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Clinical Trial Summary

A randomized, controlled, open-label, dose-exploration study to assess the effectiveness and safety of Lipovirtide combined with nucleoside drugs in HIV-infected patients who have not received antiviral treatment before.


Clinical Trial Description

multiple sites, randomized, open-label, controlled study design. 64 eligible subjects will be enrolled in this study, and they will be randomly assigned to each group in a 1:1:1:1 proportion, 16 subjects in each group. Each site will compete to enroll subjects. The 4 groups are as follows: Group A:Lipovirtide 10mg+3TC+TDF(LP-80:once a week;3TC+TDF:once daily); Group B:Lipovirtide 40mg+3TC+TDF(LP-80:once a week;3TC+TDF:once daily); Group C:Lipovirtide 60mg+3TC+TDF(LP-80:once every 2 weeks;3TC+TDF:once daily); Group D:DTG +3TC + TDF(once daily). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06061536
Study type Interventional
Source Shanxi Kangbao Biological Product Co., Ltd.
Contact Ping Ma, Doctor
Phone +8615922124490
Email mapingtianjin@163.com
Status Recruiting
Phase Phase 2
Start date November 2, 2023
Completion date October 30, 2024

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