CompletedNot applicableNCT00096850
Safety, Tolerability, and Blood Levels of Ritonavir-Boosted Atazanavir and Rifampin When Taken Together in HIV Uninfected Adults
Studying Primary genito-urinary 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
- National Institute of Allergy and Infectious Diseases (NIAID)
- Principal Investigator
- David W. Haas, MD, M.DInfectious Diseases, Vanderbilt University Medical Center
- Intervention
- Atazanavir(drug)
- Enrollment
- 18 enrolled
- Eligibility
- 18-55 years · All sexes
- Timeline
- 2007
Study locations (3)
- Stanford CRS, Palo Alto, California, United States
- The Ohio State Univ. AIDS CRS, Columbus, Ohio, United States
- Vanderbilt Therapeutics CRS, Nashville, Tennessee, United States
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.
Open NCT00096850 on ClinicalTrials.govOther trials for Primary genito-urinary tuberculosis
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