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Study to Evaluate Pharmacokinetic and Safety of Albuvirtide Between Intravenous Drip and Intravenous Injection

HIV/AIDS Clinical Trial

Official title:
Study to Evaluate Pharmacokinetic and Safety of Albuvirtide Between Intravenous Drip and Intravenous Injection

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, B and 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 min or by iv bolus for 0.5 min or 3 min, respectively. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05206019
Study type Interventional
Source Frontier Biotechnologies Inc.
Contact
Status Completed
Phase Phase 1
Start date February 16, 2022
Completion date May 2, 2022
View Details
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