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Clinical Trial Summary

The purpose of this study is to determine whether prophylaxis with micafungin is effective in the induction chemotherapy for newly diagnosed acute leukemia patients.


Clinical Trial Description

Medically fit patients with newly diagnosed acute leukemia received 50 mg micafungin intravenously once daily from the initiation of first induction chemotherapy to recovery of neutrophil count, suspected fungal infection, or unacceptable drug-related toxicity. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02440178
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase Phase 2
Start date September 19, 2015
Completion date June 1, 2017

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