This study is designed as two sequential trials. The first is a phase I open label trial to evaluate the safety and tolerability of MAT2203. The maximal tolerated and non-toxic daily dose,will then be moved forward into a multi-day safety trial. The Phase II trial will investigate toxicity and early fungicidal activity (EFA) of MAT2203 with flucytosine.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Highest dose tolerated without inducing vomiting
Timeframe: 7 days
Evidence of fungicidal activity
Timeframe: 2 weeks