1,050
Participants
Start Date
May 9, 2025
Primary Completion Date
January 31, 2028
Study Completion Date
June 30, 2028
HS-20122(Phase 1a:Dose Escalation)
Intravenous (IV) administration of HS-20122 ; Participants will continue treatment until the end of the study in the absence of unacceptable toxicities and confirmed disease progression.
HS-20122(Phase 1b:Dose Expansion )
travenous (IV) administration of HS-20122 ; Participants will continue treatment until the end of the study in the absence of unacceptable toxicities and confirmed disease progression.
Hansoh BioMedical R&D Company
INDUSTRY