drugset / Trial / NCT02182310

Assessment of the Effect of BI 201335 on the QT Interval in Healthy Female and Male Subjects

NCT02182310

Phase 1 Completed 56 enrolled Boehringer Ingelheim
RandomizedCrossoverDouble-blindTreatment

Summary

To demonstrate that BI 201335 does not prolong the QT interval more than placebo. To assess the tolerability of 1200 mg of BI 201335 as single dose in female subjects (double-blind, randomised, placebo-controlled) before inclusion of female subjects in the cross-over part of the trial.

Timeline

Start
2008-06
Primary completion
2008-10
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Faldaprevir Small molecule 480 mg
Subject Faldaprevir Small molecule 1200 mg
Comparator Moxifloxacin Small molecule

Indications

No indication recorded.