An Open-Label, Multicenter, Phase 1b/2 Study of the Safety andEfficacy of KRT-232 Combined with Ruxolitinib in Patients withPrimary Myelofibrosis (PMF), Post–Polycythemia Vera MF (Post–PV-MF), Or Post–Essential Thrombocythemia MF (Post-ET-MF)Who H
MD Anderson Study Status
This is a phase 1b/2 study of KRT-232 combined with ruxolitinib in subjects with MF who have a suboptimal response after at least 18 weeks of treatment with ruxolitinib. The primary objective of the study is to determine a recommended phase 2 dose (RP2D) of KRT 232 in combination with ruxolitinib.
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Phone Number: 1-877-MDA-6789
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