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Hmmm it appears misiu said "normal" Fedex---
Yes they send by FedEx,
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=165394507
Says here---
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8 °C for one week. Store at -20 to -80 °C for twelve months from the date of receipt.
Target Information
Leronlimab (PRO140) is a humanized IgG4 monoclonal antibody that can target to block chemokine receptor 5 (CCR5), a cell receptor used in HIV infection, tumor metastasis, and immune signal transduction Play multiple roles.
https://www.thermofisher.com/antibody/product/Leronlimab-Antibody-Recombinant-Monoclonal/MA5-42195#:~:text=Use%20a%20manual%20defrost%20freezer%20and%20avoid%20repeated,for%20twelve%20months%20from%20the%20date%20of%20receipt.
FedEx says---
Cold shipping package provided by FedEx
Cold shipping package provided by FedEx can keep your temperature-sensitive shipments between 2°C and 8°C (35°F and 46°F) for 48 or 96 hours* without the weight, hassle and expense of using dry ice or gel packs.
https://www.fedex.com/en-us/shipping/temperature-control/refrigerated-cold-shipping.html
Jet Flight? FedEx? Somebody is lying---
Black-Ops:
FDA ((((((((FULL HOLD)))))))) still intact?
Yes or no?
Thanks fd, the timelines dont lie...36 minutes from article posted on Zerohedge to pumped with link included here on this message board in the middle of the night.
Precision coordination involving both participants from start to finish indeed.
How prophetic--- Please read my last post ,
Interesting timeline here---
36 minutes from story published to story touted here on this message board:
Um, dolph, tell the truth, dont lie, did she let you know she had been contacted and asked permission to publish her story?
Stop lying...you dont know who "chessmaster" is and if you did you wouldnt cough him up.
Too late dolph, the word is out.
Admitting she colluded with a professional tout before the article was posted, never mentioned anything about it, and then was the first person on this msg board to post a link to the article...
Looks like securities fraud to me too.
(a SEC violation)--- Without a doubt.
LOL! misipoo got a 30 day time out in Ihub jail.
LAUGHING
OOOPS! I remember Senior Admin Shelly saying there is a zero tolerance policy on doxxing.
Lets see if misi baby limps back on the playing field.
LAUGHING
2 year old maps from internet randos wont do you much good so who is "chessmaster" the author in the Zerohedge paid pump which you didnt say anything about until you furnished the link AFTER the article was published?
Hmmm, no "chessmaster" aliases on Ihub so who is it?
As of right now, all roads lead to d0lphintom.
Um, misiu, just one more thing...
How was the author "chessmaster" able to get in contact with you?
Did he look in the phone book under "misiu143" and find it?
Is "chessmaster" your buddy "d0lphintom"?
We know hes a professional writer of books involving stocks charts and what nots...and hes repeatedly admitted having discussions with you via telephone.
Need the links?
Who exactly is "chessmaster" (the author) or did you even ask?
If you didnt ask, why didnt you want to know?
Did the author of the article describe himself as "chessmaster" to you or did he divulge his true identity?
If so, who exactly is "chessmaster"?
Were you compensated for your efforts/contributions to the article?
Why didnt you tell this board a PAID article was about to hit Zerohedge at the same time you were "supposedly" contacted to do the article?
So you knew well in advance the PAID article was going to be published on Zerohedge and the first poster on this CYDY message board to mention the Zerohedge article is that correct?
So by your own admission you were directly involved in the publishing of a paid article that was eventually removed from the Zerohedge website is that correct?
This is what Zerohedge says by their own admission what they are in the business of doing----
And I quote:
Lemme get this straight...so you as the "mother" described in the article has absolutely no idea why the article was scrubbed?
Zerohedge (or their lawyers) never contacted you and advised you as to the reason the article was removed?
Why was this article scrubbed from the Zerohedge website?
Was it fact checked for truthfulness and found out to be a lie?
Leronlimab Anecdotes - A Patient's Perspective - Beating the System
BY CHESSMASTER
THURSDAY, AUG 12, 2021 - 22:03
CytoDyn, appears to be the only biotech company with a proven treatment in a large randomized controlled trial for severe and critical COVID-19. Proven means their drug reduced 14 day mortality by 82% in a phase 3 clinical trial. Proven doesn't mean the drug is approved by the FDA because they asked for more data. This is the rub because it's proven, but not approved and because of that the company has been under constant assault and criticism for how the management team has been handling the clinical trials. Their leading drug candidate is called leronlimab and is branded as Vyrologix and it has single handedly taken dying from COVID-19 off the table. Many of the critics of the Company are shareholders and in one special case a group of shareholders that called themselves Advancing Leronlimab and used what the Company described and illegal tactics to challenge the board of directors. Luckily for patients around the world their bid for greed and avarice failed.
When you put aside the greed and take a hard look at the company, their mission statement is to save lives and of course maximize shareholder value. This management team may be tiny in comparison to most biotechs, but enormous in terms of heart. This team actually cares for patients personally and at one time in the pandemic had the largest number of compassionate use approvals. The truth is that there’s only one reason for breaking a record for compassionate use and it has to do with the viability of the treatment. Many that have gotten either compassionate use or the rarely used Right to Try approvals have interfaced with top management as they worked tirelessly to get the approvals processed as quickly as possible.
Shareholders that have a hard time understanding how a drug with so much potential isn't approved by now don't understand how challenging the drug development process is, and they certainly don’t understand a management that seems to put patients’ lives first. At CytoDyn the CEO has gotten himself personally involved in pushing the process of many Emergency IND’s and compassionate use requests. This is not a normal thing that people are likely to see at any other biotech on the globe. The corporate culture really values human life and seems to do anything they can to preserve it.
Leronlimab has saved many lives. A very recent anecdotal report of another life saved by leronlimab underscores the importance of how truly revolutionary this drug could become. In order to preserve the privacy of the patient no identifying details will be used. Approximately 2 weeks ago a mother in the medical field was talking to her grown son who is also in the medical field and noticed over the phone that he sounded sick and nasally. The son indicated that he just had a bad cold and that something was going around because he thought since all people were all wearing masks for so long that their natural immunity was compromised and colds were on the rise. The mom was skeptical of the answer and made him take a home covid test from the pharmacy. Although he tested positive, the mom was well versed in treatment options and was prepared. She pumped him up with ivermectin, vitamins and eventually resorted to hydroxychloroquine. Nothing seemed to work, and after a couple of days his oxygen levels eventually dropped into the mid 70’s forcing him to call an ambulance. When he arrived he found himself in an unfortunate situation. The Floridian healthcare system was experiencing a surge and was overrun with patients. After many hours of waiting he was diagnosed via a chest X ray having double lobe pneumonia, no treatment was administered and the son found his way back home after picking up a canister of oxygen to use at home. During his wait in the Emergency room he was not provided water, or intravenous fluids, or a bed to lay down on. Despite his use of oxygen at home his oxygen levels continued to deteriorate to 74%. He could barely breathe or talk. This put him at severe risk of dying, he needed to get back to the hospital. The surrounding hospitals were all full capacity so the resourceful mom called around looking for open beds. Eventually he was admitted to another hospital with a compassionate doctor leading the treatment. The first treatment offered was Remdesivir and that was patently rejected by the mom who read the reports and understood it was not appropriate for her son's situation. This was a cytokine storm not a viral infection. She made it known that she wanted leronlimab to be used for her son. Instead of saying no, the doctor suggested they try one of the approved options like tocilizumab first and see if there was any change before they go the Right to Try route. After 3 days of seeing continued deterioration the Right to Try paperwork was signed by the doctor. The drug made it to the hospital the very next day. This was very A-typical because the mom was completely prepared and was on top of the communication.
Before taking leronlimab the patient was on high flow oxygen consuming between 6 – 10 liters. Since leronlimab is a subcutaneous shot it takes time to enter the bloodstream and she cautioned her son to remain patient. After administration it took two hours before there was a change in his status. The patient was able to talk better and had a more productive cough and the oxygen saturation levels started to increase. After 4-5 hours oxygen levels improves so much high flow oxygen was removed and reduced to the nasal cannula. The patient's strength was coming back and he felt like leaving the hospital, but there was also pressure for him to leave to make room for the sick that were in the hallways. The patient was ultimately discharged 26 hours after being injected with leronlimab, and went home with instructions to use oxygen as needed and report back if there was a worsening of conditions.
All these anecdotal patients that took leronlimab, which numbers over 100 understand one truth. The drug works and works extremely well and in most cases quickly. The last thing these patients care about is the greed involved in developing a drug and the he said she said minutia in the boardroom. They welcome a CEO and a company with a refreshing attitude that just wants to save lives. Critically ill patients have been abandoned by both the FDA with their draconian policies and politicians whom seem to be more concerned about mandating vaccines and masks. Team CytoDyn and Hero moms need to be celebrated whenever possible.
The measures to curb the pandemic failed with over 620,000 American in body bags. Initial estimates were 200,000. History will eventually reflect upon how many lives that could have been saved if leronlimab was approved sooner. There is still a long approval road ahead for leronlimab in the United States, but Brazil has their own pivotal trial starting imminently and may be the first beneficiary of a COVID drug that takes dying off the table and flattens the curve.
The situation in Florida with respect to available ICU beds is really bad and here sits a drug that saves the lives of almost everyone it touches. It also has the potential to seriously flatten the curve in hard hit areas because if all the people sitting in the hallways were given this very safe drug they might actually go home like this patient did. People need to know about this drug and the process required to get it. Right now it's only available via Right to Try since it doesn't have its EUA approval or any active clinical trial sites in the USA. Eventually the FDA will come around to approving this drug but in the meantime it's pointless to provoke the FDA and try to force an approval. That's been tried before and has failed. People just need to work within the system to get the drug for your loved ones should they need it. The hero mom in this story was well educated and prepared on what to do in case of this eventuality. Advanced preparedness seems to be partly responsible for the happy ending. So the lesson learned here is that there is no substitute for preparation. It's clear that this drug takes dying off the table and when politicians decide they've seen enough body bags then maybe this drug will see the light of day for use in COVID-19 in the United States.
Right to Try is the only way to access leronlimab and take dying off the table for severe to critical patients. The only hitch is that you have to ask for it and you have to get a doctor at the hospital willing to step up. These anecdotal reports are just whispers right now, but they will turn into a thunderous call to action as the pandemic worsens and news of the drugs success continues to spread.
The "twins" story show up in a online website aimed at the investing public?
Leronlimab Anecdotes - A Patient's Perspective - Beating the System
BY CHESSMASTER
THURSDAY, AUG 12, 2021 - 22:03
CytoDyn, appears to be the only biotech company with a proven treatment in a large randomized controlled trial for severe and critical COVID-19. Proven means their drug reduced 14 day mortality by 82% in a phase 3 clinical trial. Proven doesn't mean the drug is approved by the FDA because they asked for more data. This is the rub because it's proven, but not approved and because of that the company has been under constant assault and criticism for how the management team has been handling the clinical trials. Their leading drug candidate is called leronlimab and is branded as Vyrologix and it has single handedly taken dying from COVID-19 off the table. Many of the critics of the Company are shareholders and in one special case a group of shareholders that called themselves Advancing Leronlimab and used what the Company described and illegal tactics to challenge the board of directors. Luckily for patients around the world their bid for greed and avarice failed.
When you put aside the greed and take a hard look at the company, their mission statement is to save lives and of course maximize shareholder value. This management team may be tiny in comparison to most biotechs, but enormous in terms of heart. This team actually cares for patients personally and at one time in the pandemic had the largest number of compassionate use approvals. The truth is that there’s only one reason for breaking a record for compassionate use and it has to do with the viability of the treatment. Many that have gotten either compassionate use or the rarely used Right to Try approvals have interfaced with top management as they worked tirelessly to get the approvals processed as quickly as possible.
Shareholders that have a hard time understanding how a drug with so much potential isn't approved by now don't understand how challenging the drug development process is, and they certainly don’t understand a management that seems to put patients’ lives first. At CytoDyn the CEO has gotten himself personally involved in pushing the process of many Emergency IND’s and compassionate use requests. This is not a normal thing that people are likely to see at any other biotech on the globe. The corporate culture really values human life and seems to do anything they can to preserve it.
Leronlimab has saved many lives. A very recent anecdotal report of another life saved by leronlimab underscores the importance of how truly revolutionary this drug could become. In order to preserve the privacy of the patient no identifying details will be used. Approximately 2 weeks ago a mother in the medical field was talking to her grown son who is also in the medical field and noticed over the phone that he sounded sick and nasally. The son indicated that he just had a bad cold and that something was going around because he thought since all people were all wearing masks for so long that their natural immunity was compromised and colds were on the rise. The mom was skeptical of the answer and made him take a home covid test from the pharmacy. Although he tested positive, the mom was well versed in treatment options and was prepared. She pumped him up with ivermectin, vitamins and eventually resorted to hydroxychloroquine. Nothing seemed to work, and after a couple of days his oxygen levels eventually dropped into the mid 70’s forcing him to call an ambulance. When he arrived he found himself in an unfortunate situation. The Floridian healthcare system was experiencing a surge and was overrun with patients. After many hours of waiting he was diagnosed via a chest X ray having double lobe pneumonia, no treatment was administered and the son found his way back home after picking up a canister of oxygen to use at home. During his wait in the Emergency room he was not provided water, or intravenous fluids, or a bed to lay down on. Despite his use of oxygen at home his oxygen levels continued to deteriorate to 74%. He could barely breathe or talk. This put him at severe risk of dying, he needed to get back to the hospital. The surrounding hospitals were all full capacity so the resourceful mom called around looking for open beds. Eventually he was admitted to another hospital with a compassionate doctor leading the treatment. The first treatment offered was Remdesivir and that was patently rejected by the mom who read the reports and understood it was not appropriate for her son's situation. This was a cytokine storm not a viral infection. She made it known that she wanted leronlimab to be used for her son. Instead of saying no, the doctor suggested they try one of the approved options like tocilizumab first and see if there was any change before they go the Right to Try route. After 3 days of seeing continued deterioration the Right to Try paperwork was signed by the doctor. The drug made it to the hospital the very next day. This was very A-typical because the mom was completely prepared and was on top of the communication.
Before taking leronlimab the patient was on high flow oxygen consuming between 6 – 10 liters. Since leronlimab is a subcutaneous shot it takes time to enter the bloodstream and she cautioned her son to remain patient. After administration it took two hours before there was a change in his status. The patient was able to talk better and had a more productive cough and the oxygen saturation levels started to increase. After 4-5 hours oxygen levels improves so much high flow oxygen was removed and reduced to the nasal cannula. The patient's strength was coming back and he felt like leaving the hospital, but there was also pressure for him to leave to make room for the sick that were in the hallways. The patient was ultimately discharged 26 hours after being injected with leronlimab, and went home with instructions to use oxygen as needed and report back if there was a worsening of conditions.
All these anecdotal patients that took leronlimab, which numbers over 100 understand one truth. The drug works and works extremely well and in most cases quickly. The last thing these patients care about is the greed involved in developing a drug and the he said she said minutia in the boardroom. They welcome a CEO and a company with a refreshing attitude that just wants to save lives. Critically ill patients have been abandoned by both the FDA with their draconian policies and politicians whom seem to be more concerned about mandating vaccines and masks. Team CytoDyn and Hero moms need to be celebrated whenever possible.
The measures to curb the pandemic failed with over 620,000 American in body bags. Initial estimates were 200,000. History will eventually reflect upon how many lives that could have been saved if leronlimab was approved sooner. There is still a long approval road ahead for leronlimab in the United States, but Brazil has their own pivotal trial starting imminently and may be the first beneficiary of a COVID drug that takes dying off the table and flattens the curve.
The situation in Florida with respect to available ICU beds is really bad and here sits a drug that saves the lives of almost everyone it touches. It also has the potential to seriously flatten the curve in hard hit areas because if all the people sitting in the hallways were given this very safe drug they might actually go home like this patient did. People need to know about this drug and the process required to get it. Right now it's only available via Right to Try since it doesn't have its EUA approval or any active clinical trial sites in the USA. Eventually the FDA will come around to approving this drug but in the meantime it's pointless to provoke the FDA and try to force an approval. That's been tried before and has failed. People just need to work within the system to get the drug for your loved ones should they need it. The hero mom in this story was well educated and prepared on what to do in case of this eventuality. Advanced preparedness seems to be partly responsible for the happy ending. So the lesson learned here is that there is no substitute for preparation. It's clear that this drug takes dying off the table and when politicians decide they've seen enough body bags then maybe this drug will see the light of day for use in COVID-19 in the United States.
Right to Try is the only way to access leronlimab and take dying off the table for severe to critical patients. The only hitch is that you have to ask for it and you have to get a doctor at the hospital willing to step up. These anecdotal reports are just whispers right now, but they will turn into a thunderous call to action as the pandemic worsens and news of the drugs success continues to spread.
Yes kg, I mustve struck a nerve because misi baby went crazy with that post.
Im only trying to help. Maybe she realized she needs to seek the professional mental help she so desperately needs.
Thank you for admitting I was telling the truth in my previous post.
if only EUA was given to our critical , as it should be Based on what data? Pump PRs and videos?
As a doctor, what statistical medical evidence says leronsaline shouldve been given an emergency use authorization?
On your say so only? With no evidence? There are rules applied as to EUA approval. RULES!
Case in point...when we we both moderating this board and I had to re-delete over 100 times on at least a couple of posts that you insisted on reinstating. You werent following the guidelines of the rules, you decided on your own that one of your pumper buddies post should stand regardless is if violated the RULES or not.
Admins had to step in and permanently delete those post and eventually got tired of your "episodes" and removed you from being a mod.
You tried the same shit with Janet Woodcock, that backfired and you moved on to Zerohedge.
Folks that know you personally reading this post will say "yep, thats her alright".
Go ahead, say Im lying about this, go ahead.
Yup kg, thats gotta be the worst step-by-step tutorial in the history of mankind.
Almost as bad as a "doctor" seeking medical procedure from an internet stock message board on how to get leronsaline.
Indeed kgro, a "doctor" refusing to help their fellow man in dire need by NOT posting a step by step tutorial on how to receive a drug via the Right To Try Act.
Harrasing Janet Woodcock, lazarus boy story, Calissio, Zerohedge article, etc., same name keeps popping up.
Good luck.
He fessed up and said the twins were "mythical".
Any chance the DOJ has subpoenaed information regarding your lazarus boy story?
Cmon, stop the bullshit. If you go the the hospital for a broken finger theyre going to give you a prescription for pain before they send you out the door.
Like I said you will be considered to be a LIAR until proven otherwise.
Um, misiu, all youre doing is repeating the same story without providing any proof.
Lets say I was hospitalized and was given a prescription.
To prove Im not a liar at the very minimum I would provide a screen shot of the prescribed drug (personal info redacted) with the date of the prescription.
Face it, without proof of your story you are considered to be a liar until proven otherwise.
that our drug saved my son life. My story is true , and hopefully one of this days Sec will react to all this stories posted here by us all , and see which stories are true , and which just to manipulate other shareholders
Lets say the SEC asks you for proof to confirm leronsaline saved your sons life.
Can you provide proof? If you cant they might see your yodeling as an attempt to manipulate the stock.
Marinade on that.
Bags aint happy thats for sure. Leronsaline no better than placebo---
PROVE kgro gave this junk to his twins.
Sure, he said it, now you PROVE that he actually did it...you stupid f-ing idiot.
Yes kgro, and other facts like a drug no better than saline and these idiots think this swill is the answer to saving humanity.
Big salary insiders prolly LAUGHING.
Dr NP.....didn’t write papers .. Um, moosiu, do you say dumb shit/lie for attention or for people to chit chat with you online?
And there ya have it folks... 20.5% vs 21.6% is basically the same.
Thanks for proving leronsaline is no better than placebo.
Just answer the goddam question and quit pretending to be confused.
Is the placebo percentage higher or lower?
The other pumper was smart enough to not reply...YOU on the other hand chose to compound your ignorance.
And as kgro pointed out in regards to the mITT shit, this is what the DD says about that---