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Re: Venture_Cap post# 117800

Friday, 09/18/2020 9:06:21 PM

Friday, September 18, 2020 9:06:21 PM

Post# of 233567
May just get monetized across the pond. Something may happen really soon in this regard> CytoDyn Inc. (OTCQB: CYDY) announced earlier this month that the Medicines & Healthcare product Regulatory Agency (MHRA) of the U.K. government requested a meeting with CytoDyn on September 9, 2020 to discuss the Company's request for Fast Track approval of leronlimab to treat COVID-19 patients with mild-to-moderate symptoms based upon the trial's Top-line Report and additional eIND data. On the suggestion of the MHRA, CytoDyn will submit its current Phase 3 CD12 study for severe-to-critical COVID-19 patients in the UK to the Urgent Public Health (UPH) Research scheme to receive possible financial support from the trial sites and the government, if the UPH deems the Company's CD12 trial an urgent health issue
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