Study #2020-0738
A Phase 2, Open-label, Multicenter Study of TL-895 in Subjects with Relapsed/Refractory Myelofibrosis, Janus Kinase Inhibitor Intolerant Myelofibrosis and Janus Kinase Inhibitor Treatment Ineligible Myelofibrosis
MD Anderson Study Status
Enrolling
Treatment Agent
TL-895
Description
This study evaluates TL-895, a potent, orally-available and highly selective irreversible tyrosine kinase inhibitor for the treatment of Myelofibrosis. Participants must be relapsed/refractory (e.g., having failed prior therapy), intolerant, or ineligible to receive JAKi treatment.
Information and next steps
Disease:
Myelofibrosis
Study phase:
II
Physician name:
Srdan Verstovsek
Department:
Leukemia
For general questions about clinical trials:
1-877-632-6789
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