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LBH589 (Panobinostat) for the Treatment of Myelofibrosis

Primary Myelofibrosis Clinical Trial

Official title:
A Phase I/II Open Label Study of LBH589, a Novel Histone Deacetylase Inhibitor (HDACi), in Patients With Primary Myelofibrosis (PMF) and Post-polycythemia/Essential Thrombocythemia Myelofibrosis (Post-PV/ET MF)

Clinical Trial Summary

LBH589 is an oral drug that targets the myelofibrosis cells in the bone marrow and induces cell death by allowing for the expression of certain suppressed genes that are important in regulating cell survival. Based on laboratory studies, the hypothesis is that this drug will selectively kill the stem cells responsible for causing myelofibrosis and result in reduction in spleen size and ultimately restoration of normal bone marrow function.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01298934
Study type Interventional
Source Icahn School of Medicine at Mount Sinai
Contact
Status Unknown status
Phase Phase 1/Phase 2
Start date September 2009
Completion date July 2015
View Details
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