CompletedPhase 3NCT02563327
Pharmacokinetic and Pharmacodynamic Study of High-Dose Rifapentine and Moxifloxacin for Treatment of Tuberculosis
Studying Tuberculosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Centers for Disease Control and Prevention
- Principal Investigator
- Rada Savic, PhDUniversity of San Francisco School of Pharmacy, San Francisco, CA
- Intervention
- Rifapentine(drug)
- Enrollment
- 53 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2016 – 2021
Study locations (3)
- University of Texas Health Science Center at, San Antonio, Texas, United States
- Joint Clinical Research Centre/ Makerere Univ Med Sch, Kampala, Uganda
- National TB Program, Hanoi, Vietnam
Collaborators
Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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