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Algorythms don't have fat fingers.
RS worries are killing this. Shorts taking advantage.
If this is the case this will be back over $3 in very short order. A link would be great or shorting HF names.
Amen to that porky, this could be over .60 by Friday...Someone has been quietly accumulating down here and the price will follow. IMO
Holding up nicely above the 20MA with great volume.....
Buyers are confident today..
Nice to be back in the 40s...woohoo
You may be right but I doubt if it drops below .05.
If this opens and shows strength above the 20MA tomorrow I am a buyer.
The 10MA will cross the 20, and the 50MA will cross the 200. Both of these will cross tomorrow! I think fundamentals and TA are converging here to set us up for a nice run.
But then again this is pennyland and things can get ugly in a heartbeat.
JMO of course...GL
$ONTY Golden cross shaping up on the daily!!?
Rolling into a stellar ASCO. Could be glorious!
GLTA
Find yourself a wiz-bang chartist and you might be successful.. LOL
LOL, exactly
Yes, a PR with Epilepsy data, followed by a PR announcing a partnership later in the week or following week. We know big pharma has tried and failed with Alzheimers and when they want something they go shopping or make deals. We are in the right place at the right time. I am still buying..
I miss Raging Bull, had alot of good times over there years ago:)
Its like Ravenhome now......:(
Falling like a rock?
Tristar web site is all screwed up. Really needs work.
Good info landing here on Friday......
diversifying
Australian vid from feb. this year. Anavex info at 4:35. Potential market worldwide is 13-67B$.
Dementia, Alzheimer's, & Anavex / The Feed
$AVXL Watching for run this week into fridays epilepsy news.
$AVXL Epilepsy news expected on Friday.
AVXL could run hard this week into fridays epilepsy news, watch or play.
AVXL The week ahead should be interesting!!
39 is here, 40 would make for a nice serene weekend.
This low floater looks interesting especially with the approval and sales in China. This should be getting alot more attention than it is at the moment.
gap at 3 must fill......we have plenty of time
I hope you do make alot of money. I just dont think you're going to make it here for a long time. The average decision time for a De Novo submission is 482 days. That is an eternity holding a bag in sub-penny land. IMO
You may have a longer wait for an FDA decision than you expect.
De Novo
The De Novo process has been around since the implementation of the FDA Modernization Act of 1997 (FDAMA). The FDAMA was intended to help improve the efficiency of bringing low-risk medical devices to market, allowing for simpler reclassification of devices that were classified as Class III due to the lack of a suitable predicate. The section of the FDAMA that handled this aspect of medical device classification (Section 513(f)(2)) became known as the De Novo process.
De Novo is a two-step process that requires a company to submit a 510(k) and complete a standard review, including an analysis of the risk to the patient and operator associate with the use of the device and the substantial equivalence rationale. Once that has been accomplished, and the medical device in question has been determined to be Not Substantially Equivalent (NSE) by the FDA, the product is automatically classified as a Class III device. The manufacturer can then submit a request for evaluation of Automatic Class III designation to have the product reclassified from Class III into Class I or Class II. The FDA will review the device classification proposal and either recommend special controls to create a new Class I or II device classification or determine that the product is a Class III device. If FDA determines that the level of risk associated with the use of the device is appropriate for a Class II or Class I designation, then the product can be cleared as a 510(k) and FDA will issue a new classification regulation and product code. This also adds the device in question to the predicate pool, which in turn broadens the market for other medical device companies considering products in a similar therapeutic area. If the device is not approved through De Novo, then it must go through the standard premarket approval (PMA) process for Class III devices.
Tacked on to the 510(k) review times, devices traveling the De Novo pathway average 482 days of review time from beginning to end.
Further compounding the delays associated with De Novo is the fact that the entire process resembles a procedural “black hole.” The FDA is not required to provide any updates concerning the status of a De Novo application, nor is there any simple way for medical device manufacturers to track a De Novo submission on their own.
De Novo is rare in the realm of low-risk medical devices – a mere 54 products took this particular route between 1998 and 2009. Given the extensive delays associated with the process, MDCI advises medical device companies to consider all other market approval pathways before deciding on to pursue a De Novo reclassification.
Are we going to fill the gap low 3s?..Oh yes, there will be fillage
With OS 1.8B Do you people think this will ever see silver? I know, I know, FDA and all that but the SS is horrendous!! seriously
The RS cheerleaders have vanished as well, it figures. Been thru a few and didnt want to go thru another. Broke even but thats all I did. The real shame here IMO is after all this time, the hope, the great press, the life saving HP, darpa, the speeches, plans, and conferences,.. JJ is really just another penny stock ceo with his head too far up his own backside to give any thought to the share holders who believed he might be the real deal.
That said, I have moved on and am removing this disappointment from my watchlist. Alot of good folks here, hope all of you land on your feet somewhere very green! GLTA
Alex125, you might try optionsXpress.
optionsXpress
Are SS numbers in info box accurate? TIA
Can they legally sit on material info, good or bad, while announcing and executing an RS in such a quick manner as this?
An RS is devastating to share holders, I dont care how high it flys. If management is doing its job there will be no need for such cheap tricks. With CTE results and Hepc treatment with HP this will get all the 'big boy' attention it needs. I hope this is what JJ is thinking about and working for every day. Without solid sales and positive developments, an RS is simply theft. IMO
"(VTL) with a market cap of $504M", SP closing in on 26./share.
The target market is such a tiny percent of the population compared to Aethlon? THAT is what you would call 'execution'. I'm beginning to wonder if JJ is not 90% dreamer, 9% bs'r, and 1% executor because I'm not seeing the level of execution around here that there should be with such a game changing device.
Life saving device............................check
tons of good news and attention...............check
world in need of said device..................check
execution.....................................
"CYTOSORB DUMMY".....LOL
Filters were provided for trials at company expense. The import tax still had to be paid. Your months-long BS campaign isnt working here gary. The new nick really suits you.
Getting??, Ive been in stitches for weeks!..LOL
Pathetic isnt it. He is in the competitors stock and is upset about all the great achievements Aethlon has made in the past few months. My question is... if csto has Euro approval, why hasnt their filter been used on any patients? And it really is to bad about their recent RS. I guess I can see why he would be a little preturbed.
"We", as in "we who are expecting something other than a fluff pr about a patient leaving the hospital", we.
Not the news weve been expecting.
Just say no to drugs.....
And YES to the hemopurifier!!
Drugs are not the solution to everything and just create more problems in the long run.