Two-week survival in Cohort 4 (all-oral regimen) was 95% in 40 patients receiving MAT2203
Mean Early Fungicidal Activity (EFA) of the rate of yeast clearance in cerebrospinal fluid exceeded the prespecified primary endpoint threshold of >0.20 CFU/mL, CSF/day
Favorable safety and tolerability data support longer-term use of MAT2203 with no evidence of kidney toxicity seen with 6 weeks of oral MAT2203 treatment
Overall survival data from Cohorts 2 and 4 of EnACT trial (Cohorts 1 and 3 were safety lead-ins) provide clinically meaningful evidence of the safety and efficacy of MAT2203 for both a step-down indication and an all-oral treatment regimen for cryptococcal meningitis
Phase 3 registration trial of MAT2203 for treatment of cryptococcal meningitis to commence Q1 2023
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