GSK plcFDA approval of Utebzi expands GSK's anti-infectives portfolio with a novel oral carbapenem.
The US Food and Drug Administration has approved Utebzi, an oral antibiotic developed by GSK and Spero Therapeutics, for adults with complicated urinary tract infections who have limited or no alternative oral treatment options. Utebzi is the first and only oral carbapenem antibiotic approved in the US, offering an alternative to intravenous therapy for a condition that affects more than 3 million people annually and where treatment failure impacts up to 34% of patients. The approval is based on the PIVOT-PO phase III trial, which showed non-inferiority of oral tebipenem pivoxil compared to intravenous imipenem-cilastatin, with overall success rates of 58.5% and 60.2% respectively. GSK expects Utebzi to be available to US patients by the end of 2026, building on its anti-infectives portfolio through an exclusive global licensing agreement with Spero Therapeutics, excluding select Asian territories.
GSK plcFDA approval of Utebzi expands GSK's anti-infectives portfolio with a novel oral carbapenem.
Spero Therapeutics IncFDA approval of Utebzi, Spero's partnered drug, is a regulatory milestone enabling commercialization.