drugset / Trial / NCT02765724

Determine Pacritinib Pharmacokinetics in Impaired Hepatic Patients and Healthy Subjects

NCT02765724

Phase 1 Completed 28 enrolled CTI BioPharma SGS S.A. · collab
Non-randomizedParallel-groupOpen-labelOther

Summary

This is an open-label, parallel-group, single-dose study of the PK and safety of 400 mg pacritinib administered orally to patients with stable chronic liver disease and healthy control subjects.

Timeline

Start
2015-01
Primary completion
2015-06
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Pacritinib Small molecule 400 mg Oral

Indications