The primary objective of this study is to test the hypothesis that once-daily infusions of LY333328 provide clinically successful treatment equivalent to that of Vancomycin in patients hospitalized on the Surgical Service with complicated gram-positive bacterial skin infections. The secondary objectives of this study are to: compare the safety parameters among the treatment regimens; characterize population pharmacokinetics of the study drug in patients, and to explore potential factors that may influence variability of pharmacokinetics; and to explore the association of pharmacokinetic variables with efficacy and safety parameters. The GCRC nursing staff obtain and process the samples for the pharmacokinetic study when the investigator's team not available.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000083-38
Application #
6415087
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1974-10-01
Project End
2002-11-30
Budget Start
Budget End
Support Year
38
Fiscal Year
2000
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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