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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04404049
Study type Interventional
Source UBP Greater China (Shanghai) Co., Ltd
Contact
Status Not yet recruiting
Phase Phase 2
Start date December 1, 2023
Completion date June 30, 2025

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