This study assess the safety, tolerability, and efficacy in reducing viral load and proviral DNA of UB-421 administered as an add-on to the ART in ART-experienced viremic HIV-1 subjects.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Monoclonal antibody by IV infusion plus standard ART
Standard ART
treatment related TEAEs
the incidence of Grade 3 drug-related treatment-emergent adverse events
Time frame: 16 Weeks
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