drugset / Trial / NCT02807207

To Evaluate the Cardiac Safety and PK Following a Single Oral Dose Administration of Pacritinib in Healthy Subjects

NCT02807207

Phase 1 Completed 42 enrolled CTI BioPharma Covance · collab
RandomizedCrossoverTriple-blindOther

Summary

The primary objective is to evaluate the cardiac safety of a single oral dose (400 mg) of pacritinib compared to placebo on the QT calculated using the Fridericia correction (QTcF) interval in healthy subjects.

Timeline

Start
2014-10
Primary completion
2014-12
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Moxifloxacin Small molecule 400 mg
Subject Pacritinib Small molecule 400 mg Oral

Indications

No indication recorded.