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Clinical Trial Summary

The primary objective of this study was to collect additional safety of INC424 in patients with Primary Myelofibrosis, Post Polycythemia Myelofibrosis or Post-essential Thrombocythemia Myelofibrosis, who either received prior treatment with commercially available agents or who have never received treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01493414
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 3
Start date August 16, 2011
Completion date January 26, 2017

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