Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
if you think lymphoseek is something ... you should look into their RIGS product (given that its still 1-3 years away)
$NEOP on bloomberg raido today .. a MUST listen .. http://bit.ly/g1OeEW
thanks for the info. I saw the product, tutorials, and the users guide... It is very clear they are years and hundreds of millions farther ahead of $ECTE
I will walk away with my profits
thanks
Yeah, I've been in them since last year in april/may sometime ... i know the company inside and out and believe that lymphoseek will achieve successful results for neo3-09
I will take some off the top after successful p3, but not that much... prob down to 45-50% of my portfolio until nda submission (which according to bupp in the latest CC which i was on .. will be about 4 weeks later)
I bought more NEOP earlier today @ 3.23 to bring my avg up to 2.29
Update on Pct of my Portfolio holdings-- $amrn 8.99%, $ista 14.81%, $neop 63.77%, $sppi 5.07%, cash 0.09%, unsettled cash 7.26%
Sold out ... couldnt let a profit slip away ended up a little over 40%
WBB Securities giving $NEOP a Strong Buy Rating and 12 Month price of $7.50 http://bit.ly/gtHK4Z
thanks to colorofmoney's input on twitter, I'm reconsidering my strategy for ECTE.OB. I still strongly believe that approval for the device will be 4-5 weeks from now ... but now I am skeptical on its sales potential unless i find something to clear that up
so, i may just sell most of my shares after approval or once it reaches a level to where im comfortable with my profits... we'll see
thanks pcrutch and colorofmoney for your vital inputs.
Yeah I saw this earlier ..this is about the 3rd time he talks them up (just like he has done for NEOP btw), Uri is very good with his picks. In short term, the skinprep system will be approved and will make a lot of money...
My long term play is based on their next product release which is about 1-2 years away + earnings on their first product.
Yeah, this one is going to be a longer term play for me .. I actually bought more yesterday @ 3.36 so brought up my avg a little
thanks buddy
For $ECTE.OB(3.39), to address (1) and (4) you can skip the the portion in BOLD
What if you could somehow inject drugs without a needle? A company called Echo Therapeutics has been working on this very problem, and took a small step forward yesterday when it received comments from the FDA. It anticipates approval in time to launch its product, called "Prelude," later this year.
For the time being, Echo is focusing on the problem of speeding up the effects of Lidocaine, a common topical numbing agent. Echo claims to have demonstrated that its device drastically shortens the time it takes for topical 4% lidocaine cream to produce its numbing effects, from about an hour on untreated skin to just a few minutes on Prelude-treated skin.
The Prelude device sits on the skin, measuring the thickness of the dead skin layer (which might be as high as 25 microns, or as low as 10). Then the device engages, its tip spins, and shaves off the dead skin, explains Echo's CEO Patrick Mooney. The very moment it reaches live skin, it stops. "You sit a couple of microns away from blood vessels" at that point, he tells Fast Company. "Now you can deliver drugs."
One reason why ultimate FDA approval of this device seems likely is that it already approved an earlier version, Soniprep, back in 1994, following its invention by MIT's Robert Langer. But Echo doesn't market Soniprep anymore; Mooney likens it to one of those briefcase-sized cell phones from circa 1991, compared with the Prelude. Another reason Mooney is more excited about this version of the device is that he's settled on a more profitable business model--one where he gives the device away basically at cost, then reaps profits by supplying disposable tips. "The razor blade business model is a much better business model," he says. "The potential theoretical market opportunity is multiple billions of dollars. There were 1.3 million botox injections last year"--a procedure that could be made less painful with the use of the Prelude and lidocaine. Echo has a corporate partner in the Michigan-based Ferndale Pharma Group, which makes the lidocaine cream. Ferndale will sell the device for Echo, bundled with its own 4% lidocaine cream.
Of course, once you open up a portal to the capillaries, you potentially open a two-way street. Not only could the device enable drug delivery, it could also enable the extraction of information. To that end, Echo has also developed something it's calling "Symphony." (Notice a pattern? That beautiful dead-skin-shaving process is just like a "prelude" to a symphony, don't you think?) Once the dead skin is removed, Symphony can track glucose levels in diabetes patients via a remote monitoring system, and can warn of the onset of hypo- or hyperglycemia.
That whole getting-things-in-and-out-of-the-body thing has traditionally been one of the more unpleasant parts of medicine; with a painless new portal, Echo does seem to be onto a good idea here. When Fast Company recently spoke to Mooney, he was "cautiously optimistic" about FDA approval; the recent milestone reached only reinforces that optimism, and he thinks that Echo should finally be bringing in revenue soon.
link: http://bit.ly/hKBnwc
EDIT: Also I highly recommend you listen to this replay of a interview with Robert Langer regarding Echo's products http://www.lifetechcapital.com/echo.htm
$NEOP.OB 136% increase since Oct posting.
This is not a momentum play, a speculative play, or technical play. I invested in the company based on the success of their soon to be marketed product, Lymphoseek.
RIGS updates/PR's and the AMEX listing was just a bonus.
thanks buddy. There is still a huge upside still left for $ECTE.OB IMO.
$ECTE.OB (3.06) Echo Therapeutics Announces Commercial Launch of Preludeâ„¢ on Track http://bit.ly/gwBqAX
here's the filing
http://bit.ly/hg8WsN
(1) 510(k) "plays" typically dont do very well, since the FDA usually takes quite a bit of time in their decision. If this device is as revolutionary as it sounds, I am sure the FDA will take their time. See CXM for an example of a major 510k dud.
- agreed, there is mixed data out there on whether they would only have to wait the 90 days or actually wait for fda clearance. I'm emailing their IR this week to confirm these mixed reports...
(2) Lots of companies got those grants, not a big deal.
- agreed
(3) They will need a major partner/distributor to put this product out there.
- Echo Therapeutics has two licensing partnerships which validate the Symphonyâ„¢ technology platform:
Handok Pharmaceuticals: The Symphony™ tCGM was licensed in South Korea to Handok Pharmaceuticals, the largest diabetes pharmaceutical company in South Korea. Specifically, on June 15, 2009 Handok paid a licensing fee of approximately $600,000 and will pay Echo Therapeutics milestone payments upon receipt of US FDA clearance of Symphony and upon the first commercial sale of Symphony in South Korea. Handok will also pay a royalty on net sales of Symphony and additional milestone payments based on Handok’s achievement of certain other targets. Handok is responsible for all product development fees and costs, and for all regulatory filings, for the final development of Symphony in South Korea.
Ferndale Pharma Group: The Prelude™ SkinPrep device was licensed to Ferndale Pharma Group to develop and market for skin preparation prior to the application of a topical analgesic or anesthetic cream for local dermal anesthesia or analgesia prior to a needle insertion or IV procedure in North America and the U.K. Specifically, on May 27, 2009, Ferndale Pharma Group paid a licensing fee of $750,000 and will pay Echo Therapeutics a milestone payment of $750,000 90 days after US FDA 510(k) medical device clearance of Prelude. Ferndale will also pay an escalating royalty on net sales and milestone payments based on Ferndale’s achievement of certain net sales targets, as well as guaranteed minimum royalties, totaling an additional $12.6 million. Ferndale is responsible for all product development fees and costs, and for all regulatory filings, for the final development of Prelude in North America and the U.K
(4) Do they have a previously approved device that is similar? Otherwise your other statement about the 90 days doesnt matter.
- goes back to q(1)
(5) You also have to consider that this is an OTC stock and will be for sometime, so it really limits the potential bang on approval. Institutions can't really invest in OTCs, unless they're very legit companies.
- agreed on the comments .. however, there are exceptions. I believe this company to be one of those exceptions such as NEOP.OB.
Not to rain on their parade, but what I want to see is some of their clinical results. These matter more than some CNBC spotlight.
- I post on these boards because of the class of investors that lurk here such as yourself. All of us are here for the same reason, and that is to make some money. So I welcome any criticism/DD/reports/research tools/etc that ya'll can provide.
Anyway, here is a link to a Institutional Research conducted by LifeTech Capital
http://bit.ly/ijiPBe
More DD on $ECTE.OB...
Uri Landesman on ECTE.OB (approx @ 7:18)
http://bit.ly/fgw6nW
ECTE.OB PR in DiabetesHealth.com
http://bit.ly/fPXY58
ECTE.OB wins Federal Research Grant
http://bit.ly/giR8qw
Uri Landesman on Squakbox mentioning ECTE.OB (approx @ 2:00)
http://bit.ly/hORy47
thanks, bud dude, can you spell check man? no one will ever take you seriously...
$ECTE.OB (3.01) - Short YouTube video presentation from last year http://bit.ly/gKt0rm . If this doesn't convince you to invest, then not much else would. FYI, I'm still kicking myself for not buying them on 1/6 (1.50's PPS) when I had an opportunity.
This is a medical device. They submitted the 510k almost 90 days ago (feb 9th is the 90th day). Here's a quote from a PDF on their website:
"Device companies are able to file an abbreviated request for marketing clearance when they are
upgrading existing technologies. Once filed, the FDA has 90 days to require further information. If they
do not respond, the company is automatically able to begin selling the newer form of their product."
link to pdf: http://bit.ly/fhe3nR
np bud,
Right now i'm holding $neop.ob, $astm, $ista, and $amrn
I'm really liking $ISTA's movement in the last couple of days since last friday's sell off
keep an eye on $DEPO in the AH and make sure they dont unload some bad news of some sort ... that sell off today was very strange in my opinion
after the insider sell off a week or so ago when the ABT thing happened, I wasnt staying around with my remaining 20% shares to find out why it occurred... so I finished selling off during that share dump ... wish the best for the rest of you
$NEOP.OB (2.80) +78% increase so far my earlier post ... so far its looking like the 4-5 pps range is imminent
Perhaps at first it will be bad, but depending on whether the FDA will work with MNKD or not, they may have caught a break....
According to what I'm reading, they already have a ongoing trial that already includes the 12 weeks of stable dosing and are going to investigate whether the FDA will allow this trial to be modified in order to suffice the CRL requirements.
yes, and it smells totally fishy ... stay away on this one in my opinion....
ZLC (5.44) up 70%~ from this post http://investorshub.advfn.com/boards/read_msg.aspx?message_id=57425948
NEOP.OB (2.32) up 48%~ from this post
http://investorshub.advfn.com/boards/read_msg.aspx?message_id=55579830
other investments: GERN, ASTM
watching: MNKD (depending on updated short interest, thinking bear raid if approved), VVUS
$PLX (9.74) - As an FYI, last time they had a S-3, here's how it ended soon after .. http://www.streetinsider.com/r/3054948
the HFT's
ZLC (4.66) (non fda) - and Moving higher .. up 47% from my last post
GERN (5.30) -- cashed out from my 5.07 entry ... thought it would be up higher by now but oh well
NEOP (1.94) -- Bought more and may buy more if it dips
CYTK - im going to take a guess that one of the institutions sold off some cytk today. That is the only explanation for the big drop of pps.... just my 2 cents worth
VVUS (9.26) up about 30% ish from my last post on 12/3
http://investorshub.advfn.com/boards/read_msg.aspx?message_id=57340773
(Non-FDA) ZLC (3.50) Up about 10% from my latest post on 12/6
http://investorshub.advfn.com/boards/read_msg.aspx?message_id=57425948
CYTK - this is what I was concerned about when I said I was cautious about it ... a 30%ish run up going into a weekend for phase 2 data was not what I wanted to do .. sorry for ya'll that lose money on this trade
is it just me or are the the weekend study/fda play results always seem to yield to a not so good monday morning trading session?
AVNR - For those of you wondering what was up with AVNR today, it was leaked info about T Row buying more shares
Looking at the document below shows their total number of shares to be 16,109,800. So they probably added a few million today...
Link
I'm tempted but I'm also cautious ... its ran up already close to 30% if I'm not mistaken. I don't believe there's much more room for improvement vs the downside... just my honest opinion..
I do hate that I was in a conf call during sheff's alert though.... oh well
I have about 45% of my portfolio in NEOP. Excellent potential. Thanks for the update
Regarding MNKD, based on experiences this year with POZN & AVNR .. anyone else going to place a low bid in prep for a bear raid?
GERN: 5.07 (bought a starter position at 5.07)
Geron Corp. said Tuesday it is offering about 17.4 million shares of its common stock in a public offering.
Menlo Park-based Geron (NASDAQ:GERN) said the shares are being offered at $5 each and it expects to raise about $87 million.
The offering is expected to close on or about Dec, 10, and underwriters were granted a 30-day option to purchase up to an additional 2.6 million shares to cover over-allotments, if any.
Geron intends to use the proceeds from the offering for research and development, including clinical trials for its product candidates, clinical development of product candidates it has in-licensed, and other general corporate purposes.
J.P. Morgan Securities LLC and Lazard Capital Markets LLC are acting as joint book-running managers of the offering. Rodman & Renshaw LLC, Roth Capital Partners LLC and WBB Securities LLC are acting as co-managers of the offering.
Read more: Geron plans to raise $87M in stock sale | Silicon Valley / San Jose Business Journal
My guess is the same reason I bought only a small position (bought @ .32 & sold @ .382) ... earlier this year people have lost a lot of money in SSNS so public sentiment for this one is not real high
FYI, I know Ameritrade did not have not had any more shares to short for a few weeks now on OREX. I gave up calling to check daily. GL with that.
(Non FDA) - NYSE: ZLC (3.17 Zale Corporation). Keep a watch on this one could be a 2-5 bagger by end of 1q in 2011. I expect better numbers in their 2010 4q & 2011 1q then the 3q numbers they recently reported