31, 2029
HS-20093
Subjects in experimental arm will be given HS-20093 intravenously at a dose of 8.0 mg/kg every 3 weeks, until disease progression or until other criteria for treatment discontinuation are met.
Hansoh BioMedical R&D Company
INDUSTRY