Condition: Pulmonary Tuberculosis · Sponsor: Centers for Disease Control and Prevention
This Phase 2, multicenter, open-label clinical trial evaluated the antimicrobial activity and safety of rifapentine-containing regimens during the intensive phase of pulmonary tuberculosis treatment. Participants were randomized to receive either a standard rifampin-based regimen (RHZE) or a rifapentine-substituted regimen (PHZE). An extension study evaluated higher daily doses of rifapentine (10, 15, and 20 mg/kg). The primary endpoint was sputum culture conversion at 8 weeks. Secondary outcomes included time to culture conversion, safety, and treatment discontinuation.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
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| Central Arkansas Veterans Health System | Little Rock, Arkansas, United States | — |
| LA County/USC Medical Center | Los Angeles, California, United States | — |
| University of Southern California Medical Center | Los Angeles, California, United States | — |
| University of California at San Diego | San Diego, California, United States | — |
| University of California, San Francincisco | San Francisco, California, United States | — |
| Denver Department of Public Health and Hospitals | Denver, Colorado, United States | — |
| Washington DC Veterans Administration Medical Center | Washington D.C., District of Columbia, United States | — |
| Emory University School of Medicine | Atlanta, Georgia, United States | — |
| Chicago VA Medical Center (Lakeside) | Chicago, Illinois, United States | — |
| Northwestern University | Chicago, Illinois, United States | — |
| Hines VA Medical Center | Hines, Illinois, United States | — |
| Johns Hopkins University School of Medicine | Baltimore, Maryland, United States | — |
+ 17 more locations — full list on the registry record.
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