Oritavancin Versus IV Vancomycin for the Treatment of Participants With Acute Bacterial Skin and Skin Structure Infection (SOLO I)

PHASE3CompletedINTERVENTIONAL
Enrollment

968

Participants

Timeline

Start Date

December 31, 2010

Primary Completion Date

October 31, 2012

Study Completion Date

November 30, 2012

Conditions
Wound InfectionAbscessSystemic InflammationCellulitis
Interventions
DRUG

Single-Dose IV Oritavancin Diphosphate

Oritavancin was administered as a single IV dose.

DRUG

IV Vancomycin

Intravenous vancomycin was administered for a minimum of 7 days and up to a maximum of 10 days.

DRUG

Placebo

Intravenous placebo was administered thereafter, for a minimum of 7 days and up to a maximum of 10 days (oritavancin and placebo).

Trial Locations (1)

91911

Sharp Chula Vista Medical Center, Chula Vista

Sponsors
All Listed Sponsors
lead

Melinta Therapeutics, Inc.

INDUSTRY