drugset / Trial / NCT04884191

Phase 2 Study: An Open-Label, Randomized, Phase 2 Dose-Finding Study of Pacritinib in Patients With Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis, or Post- Essential Thrombocythemia Myelofibrosis Previously Treated With Ruxolitinib

NCT04884191

Phase 2 Completed 165 enrolled CTI BioPharma
RandomizedParallel-groupOpen-labelTreatment

Summary

This was an open-label, randomized, dose-finding study in patients with primary or secondary MF (Dynamic International Prognostic Scoring System \[DIPSS\] risk score of Intermediate-1 to High-Risk) who were previously treated with ruxolitinib. The study was designed to support a pacritinib dosage selection decision with evaluation of 3 dosages.

Timeline

Start
2017-07-31
Primary completion
2019-09-04
Completion
2019-09-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Pacritinib Small molecule 100 mg
Subject Pacritinib Small molecule 200 mg