Protocol No
KARTOS-KRT-232-101-MF
Principal Investigator
Laura Michaelis
Phase
II
Summary
This study wants to find out whether the investigational drug, KRT-232, reduces the symptoms of myelofibrosis, and whether it causes any problems (side effects).
Description
KRT-232 in Subjects With PMF, Post-PV MF, or Post-ET MF Who Have Failed a JAK Inhibitor
Participating Institutions
Froedtert Hospital
Status
OPEN TO ACCRUAL
Sub Category
ClinicalTrials.gov