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I believe the original conversations with Diwan stated that once the building purchase was completed it would take about six months to have the cGMP ready to produce CIDES. I seem to remember a Sept./Oct. 2012 timeframe. Up to that point, the current labs can produce sufficient materials to complete toxicology and pharmacology studies required to file the NDA. Seymour also stated that the entire lab would be fabricated off-site, trucked in, and installed in a couple of weeks. We'll see.
Are you telling me that if it walks like a duck and quacks like a duck........
Is there animosity or antagonism between Seymour and Erhlich over his departure? If so, do you think that has any impact on Menon's support of NNVC?
Is there any business relationship between Cellceutix (CTIX) and the principals of NNVC? Leo Erhlich was CFO at NNVC and left under a cloud with his ten million founders shares. I believe that Kard Scientific is associated with them as well.
Drip, drip, drip.......
That particular gentleman does not speak for the board or shareholders at large. He certainly doesn't speak for me.
How long can it possibly take to pull out a calendar and pick one of three dates. Another great example of our government in action. I'm reminded of that greatest of oxymorons, "Hi, we're from the government and we're here to help you."
The law of large numbers makes it true.
There are a hundred million shares floating around unaccounted for. Some of that is smart money.
If offered as compassionate treatment for a dying man, could Rabicide be administered to the rabies victim?
My bad. I forgot to check the market schedule before I commented. I must remember to only comment AFTER my first cup of coffee.
I really thought there would be an announcement of a date for the FDA meeting today. It has been thirty days since the original information. After six years one should get used to disappointments with NNVC timeliness.
I pray that one day the names of Anil Diwan and Eugene Seymour will be mentioned in the same hallowed terms as Alexander Fleming. Happy New Year to all.
Hawaii in 2013?
I believe they have thirty days to reply and sixty days to schedule a meeting/call. I'm sure that if they have responded it's not something NNVC wants to release into the doldrums of the last week of the year.
Happy New Year to all. May it be a good one for NNVC.
Congratulations!!! Now the long slog to 3rd phase approval begins. Allan's 2014/15 still looks good. See everyone in Hawaii in 2013.
If Diwan, Seymour , Theracour or any other insider or 5% stockholder were selling, wouldn't they be required to report it under SEC rules?
I didn't say they did. I simply asked you for your reasoning and you gave it to me. Thank You.
What is your basis for stating that Seaside must sell their shares? They can do as they please. I imagine they are holding some shares for long term appreciation. They must believe in the technology to have invested in the first place.
Welcome back Keltoi, you were missed, you cantankerous old curmudgeon.
How do you know ES and AD are not working every day? Remember, you are not a participant.
If one chooses it to be.
I am not criticizing the company or its management. I am frustrated that the call hasn't been made, but I am confident it will be when the dossier is ready. In the meantime as a non-participant investor, I can only wait and encourage the participants. It adds nothing to the dialogue to continually harp on the same old canards unless it is your motivation to disrupt the market for your own pecuniary gain.
Anyone who is not inside the company and working on the problem.
NNVC has tested its viricide on 3500+ animals with 100% positive test results, they have done this with minimum investment and dilution when compared with other pharmaceutical start-ups. They are well ahead of the curve when compared to other vaccine related developments. I think that speaks more to the issue than uninformed criticisms by non-participants.
That may be one of the most ludicrous posts I have ever seen. Anil Diwan created this biologic and is working diligently to get it to market. What have you done?
Amen, Doc.
And to you Kelt. Life is too short to focus on the negatives.
Quantify moments.
In a reply to someone's email, Dr. Seymour said that everything was now in BCG's hands and the submission timing depended on BCG finishing the dossier. That was two or three months ago.
The way it was stated was very confusing. Since this is the NNVC board, I assumed you were referring to NNVC.
Doc, you speak of this as fact. How could you know this without receiving inside information? I hope you are right.
Uh-Oh Doc. Looks like you might have jinxed us.
There is an excellent article in Time Magazine for Nov. 2nd. It deals with organizations trying to find and deal with newly mutant viruses that can jump from animals to humans. The goal is to head-off a new viral pandemic like the 1918 Spanish flu which killed nearly 100,000,000 people worldwide.
Perleman has been involved in many scandals. Check out his bio.
As frustrated as I get with the glacial pace of NNVC, I must assume that they, as the experts in drug development and in relations with the FDA, know what they are doing. They must be as anxious as any of us "IHUB boarders" to see their fifteen years of work come to fruition. I will now go back to sleep and await a positive announcement from DR. Seymour.
What is the basis for that date?
It seems that everytime NNVC gets a little headwind, management comes along and does something to knock it down. When will it ever end?
The Pfizer person said that NNVC does not yet have "proof of concept" for Viricides. Does that come with a successful Phase 1 trial or must one get further down the testing path?
Does this mean that process and prodecure are more important to the FDA than the relief of human suffering?
Here we go again. When NNVC detractors can't find anything factual to criticize they dredge up the old canards against Dr. Menon. Different aliases, same old story.