63
Participants
Start Date
August 31, 2025
Primary Completion Date
December 31, 2027
Study Completion Date
December 31, 2028
HS-20093
Intravenous (IV) administration of HS-20093 Q3W; Participants will continue treatment until the end of the study in the absence of unacceptable toxicities and confirmed disease progression.
HRS-5041
HRS-5041 was given oral administration, QD, at a 21-day cycle.
Hansoh BioMedical R&D Company
INDUSTRY