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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 (Cohorts 1-3) or Indolent Systemic Mastocytosis (Cohort 5). Participants must be diagnosed with Myelofibrosis and be relapsed/refractory (e.g., having failed prior therapy), intolerant, or ineligible to receive JAKi treatment, or be diagnosed with Indolent Systemic Mastocytosis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04655118
Study type Interventional
Source Telios Pharma, Inc.
Contact John Mei
Phone 650-542-0136
Email jmei@teliospharma.com
Status Recruiting
Phase Phase 2
Start date October 22, 2020
Completion date December 31, 2025

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