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Completed Phase 3 Interventional Results available

Study to Compare Delafloxacin to Moxifloxacin for the Treatment of Adults With Community-acquired Bacterial Pneumonia

ClinicalTrials.gov ID: NCT02679573

Public ClinicalTrials.gov record NCT02679573. 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, 12:04 PM 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 3, Multicenter, Randomized, Double-Blind, Comparator-Controlled Study to Evaluate the Safety and Efficacy of Intravenous to Oral Delafloxacin in Adult Subjects With Community-Acquired Bacterial Pneumonia

Brief summary

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

The purpose of this study is to evaluate the safety and efficacy of delafloxacin compared to moxifloxacin in the treatment of adult patients with community-acquired pneumonia.

Study identification

NCT ID
NCT02679573
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Melinta Therapeutics, Inc.
Industry
Enrollment
860 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Dec 14, 2016 (Actual)
Primary completion
Jul 31, 2018 (Actual)
Completion
Aug 7, 2018 (Actual)
Last update posted
Feb 27, 2020

2016 – 2018

United States locations

U.S. sites
25
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
Melinta 306 Study Site Montgomery Alabama 36106 —
Melinta 306 Study Site Newark Delaware 19718 —
Melinta 306 Study Site Coral Gables Florida 33134 —
Melinta 306 Study Site DeBary Florida 32713 —
Melinta 306 Study Site DeLand Florida 32720 —
Melinta 306 Study Site Fort Myers Florida 33901 —
Melinta 306 Study Site Miami Florida 33126 —
Melinta 306 Study Site Miami Florida 33185 —
Melinta 306 Study Site Louisville Kentucky 40202 —
Melinta 306 Study Site Natchitoches Louisiana 71457-6215 —
Melinta 306 Study Site Baltimore Maryland 21201 —
Melinta 306 Study Site Boston Massachusetts 02115 —
Melinta 306 Study Site Burlington Massachusetts 01805 —
Melinta 306 Study Site Saint Paul Minnesota 55104 —
Melinta 306 Study Site St Louis Missouri 63110 —
Melinta 306 Study Site Butte Montana 59701 —
Melinta 306 Study Site Omaha Nebraska 68124 —
Melinta 306 Study Site Newark New Jersey 07102 —
Melinta 306 Study Site Buffalo New York 14215 —
Melinta 306 Study Site Charlotte North Carolina 28203 —
Melinta 306 Study Site Cleveland Ohio 44106-5029 —
Melinta 306 Study Site Dayton Ohio 45402 —
Melinta 306 Study Site Rapid City South Dakota 57702 —
Melinta 306 Study Site Franklin Tennessee 37067 —
Melinta 306 Study Site Corsicana Texas 75110 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 65 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02679573, 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 27, 2020 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02679573 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →