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Completed Phase 3 Interventional Results available

A Study in Adolescent and Adult Female Participants to Evaluate Clinical Symptom Improvement and the Safety of Gepotidacin During Treatment of Uncomplicated Urinary Tract Infections (Acute Cystitis)

ClinicalTrials.gov ID: NCT06597344

Public ClinicalTrials.gov record NCT06597344. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 1:14 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3b, Open-label, Single-arm Study in Adolescent and Adult Female Participants to Evaluate Clinical Symptom Improvement and the Safety of Gepotidacin During Treatment of Uncomplicated Urinary Tract Infections (Acute Cystitis)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The study will be conducted to evaluate the clinical symptom improvement and safety of oral gepotidacin for treatment of uncomplicated UTI (acute cystitis) in adolescent and adult female participants.

Study identification

NCT ID
NCT06597344
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
97 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2, 2024 (Actual)
Primary completion
Mar 10, 2025 (Actual)
Completion
Mar 10, 2025 (Actual)
Last update posted
Feb 11, 2026

2024 – 2025

United States locations

U.S. sites
22
U.S. states
8
U.S. cities
20
Facility City State ZIP Site status
GSK Investigational Site Modesto California 95350-5365 —
GSK Investigational Site Pasadena California 91101-2453 —
GSK Investigational Site San Diego California 92120-5259 —
GSK Investigational Site Valencia California 91355 —
GSK Investigational Site Miami Florida 33135 —
GSK Investigational Site Ormond Beach Florida 32174-6302 —
GSK Investigational Site Palm Springs Florida 33406-7671 —
GSK Investigational Site Palm Springs Florida 33461 —
GSK Investigational Site Plant City Florida 33563-4202 —
GSK Investigational Site Sweetwater Florida 33172-2741 —
GSK Investigational Site West Palm Beach Florida 33409-3401 —
GSK Investigational Site West New York New Jersey 07093-2622 —
GSK Investigational Site New York New York 10016-7313 —
GSK Investigational Site Dayton Ohio 45424 —
GSK Investigational Site Forney Texas 75126-4174 —
GSK Investigational Site Houston Texas 77036 —
GSK Investigational Site Houston Texas 77087 —
GSK Investigational Site Kingwood Texas 26537 —
GSK Investigational Site Mesquite Texas 75149 —
GSK Investigational Site Missouri City Texas 77459-4756 —
GSK Investigational Site Bountiful Utah 84010-4943 —
GSK Investigational Site Morgantown West Virginia 26501 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06597344, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 11, 2026 · Synced Oct 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06597344 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →