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I am excited, I wonder if we see pr this week, and what sp will do once it hits.
Hope your right! "Should" be this week but if not it will be soon imo. A lot in the works for avvh, and it's exciting, but those who sell for pennies profit could be crying crocodile tears by end of July.
I agree, I got in IQST at .09 and got lucky to get out at $1.80 after it hit $2.00. I think this will be a lot better than that, go AVVH.
I apologize, I am not trying to be in any way a "doubter". I should have expressed my thoughts better. I have followed for a few months, and just recently jumped in at .065, and am excited for the future. As far as investing what I am comfortable with, I'm fine with it. This is my first experience with a custodianship and I'm not sure of possibilities is what I'm saying.
I hope risks are worth it. I jumped in with a large investment,(for me 10% of portfolio). Is there any way that the merger will not happen? Is it possible the share cancellation will be voided? I am excited about possibilities, but very nervous as well. I've read up on Gold Quest, and understand they are the real deal, but still would like a little more than a couple tweets for confirmation.
Truthfully I would be very happy if we reached $1 by eoy. That's more than 10x where we are now!
Glad to have found this. Potential here is overwhelming! This could get to $5 by eoy.
FDA approved Biogen's alz drug without evidence of it's efficacy and against review committee's recomendation. Why do people say leronlimab must meet any kind of a level efficacy as an argument against it's approval? If people want to try it, it should be made available, and let the free market decide imo.
Who wants to enroll in a trial if the drug is available? Why does leronlimab need to meet stat sig? It is irrelevant according to FDA. Just sell what you want and let the free market determine if your drug will be successful.
Pumping is just as bad as bashing. People buy on the hype, and when news doesn't happen they sell to MM's at a loss. Let's keep it real.
No shorting, just people tired of waiting. Lot's of pumping, and no news gets old. Reality is IF and that's a mountain of a if, there is a merger it may go to .10-.15 cents imo.
Been watching for a bit, joined the party at .068, any idea when we hear news regarding Gold Quest? Will this be a merger, or is it possible that a new company is formed?
Misiu143, I agree that this is only beginning. I don't understand when I read posters who scream there is no revenue yet, how can they think they are affecting any thought process of individuals who read their post, other than they will shake their head is disbelief. IMO Indonesia and Malaysia are in contact with Chiral and asking questions. It is only a matter of time. GLTA
I am becoming more convinced that FDA and BP will do to CytoDyn what GM and politicians did back then. Hate to say it, but saying odds are against leronlimab being approved, is like saying odds are against me flying to the moon. I love the science, just saying what I think.
Yes it is good news. However until profits are realized, volume will remain low and mm's will continue owning price.
Why can't they say "has been submitted"! Why all the pomp and circumstance about plans to submit? We've all heard about it, just get it started already! Certainly contributes to the uncertainty surrounding this stock. If it's going to be in a few days, wait until it happens, then pr it, otherwise be quiet, it doesn't help.
Misiu143 do you think a statement from CytoDyn saying something like " we appreciate the FDA and their efforts to find thereaputics to treat covid19, and we plan on having trials in Brazil at Albert Einstein hospital which will have our preferred 4 dose regimen with severe and critical patients to address the issues in cd12 trial". There was a post on another mb to this effect. Do you think a response would be wise?
FDA's decision not to include 4 doses for CD12 trial is what prompted many longs to petition FDA. I know that you feel that longs are "pestering" and their concerns for unfairness are putting the chance of approval from US FDA at risk, but I ask you, if the trial was approached with the same method as Remdesivir where they had the flexibility to change end points and dosing, do you really believe that leronlimab would not prove superior? Every other country and WHO are all calling for an end to treatment with Remdesivir, yet the US continues to use this drug. So since it appears that leronlimab was treated unfairly, do you honestly believe that the approach by many doctors and members of this board can cause any more harm. FDA has shown that they are corrupt imo, not only from the design of the CD12 trial where 4 doses was not allowed, but from the timing of the pr that was put out during market hours. If you believe otherwise, then you have a short interest to satisfy imo and are unworthy of any further conversation.
Misiu143 you are truly a hero. I sincerely hope this has a positive impact on people of influence within the FDA. What is your realistic expectation?
Scooter, so what would your response be to those people who have been "data mining" if results from Brazil with 4 doses turn out to be stat sig for entire critical group at interm analysis? As you are very aware, the claim that 4 doses for cd12 was denied, and many claim it caused the failure. Do you feel that Brazil should grant EUA with those results?
I was under impression that trial had to be done first in India.
Misiu143 if trials are successful and Brazil grants EUA at interm analysis, what will FDA's response be? If trial is stat sig with the number of patients, how can they ignore it? Could India grant EUA from those results?
What would be significant? 10 thousand vials? When?
Any mention of India in CC?
What happened to 28 receiving csp? No word on them. When are we expecting results?
Even MacLeod cannot sell leronlimab unless given the CSP or EUA by government. I don't see that happening imo.
Daemon57, respect it doesn't say anything about a sale. It says that Macleods has "the exclusive right to distribute Vyrologix for COVID-19 in India for a three-year period in accordance with the treatment protocols approved under the applicable CSP or EUA". It has to be approved! I have a hard time seeing that anytime soon imo.
Will there even be a trial in Brazil? Will CytoDyn have enough money to get it done?
Below $1 without sales pr by end of week imo.
What are chances of revenue this year? None imo, as all countries mentioned as being interested have been put on notice. Possible BO at sub $2 possible is on the horizon.
No EUA from Philippines is being broadcasted. There is some nefarious activity going on here. I'm sure now Philippines is off the table. I wonder also about India. What will their FDA do, give money for a drug that received such an open rebuke? Hard to fathom. Even if Brazil goes ahead with planned trials, I doubt that interm results will bring EUA. Very long road to revenue for CytoDyn it seems. Well timed and planned by FDA ant the bequest of BP I'm sure.
I believe this is for the benefit of Philippines FDA. No EUA allowed. Just a reminder who is boss.
I thought CytoDyn said they were giving away 400 vials. Why do you think the 150 patients who have been treated were not part of this group. I still don't think any PO has been signed, regardless of the distribution agreement with Chiral. You think NP told the truth regarding revenue, well I don't imo.
As CEO he doesn't get a pass for "spewing" material info. It is lying and he should be held accountable
Daemon57, now with no revenue this past week, what are your realistic expectations for the near future? Is there any chance for leronlimab with NP as CEO in your opinion? A lot of promises, but never coming through is the pattern I see and it doesn't bode well for the sp without a BO imo.
I believe something of substance, i.e. EUA or PO produced, then we will be under $2 by end of next week imo.
Just show me da money. Don't talk about it, do it or be quiet.
With all that he has said that have been flat out lies, do you believe this??? I don't. I do believe he is trying to find a way to pump up sp for personal reasons, and he thinks that shareholders can't see through the bs. Just announce EUA or PO, if not, be quiet.
There needs to be a BO period.
As far as NP is concerned, don't say anything more until contract signed. Stop lying! You can't say "I hope so" 50 times without results and expect any kind of respect. If you can't run with the big dogs, stay on the porch. NP needs to leave for leronlimab to reach it's full potential imo.