CytoDyn included in this PR Newswire article: h

CytoDyn included in this PR Newswire article:

https://invest.ameritrade.com/grid/p/site#r=j...105p3305-1

Quote:

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CytoDyn Inc. (OTCQB: CYDY) a late-stage biotechnology company developing leronlimab (PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, recently announced a comprehensive update and overview of the therapeutic indications from over 30 COVID-19 patients recently treated with leronlimab in over 4 hospitals and clinics throughout the country. More than 25 hospitals, to date, have requested participation in the Company's trials.

Patient enrollment in the Company's two clinical trials and Emergency Investigational New Drug (EIND) is as follows: 1) More than 25 patients have been administered leronlimab under EINDs authorized by the U.S. Food and Drug Administration (FDA); 2) Rate of response in mild-to-moderate patients under EIND has been very promising with the first five patients treated being removed from oxygen; 3) As of last week, 12 patients have been treated in the Phase 2 trial for mild-to-moderate COVID-19 indications and, because it is a double-blinded, placebo-controlled trial, results are not yet available; and 4) First site cleared to enroll patients in Phase 2b/3 beginning today.

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I realize some of this is a replay from the company PR and in fact the Phase 2b/3 trial actually began yesterday.... but CytoDyn is in the running....