drugset / Trial / NCT00719836

A Phase 1/2 Study of SB1518 for the Treatment of Advanced Myeloid Malignancies

NCT00719836

Phase 1/2 Completed 76 enrolled S*BIO
NaSingle-groupOpen-labelTreatment

Summary

This study consists of two phases: the first portion of the study is a Phase 1 dose escalation study to determine the maximum tolerated dose and the dose limiting toxicities of SB1518 when given as a single agent orally once daily in subjects with advanced myeloid malignancies; the second portion of the study is a Phase 2 study to define the efficacy and safety profile of single-agent SB1518 at the recommended dose in subjects with chronic idiopathic myelofibrosis (CIMF).

Timeline

Start
2008-08
Primary completion
2012-01
Completion
2012-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Pacritinib Small molecule 100 mg Oral
Subject Pacritinib Small molecule 400 mg Oral
Subject Pacritinib Small molecule 500 mg Oral
Subject Pacritinib Small molecule 600 mg Oral