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GREAT POST JJAAMMAANN!! New traders take heed.
Sweet!! Nothing like an unexpected positive surprise in the form of $.
I was in shock when I saw this bounce to .004 in December...even more so now.
There are some strong hands holding and it's not just I flub money.
VOTE FOR 500,000,000 SHARE INCREASE coming in a few weeks!!!
Good luck!!
No one to blame for the selling more than GC himself from constant lies.
I've been in since 2014 actually....riding SAMP free shares.
Welcome to you!
300 posts a day on every promo board on the site is going to attract people that will occasionally sell shares for profit.... It's not always an MM.
Double to Triple zero anyone? So pathetic....
OUCH!! Big dumps at .11
looks like more toxic shares hitting the market!
The toxic debt won't let this go higher.
500 mil new shares next month too...
Most traders here will be long gone by then... as well as their money.
Warning to all new traders...stay away.
Everything active except the share price.
Toxic shares can be dumped at any moment so you will get NO traction.
.05 next week IMO
29.40 in reality was 19 cents before 1 share for 150 split. So much toxicity the EPA is probably on it. Another 500 million shares soon! If you like cheats and lies stick around you'll love AMBS! 2 years ago this was at .12 but 150 times more valuable.
Good luck all. You may squeeze out a bag or two before more toxic shares deplete this further.....but then run!!!
Brilliant chart....LMAO.
JP...I wouldn't even waste my time dissing a company this pathetic.
Hopefully there is a hell because Gerald will be there.
Time to move on buddy!
Seen USAR?
Somewhere around .009
Press Releases
Amarantus Announces Results of Annual Meeting
Download as PDF
SEPTEMBER 03, 2015
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, ratified the appointment of Marcum LLP as the Company's independent auditors for the year ending December 31, 2015, and approved an amendment to the Company's Articles of Incorporation to increase the Company's authorized shares of common stock from 13,333,334 to 35,000,000.
Amarantus Announces First Patient Dosed in Eltoprazine Phase 2b Study for Treatment of Parkinson's Disease Levodopa-Induced Dyskinesia
Top-Line Phase 2b Results Expected in 1H 2016
SAN FRANCISCO and GENEVA, July 20, 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 the first patient has been dosed in the Phase 2b clinical study of the Company's lead neurology therapeutic candidate eltoprazine for the treatment of Parkinson's disease levodopa-induced dyskinesia (PD-LID).
"The start of patient dosing in this Phase 2b trial represents a further important milestone in our clinical development program for the treatment of PD-LID. Eltoprazine has the potential to be an impactful therapy for individuals with Parkinson's disease taking levodopa-based products," said David A Lowe, Ph.D., Member of the Board of Amarantus BioScience Holdings, Inc.
Patient dosing was initiated by principal investigator Stuart H. Isaacson, M.D., Director of the Parkinson's Disease and Movement Disorders Center of Boca Raton, a nationally recognized leading clinical research institution renowned for its testing of new treatments for improving the symptoms of Parkinson's disease and decelerating its progression.
Gerald E. Commissiong, President and CEO of Amarantus BioScience Holdings, Inc., added, "With this study now underway, the Company's clinical development team will now focus on the initiation of our upcoming Phase 2 clinical study of ESS for the treatment of severe burns, expected to open this quarter at a US military center."
The multi-center, 60-subject Phase 2b study in individuals with Parkinson's disease is a double-blind, placebo-controlled, four-way crossover, dose range finding, clinical trial designed to evaluate dose response effect of repeated eltoprazine dosing on safety, tolerability and dyskinesia severity using state-of-the-art rating scales, diaries and motion sensors. The Company expects to report top-line results from the eltoprazine Phase 2b study in the first half of 2016.
PD-LID is an abnormal involuntary, movement disorder resulting from prolonged levodopa-based therapy, the most commonly prescribed treatment for Parkinson's disease. PD-LID occurs in approximately 60-80% of Parkinson's patients and is one of the most difficult problems facing people with the disease. This dyskinesia can be severely disabling and impact quality of life by prohibiting the ability to perform routine daily functions.
Additional study sites throughout the United States and Europe will be forthcoming. For patients and physician interested in enrollment information for the Phase 2b clinical study with eltoprazine for the treatment of PD-LID please visit clinicaltrials.gov and use identifier: NCT02439125.
Good call!
Amarantus Completes Acquisition of ESS From Lonza for the Treatment of Severe Burns
Download PDF
Amarantus Now Has Full Ownership of Cutanogen Corporation, Which Has Exclusive Worldwide License to Orphan Drug Product Candidate Engineered Skin Substitute (ESS)
SAN FRANCISCO and GENEVA, July 15, 2015 (GLOBE NEWSWIRE) -- Amarantus BioScience Holdings, Inc. (OTCQX:AMBS), a biotechnology company focused on developing therapeutic and diagnostic products for diseases in the areas of neurology, psychiatry, ophthalmology and regenerative medicine, announced that it has completed the acquisition of Cutanogen Corporation ("Cutanogen") from Lonza Walkersville, Inc. ("Lonza"), a subsidiary of Lonza Group Ltd. Cutanogen has an exclusive worldwide license to intellectual property rights associated with Engineered Skin Substitute ("ESS"), an autologous full thickness skin replacement product in development for the treatment of severe burns. ESS has received orphan drug designation from the U.S. Food and Drug Administration for the treatment of hospitalized patients with deep partial and full thickness burns requiring grafting. With this agreement, Amarantus has engaged Lonza via a long-term services agreement to manufacture ESS under Good Manufacturing Practices for human clinical trials, and subsequent commercial distribution.
"The completion of the acquisition of Cutanogen from Lonza represents a cornerstone of Amarantus' therapeutics acquisition strategy as the company prepares for its upcoming listing on a national exchange," said Gerald E. Commissiong, President & CEO of Amarantus. "ESS is a potentially revolutionary solution for the treatment of severe burns that has demonstrated initial human proof-of-concept in an investigator-initiated setting. Going forward, Amarantus plans to take this program through a stringent corporate-sponsored regulatory development program under an already open IND with the FDA, to gain marketing approval, initially for the treatment of severe burns in the United States. The company intends to work closely with US regulatory authorities under the orphan drug designation pathway to achieve this objective."
Details regarding the financial components of the transaction are available on Form 8-K filed with the Securities Exchange Commission ("SEC") and may be accessed on the SEC's website at www.sec.gov.
Maxim Group, LLC served as M&A advisor to Amarantus on the transaction.
12,200 on bid 6.39
Amarantus Announces Presentation of Eltoprazine Phase 1/2a Clinical Data at the 19th International Congress of Parkinson's Disease and Movement Disorders
- Poster Presentation on June 15, 2015 from 12:30-2:00 p.m. PDT -
SAN FRANCISCO and GENEVA, June 15, 2015 (GLOBE NEWSWIRE) -- Amarantus BioScience Holdings, Inc. (OTCQB:AMBSD), a biotechnology company focused on developing therapeutic and diagnostic products for neurological disorders and orphan indications, announced that data from the Phase 1/2a clinical study of eltoprazine for the treatment of Parkinson's disease levodopa-induced dyskinesia (PD-LID) has been accepted for presentation at the 19th International Congress of Parkinson's Disease and Movement Disorders being held June 14-18, 2015, in San Diego, CA.
Professor Per Svenningsson, M.D., Ph.D., of the Centre for Molecular Medicine at Karolinska Institutet, will present poster number 331 entitled, "Single oral treatment with the 5-HT1A/B agonist, Eltoprazine, counteracts L-dopa-induced dyskinesias in Parkinson's disease: A phase I/IIA, double-blind, randomized, placebo-controlled, dose-finding study," on Monday, June 15, 2015, from 12:30-2:00 p.m. PDT in the Coronado Ballroom of the Manchester Grand Hyatt.
Further, poster number 331 has been selected for a guided poster tour with Professor Svenningsson. Guided Poster Tour 16 entitled, "Parkinson's Disease: Neuropharmacology," will be held at Harbor G, 2nd Level, Harbor Tower from 12:00-3:30 p.m. PDT on Thursday, June 18, 2015.
Eltoprazine is a small-molecule 5-HT1A/1B serotonin receptor agonist, investigational drug candidate, with a well-established safety profile. A Phase 1/2a dose-finding study was conducted with eltoprazine to determine its effect against levodopa-induced dyskinesia, in patients with Parkinson's disease. The double-blind, randomized, placebo-controlled clinical study was led by Professor Svenningsson, Professor Anders Björklund, Ph.D., Faculty of Medicine at Lund University, and Professor Håkan Widner, M.D., Ph.D., Faculty of Medicine at Lund University. The study was partially supported by a grant from The Michael J. Fox Foundation for Parkinson's Research.
Amarantus previously announced that it will commence a multi-center, 60-subject Phase 2b study in individuals with PD-LID before the end of the June 2015. The study will be a double-blind, placebo-controlled, four-way crossover, dose range finding, clinical trial designed to evaluate dose response effect of repeated eltoprazine dosing on safety, tolerability and dyskinesia severity using state-of-the-art rating scales, diaries and motion sensors (ClinicalTrials.gov Identifier: NCT02439125). Pharmacokinetics and pharmacodynamics will also be evaluated. The Company expects to report top-line results from this Phase 2b study in the second quarter of 2016.
About Eltoprazine
- Presentation and Webcast on May 28, 2015, at 9:00 a.m. EDT -
SAN FRANCISCO and GENEVA, May 26, 2015 (GLOBE NEWSWIRE) -- Amarantus BioScience Holdings, Inc. (OTCQB:AMBS), a biotechnology company focused on developing therapeutic and diagnostic products for neurological disorders and orphan indications, announced that it will be presenting at the Fourth Annual SeeThru Equity Microcap Investor Conference being held May 28, 2015, at Convene Grand Central, New York, NY.
Gerald E. Commissiong, President & CEO of Amarantus, will provide a corporate overview and an update on the clinical development of the Company's lead therapeutic product candidate eltoprazine for the treatment of Parkinson's disease levodopa-induced dyskinesia (PD-LID), on Thursday, May 28, 2015, at 9:00 a.m. Eastern Time.
A live webcast of the presentation may be accessed via the News and Events page of the Investor Relations section of the Amarantus corporate web site under the IR Calendar at www.amarantus.com. The webcast replay will be available approximately two hours after the presentation ends and will be archived for 30 days.
About the Fourth Annual SeeThru Equity Microcap Investor Conference
SeeThru Equity is the premier and unbiased provider of microcap equity research and institutional and high net worth investor focused conferences. Since its inception in 2011, the firm has grown to over 125 companies under coverage and has successfully hosted 14 investor conferences. The Fourth Annual Microcap Investor Conference brings together over 60 presenting companies and 600 attendees. The conference offers detailed presentations, targeted one-on-one meetings and numerous networking opportunities.
Amarantus to Present at the Fourth Annual SeeThru Equity Microcap Investor Conference on May 28, 2015
Great example here! 20% gain the day of RS. 1 - 125 split.
Update on Advaxis Announces 1-for-125 Reverse Stock Split and Decrease in Authorized Shares of Common Stock
Download PDF
PRINCETON, N.J.-- Advaxis, Inc., (OTCQB: ADXS and ADXSD), a leader in developing the next generation of immunotherapies for cancer and infectious diseases, announced that the closing price of its stock was $5.87 on July 15, 2013, the first day of trading on a post reverse split basis, an increase of approximately 20% from the previous closing price of $4.875. This release updates the release “Advaxis Announces 1-for-125 Reverse Stock Split and Decrease in Authorized Shares of Common Stock” issued Monday, July 15. The original release follows:
Advaxis, a leader in developing the next generation of immunotherapies for cancer and infectious diseases, announced today a 1-for-125 reverse stock split of its common stock and a decrease in the number of its authorized shares of common stock from 1,000,000,000 to 25,000,000. The reverse stock split and the decrease in the number of authorized shares of common stock were authorized by Advaxis’ stockholders at the annual meeting of stockholders held on June 14, 2013.
Advaxis’ shares of common stock will trade on a post-split basis beginning on July 15, 2013. The ticker symbol will not change although a “D” will be appended to the trading symbol (ADXSD) for 20 trading days to alert the public regarding the reverse stock split. The new CUSIP number for Advaxis’ common stock post-reverse stock split will be 007624 208.
At the effective time of the reverse stock split, every 125 shares of Advaxis’ issued and outstanding common stock will automatically be combined into 1 issued and outstanding share of common stock without any change in the par value of the shares. This will reduce the number of outstanding common shares of Advaxis from approximately 609 million to approximately 4.9 million. Additional information can be found in a Form 8-K to be filed with the Securities and Exchange Commission.
“The reverse stock split does not fundamentally change stockholder value or the market capitalization of Advaxis, but we believe increasing the price per share will make our stock more attractive to a broader range of institutional and other investors and ultimately increase stockholder value,” commented Thomas A. Moore, Chairman and Chief Executive Officer of Advaxis.
Proportionate voting rights and other rights of common stockholders will not be affected by the reverse stock split, other than as a result of the cashing out of fractional shares. Stockholders who would otherwise hold a fractional share of common stock will receive a cash payment in lieu of a fractional share. The outstanding preferred stock will not be affected by the reverse stock split.
It is not necessary for stockholders to exchange their existing stock certificates for new stock certificates in connection with the reverse stock split, although stockholders may do so if they wish. Please direct any questions you might have concerning the reverse stock split to your broker or our transfer agent, Securities Transfer Corporation, by calling 469-633-0101, ext. 112, or emailing sanchez@stctransfer.com.
SGT Pepper is WRONG...the stock will have the letter D attached to it for 20 days from the date of designation to signify a reverse split is taking place. It does not stop trading.
.
Jason Napodano, CFA
@JNapodano
I think the $AMBS R/S signifies a real interest in spinning off AMDX, this way both are NASDAQ listed, or AMDX can be sold for more $.
Less than 2 % of the outstanding traded...not bad IMO
Shorts are in every market but the naked shorting will be mostly history.
If we only have 7 million shares and the price is 7.50 the market cap is still only 52,500,000.
This could trade up to $22.50 just as easily IMO. to make Market cap 157,500,000 pending announcements.
Not using authorized shares. just issued and outstanding. 1,050,000 /150
If converted at .05 it will translate to $7.50 a share
7mil x 150 = 1,050,000
Following the reverse split, there will be approximately 7 million common shares outstanding.
As a result of the stock split, every 150 shares of issued and outstanding common stock will be converted into 1 share of common stock. Upon FINRA approval the Company's common stock will temporarily trade on the OTCQB under the symbol "AMBSD," for a period of 20 trading days after which time the symbol will revert back to AMBS. The temporary "D" at the end of the Company's stock symbol signifies that the reverse stock split has occurred. Following the reverse split, there will be approximately 7 million common shares outstanding.
Amarantus Effects Capital Restructuring in Anticipation of National Exchange Listing
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-Company Announces 1-for-150 Reverse Stock Split-
SAN FRANCISCO and GENEVA, May 22, 2015 (GLOBE NEWSWIRE) -- Amarantus BioSciences Holdings, Inc. (OTCQB:AMBS), a biotechnology company focused on developing therapeutic and diagnostic products for neurological disorders and orphan indications, announced that it has implemented a 1-for-150 reverse stock split of its common stock. Trading on a split adjusted basis will occur upon final approval from FINRA. A new CUSIP number for the common shares will be issued in connection with the reverse split.
"With our Company having recently achieved a number of important scientific and business milestones, we are confident that we have built a solid foundation for Amarantus and are now ready to take the steps necessary to elevate our Company to the next level. Achieving an up-listing to a national stock exchange this year is an integral part of our overall corporate strategy to maximize the value of Amarantus and this reverse stock split is an important step in enabling the Company to achieve that goal," said Gerald E. Commissiong, President & CEO of Amarantus. "We remain committed to advancing Amarantus to its next phase of growth in order to unlock the true value and potential of our Company. We are confident that our Company will now be better positioned for appreciation through increased visibility and the deliberate expansion of the shareholder base as we achieve important value building milestones in our therapeutic and diagnostics divisions."
"The core fundamentals of Amarantus have never been stronger, with the upcoming initiation of our Phase 2b clinical study of our lead product candidate, eltoprazine, in Parkinson's disease levodopa-induced dyskinesia and the pending strategic transaction in our diagnostics division. In addition, we believe the potential addition of the clinical-stage orphan candidate ESS, as part of the potential acquisition of Cutanogen Corporation from Lonza, will complement our orphan preclinical MANF programs, while adding a second clinical-stage therapeutic program to bolster our pipeline. Further, the Company has made significant progress in the evaluation of strategic options for our wholly-owned subsidiary Amarantus Diagnostics, and we expect to begin the implementation phase shortly, with a view of potentially returning capital to shareholders in 2015," commented Robert Farrell, Chief Financial Officer of the Company.
"Taken together, we believe the pending catalytic events in both our therapeutics and diagnostics divisions provide a sound rationale for us to begin participating in the broader capital markets, so that our shareholders may begin to realize value from our rich pipeline. With this, management and the Board believe now is the right time to move forward with our uplisting strategy in earnest," concluded Mr. Farrell.
As a result of the stock split, every 150 shares of issued and outstanding common stock will be converted into 1 share of common stock. Upon FINRA approval the Company's common stock will temporarily trade on the OTCQB under the symbol "AMBSD," for a period of 20 trading days after which time the symbol will revert back to AMBS. The temporary "D" at the end of the Company's stock symbol signifies that the reverse stock split has occurred. Following the reverse split, there will be approximately 7 million common shares outstanding.
All fractional shares created by the reverse stock split will be rounded to the nearest whole share. If the fraction created is one half or less, it will be rounded down to the nearest whole share. If the fraction is more than one half, it will be rounded up to the nearest whole share. Each shareholder will get at least one share.
The Company's transfer agent, VStock Transfer, LLC, will adjust its records to reflect each shareholder's post-split position. Share adjustments to physical stock certificates can be made upon surrender of the certificate to the transfer agent. Please contact VStock Transfer, LLC for further information at (212) 828-8436 or toll-free at (855)-9VSTOCK FREE or by email at info@vstocktransfer.com.
SAN FRANCISCO and GENEVA, May 21, 2015 (GLOBE NEWSWIRE) -- Amarantus BioScience Holdings, Inc. (OTCQB:AMBS), a biotechnology company focused on developing therapeutic and diagnostic products for neurological disorders and orphan indications, announced that it has entered into a clinical trial agreement with Chiltern International (Chiltern), a leading global contract research organization (CRO), to manage the clinical research and monitoring program services for the Phase 2b study of eltoprazine in Parkinson's disease levodopa-induced dyskinesia (PD-LID).
The Company also announced that it has completed its clinical investigator meetings in both the United States and European Union and is on track to commence enrollment and dosing for the 60-patient international, multi-center PD-LID study in the second quarter of 2015.
"We selected Chiltern as our CRO partner for PD-LID Phase 2b development because of their proven excellence in quality and reliability in drug development along with their exceptional expertise in the managing the comprehensive and extensive international clinical study regulatory requirements," said Gerald E. Commissiong, President & CEO of Amarantus. "Now that our investigator meetings have been completed in both the U.S. and the EU, we are ready to commence the eltoprazine dose response, efficacy and safety trial this quarter. The expansion of our team, via our collaboration with Chiltern, will allow us to advance the PD-LID program as efficiently and quickly as possible. The next step is to initiate our first clinical site and begin screening patients for enrollment in the study."
Chiltern will manage all clinical activities related to the Phase 2b eltoprazine study including clinical trial site approval and authorization, investigator and staff training, patient recruitment, timeline and budget monitoring, centralized program tracking systems, regulatory controls and responsibilities, data monitoring committee organization and administration, and trial data quality control and final data lock.
Dr. Jim Esinhart, CEO of Chiltern, added, "Our mission is to provide premier CRO services to innovative and forward-thinking biopharmaceutical companies. As such, we are pleased to partner with Amarantus and manage the initiation of their Phase 2b study with eltoprazine. We recognize that PD-LID can be severely disabling and impact quality of life for Parkinson's patients and utilizing our award-winning trial management program and over 30 years of industry expertise, we look forward to advancing eltoprazine to its next level of clinical development and one-step closer to fulfilling its therapeutic potential for patients with PD."
The Phase 2b eltoprazine trial is a double-blind, placebo-controlled, four-way crossover, dose range finding, clinical study designed to evaluate dose response effect of repeated eltoprazine dosing on safety, tolerability and dyskinesia severity using state-of-the-art rating scales, diaries and motion sensors. Pharmacokinetics and pharmacodynamics will also be evaluated.
About Chiltern International
Chiltern is a leading global CRO that listens to client needs in order to customize solutions for the Biopharma industry. With 33 years in service, Chiltern delivers from three specialized business units: Chiltern Biopharma, with deep therapeutic expertise for respiratory, anti-infectives / vaccines, ophthalmology, dermatology and other specialty areas; Chiltern Oncology, led by physicians, scientists and clinicians to uniquely manage all phases of hematologic and oncologic clinical drug development; and Chiltern Source, a world leader in tailored relationships for FSP, resourcing and staffing solutions. Chiltern's 2,200 engaged professionals work across 45 countries to deliver flexible, responsive solutions that are "Designed Around You". Further information is available at: http://www.chiltern.com.
About Eltoprazine
Eltoprazine is a small molecule 5HT1A/1B partial agonist in clinical development for the treatment of Parkinson's disease levodopa-induced dyskinesia (PD-LID) and adult attention deficit hyperactivity disorder (ADHD). Eltoprazine has been evaluated in over 680 human subjects to date, and has a well-established safety profile. Eltoprazine was originally developed by Solvay Pharmaceuticals for the treatment of aggression. Upon Solvay's merger with Abbott Pharmaceuticals, the eltoprazine program was out-licensed to PsychoGenics. PsychoGenics licensed eltoprazine to Amarantus following successful proof-of-concept trials in PD-LID and adult ADHD.
About Parkinson's Disease and Levodopa-Induced Dyskinesia (PD-LID)
Parkinson's disease is a chronic, progressive neurodegenerative disorder that causes motor symptoms such as tremors, rigidity and slowed movements as well as non-motor symptoms including cognitive impairment, mood disorders and autonomic dysfunction. The Parkinson's Disease Foundation estimates that there are approximately one million people living with Parkinson's disease in the United States and seven to 10 million PD patients worldwide. The most commonly prescribed treatments for Parkinson's disease are levodopa-based therapies. In the body, levodopa is converted to dopamine to replace the dopamine loss caused by the disease. As dopamine neurons in the brain are lost the therapeutic efficacy of levodopa attenuates, and increased use is associated with a side effect of dyskinesias. These are involuntary, uncontrollable and often exaggerated and jerky movements. They are distinct from the static, rhythmic tremor as a symptom of Parkinson's disease. Levodopa-induced dyskinesia can be severely disabling, rendering patients unable to perform routine daily tasks.
Amarantus Enters Into CRO Agreement With Chiltern International to Commence Phase 2b Clinical Development of Eltoprazine in Parkinson's Disease Levodopa-Induced Dyskinesia
http://ir.amarantus.com/company-news/detail/1995
It bounced almost 20 % higher off the low. It was quick but was a bounce none the less.
Do you seriously think a few enthusiastic posters here is what made this rally the last few days?? A pump and dump is a scam with no viable business and an intent to scam people.
Just because some people, most of whom have held this for years were excited to see some positive movement does not make this a pump and dump nor make them snake oil peddlers.
7 or higher is coming...
Do you seriously think a few enthusiastic posters here is what made this rally the last few days?? A pump and dump is a scam with no viable business and a intent to scam people.
Just because some people, most of whom have held this for years were excited to see some positive movement does not make this a pump and dump nor make them snake oil peddlers.
7 or higher is coming...
Sell and buy APPL.