Mr. Andrew Rae reports

ICO THERAPEUTICS ANNOUNCES DOSING OF FIRST FULL COHORT IN SECOND ORAL AMPHOTERICIN B STUDY

All subjects in the first of two cohorts in iCo Therapeutics Inc.'s phase 1b study have received the first dose of oral amphotericin B. Dosing will occur over a period of 10 days. One additional cohort is expected to be dosed in Q1 2020, followed by the initiation of a phase II study comparing oral amphotericin B with fluconazole in a head-to-head study in vulvovaginal candidiasis in Q2 2020.

All subjects in the phase 1b study will be dosed for 10 consecutive days with additional 10 days of follow-up (for a total of 20 days). Two doses of oral amphotericin B (100 milligrams and 400 mg), showing promising pharmacokinetic outcomes in the previous phase 1 trial (using a single dose only), will be used in the phase 1b study. Extensive safety and pharmacokinetic testing will also be performed throughout the study to indicate which dose might be the safest and effective for future trials in patients with fungal diseases.

About iCo Therapeutics Inc.

iCo Therapeutics identifies existing development stage assets for use in underserved ocular and infectious diseases.

We seek Safe Harbor.