Meropenem and vaborbactam

(Vabomere®)

Meropenem and vaborbactam

Drug updated on 9/4/2024

Dosage FormInjection (intravenous; 2 g/vial [1 g meropenem (equivalent to 1.14 g meropenem trihydrate) and 1 g vaborbactam])
Drug ClassAntibacterials
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of patients 18 years and older with complicated urinary tract infections (cUTI) including pyelonephritis caused by designated susceptible bacteria.

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Summary
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  • Vabomere (meropenem and vaborbactam) is indicated for the treatment of patients 18 years and older with complicated urinary tract infections (cUTI), including pyelonephritis caused by designated susceptible bacteria.
  • This summary is based on the review of two systematic review(s)/meta-analysis(es). [1-2]
  • The intervention group demonstrated a higher Clinical Cure Rate (CCR) at Test of Cure (TOC) compared to the control group (83.6% vs. 80.3%, OR 1.37, 95% CI 1.08-1.74, P=0.01), and a higher microbiological eradication rate at TOC (77.7% vs. 67.2%, OR 1.79, 95% CI 1.46-2.20, P<0.00001).
  • Meropenem/vaborbactam (MV), ertapenem (ETPM), and biapenem (BAPM) were associated with higher clinical and microbiological treatment success rates compared to other carbapenems, with doripenem (DOPM) showing lower clinical treatment success rates.
  • Meropenem/vaborbactam (MV) was particularly effective in treating complicated urinary tract infections (cUTI) caused by carbapenem-resistant uropathogens, making it a significant option for this specific population subgroup.
  • No significant difference in the risk of treatment-emergent adverse events (AEs) between the intervention and control groups was observed (OR 0.95, P=0.57).
  • Meropenem/vaborbactam (MV) and imipenem/cilastatin (IC) had higher risks of adverse events compared to other carbapenems.
  • There is no population type or subgroup information available in the reviewed studies.