This concerns you,,
5K people will die every day until an effective therapeutic is approved for COVID. Leronlimab has demonstrated that it could save 4K of them but it is being intentionally suppressed. Leronlimab has the potential to disrupt a pharmaceutical company with a market cap of $90b and obsolete much of their product line. To this company, suppressing or owning Leronlimab is a matter of corporate survival.
The millions that have died from COVID didn’t volunteer and you can’t control your fate any more than they did. 5 thousand will die today and every day for the foreseeable future. 4 thousand of them could have been saved by Cytodyn and their new drug Leronlimab*! Unfortunately, Cytodyn is a very small Biotech (22 employees) still in the pre-revenue phase and it is fighting a monumental battle against one particular goliath of a Big Pharma ($90b market cap) to get Leronlimab to the public. The byproduct of this battle has been hundreds of thousands of avoidable deaths and the battle is still raging with no end in sight.
All sports employ scouts to find the best talent in order to not only improve their team but to eliminate playing against them. Big Pharma employs the exact same tactic and a scout discovered a drug that has the potential to be on par with any of the greatest therapeutic discoveries in history, Penicillin included! Historically, BP attempts to gain ownership of the new rising star by partnering or buyout. Knowing they have a drug with the potential for hall of fame revenues, Cytodyn is not interested in sharing the proceeds from a drug that will sell itself. Accordingly, a deliberate, well thought out, comprehensive plan to suppress Leronlimab and keep Cytodyn from revenues was executed in an attempt for a hostile takeover. The evidence against BP in this battle is beyond the scope of this letter because it is too expansive to detail in this format. I can say it ranges from government coercion, CYDY stock manipulation (over 70 lawsuits from fictious firms-that has to be a record!), media suppression and foreign government interference. This war includes everything from crowd control on social media to the highest levels of government. Never in history has a company who is tasked with the well-being of humanity killed so many to stay in business. The fight is on to not only own this future legend but to not compete against it. I’ve outlined a few of the events I’ve observed in the year I’ve been invested in my open letter** to President Biden that proves BP suppression of Cytodyn. Goliath is in a fight for existence during a pandemic and they are doing everything in their power to keep Cytodyn from revenues. I can’t overstress that this battle has caused the deaths of hundreds of thousands of people that could have been saved and these people believed this very company would save them. The death toll will grow every day by approximately 5k until the FDA issues the EUA the world desperately needs!
In the interest of brevity please consider that if something is blatantly obvious, certainly, there is more buried beneath. The tip of this Iceberg exposed itself late last year when the FDA, in response to a trial protocol request by Cytodyn for 4-doses in their CD12, rejected that request and directed 2-doses over 2 weeks. The sole purpose of that unfounded rejection was to handicap the trial, prevent an EUA, and to delay revenues for Cytodyn. Once Leronlimab is EUA’d the war ends, Cytodyn wins and Goliath dies slowly over the next 5-10 years.
One of the primary considerations in trial design and protocol is safety. The move to reject a 4-dose protocol is not only a complete reversal of a previous FDA decision on Leronlimab’s safety, it represents the opposite end of the stick. The FDA previously determined that Leronlimab was safe enough to be self-injected at home on a weekly basis. That represents the ultimate vote of confidence by the FDA for a new drug.
To not only refuse a request for 4 doses to a dying person in an ICU hospital setting but to tell them they can only have 2 does when people have taken 100’s of doses at home, some for 6 years, defies any medical or scientific justification and is a complete reversal of an established safety protocol. How do you justify telling one group you can take hundreds of doses at home spanning years and another group dying in an ICU: sorry, only 2 doses for you? What kind of pressure was being applied by Goliath to the persons who made the decision to change a standing policy and kill hundreds of thousands?
Hundreds of thousands are drowning in their own bodies and the FDA is holding the life preserver that could save 80%*** of them yet they won’t throw it!
Due to the scale of avoidable death and the fact that it will continue globally, it is the responsibility of Congress to Investigate.
Getting Congress to investigate is up to you. If you are reading this letter, you have a responsibility to everyone you love to spread this word as far and wide and as fast as you can because your life may depend on it one day and if you wait until it does, it’s too late. Do it for the kids that are now dying from COVID. Copy, paste and edit this letter**** then send to every government official you can, send the link to this letter via social media and encourage participation-5 minutes a day to possibly save someone you love from a fate that is out of their control. It will become part of my morning routine until the investigation is announced, I can only hope I’m not doing it alone.
A company with a $90b market cap is not going to roll over and die, it is not going to fight fair, it doesn’t care who dies and it will never stop fighting for its existence. The only way to win this battle is by Cytodyn achieving revenues and by producing as much Leronlimab as it can, as fast as it can. This is the equivalent of a high school football team (no offense CYDY team, you’re all awesome) against the Buccaneers at the top of their game and every down is played at 100%, no mercy and no Refs. It is up to you to reach Congress***** and the only way to do that is by a social storm of outrage, tell Congress you want Goliath held accountable once the evidence is revealed. Every day matters to the dying, the life you help save could be your own. The entire world should know this is happening because everybody is at risk!
This concerns you,,
5K people will die every day until an effective therapeutic is approved for COVID. Leronlimab has demonstrated that it could save 4K of them but it is being intentionally suppressed. Leronlimab has the potential to disrupt a pharmaceutical company with a market cap of $90b and obsolete much of their product line. To this company, suppressing or owning Leronlimab is a matter of corporate survival.
Millions have died from COVID! They didn’t volunteer and neither can you control your fate any more than they. Five thousand people will die today and every day for the foreseeable future until an effective therapeutic is approved. Four thousand of them, a full 80% could have been saved* by Cytodyn and their new drug Leronlimab**. However, anecdotal evidence suggests Big Pharma is Coercing the FDA into suppressing this drug. Cytodyn is a very small Biotech (22 employees) still in the pre-revenue phase. It is fighting a monumental battle against one particular goliath of a Big Pharma ($90b market cap) to get Leronlimab to the public. Hundreds of thousands of avoidable deaths are the collateral byproduct of this battle which rages on with no end in sight.
As sports teams scout talent so does Big Pharma. As talent goes, Leronlimab has the potential to be on par with any of the greatest therapeutic discoveries in history - Penicillin included! The list of potential indications for this amazing molecule includes over 20 auto-immune deficiencies, multiple cancers, HIV and NASH among other life-threating diseases. Coupled with an almost unheard-of pharmaceutical safety profile (zero SAEs in over 1200 patients) you have the making of a multi-billion dollar per year drug for Cytodyn.
Since Goliath was unable to reach a deal to partner or buyout Cytodyn, it would appear they have executed a plan for a hostile acquisition of Leronlimab. A highly questionable, long standing policy reversal with respect to safety as it pertains to dosing Leronlimab leads one to ask, was the FDA complicit in this plan?
In a four-year HIV trial, the FDA approved hundreds of patients to self-inject on a weekly basis (FDA’s ultimate safety endorsement). Some patients injected 100’s of weekly doses spanning almost 7 years! The FDA rejection of Cytodyn’s request for 4-doses in its phase 3 CD12 trial application (COVID severe/critical) and the subsequent limiting of the protocol to 2-doses handicapped the trial and prevented Statistical Significance. (In addition, the FDA denied Cytodyn the ability to ‘age adjust’ trial data for an uneven distribution of high risk, over age 65 patients in the trial, which would have resulted in Stat Sig). The rationale for that deadly decision must be explained considering the FDA approved a subsequent request for 8 weekly doses in the COVID-19 Long Haulers Study. Cytodyn requested an EUA but was denied due to the results of the 2-dose restriction in CD12. An EUA would have ended the ongoing hostile takeover attempt on Cytodyn and more importantly saved hundreds of thousands of lives.
Due to the scale of avoidable death from this single abhorrent decision, Congress must Investigate. How can the FDA justify telling one group you can take hundreds of weekly doses at home spanning years, yet deny another group dying in an ICU: sorry, only 2 doses for you, then turn around and approve 8 weekly doses to a third group? The FDA withheld 2 additional doses of a potentially lifesaving drug whose worst side effect is headache and diarrhea without scientific or medical justification. Has Goliaths’ massive lobby coerced FDA decision makers, forcing a reversal of a safety endorsement that spanned 7 years - a decision that has resulted in hundreds of thousands of avoidable deaths?
Getting Congress to investigate is up to all of us. If you are reading this letter, you have a responsibility to everyone you love to spread this word as far and wide, and as fast as you can. Your life may depend on the action you take today. Waiting until you or a loved one needs Leronlimab will be too late. Copy, paste and edit this letter*** then send it to every government official you can. For further reference please see my open letter**** to President Biden.
Respectfully submitted,
Alan Hassall
Capt. FedEx Retired
* https://bit.ly/3b9Awfc
** https://bit.ly/3eZDm7q
*** https://bit.ly/3h9LTHv
**** https://bit.ly/3erX5hd
