UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of Report (Date of earliest event reported):
January 15, 2015
AMARANTUS BIOSCIENCE HOLDINGS, INC.
(Exact name of registrant as specified in
its charter)
Nevada |
000-55016 |
26-0690857 |
(State or other jurisdiction of
incorporation or organization) |
(Commission File Number) |
IRS Employer
Identification No.) |
655 Montgomery Street, Suite 900
San Francisco, CA |
94111 |
(Address of Principal Executive Offices) |
(Zip Code) |
(408) 737-2734
(Registrant’s telephone number, including
area code)
Check the appropriate box below if the
Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
| ¨ | Written
communications pursuant to Rule 425 under the Securities Act |
| ¨ | Soliciting
material pursuant to Rule 14a-12 under the Exchange Act |
| ¨ | Pre-commencement
communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| ¨ | Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
On January 15, 2015,
Amarantus BioScience Holdings, Inc. (the “Company”) released a press release which reported that the Company received
positive top-line results of its LP-002 study of the Lymphocyte Proliferation Test (LymPro Test(R)) blood diagnostic
for Alzheimer's disease. A copy of the press release is attached hereto as Exhibit 99.1.
Also, on January
15, 2015, the Company issued a press release with respect to the Company’s entry into an exclusive option agreement with
Georgetown University, which option agreement was disclosed by the Company in its Form 8-K filed on January 15, 2015.
A copy of the press release is attached hereto as Exhibit 99.2.
| Item 9.01 | Financial Statements and Exhibits. |
(d) Exhibits
Exhibit No. |
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Description |
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99.1
99.2 |
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Press release dated January 15, 2015
Press Release dated January 15, 2015 |
SIGNATURES
Pursuant to the requirements
of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned
thereunto duly authorized.
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AMARANTUS BIOSCIENCE HOLDINGS, INC. |
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Date: January 15, 2015 |
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By: |
/s/ Gerald E. Commissiong |
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Name: Gerald E. Commissiong |
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Title: Chief Executive Officer |
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Exhibit 99.1
Amarantus Announces Positive Data From 140 Subject LP-002
Clinical Study of LymPro Test(R) Confirming Statistically Significant Markers for Alzheimer's
SAN FRANCISCO and GENEVA, Jan. 15, 2015 (GLOBE NEWSWIRE) --
Amarantus BioScience Holdings, Inc. (AMBS), a
biotechnology company focused on the development of diagnostics for neurology and therapeutic products in the areas of neurology,
psychiatry, ophthalmology and regenerative medicine, reported positive top-line results of its LP-002 study of the Lymphocyte
Proliferation Test (LymPro Test(R)) blood diagnostic for Alzheimer's disease (AD). Results from the 140-subject study
demonstrated that multiple individual biomarkers achieved statistically significant results to correctly identify patients with
AD from healthy controls. The company recently completed 'Fit-for-Purpose' assay validation for LymPro at Icon Central Laboratories
in Farmingdale, NY, enabling the assay to be offered to the pharmaceutical industry for evaluation in therapeutic Alzheimer's
clinical trials. Biomarker services using LymPro Test biomarker data are now available to the pharmaceutical industry for Investigational
Use Only (IUO) in pharmaceutical therapeutic clinical development programs.
In addition, the company identified a new, undisclosed biomarker
that correlates with AD diagnosis in the LP-002 study (p<0.0001). This new marker could become a central component of a multivariate
algorithm (LymPro Score) that is currently being analyzed by company scientists to deliver a simplified assessment of an individual's
likelihood of having Alzheimer's disease.
"LymPro represents an innovative approach to improving
the diagnosis of Alzheimer's disease by measuring a fundamental aspect of disease biology," said Gerald E. Commissiong, President
& CEO of Amarantus. "The fact that LymPro has the ability to distinguish patients with early stage AD from control subjects
will be important to the pharmaceutical industry engaged in Alzheimer's research. We believe LymPro will have an important impact
on future therapeutic drug development programs enabling pharmaceutical companies the opportunity to both enrich clinical trial
populations, as well as monitor relevant biology in AD subjects."
In the 140-subject study assessing 71 patients with mild-to-severe
AD versus a control group of 69 healthy subjects, the expression of the marker CD69 on specific subpopulations of lymphocytic cells
was statistically significantly lower in the AD groups versus the control group, as measured under two different mitogenic stimulation
conditions (LymPro Version 1 and LymPro Version 2). The LymPro Version 1 assay replicated previous published work, most notably
with the CD19+ positive lymphocytes (p=0.0005), confirming published literature. Each of the three stages of Alzheimer's disease
showed significant differences in marker expression as compared to healthy controls.
In addition, after further analysis of a 44 subject 7-year longitudinal
retrospective study including a patient record clinical data assessment over time, LymPro was able to distinguish Alzheimer's disease
from Parkinson's and vascular dementias with a sensitivity of 94% and specificity of 65% (p=0.0002). This is of importance because
it may assist pharmaceutical companies in distinguishing dementia of the Alzheimer's type from dementia of a different etiology.
A copy of a corporate presentation reviewing the data is available
online on the company's website at http://ir.amarantus.com/presentations.
As described in the published literature, CD69 is a protein
expressed when lymphocytic blood cells are undergoing proliferation, and is considered an early marker of cell division. Low levels
of CD69 under cell division conditions in AD patients is indicative of lymphocytic cell cycle dysregulation and a surrogate marker
for the neuronal cell cycle dysregulation that has been observed in the brains of AD patients at autopsy.
"Not only is LymPro a consistent and reliable tool in diagnosing
Alzheimer's disease, having completed 'Fit-for-Purpose' assay validation at Icon, it may now be used to enrich inclusion criteria
in pharmaceutical clinical studies," said Colin Bier, Chief Development Officer of Amarantus Diagnostics, the company's newly
created wholly-owned subsidiary. "Use of the LymPro Test will likely mitigate principal investigators' risk of selecting the
wrong patients for inclusion in clinical studies of Alzheimer's therapeutics."
Amarantus intends to publish data from these studies in peer-reviewed
journals as well as present them at various scientific congresses throughout the course of 2015.
About Alzheimer's disease
According to the Alzheimer's Association, it is estimated that
over 5.4 million people in the United States suffer from Alzheimer's disease. Over 500,000 patients are diagnosed annually, with
nearly one-in-eight older Americans affected by the disease. Alzheimer's disease is the third leading cause of death in the United
States. The cost of unpaid care in the United States is estimated at over $210 billion annually. Total payments for care are estimated
at over $200 billion annually, including $140 billion in cost to Medicare and Medicaid. Alzheimer's expenditures in the United
States are expected to exceed $1.2 trillion by 2050. There is no cure or effective treatment for Alzheimer's disease. Worldwide,
about 35.6 million individuals have the disease and, according to the World Health Organization, the number will double every 20
years to 115.4 million people with Alzheimer's by 2050.
About LymPro Test(R)
The Lymphocyte Proliferation Test (LymPro Test(R))
is a diagnostic blood test that determines the ability of peripheral blood lymphocytes to withstand an external mitogenic stimulation
that induces them to enter the cell cycle. It is believed that certain diseases, most notably Alzheimer's disease, are the result
of compromised cellular machinery that leads to aberrant cell cycle re-entry by neurons. LymPro is unique in the use of peripheral
blood lymphocytes (PBLs) as a surrogate for neuronal cell function, suggesting a common immune-based relationship between PBLs
and neurons in the brain.
About Amarantus BioScience Holdings, Inc.
Amarantus BioScience Holdings (AMBS) is a biotechnology company
developing treatments and diagnostics for diseases associated with neurodegeneration and protein misfolding-related apoptosis.
AMBS has licensed Eltoprazine, a Phase 2b ready small molecule indicated for Parkinson's disease Levodopa-induced dyskinesia and
adult ADHD. AMBS has an exclusive worldwide license to the Lymphocyte Proliferation test, (LymPro Test(R)), which was
developed by Prof. Thomas Arendt, Ph.D., from the University of Leipzig, for Alzheimer's disease and owns the intellectual property
rights to a therapeutic protein known as mesencephalic-astrocyte-derived neurotrophic factor ("MANF") and is developing
MANF-based products as treatments for brain and ophthalmic disorders. AMBS also owns intellectual property for the diagnosis of
Parkinson's disease (NuroPro) and the discovery of neurotrophic factors (PhenoGuard(TM)).
In November 2014, AMBS entered into an exclusive option agreement
with Lonza Walkersville, Inc., a subsidiary of Lonza Group Ltd., to acquire Cutanogen Corporation, a subsidiary of Lonza Walkersville,
to develop Engineered Skin Substitute (ESS-W), an autologous skin replacement product for the treatment of Stage 3 and Stage 4
intractable severe burns.
On January 12, 2015, AMBS announced the acquisition of DioGenix,
Inc., a specialized neuro-diagnostics company, and owns the rights to MSPrecise(R), a proprietary next-generation DNA
sequencing (NGS) assay for the identification of patients with relapsing-remitting multiple sclerosis (RRMS) at first clinical
presentation. For further information please visit www.Amarantus.com, or connect with
the company on Facebook, LinkedIn, Twitter
and Google+.
Forward-Looking Statements
Certain statements, other than purely historical information,
including estimates, projections, statements relating to our business plans, objectives, and expected operating results, and the
assumptions upon which those statements are based, are forward-looking statements. These forward-looking statements generally are
identified by the words "believes," "project," "expects," "anticipates," "estimates,"
"intends," "strategy," "plan," "may," "will," "would," "will be,"
"will continue," "will likely result," and similar expressions. Forward-looking statements are based on current
expectations and assumptions that are subject to risks and uncertainties which may cause actual results to differ materially from
the forward-looking statements. Our ability to predict results or the actual effect of future plans or strategies is inherently
uncertain. Factors which could have a material adverse effect on our operations and future prospects on a consolidated basis include,
but are not limited to: changes in economic conditions, legislative/regulatory changes, availability of capital, interest rates,
competition, and generally accepted accounting principles. These risks and uncertainties should also be considered in evaluating
forward-looking statements and undue reliance should not be placed on such statements.
Contact:
Investor Contact:
Jenene Thomas
Jenene Thomas Communications, LLC
Investor Relations and Corporate Communications Advisor
T: (US) 908.938.1475
E: jenene@jenenethomascommunications.com
Media Contact:
Planet Communications
Deanne Eagle, Media Contact
T: (US) 917.837.5866
Exhibit 99.2
Amarantus Announces Exclusive Option Agreement With Georgetown
University to License Patent Rights for Blood Based Biomarkers for Alzheimer's Disease
SAN FRANCISCO and GENEVA, Jan. 15, 2015 (GLOBE NEWSWIRE) --
Amarantus BioScience Holdings, Inc. (AMBS), a
biotechnology company focused on the development of novel diagnostic tests in neurology and therapeutic products in the areas
of neurology, psychiatry, ophthalmology and regenerative medicine, announced that it has executed a one-year, exclusive option
agreement with Georgetown University to enter into a license for the patent rights related to certain blood based biomarkers for
memory loss that Georgetown University and University of Rochester jointly own. Amarantus will be required to achieve timely milestones
including providing Georgetown with development and commercialization plans for the biomarkers, share information related to Amarantus'
diagnostic assets, CLIA validation of biomarkers, recruitment of a senior executive to lead Amarantus' diagnostics division and
other requirements as defined in the agreement.
"The evaluation of the memory loss-related biomarkers from
Georgetown University and University of Rochester are part of our continuing plan to be the world's premier Alzheimer's blood-based
diagnostic company in the world," said Gerald E. Commissiong, President & CEO of Amarantus. "There are six patents
covered in the agreement with Georgetown University. The technologies are based on metabolic, genetic and exosomal biomarkers.
We believe these may hold additional potential for identifying distinguishing factors in dementia and Alzheimer's disease that
will be complementary to our current cell cycle dysregulation platform with LymPro(R) Test. With the potential addition
of these biomarkers to our Alzheimer's diagnostics portfolio, we are positioning ourselves to be able to serve the pharmaceutical
clinical trial community with all three modalities (cell cycle dysregulation, lipidomics and exosomes) that will streamline their
efforts to recruit and monitor subjects enrolling in Alzheimer's therapeutics clinical studies, in addition to bringing to market
blood diagnostics for Alzheimer's disease that will help individuals and nations implement robust screening initiatives to accurately
diagnose Alzheimer's disease."
"The preclinical state of the disease when one is asymptomatic
offers a window of opportunity for potential disease-modifying intervention such as medications," stated Howard Federoff,
MD, PhD, Executive Vice President for Health Sciences at Georgetown University Medical Center and Executive Dean of Georgetown's
School of Medicine, and one of the inventors of the technology. "It will be critical to have biomarkers such as these for
large-scale screening to identify at-risk individuals in order to test therapeutic agents that might delay or prevent the emergence
of the disease. This will ultimately be hugely important to patients and their families."
During the option period, Amarantus has been granted rights
to internally evaluate the biomarkers. The biomarkers are based on technologies entitled, "Blood Based Biomarkers for Memory
Loss" developed in the course of research performed by Drs. Howard Federoff, Massimo Fiandaca, Amrita Cheema, Yuriv Gusev,
and Xiaogang Zhong at Georgetown University and Dr. Mark Mapstone at University of Rochester.
About Alzheimer's disease
According to the Alzheimer's Association, it is estimated that
over 5.4 million people in the United States suffer from Alzheimer's disease. Over 500,000 patients are diagnosed annually, with
nearly one-in-eight older Americans affected by the disease. Alzheimer's disease is the third leading cause of death in the United
States. The cost of unpaid care in the United States is estimated at over $210 billion annually. Total payments for care are estimated
at over $200 billion annually, including $140 billion in cost to Medicare and Medicaid. Alzheimer's expenditures in the United
States are expected to exceed $1.2 trillion by 2050. There is no cure or effective treatment for Alzheimer's disease. Worldwide,
about 35.6 million individuals have the disease and, according to the World Health Organization, the number will double every 20
years to 115.4 million people with Alzheimer's by 2050.
About Amarantus BioScience Holdings, Inc.
Amarantus BioScience Holdings (AMBS) is a biotechnology company
developing treatments and diagnostics for diseases associated with neurodegeneration and protein misfolding-related apoptosis.
AMBS has licensed Eltoprazine, a Phase 2b ready small molecule indicated for Parkinson's disease Levodopa-induced dyskinesia and
adult ADHD. AMBS has an exclusive worldwide license to the Lymphocyte Proliferation test, (LymPro Test(R)), which was
developed by Prof. Thomas Arendt, Ph.D., from the University of Leipzig, for Alzheimer's disease and owns the intellectual property
rights to a therapeutic protein known as mesencephalic-astrocyte-derived neurotrophic factor ("MANF") and is developing
MANF-based products as treatments for brain and ophthalmic disorders. AMBS also owns intellectual property for the diagnosis of
Parkinson's disease (NuroPro) and the discovery of neurotrophic factors (PhenoGuard(TM)).
In November 2014, AMBS entered into an exclusive option agreement
with Lonza Walkersville, Inc., a subsidiary of Lonza Group Ltd., to acquire Cutanogen Corporation, a subsidiary of Lonza Walkersville,
to develop Engineered Skin Substitute (ESS-W), an autologous skin replacement product for the treatment of Stage 3 and Stage 4
intractable severe burns.
On January 12, 2015, AMBS announced the acquisition of DioGenix,
Inc., a specialized neuro-diagnostics company, and owns the rights to MSPrecise(R), a proprietary next-generation DNA
sequencing (NGS) assay for the identification of patients with relapsing-remitting multiple sclerosis (RRMS) at first clinical
presentation. For further information please visit www.Amarantus.com, or connect with
the company on Facebook, LinkedIn, Twitter
and Google+.
Forward-Looking Statements
Certain statements, other than purely historical information,
including estimates, projections, statements relating to our business plans, objectives, and expected operating results, and the
assumptions upon which those statements are based, are forward-looking statements. These forward-looking statements generally are
identified by the words "believes," "project," "expects," "anticipates," "estimates,"
"intends," "strategy," "plan," "may," "will," "would," "will be,"
"will continue," "will likely result," and similar expressions. Forward-looking statements are based on current
expectations and assumptions that are subject to risks and uncertainties which may cause actual results to differ materially from
the forward-looking statements. Our ability to predict results or the actual effect of future plans or strategies is inherently
uncertain. Factors which could have a material adverse effect on our operations and future prospects on a consolidated basis include,
but are not limited to: changes in economic conditions, legislative/regulatory changes, availability of capital, interest rates,
competition, and generally accepted accounting principles. These risks and uncertainties should also be considered in evaluating
forward-looking statements and undue reliance should not be placed on such statements.
Contact:
Investor Contact:
Jenene Thomas
Jenene Thomas Communications, LLC
Investor Relations and Corporate Communications Advisor
T: (US) 908.938.1475
E: jenene@jenenethomascommunications.com
Media Contact:
Planet Communications
Deanne Eagle, Media Contact
T: (US) 917.837.5866
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