Home » FDA Approves Merck’s Recarbio for Hospital-Acquired Pneumonia
FDA Approves Merck’s Recarbio for Hospital-Acquired Pneumonia
The FDA has approved Merck’s Recarbio (imipenem-cilastatin and relebactam) to treat hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia in patients ages 18 years and older.
The approval was based on the results of a phase 3 clinical trial, in which Recarbio demonstrated noninferiority to piperacillin-tazobactam in 28-day mortality and clinical response at early follow-up.
Recarbio was previously approved for treatment of complicated urinary tract infections and complicated intra-abdominal infections in patients with limited or no alternative treatment options.
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