Start Date
April 1, 2025
Primary Completion Date
December 31, 2025
Study Completion Date
December 31, 2025
UB-421
Subjects will receive 13 doses of the UB-421 by intravenous infusion at 25 mg/kg bi-weekly (Cohort 2, 26 weeks).
current standard HAART treatment
Subjects will receive current standard HAART treatment as the active control group.
Beijing Youan Hospital,Capital Medical University, Beijing
Lead Sponsor
United BioPharma
INDUSTRY