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Completed Phase 2 Interventional

TBTC Study 27: Moxifloxacin vs Ethambutol for TB Treatment

ClinicalTrials.gov ID: NCT00140309

Public ClinicalTrials.gov record NCT00140309. 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 Jun 26, 2026, 9:47 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

TBTC Study 27: An Evaluation of the Activity and Tolerability of Moxifloxacin During the First Two Months of Treatment for Pulmonary Tuberculosis--A Double-Blind, Randomized, Multicenter Study by the Tuberculosis Trials Consortium

Study identification

NCT ID
NCT00140309
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Centers for Disease Control and Prevention
Federal
Enrollment
350 participants

Conditions and interventions

Interventions

  • moxifloxacin (with isoniazid, rifampin, pyrazinamide) 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
Jun 30, 2003
Primary completion
Not listed
Completion
Nov 30, 2005
Last update posted
Mar 18, 2007

2003 – 2005

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
University of Southern California Medical Center Los Angeles California 90033
University of California at San Diego San Diego California 92103
University of California, San Francisco San Francisco California 94110
Denver Public Health Department Denver Colorado 80204
Washington DC Veterans Administration Medical Center Washington D.C. District of Columbia 20422
Emory University School of Medicine Atlanta Georgia 30303
Hines Vetrans Administration Medical Center Hines Illinois 60141
Johns Hopkins University Baltimore Maryland 21231
Boston University Medical Center Boston Massachusetts 02118
New Jersey School of Medicine Newark New Jersey 07107
New York University School of Medicine New York New York 10016
Columbia University New York New York 10032
Harlem Hospital Center New York New York 10037
Veterans Administration Tennessee Valley Health Care System Nashville Tennessee 37232
University of North Texas Health Science Center Fort Worth Texas 76104
Houston Veterans Administration Medical Center Houston Texas 77030
Audie L Murphy Memorial Veterans Administration Medical Center San Antonio Texas 78284
Seattle-King County Health Department 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00140309, 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 Mar 18, 2007 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00140309 live on ClinicalTrials.gov.

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