drugset / Trial / NCT02227017

Relative Bioavailability of Tipranavir (TPV)/Ritonavir (RTV) at Steady State Administered as Oral Solutions vs. Capsules in the Fed and Fasted State in Healthy Volunteers

NCT02227017

Phase 1 Completed 35 enrolled Boehringer Ingelheim
Non-randomizedCrossoverOpen-labelTreatment

Summary

Study to establish the relative bioavailability of the TPV oral solution formulation (500 mg coadministered with RTV oral solution 200 mg) to the TPV capsule formulation (500 mg coadministered with RTV capsules 200 mg), with both treatments at steady-state under fasted and fed conditions in healthy male and female volunteers.

Timeline

Start
2006-02
Primary completion
2006-04
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Ritonavir Other / unclassified 200 mg Oral
Subject Tipranavir Small molecule 500 mg Oral

Indications

No indication recorded.