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Evaluate the Pharmacokinetics and Safety of EXPAREL® Following Subcutaneous Administration in Healthy Chinese Subjects

Healthy Subjects Clinical Trial

Official title:
A Phase 1, Open Label Study to Evaluate the Pharmacokinetics and Safety of EXPAREL® Following Subcutaneous Administration in Healthy Chinese Subjects

Clinical Trial Summary

This is a single-center, open-label, single-dose study to evaluate the safety, pharmacokinetics in healthy subjects

Clinical Trial Description

This is a phase I, open-label, single-dose in healthy subjects conducted at single center.The objectives are to evaluate the metabolic and safety profile of EXPAREL®. Each volunteer will receive one dose of the investigational drug via subcutaneous injection at multiple points during the study period. Study duration is around 54 days, including screening, confinement, ambulatory visit and a phone follow up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04158102
Study type Interventional
Source Nuance Pharma (shanghai) Co., Ltd
Contact
Status Completed
Phase Phase 1
Start date November 7, 2019
Completion date December 26, 2019
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