drugset / Trial / NCT00146328

Rollover Trial Safety and Tolerability of Combination Tipranavir and Ritonavir Use in HIV 1 Infected Subjects

NCT00146328

Phase 2/3 Completed 997 enrolled Boehringer Ingelheim
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The objective of this study is to determine the long term safety and tolerability of multiple oral doses of tipranavir (Aptivus) and ritonavir with a focus on the long term safety of the development dose (500 mg tipranavir/200 mg ritonavir BID) when administered with other antiretroviral medications.

Timeline

Start
2001-04
Primary completion
2008-05
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Tipranavir Small molecule 500 mg Oral