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Clinical Trial Summary

The purpose of the study is to identify the recommended Part 2 dose (R2PD) of imetelstat in combination with ruxolitinib in participants with myelofibrosis (MF) in Part 1, and to evaluate the safety and clinical activity of the R2PD of imetelstat in combination with ruxolitinib in participants with MF in Part 2.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05371964
Study type Interventional
Source Geron Corporation
Contact Tymara Berry, MD
Phone 650-473-7794
Email myf1001-info@geron.com
Status Recruiting
Phase Phase 1
Start date May 4, 2022
Completion date August 2027

See also
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