Evaluating oritavancin for Gram-positive infections: a systematic review of on-label and off-label use

Alex Soriano1,2,3, Carlo Tascini4, Marco Falcone5

  • 1Infectious Diseases Service, Hospital Clínic Barcelona, University of Barcelona, Spain.

Drugs in Context
|March 27, 2026
PubMed
Abstract

Insights

Oritavancin effectively treats acute bacterial skin infections and shows promise for difficult Gram-positive infections like osteomyelitis. Further research is needed to optimize dosing for off-label uses.

Area of Science:

  • Infectious Diseases
  • Pharmacology
  • Clinical Medicine

Background:

  • Oritavancin is a lipoglycopeptide antibiotic for acute bacterial skin and skin structure infections (ABSSSI).
  • It has potential for treating challenging Gram-positive infections, including osteomyelitis, bacteraemia, and endocarditis.
  • This review assesses oritavancin's efficacy, safety, and clinical application in both approved and unapproved indications.

Purpose of the Study:

  • To systematically review the efficacy and safety of oritavancin.
  • To evaluate its clinical use in on-label and off-label indications.
  • To assess its potential as a treatment alternative for difficult Gram-positive infections.

Main Methods:

  • Searched MEDLINE and CENTRAL databases from 2011 to 2024.
  • Included randomized trials, retrospective cohorts, case series, and real-world evidence.
  • Assessed risk of bias using Critical Appraisal Skills Programme (CASP) tools.

Main Results:

  • Twenty-five studies were included, covering ABSSSI (n=2311) and off-label uses (n=692).
  • Oritavancin showed clinical cure rates of 79.6-83.3% for ABSSSI in RCTs, comparable to vancomycin.
  • Clinical success rates ranged from 85-88% for ABSSSI and 70-100% for off-label uses; adverse events were mostly mild to moderate.

Conclusions:

  • Oritavancin is effective for ABSSSI.
  • It shows promise for selected Gram-positive off-label indications needing prolonged therapy.
  • Standardized dosing and prospective trials are necessary for optimal off-label regimens.

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