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Pharmacotherapy. 2014 Sep;34(9):891-900. doi: 10.1002/phar.1458. Epub 2014 Jul 3.

Single- and multiple-dose pharmacokinetics and absolute bioavailability of tedizolid.

Author information

1
Cubist, San Diego, California.

Abstract

OBJECTIVES:

Tedizolid phosphate is a novel antibacterial under investigation for the treatment of gram-positive infections. This study was conducted to assess the pharmacokinetics, safety, and tolerability of intravenous tedizolid phosphate as well as the oral bioavailability of tedizolid phosphate.

DESIGN:

Double-blind, single-ascending dose, multiple-dose pharmacokinetics study, as well as tolerability and open-label crossover studies.

SETTING:

Single center in the United States (Covance Clinical Research Unit, Madison, WI) between September 2009 and January 2010.

PARTICIPANTS:

Ninety healthy volunteers.

INTERVENTION:

Single intravenous (IV) doses of tedizolid phosphate 50 mg (lead-in) and 100-400 mg. Single oral and IV dose of tedizolid phosphate 200 mg in crossover fashion. Multiple IV doses of tedizolid phosphate 200 and 300 mg for up to 7 days.

MEASUREMENTS AND MAIN RESULTS:

A dose-dependent increase was observed in the maximum plasma concentration (1.2-5.1 μg/ml) and the area under the concentration-time curve (17.4-58.7 μg × hr/ml) of tedizolid (the microbiologically active moiety of tedizolid phosphate) after single IV doses of tedizolid phosphate 100-400 mg. Administration of IV tedizolid phosphate 200 mg once/day for 7 days resulted in minimal (28%) tedizolid accumulation. The absolute oral bioavailability of tedizolid after a single 200-mg dose of tedizolid phosphate was 91%; pharmacokinetic parameters of tedizolid were similar with oral and IV administration. Treatment-related adverse events occurred in 41% of subjects. Most adverse events were related to infusion site and became more frequent with multiple dosing. In an additional 3-day tolerability study, IV tedizolid phosphate 200 mg and placebo were similarly tolerated, based on visual infusion phlebitis scores.

CONCLUSION:

These results from a population of healthy volunteers support once/day dosing of tedizolid phosphate 200 mg with both the oral and IV formulations, without the need for dose adjustment when switching administration routes.

TRIAL REGISTRATION:

ClinicalTrials.gov NCT00983255.

KEYWORDS:

intravenous; pharmacokinetics; tedizolid phosphate

PMID:
24989138
PMCID:
PMC4260119
DOI:
10.1002/phar.1458
[Indexed for MEDLINE]
Free PMC Article

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