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Clinical Trial Summary

The purpose of this study is to compare the safety, pharmacokinetics, and efficacy of oral SCY-078 vs. standard-of-care following initial intravenous echinocandin therapy in the treatment of invasive candidiasis.


Clinical Trial Description

Patients will receive initial intravenous (IV) echinocandin therapy. Patients who are eligible for randomization will receive SCY-078 500-mg orally, SCY-078 750-mg orally, or standard-of-care. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02244606
Study type Interventional
Source Scynexis, Inc.
Contact
Status Completed
Phase Phase 2
Start date September 2014
Completion date August 2016

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