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Completed Phase 3 Interventional Results available

Study to Compare Lefamulin to Moxifloxacin for the Treatment of Adults With Pneumonia

ClinicalTrials.gov ID: NCT02813694

Public ClinicalTrials.gov record NCT02813694. 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 Jul 22, 2026, 8:49 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 3, Randomized, Double-Blind, Double-Dummy Study to Compare the Efficacy and Safety of Oral Lefamulin (BC 3781) Versus Oral Moxifloxacin in Adults With Community-Acquired Bacterial Pneumonia

Study identification

NCT ID
NCT02813694
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Nabriva Therapeutics AG
Industry
Enrollment
738 participants

Conditions and interventions

Interventions

  • lefamulin Drug
  • Moxifloxacin Drug

Drug

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
Jul 31, 2016
Primary completion
Dec 31, 2017
Completion
Dec 31, 2017
Last update posted
Oct 22, 2019

2016 – 2018

United States locations

U.S. sites
25
U.S. states
13
U.S. cities
23
Facility City State ZIP Site status
1080 Beverly Hills California
Site 1065 Fresno California 93701
1078 Northridge California
Site 1072 Oxnard California 93030
Site 1070 Sacramento California 95817
1079 Sherman Oaks California
Site 1053 Sylmar California 91342
Site 1064 DeBary Florida 32713
Site 1052 DeLand Florida 32720
1076 Miami Florida
Site 1051 Michigan City Indiana 46360
Site 1057 Natchitoches Louisiana 71457
Site 1073 New Bedford Massachusetts 02740
Site 1055 Detroit Michigan 48201
Site 1062 Detroit Michigan 48235
Site 1068 Royal Oak Michigan 48073
Site 1058 St Louis Missouri 63110
Site 1054 Butte Montana 59701
Site 1067 Lima Ohio 45801
Site 1056 Rapid City South Dakota 57702
1077 Hendersonville Tennessee
Site 1060 Houston Texas 77070
Site 1069 Houston Texas 77093
Site 1066 Splendora Texas 77372
Site 1059 Charlottesville Virginia 22908

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 130 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02813694, 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 Oct 22, 2019 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02813694 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →