Replies to post #204285 on Cytodyn Inc (CYDY)

[justdafactss]

New Proactive video on the way---

Additionally, we request that your submission include a comprehensive plan of action to disseminate truthful, non-misleading, and complete corrective communication(s) about the concern(s) discussed in this letter. The corrective communication(s) should be disseminated to the audience(s) that received the promotional communication(s) identified in the opening paragraph of this letter. OPDP recommends that corrective communication(s) include a description of the promotional communication(s) identified in this letter, which misbrand leronlimab; include a summary of the concern(s) described in this letter; and provide information to correct each of these concern(s). Corrective communication(s) should be free of promotional claims and presentations. To the extent possible, corrective communication(s) should be distributed using the same media, and generally for the same duration of time and with the same frequency as the promotional communication(s) identified in the opening paragraph of this letter.
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/cytodyn-inc-626957-02112022

[Bill_ENG]

I'm sure many are hoping to create a selloff with a new FDA letter...

Hence the reason why the 4,000,000 shares that were returned last week were borrowed this morning.

I don't think the shorts or the 13D remnants or the BP minions understand the current holders of Cytodyn stock.

jmo

[StealthGold]

You still thinking there is a secret partnership?

[Rockleo]

Monroe..My 2 Cents..!!!

My interpretation of today’s letter is vastly different from anyone else’s..!!!

The FDA admitted our Day 7 and Day 14 Mortality benefit of 78% and 82% respectively..Compared to Standard of Care..!!! FOR SEVERE TO CRITICAL COVID PATIENTS..!!!

PERIOD..!!!

The FDA did not deny this fact..!!! OR..Call it false..!!!

I believe the FDA is trying to focus the attention of the World Medical Community on these two critical days..To see if the Brazil Trials replicate these outstanding findings..!!!

If the results of our Brazil Trials are similar to our FDA scrutinized CD12 Trial on Day 7 and Day 14..!!!

AND..!!!

With the administration of Dose 3 and 4 ..On Day 14 and Day 21..!!!

The World see’s the Mortality benefit being sustained…All the way to Day 30.!!!

Well..!!!