Pharmacokinetics of Apricitabine and Tipranavir When Dosed Alone or Together
Completed · Phase 1
Conditions studied: HIV Infection
In brief
The aim of the study is to see if apricitabine or tipranavir affect the levels of each other in the blood (pharmacokinetic interaction) when they are dosed together.
Key facts
- Study ID
- NCT00352066
- Run by
- Avexa
- People needed
- 18
- Starts
- 2006-07-01
- Expected to finish
- 2006-08-01
- Last updated by the study team
- 2011-06-23
Who can join
Age: 18 and older, up to 40. Sex: male. Healthy volunteers: accepted.
You may qualify if…
- healthy males 18-40 years old
- non-smokers
- no clinically significant medical history
You may not qualify if…
- current or relevant previous medical history of significance
- hepatitis B, hepatitis C, or HIV positive
- current use of prescription or OTC medications
- use of illicit substances or alcohol (>14 drinks/week)
Where it is running
- Jasper Clinic Inc — Kalamazoo, Michigan, United States
Full record on ClinicalTrials.gov
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