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Re: roiresearch post# 329955

Wednesday, 10/28/2020 9:13:37 AM

Wednesday, October 28, 2020 9:13:37 AM

Post# of 402939
Questions I have based on the pre-ind and written responses received

IPIX: In the application, the Company has requested regulatory guidance on its planned Phase 2, randomized, double-blind, placebo-controlled, multi-center study to evaluate the efficacy and safety of Brilacidin in hospitalized patients with COVID-19. Target enrollment is 120 patients, with a planned interim analysis.

1) what was the FDA recommendation
2) is IPIX in agreement with FDA's recommendation

These are 2 very strong pieces of information left out of IPIX's PR that would have given investors the insight as to when human trials will begin




the above is all IMHO (consider this my safe harbor statement)

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