Two months after its urogenital gonorrhea antibiotic hit the primary endpoint in a registrational trial, GSK is providing a closer look at results as it gears up for regulatory filings in 2025.
The Phase 3 EAGLE-1 trial compared GSK’s antibiotic with standard-of-care ceftriaxone plus azithromycin in 600 people with uncomplicated urogenital gonorrhea. In the primary endpoint of microbiological response at the test-of-cure visit three to seven days after treatment, gepotidacin achieved a 92.6% success rate versus 91.2% for control, per a Wednesday release. The p-value of the non-inferiority endpoint was not disclosed.
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