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News from Finanznachrichten.de June 18,
2007
StemCells, Inc. Announces Important
Milestone in Batten Disease Clinical Trial
StemCells, (Nachrichten) Inc. (NASDAQ:
STEM) today announced that the Phase I clinical trial of its
proprietary HuCNS-SC™ product candidate (purified human neural
stem cells) has successfully completed enrollment of the low-dose
cohort and will proceed to the high-dose cohort. This trial is
designed to evaluate the safety and preliminary efficacy of the
HuCNS-SC product candidate as a treatment for infantile and late
infantile
neuronal ceroid lipofuscinosis (NCL), also often referred to
as Batten disease. To date, three patients out of a planned total of
six have been transplanted with HuCNS-SC cells. A review of the
trial data to date, conducted by an independent Data Safety
Monitoring Committee comprised of experts in pediatric neurosurgery,
pediatric neurology, solid organ transplantation, and genetics, has
identified no safety issues that would preclude advancing the trial
to the next dose level.
“This is a significant milestone for the trial and StemCells, Inc.
We are halfway through the planned enrollment in the first
FDA-approved clinical investigation of purified human neural stem
cells. The first patient enrolled in the trial has now reached the
halfway point of the study and completed a number of important
assessments. To date, all three patients have tolerated the
transplantation and have returned home,“ť said Stephen Huhn, M.D.,
F.A.C.S., F.A.A.P., Vice President and Head of the Neural Program of
StemCells, Inc. “We are encouraged by the progress of the trial, but
remain mindful of the difficult challenges involved with the
development of novel therapeutics. We are also grateful for the
participation of the families in this study and the commitment of
the research staff at OHSU. Batten disease is a terrible affliction,
and this trial is the first step on the path toward a treatment for
this devastating disease and potentially other lysosomal storage
disorders.“ť
The clinical trial is being led by co-principal investigator Robert
Steiner, Vice Chairman of Pediatric Research at Doernbecher
Children's Hospital, and Professor of Pediatrics and Molecular&Medical
Genetics in the OHSU School of Medicine; co-principal investigator
Nathan Selden, Campagna Associate Professor of Pediatric
Neurological Surgery and Head of the Division of Pediatric
Neurological Surgery, Doernbecher and OHSU School of Medicine;
co-investigator Thomas K. Koch, M.D., F.A.A.P., F.A.A.N., Director
of Pediatric Neurology and Professor of Pediatrics and Neurology at
Doernbecher, OHSU School of Medicine; and co-investigator Amira
Al-Uzri, M.D., M.C.R., associate professor of pediatrics (pediatric
nephrology and hypertension), and director of the pediatric kidney
transplant program at Doernbecher Children's Hospital, OHSU School
of Medicine.
About Neuronal Ceroid Lipofuscinosis (Batten Disease)
Neuronal ceroid lipofuscinosis is a fatal neurodegenerative disorder
brought on by inherited genetic mutations. The disorder afflicts
infants and young children, and the three most common forms of NCL“”infantile,
late infantile and juvenile onset“”are often referred to as Batten
disease. All forms have the same basic cause“”lack of a lysosomal
enzyme“”and have similar progression and outcome. Children with NCL
suffer seizures, progressive loss of motor skills, sight and mental
capacity, eventually becoming blind, bedridden and unable to
communicate.
Infantile or late infantile NCL is brought on by inherited mutations
in the CLN1 gene, which codes for palmitoyl-protein thioesterase 1
(PPT1) or in the CLN2 gene, which codes for tripeptidyl peptidase I
(TPP-I), respectively. The consequence of these gene mutations is
either a defective or missing enzyme that leads to accumulation of
lipofuscin-like fluorescent inclusions in various cell types. These
non-degraded lysosomal inclusions accumulate to the point of
interference with normal cellular function and ultimately lead to
the pathological manifestations of the disease. One way to treat the
disease is to provide the brain with a replacement source of
functional enzyme that can be taken up by the enzyme-deficient cells.
About HuCNS-SC™ Cell-Based Therapeutic
StemCells' HuCNS-SC cell-based therapeutic product candidate is
purified human neural stem cells prepared under controlled
conditions. When HuCNS-SC cells are transplanted into the brain of a
mouse model developed to mimic the human form of infantile NCL, the
cells spread throughout the brain and produce the missing lysosomal
enzyme. The enzyme level increases and continues to do so over time
after the transplant. Thus, placement of HuCNS-SC cells in
appropriate places in the brain provides the prospect of long-term
delivery of the missing lysosomal enzyme. In laboratory studies,
HuCNS-SC cells also produce the lysosomal enzyme missing in late
infantile NCL, the other subtype being studied in the clinical
trial. The production of both enzymes by HuCNS-SC cells provides a
scientific rationale for enzyme replacement and cellular rescue in
these two subtypes of NCL.
About StemCells, Inc.
StemCells, Inc. is a clinical-stage biotechnology company focused on
the discovery, development and commercialization of cell-based
therapeutics to treat diseases of the nervous system, liver and
pancreas. The Company's programs seek to repair or repopulate neural,
liver or other tissue that has been damaged or lost as a result of
disease or injury. StemCells has pioneered the discovery and
development of HuCNS-SC cells, its highly purified population of
human neural stem cells. The cells are expandable into cell banks
for therapeutic use, which offers the potential of using normal,
non-genetically modified cells as cell-based therapeutics. StemCells
owns or has exclusive rights to more than 50 issued or allowed U.S.
patents and more than 150 granted or allowed non-U.S. patents.
Further information about the Company is available on its Web site
at www.stemcellsinc.com.
About OHSU and Doernbecher Children's Hospital
Oregon Health&Science University is the state's only health and
research university, and Oregon's only academic health center. OHSU
is Portland's largest employer and the fourth largest in Oregon (excluding
government), with more than 12,000 employees. OHSU's size
contributes to its ability to provide many services and community
support activities not found anywhere else in the state. It serves
189,000 patients annually, and is a conduit for learning for more
than 3,400 students and trainees. OHSU is the source of more than
200 community outreach programs that bring health and education
services to every county in the state.
As a leader in research, OHSU earned $294 million in research
funding in fiscal year 2006. OHSU serves as a catalyst for the
region's bioscience industry and is an incubator of discovery,
averaging one new breakthrough or innovation every three days, with
more than 3,500 research projects currently under way. OHSU
disclosed 116 inventions in 2006 alone, and OHSU research resulted
in 28 new spinoff companies since 2000, most of which are based in
Oregon.
Doernbecher Children's Hospital, a division of Oregon Health&Science
University, is a world-class academic health center that each year
cares for more than 56,000 patients from across the United States.
In the most patient- and family-centered environment, children
receive outstanding cancer treatment, specialized neurology care,
highly sophisticated heart surgery, and care in many other pediatric
specialties. In addition to several locations in the Portland
metropolitan area, Doernbecher's pediatric experts travel throughout
Oregon and southwest Washington providing pediatric specialty care
at 13 outreach clinics.
Apart from statements of historical facts, the text of this press
release constitutes forward-looking statements regarding, among
other things, the future business operations of StemCells, Inc. (the
“Company“ť) and its ability to conduct clinical trials as well as
its research and product development efforts. The forward-looking
statements speak only as of the date of this news release. StemCells
does not undertake to update any of these forward-looking statements
to reflect events or circumstances that occur after the date hereof.
Such statements reflect management's current views and are based on
certain assumptions that may or may not ultimately prove valid. The
Company's actual results may vary materially from those contemplated
in the forward-looking statements due to risks and uncertainties to
which the Company is subject, including uncertainty as to whether
results obtained in the animal models of infantile NCL, spinal cord
injury, or other diseases and conditions will be able to be
translated into treatment for humans; uncertainty as to whether the
FDA or other applicable regulators or review boards will permit the
Company to continue clinical testing in NCL or in future clinical
trials of proposed therapies for other diseases or conditions
despite the novel and unproven nature of the Company's technology;
uncertainties regarding the timing and duration of, and enrollment
of patients in, any clinical trials; uncertainties regarding the
Company's ability to obtain the increased capital resources needed
to continue its current research and development operations and to
conduct the research, preclinical development and clinical trials
necessary for regulatory approvals; uncertainty regarding the
validity and enforceability of the Company's patents; uncertainty as
to whether HuCNS-SC and any products that may be generated in the
future in the Company's stem cell programs will prove safe and
clinically effective and not cause tumors or other side effects;
uncertainty as to whether the Company will achieve revenues from
product sales or become profitable; and other factors that are
described under the heading “Risk Factors“ť in Item 1A of the
Company's Annual Report on Form 10-K.
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