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Clinical Trial Summary

This is a single-center,randomized,open, single-dose, parallel-design study, which will be only enrolled Chinese healthy volunteers.


Clinical Trial Description

30 Chinese volunteers will be enrolled to assess the pharmacokinetic and safety of Albuvirtide in two different Administration methods. All subjects are required to collect PK blood samples before and after administration. 30 healthy subjects will be randomized into three cohorts ( cohorts A, Band C) in 1:1:1 ratio, with 10 subjects in each cohort.The subjects will receive a single dose of 320 mg of albuvirtide by iv infusion for 45 mins or by iv bolus for 0.5 min or 3 mins, respectively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05206019
Study type Interventional
Source Frontier Biotechnologies Inc.
Contact Tianning Gao, MM
Phone (+86)025-69648387
Email [email protected]
Status Not yet recruiting
Phase Phase 1
Start date February 1, 2022
Completion date July 15, 2022

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