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Clinical Trial Summary

This study evaluates TL-895, a potent, orally-available and highly selective irreversible tyrosine kinase inhibitor for the treatment of Myelofibrosis. Participants must have MF (PMF, Post PV MF, or Post ET MF) who are JAKi treatment-naïve or those who have a suboptimal response to ruxolitinib.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05280509
Study type Interventional
Source Telios Pharma, Inc.
Contact John Mei
Phone 650-542-0136
Email jmei@teliospharma.com
Status Recruiting
Phase Phase 1/Phase 2
Start date June 9, 2022
Completion date April 2027

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