This is a Phase II, randomized, open-label, multi-center, active-controlled study to assess the safety, tolerability, and efficacy of UB-421 administered as an add-on to the standard ART in ART-treated HIV-1 subjects with stably suppressed HIV-1 plasma VL. The study will be conducted at multiple study centers, designated AIDS hospitals in China.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
39
Monoclonal antibody by IV infusion plus standard ART
Monoclonal antibody by IV infusion plus standard ART
treatment related TEAEs
the incidence of Grade 3 drug-related treatment-emergent adverse events
Time frame: 48Weeks
the change of immune profiles
Change in Treg percentage in the peripheral blood
Time frame: 16Weeks
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