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Terminated Phase 2 Interventional

Efficacy and Safety Study of JNJ-32729463 Compared With Moxifloxacin for the Treatment of Subjects Requiring Hospitalization for Community-Acquired Bacterial Pneumonia

ClinicalTrials.gov ID: NCT01198626

Public ClinicalTrials.gov record NCT01198626. 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 Sep 2, 2026, 8:13 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 Randomized, Controlled, Double Blind, Multicenter, Phase 2 Study of the Safety/Tolerability and Efficacy of JNJ-32729463 Compared With Moxifloxacin for the Treatment of Subjects Requiring Hospitalization for Community-Acquired Bacterial Pneumonia (CABP) With a PORT Score of II or Greater

Brief summary

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

The purpose of this study is to determine the efficacy, safety and tolerability of JNJ-32729463 compared to moxifloxacin for the treatment of subjects requiring hospitalization for Community-Acquired Bacterial Pneumonia (CABP).

Study identification

NCT ID
NCT01198626
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Furiex Pharmaceuticals, Inc
Industry
Enrollment
32 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 Years
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
Sep 30, 2010
Primary completion
Sep 30, 2011
Completion
Sep 30, 2011
Last update posted
Dec 7, 2011

2010 – 2011

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Furiex Research Site Mobile Alabama 36608
Furiex Research Site Sylmar California 91342
Furiex Research Site Orlando Florida 32837
Furiex Research Site Vero Beach Florida 32960
Furiex Research Site Peoria Illinois 61637
Furiex Research Site Hazard Kentucky 41701
Furiex Research Site Anaconda Montana 59711
Furiex Research Site Omaha Nebraska 68131
Furiex Research Site Albueuerque New Mexico 87131
Furiex Research Site Austin Texas 78701
Furiex Research Site Austin Texas 78705
Furiex Research Site Austin Texas 78759
Furiex Research Site Longview Washington 98632

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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01198626, 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 Dec 7, 2011 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01198626 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →