drugset / Trial / NCT02192463

Relative Bioavailability of Different Oral Viramune Extended Release Formulations Compared to Viramune® Oral Suspension in Healthy Male Volunteers

NCT02192463

Phase 1 Completed 204 enrolled Boehringer Ingelheim
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Study to determine the relative bioavailability of different oral Viramune Extended Release (ER) formulations compared to Viramune® Immediate Release (IR) tablet

Timeline

Start
2006-04
Primary completion
2006-08
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Nevirapine Small molecule 200 mg Oral
Subject Nevirapine Small molecule 300 mg Oral
Subject Nevirapine Small molecule 400 mg Oral

Indications

No indication recorded.