Recarbrio is a combination of imipenem, a penem antibacterial, cilastatin, a renal dehydropeptidase inhibitor, and relebactam, a betalactamase inhibitor.
Recarbrio is specifically indicated for the following:
Recarbrio is supplied as a solution for intravenous infusion. The recommended dose is 1.25 grams (imipenem 500mg, cilastatin 500 mg, and relebactam 250 mg) administered by intravenous (IV) infusion over 30 minutes every 6 hours in patients 18 years of age and older with creatinine clearance (CLcr) of 90 mL/min or greater. A dose reduction is recommended for patients with CLcr less than 90 mL/min. The severity and location of infection, as well as clinical response should guide the duration of therapy. Please see drug label for specific dose adjustments. The recommended duration of treatment with Recarbrio is 4 days to 14 days.
The determination of efficacy and safety of Recarbrio was supported in part by the previous findings of the efficacy and safety of imipenem/cilastatin for the treatment of cIAI and cUTI. The contribution of relebactam to Recarbrio was primarily established in vitro and in animal models of infection. Imipenem/cilastatin plus relebactam was studied in cIAI and cUTI including pyelonephritis in randomized, blinded, active-controlled, multicenter trials. These trials provided only limited efficacy and safety information.
The FDA approval of Recarbrio for HABP/VABP was based on results of the pivotal Phase 3 RESTORE-IMI 2 trial that compared Recarbrio 1.25 grams (imipenem 500 mg/cilastatin 500 mg/relebactam 250 mg) to piperacillin/tazobactam 4.5 grams (PIP/TAZ, piperacillin 4000 mg/tazobactam 500 mg), each administered intravenously every six hours for seven to 14 days, for the treatment of adult patients with HABP/VABP. Recarbrio met the primary and key secondary endpoints, demonstrating non-inferiority to PIP/TAZ in 28-day all-cause mortality and clinical response at early follow-up, respectively.
Adverse effects associated with the use of Recarbrio may include, but are not limited to, the following:
alanine aminotransferase increased
aspartate aminotransferase increased
phlebitis/infusion site reactions
Recarbrio is a combination of imipenem, a penem antibacterial, cilastatin, a renal dehydropeptidase inhibitor, and relebactam, a betalactamase inhibitor. Cilastatin limits the renal metabolism of imipenem and does not have antibacterial activity. The bactericidal activity of imipenem results from binding to PBP 2 and PBP 1B in Enterobacteriaceae and Pseudomonas aeruginosa and the subsequent inhibition of penicillin binding proteins (PBPs). Inhibition of PBPs leads to the disruption of bacterial cell wall synthesis. Imipenem is stable in the presence of some beta lactamases. Relebactam has no intrinsic antibacterial activity. Relebactam protects imipenem from degradation by certain serine beta lactamases such as Sulhydryl Variable (SHV), Temoneira (TEM), Cefotaximase-Munich (CTX-M), Enterobacter cloacae P99 (P99), Pseudomonas-derived cephalosporinase (PDC), and Klebsiella-pneumoniae carbapenemase (KPC).
For additional information regarding complicated intra-abdominal and urinary tract infections or Recarbrio, please visit the Recarbrio web page.