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Clinical Trial Summary

This study is to evaluate the efficacy and safety according to incremental dosing for 8 weeks and duration of administration for 1 year in patients with high-risk essential thrombocythemia.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03232177
Study type Interventional
Source Yuhan Corporation
Contact
Status Completed
Phase Phase 4
Start date June 5, 2017
Completion date December 5, 2020

See also
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