A Study to Evaluate Pharmacokinetic, Safety, Tolerability and Relative Bioavailability of Gepotidacin in Healthy Adult Male and Female Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

March 1, 2022

Primary Completion Date

April 22, 2022

Study Completion Date

April 22, 2022

Conditions
Healthy Volunteers
Interventions
DRUG

Gepotidacin

Gepotidacin will be administered

Trial Locations (1)

89113

GSK Investigational Site, Las Vegas

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY