Ceftobiprole medocaril sodium

(Zevtera®)

Zevtera®

Drug updated on 10/17/2024

Dosage FormInjection (intravenous; 667 mg)
Drug ClassCephalosporin antibacterials
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of Adult patients with Staphylococcus aureus bloodstream infections (bacteremia) (SAB), including those with right-sided infective endocarditis
  • Indicated for the treatment of adult patients with acute bacterial skin and skin structure infections (ABSSSI)
  • Indicated for the treatment of adult and pediatric patients (3 months to less than 18 years old) with community-acquired bacterial pneumonia (CABP).

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Summary
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  • This summary is based on the review of four systematic review(s)/meta-analysis(es). [1-4]
  • Ceftobiprole demonstrated comparable clinical success rates to other antibiotics for treating acute bacterial skin and skin structure infections (ABSSSIs) in both intention-to-treat and clinical evaluable populations, with no significant difference in overall clinical response compared to vancomycin-based treatments. However, ceftobiprole was less effective in treating major cutaneous abscesses.
  • In burn patients, there is insufficient evidence to assess the effectiveness of ceftobiprole, and for children with hospital-acquired pneumonia, very low certainty of evidence precludes any meaningful conclusions on its effectiveness.
  • There is insufficient data on the safety profile of ceftobiprole in burn patients and neonates/children with hospital-acquired pneumonia, with no comprehensive safety outcomes reported. Ceftobiprole had a comparable safety profile to vancomycin-based treatments for ABSSSIs, though it was associated with a higher risk of nausea.
  • There is no population types or subgroups information available in the reviewed studies.