This study is currently not recruiting participants.

A Prospective Multicenter Open-Label Study to Assess the Pharmacokinetics and Tolerability of Telavancin at Differing Dosing Regimens in Cystic Fibrosis Adults Admitted with Acute Pulmonary Exacerbations

  • STATUS
    Not Recruiting
Updated on 19 February 2024

Summary

The purpose of this study is to understand the pharmacokinetics of telavancin in adult CF patients in order to select the appropriate dosing regimen in the special population which might differ from dosing for pulmonary infections in non-CF patients.

Description

The purpose of this study is to understand the pharmacokinetics of telavancin in adult CF patients in order to select the appropriate dosing regimen in the special population which might differ from dosing for pulmonary infections in non-CF patients.

Details
Condition cystic fibrosis
Age 100years or below
Clinical Study IdentifierTX8203
Last Modified on19 February 2024

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