drugset / Trial / NCT02833831

Study to Evaluate the Effect of ALS-008176 on Cardiac Repolarization Interval in Healthy Participants

NCT02833831

Phase 1 Completed 103 enrolled Janssen Research & Development, LLC
RandomizedCrossoverDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the effect of supratherapeutic exposures of ALS-008176 on the QT/ corrected QT interval (QTc) interval in healthy participants (Panel 2).

Timeline

Start
2016-06-02
Primary completion
2017-02-17
Completion
2017-02-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Lumicitabine Small molecule 1500 mg Oral
Subject Lumicitabine Small molecule 2500 mg Oral
Subject Lumicitabine Small molecule 3000 mg Oral
Subject Moxifloxacin Small molecule 400 mg

Indications

No indication recorded.