To Investigate the Efficacy and Safety of UB-421 Monotherapy in HIV-1 Infected Adults

PHASE3WithdrawnINTERVENTIONAL
0
Timeline

Start Date

April 1, 2025

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2025

Conditions
HIV-1 Infection
Interventions
DRUG

UB-421

Subjects will receive 13 doses of the UB-421 by intravenous infusion at 25 mg/kg bi-weekly (Cohort 2, 26 weeks).

DRUG

current standard HAART treatment

Subjects will receive current standard HAART treatment as the active control group.

Trial Locations (1)

100069

Beijing Youan Hospital,Capital Medical University, Beijing

Sponsors

Lead Sponsor

All Listed Sponsors
lead

United BioPharma

INDUSTRY