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.
Back in 2010 when Regenicin announced the deal with Lonza the stock was at $2.20 and a market cap of $185K. Since then there is DoD backing, ODD, IND, Phase 2 trial starting, other orphans, potential PRV(s) valued at $300M each, etc.
Additionally, an award from ASPR or purchase by BARDA down the road would send this through the roof where it would be too late to get in. GC mentioned on the call they presented in May and will come back next month with more data.
Many startup bios hope to have one billion dollar opp. AMBS has 4 - Dx, Elto, ESS & MANF. Not a bad problem to have.
Sell two to fund the other two?
Accelerate one to fund the other three?
Also consider if you sell one of them, what's the chances of finding an equivalent replacement asset for your pipeline a year from now when you do have extra dollars.
You could bet if they sold ESS tomorrow for $500M, there would be people bitching here how stupid that was.
That's just a fraction of highlights and just what I started noting towards the beginning. There is so much to be pulled from what GC said and the presentation.
For example, no one here even mentioned CTE. No one mentioned the slide about Lympro partnerships. I guess it's too easy to make defamatory comments about the company and poke fun at people who suffer from horrific conditions. What goes around will come around eventually.
All hands on deck for ESS. If it's truly a multi-billion dollar opportunity it's a wise decision. But who knows, maybe they sold Eltop.
I wouldn't worry about them. Some very immature posts as usual. They were all pumping this morning and sold out this afternoon. Goodbye for now. Gives me more time to continue to accumulate.
More importantly, the recording is up and running.
Here's a few notes as I'm starting to listen to it again.
- 3 orphans and two more on the way. A year ago none.
- Opportunity for PRV which are selling at a average of $300M
- ESS operating under non-diluted funding from AFRIM.
- Potential for continued support. $130M awarded just yesterday. ESS was presented to a special panel in May. The data will be presented in Q4
- First gen ESS likely and immediate benefit for patients, but other things can be added to make it truly revolutionary and expand into a number of other areas
Good to hear the shift in focus to one of the company's most valuable short and long-term assets. There is a reason why ESS was valued at $1.8 Billion four years ago, even before DoD backing, ODD, IND, Phase 2 trial starting, other orphans, potential PRV(s) valued at $300M each, etc. Hats off to management for untangling the legal mess so this product can be brought to market now.
Here's where I think the team made two errors in judgement in my opinion.
They may have planned for best case or average case timelines and execution.
Likely best case-ish. The proxy screw up, which was out of the company's control is just one example of where worse case happened. Now if they added all the contingency for worst case, people would have jumped ship anyway due to timelines being so far off.
They didn't expect the market reaction they got.
Many shareholders didn't expect it either so not many come out smart on this one. You got a handful of analysts that have done extensive analysis on the company and value it as a multiple many times higher than it is, but yet the sp is what it is. You end up with a tsunami effect of selling, shorting, conversion, whatever.
There is a link posted on a few of the boards of getting rid of the overhang before an uplist/IPO. As painful as it's been, maybe the selling is over and onward and upward. Would appear the bottom is in. Oh to be a lucky new investor jumping in now at these levels.
We'll see what GC says tomorrow.
What's your take on LPC in all of this?
If you could go back to the point in time of the company you first invested in with Lympro, not even knowing the game rules would change along the way (e.g. gold standard benchmark measurement), what would you do differently in hindsight? Keeping in mind no one has brought a Alzheimer Dx tool to market so there is no "how to" guide.
Should they have passed up ESS, put Eltoprazine on the shelf, sold Lympro early on for $10M? Wouldn't be much of a holding company or long-term business model.
Your first point had everything to do with the proxy going out late. Can't fault the company on that. In hindsight, they probably could have called an audible and pushed the date out right away, but maybe they thought they were close and was worth the risk moving forward.
Your other two points come down to which is greater. The dilution or the increasing asset value. The only question remains, do they sell something, partner or continue to hold for the gold.
Reminds me of a chicken. How long does the company hold.
Your first point had everything to do with the proxy going out late. Can't fault the company on that. In hindsight, they probably could have called an audible and pushed the date out right away, but maybe they thought they were close and was worth the risk moving forward.
Your other two points come down to which is greater. The dilution or the increasing asset value. The only question remains, do they sell something, partner or continue to hold for the gold.
Reminds me of a chicken. How long does the company hold.
The majority of shareholders with a long-term view have weighed in less than 30 days ago. I assume they are not panicking because of the value of the assets the holding company owns. Those that did panic, likely have sold and moved on.
I've already posted what ESS and the other assets are worth. A sale of ESS along would be a high multiple of the market cap today. No one saw ESS purchase coming and many said there was no way the company would close the deal.
The company has an exciting "de-risked" pipeline. If they only had one asset, then I'd be panicking.
SAN FRANCISCO and GENEVA, Sept. 3, 2015 (GLOBE NEWSWIRE) -- Amarantus BioScience Holdings, Inc. (OTCQX:AMBS), a biotechnology company developing therapeutic and diagnostic product candidates in orphan indications and neurology, announced that at its 2015 Annual Meeting of Stockholders held yesterday in New York, New York, the stockholders approved the election of Gerald Commissiong, Dr. John Commissiong, Robert Harris, Donald Huffman, Dr. David Lowe, and Dr. Joseph Rubinfeld to the Amarantus Board of Directors,
http://ir.amarantus.com/press-releases/detail/2017/amarantus-announces-results-of-annual-meeting
No imagination. I back up what I post with links. Here you go.
http://content.stockpr.com/amarantus/media/782786d417b8894297ed7f45f31a9e42.pdf
Did your lawyer recommend you keep posting on the message board, creating fake IDs, calling into Shareholder meeting pretending to be a stock analyst, posting lies on a message board and making defamatory comments. All public record even though you deleted some.
Not saying that to make you defensive, but usually lawyers may be a little risk adverse to those type of things.
At least we know why you and a few others have been 24x7 on this hoping to do a smear campaign to blackmail the company.
The irony is if you sold out, put the money into a lawyer and the stock goes up to $45 next month.
If they haven't spent all of the last 1B in pre RS terms. What's the difference if they add 3.3B?
It is funny the company went from not enough pipeline candidates to too many in actually a very short time period. People can barely keep up.
Maybe a few years from now, you are holding shares in 3 or 4 companies. Wouldn't that be nice.
You didn't say how many of the additional 1B were actually used for what. Some may have the impression that they were all used which is far from the truth.
If we bought $34M of 3 recent assets and the market cap is $17M than either the company is much smarter than the emotional retail investor or a bunch of chumps. If the people believe the latter, then they should have sold while they are ahead when the first acquisition was announced. If they spent $34M on $340M of assets, then good job. Not as great as Vivek, but he has his Mom helping out.
How many of the 1B shares were used?
How many of the 1B shares were used to fund operations?
How many of the 1B shares were used to buy high valued assets?
Depending on how you answer these questions is whether there is cause for alarm or a boy crying wolf.
Did you lose a fortune? I am sorry to hear. I have lost nothing.
So, in the last year, how many shares were added and what is the net increase in value of the assets.
You can;t go by the sp and emotional retail investors unless you are a st investor. I'll go buy the analyst.
Thanks for posting. You got some very worked up here.
So you have a young CEO in his 20's, with no BIO experience, that is running a company with 10 employees, and get this, two of which are his Mom and Brother and he buys undervalued assets and turns around and IPO's them for a exponential gain. What ever you do, don't mention what nationality he is or what country he's from.
Sounds like a class action suit to some here. LOL
Were you one of the ones that said GC would be voted out? Looks like you may be in a "minority" for a change.
Forward-looking statement
In United States business law, a forward-looking statement or safe harbor statement is a statement that cannot sustain itself as merely a historical fact. A forward-looking statement predicts, projects, or uses future events as expectations or possibilities. These statements can often be misleading, as they can be mistaken for factual statements, while they are actually speculation.
https://en.wikipedia.org/wiki/Forward-looking_statement
Keep in mind even the Fortune 100 companies say the same thing vs. high risk, high reward OTC companies.
RESEARCH REPORT UPDATE
AMBS: AMARANTUS RECEIVES ORPHAN DRUG DESIGNATION FROM THE FDA FOR MANF FOR THE TREATMENT OF RETINAL ARTERY OCCLUSION
09/14/2015
http://scr.zacks.com/News/Press-Releases/Press-Release-Details/2015/AMBS-Amarantus-Receives-Orphan-Drug-Designation-from-the-FDA-for-MANF-for-the-Treatment-of-Retinal-Artery-Occlusion/default.aspx
I guess you really don't want a real dialog about the company and rather just go back to childish name calling. Sad but true.
That's what he said...
Can can think of five ways off the top of my head. Replacing the CEO isn't one of them. People would just find the next thing to complain about.
It matters little in what I think nor do I want to be a monday morning quarterback. You were at the shm. What questions did you ask? Was this one of them?
Back in 2010 when Regenicin announced the deal with Lonza the stock popped to $2.20 and a market cap of $185K. That was at the time Dr. Joseph Rubinfeld joined the Board of Directors. After that, the company ran into all sorts of issues.
Fast forward 5 years. What's the product now worth with the litigation cleared up and all that has transpired since that date: DoD backing, ODD, IND, Phase 2 trial starting?
Pharma-economics (Savings) for burns >50% only:
Low End: (500 Patients) X ($10K Savings/day) X (60 days) = $300M
High End: (3500 Patients) X ($15K Savings/day) X (120 days) = $6.3B
June 19, 2015 - 2015 Impact Investor Conference
18:05 - "The most important thing about this asset is it as a wealth of human efficacy data that has been out there and the key opinion leading physicians love this technology. We're talking about 3 out former past presidents of the American Burn Association are going to be involved in this 10 patient phase 2 clinical study and we think there may be some means we can get an accelerated pathway from a market perspective."
20:00 - " Near term commercial opportunity . There is no competition in terms of technology that have both layers of own skin. This is the ownly technology out there. We think in the US it's a $500M market opportunity not to mention other things diabetic foot ulcers, burns that are less than 50%, 30%, as well as ultimately some kind of cosmetic opportunity..."
June 16, 2015 - BIO International Convention at 2:30 pm ET
15:00 - "We believe this program will significantly mitigate enterprise risk as well as expose us to tremendous upside because of the data that has been produced since the physician sponsored study that is publicly available ."
11/19/2014 - AMBS: ASTUTE DEAL BRINGS IN ANOTHER SHOT ON GOAL FOR AMARANTUS BIO
11/18/2014 - Amarantus Business Update Conference Call "And with ESS-W, we feel as though we have found just a tremendous opportunity."
4/10/2014 - Development of the Mechanical Properties of Engineered Skin Substitutes After Grafting to Full-Thickness Wounds
11/23/2010 - DoD awards Regenicin and Lonza $18 million to develop PermaDerm for severe burns
8/18/2010 - Regenicin Completes Acquisition of Worldwide Exclusive Know-How Technology License from Lonza Walkersville
Value of #AMBS pipeline
Engineered Skin Substitute
ESS was estimated to be worth 1.8B and that was BEFORE DoD backing, ODD, IND, Phase 2 trial starting.
MANF Ophthalmology
AGTC is in the early Ophthalmology stage similar to Amarantus...
Analyst Coverage
http://ir.amarantus.com/analyst-coverage
WallachBeth Price Target $18
http://m.briefing.com/investor/popuppages/articlepopup.aspx?articleid=ud20150714072621
SeeThruEquity: $45
http://finance.yahoo.com/news/seethruequity-initiates-coverage-amarantus-bioscience-130000691.html
Zacks: $15
http://scr.zacks.com/files/September-2-2015_AMBS_Zeng.pdf
What a difference two days make...
http://investorshub.advfn.com/boards/read_msg.aspx?message_id=116537631
RAO was also on the July agenda. Meeting minutes should be posted in a day or two. Assuming this is Amarantus which I do, it's a good sign they are back on the agenda for the following meeting vs. being sent packing.
RP seemed rather straight forward. A number of companies have submitted for RP orphan over the years. I haven't see the same activity for RAO. Actually none, but haven't spent a very long time looking. Two orphans on MANF would be incredible. One is great. Two is even better. I already posted the deal AGTC got with two orphans in ophthalmology with one reaching clinical (pipeline -> http://www.agtc.com/products)
Here's the July meeting:
Committee for Orphan Medicinal Products (COMP)
Draft agenda for the meeting on 14-16 July 2015
2.2.13. - EMA/OD/079/15
Treatment of retinal artery occlusion
Action: For adoption
Documents tabled:
Draft Summary report
http://www.ema.europa.eu/docs/en_GB/document_...189364.pdf
Here's the link to watch:
http://www.ema.europa.eu/ema/index.jsp?curl=pages/news_and_events/document_listing/document_listing_000201.jsp&mid=WC0b01ac0580028e78