GlaxoSmithKline
This study aims to evaluate the pharmacokinetic of gepotidacin in fed healthy lactating women.
Inclusion Criteria: * Participants must be healthy lactating women, 18 to 50 years of age, inclusive, at Screening. * Actively breastfeeding or expressing breast milk. * At least 28 days postpartum with a full milk supply established, and with no persistent complications from delivery (there is no maximal length of time postpartum required). * Willingness to temporarily discontinue feeding breast milk to infants from dosing through to 72 hours after dosing (approximately 3 days), with the ability to pump and provide reserve milk for bottle feeding prior to the study OR has decided to permanen…
A single oral dose of 3000 mg gepotidacin will be administered
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