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