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Clinical Trial Summary

It is a prospective, non-interventional, open-label study, in order to observe the safety and response in FLT3-ITD mutation positive AML patients who receiving sorafenib as induction, consolidation, salvage, maintenance or alleviative treatment. The duration of the study from June 2014 through May 2019, with the recruitment duration from June 2014 to May 2017. The inclusion criteria is:

1. Definitely diagnosed as AML

2. FLT3-ITD mutation has been confirmed

3. Accepting the prescription of sorafenib


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02156297
Study type Observational
Source The First Affiliated Hospital of Soochow University
Contact Jia Chen, M.D.
Phone +86 512 67781856
Email c_jerry_j@163.com
Status Recruiting
Phase
Start date June 2014
Completion date August 2022

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