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Design of Two Phase III, Randomized, Multicenter Studies Comparing Gepotidacin with Nitrofurantoin for the Treatment of Uncomplicated Urinary Tract Infection in Female Participants

Authors :
Caroline Perry
Mohammad Hossain
Marcy Powell
Aparna Raychaudhuri
Nicole Scangarella-Oman
Courtney Tiffany
Sherry Xu
Etienne Dumont
Salim Janmohamed
Source :
Infectious Diseases and Therapy, Vol 11, Iss 6, Pp 2297-2310 (2022)
Publication Year :
2022
Publisher :
Adis, Springer Healthcare, 2022.

Abstract

Abstract Background Uncomplicated urinary tract infections (uUTIs) are among the most common community-acquired infections for women worldwide. Treatment options are increasingly limited by antibiotic resistance; novel oral antibiotics are urgently needed. Gepotidacin is a novel, bactericidal, first-in-class triazaacenaphthylene antibiotic that inhibits bacterial deoxyribonucleic acid (DNA) replication by a distinct mechanism of action, which confers activity against most strains of target pathogens, such as Escherichia coli and Staphylococcus saprophyticus, including those resistant to current antibiotics. Here, we describe the designs of two near-identical phase III clinical trials (EAGLE-2 and EAGLE-3) evaluating gepotidacin for the treatment of uUTI. Methods These are phase III, randomized, multicenter, parallel-group, double-blind, double-dummy, comparator-controlled, noninferiority studies, comparing the efficacy and safety of gepotidacin to nitrofurantoin in the treatment of uUTI. Eligible participants are women aged ≥ 12 years with ≥ 2 uUTI symptoms, randomized (1:1) to receive oral gepotidacin (1500 mg) plus placebo or nitrofurantoin (100 mg) plus placebo, twice daily for 5 days. The primary therapeutic endpoint is composite clinical and microbiological efficacy, with noninferiority comparisons made in individuals with a qualifying (≥ 105 colony-forming units/mL urine) nitrofurantoin-susceptible uropathogen. Results These trials were designed in accordance with US Food and Drug Administration (2019) and European Medicines Agency (2018) guidance, particularly the composite endpoint and microbiological evaluability requirements. Across the trials ~ 5000 participants are planned to be enrolled from > 200 centers globally. Conclusions Gepotidacin represents an important potential treatment option being evaluated to address the need for novel oral antibiotics to treat uUTI. These trials are registered at ClinicalTrials.gov ( https://clinicaltrials.gov/ ) where the full protocols can be accessed under trial IDs: NCT04020341 (EAGLE-2) and NCT04187144 (EAGLE-3). Digital features This article includes a video abstract. To view digital features for this article go to https://doi.org/10.6084/m9.figshare.22015349 . Design of Two Phase III, Randomized, Multicenter Studies Comparing Gepotidacin with Nitrofurantoin for the Treatment of Uncomplicated Urinary Tract Infection in Female Participant (MP4 1,04,082 kb)

Details

Language :
English
ISSN :
21938229 and 21936382
Volume :
11
Issue :
6
Database :
Directory of Open Access Journals
Journal :
Infectious Diseases and Therapy
Publication Type :
Academic Journal
Accession number :
edsdoj.fd53b457bcd43ea86c2ad2f8d426ffa
Document Type :
article
Full Text :
https://doi.org/10.1007/s40121-022-00706-9