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Terminated Phase 3 Interventional Results available

Comparison of Delafloxacin Versus Ceftriaxone for the Treatment of Uncomplicated Gonorrhea

ClinicalTrials.gov ID: NCT02015637

Public ClinicalTrials.gov record NCT02015637. 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 24, 2026, 7:31 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 Comparative Evaluation of the Single-dose Efficacy of Oral Delafloxacin Versus the Single-dose Efficacy of an Intramuscular Injection of Ceftriaxone in Subjects With Uncomplicated Urogenital Gonorrhea

Brief summary

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

The purpose of this study is to evaluate the effects of a single oral dose of delafloxacin versus a single intramuscular injection of ceftriaxone in subjects with uncomplicated cervical, urethral, rectal, or pharyngeal gonorrhea.

Study identification

NCT ID
NCT02015637
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Melinta Therapeutics, Inc.
Industry
Enrollment
460 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
15 Years and older
Sex
All
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
Jan 23, 2014 (Actual)
Primary completion
Nov 2014 (Actual)
Completion
Dec 10, 2014 (Actual)
Last update posted
Jun 20, 2018

2014

United States locations

U.S. sites
25
U.S. states
14
U.S. cities
24
Facility City State ZIP Site status
Melinta 304 Study Birmingham Alabama 35294 —
Melinta 304 Study Site Chula Vista California 90911 —
Melinta 304 Study Site La Mesa California 91942 —
Melinta 304 Study Site Los Angeles California 90069 —
Melinta 304 Study Site San Francisco California 94103 —
Melinta 304 Study Atlanta Georgia 30308 —
Melinta 304 Study Decatur Georgia 30033 —
Melinta 304 Study Site Indianapolis Indiana 46202 —
Melinta 304 Study Site New Orleans Louisiana 70112 —
Melinta 304 Study Site Omaha Nebraska 68114 —
Melinta 304 Study Site Las Vegas Nevada 89109 —
Melinta 304 Study Site Brooklyn New York 11203 —
Melinta 304 Study Brooklyn New York 11203 —
Melinta 304 Study Site New York New York 10018 —
Melinta 304 Study Site The Bronx New York 100461 —
Melinta 304 Study Site Durham North Carolina 27701 —
Melinta 304 Study Site Greensboro North Carolina 27405 —
Melinta 304 Study Site Cleveland Ohio 44108 —
Melinta 304 Study Site Columbus Ohio 43231 —
Melinta 304 Study Site Portland Oregon 97204 —
Melinta 304 Study Erie Pennsylvania 16507 —
Melinta 304 Study Site Philadelphia Pennsylvania 191007 —
Melinta 304 Study Site Pittsburgh Pennsylvania 15213 —
Melinta 304 Study Site Houston Texas 77011 —
Melinta 304 Study Site Seattle Washington 98104 —

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 NCT02015637, 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 Jun 20, 2018 · Synced Oct 24, 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 NCT02015637 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →