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

Primary Objective

To determine the RP2D and schedule of TL-895 in each cohort. The SRC will determine the RP2D and schedule for Cohorts 1, 2 and 3 based on safety and tolerability data obtained from each arm of that cohort.

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Details
Age

Adult

Type of Study

Treatment

Locations

Outpatient CTRC
University of Colorado Hospital

Principal Investigator
Photograph of Brandon Mcmahon,  MD

Brandon Mcmahon, MD

Study ID

Protocol Number: 20-3032

More information available at ClinicalTrials.gov: NCT04655118

Categories

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