A Study to Evaluate Efficacy and Safety of Gepotidacin in the Treatment of Uncomplicated Urinary Tract Infection (UTI)

  • STATUS
    Recruiting
  • End date
    Mar 13, 2024
  • participants needed
    2500
  • sponsor
    GlaxoSmithKline
Updated on 7 October 2022
nitrite
gepotidacin
dysuria
cystitis
nitrofurantoin
acute cystitis
leukocyte esterase

Summary

The study will be conducted to evaluate the therapeutic response (combined per participant microbiological and clinical response) of oral gepotidacin compared to oral nitrofurantoin for treatment of uncomplicated UTI (acute cystitis) in adolescent and adult female participants.

Details
Condition Urinary Tract Infections
Treatment Nitrofurantoin, Gepotidacin, Placebo matching nitrofurantoin, Placebo matching gepotidacin
Clinical Study IdentifierNCT04020341
SponsorGlaxoSmithKline
Last Modified on7 October 2022

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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