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Clinical Trial Summary

The purpose of this study is to evaluate efficacy and safety of nilotinib in patients with Imatinib resistant or intolerant CML-CP or AC. Efficacy evaluation will be made by Complete cytogenetic response rate(CCyR) at 12 months after nilotinib administration.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01206088
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 4
Start date February 2009
Completion date September 2012

See also
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