drugset / Trial / NCT02182297

Safety, Tolerability, and Pharmacokinetics of BI 201335 NA in Healthy Male Subjects

NCT02182297

Phase 1 Completed 50 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of this trial was to investigate safety, tolerability, and pharmacokinetics of BI 201335 ZW after administration of single rising doses from 40 mg to 480 mg of BI 201335 NA in healthy Japanese male volunteers.

Timeline

Start
2008-04
Primary completion
2008-12
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Faldaprevir Small molecule 40 mg Oral
Subject Faldaprevir Small molecule 480 mg Oral

Indications

No indication recorded.