drugset / Trial / NCT00719836
A Phase 1/2 Study of SB1518 for the Treatment of Advanced Myeloid Malignancies
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |