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Research Round Table 2012 – Yanping Li, PhD, Assistant Professor, Transgenic Models – Video

Posted: October 31, 2012 at 10:43 pm


Research Round Table 2012 - Yanping Li, PhD, Assistant Professor, Transgenic Models
Here at The Parkinson #39;s Institute, we don #39;t only have a nationally-recognized clinic and treat thousands of patients a year, but we also have exciting laboratories that work directly with Parkinson #39;s disease and are discovering new things about the disease every day. From stem cell research to genetic mutations, hear from each of our labs about the latest findings from our brilliant scientists.From:ParkinsonInstituteViews:0 0ratingsTime:05:03More inScience Technology

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Research Round Table 2012 - Yanping Li, PhD, Assistant Professor, Transgenic Models - Video

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Stem Cell Therapeutics Announces Admission to Centre for Commercialization of Regenerative Medicine (CCRM) Consortium

Posted: October 31, 2012 at 10:43 pm

TORONTO, ONTARIO--(Marketwire - Oct 29, 2012) - Stem Cell Therapeutics Corp. (TSX VENTURE: SSS) ("the Company"), a life sciences development company for stem cell-based medicines, today reported its admission to the Centre for Commercialization of Regenerative Medicine''s (CCRM) industry consortium.

"We are the only public Canadian company to be part of CCRM''s twenty-member consortium of international leaders in the regenerative medicine arena, a consortium designed to bridge business and scientific expertise to translate stem cell-based and regenerative medicine discoveries into commercial products and therapies," said David Allan, Executive Chairman of Stem Cell Therapeutics Corp. "Participating in this consortium links us to one of the key hubs in Canada for the commercialization of this country''s extraordinary output in stem cell-based science."

The corporate objectives for repositioning the Company include the now-announced involvement with CCRM, the identification and acquisition of additional technologies that will serve to attract capital to revitalize our organization, and striving to extract value from the important patented approaches for the stimulation of endogenous stem cells from Dr. Sam Weiss on which this Company was founded. Stem Cell is pleased to announce this involvement with CCRM as well as the receipt of US$175,000 of a $250,000 arrangement with NeuroNova AB, a Swedish private company developing new therapeutics for ALS and Parkinson''s. The full payment will settle a patent interference case initiated by the United States Patent and Trademark Office under which Stem Cell has withdrawn certain pending and issued patents to treat Parkinson''s disease.

The Company further advises that two additional patient have now been enrolled in its ongoing trial in Traumatic Brain Injury at Calgary''s Foothills Hospital. These patients bring the trial to the midpoint of enrollment, restoring the prospect of the trial to meet the original timelines anticipated by the investigators after enduring a slow initial recruitment period. The Company continues to concentrate its efforts on the conclusion of its remaining objectives.

About Stem Cell Therapeutics:

Stem Cell Therapeutics Corp. (TSX VENTURE:SSS) is a Canadian commercialization receptor company in the business of developing stem cell-based therapeutics through partnerships with research institutions or technology transfer organizations. The Company''s corporate objectives include the analysis and acquisition of additional stem cell-related development opportunities and securing capital for the advancement of the licensed or acquired products. SCT has extensive expertise and experience in the stem cell biotechnology sector based on the intellectual property of Dr. Samuel Weiss in stem cell research. SCT proposes to build upon this existing pipeline of stem cell technologies by acquiring new early-stage clinical or late-stage preclinical candidates. SCT''s Traumatic Brain Injury product, NTx-428, is currently in a Phase II clinical trial. For more information, visit: http://www.stemcellthera.com

Caution Regarding Forward-Looking Information:

Certain statements contained in this press release constitute forward-looking information within the meaning of applicable Canadian provincial securities legislation (collectively, the "forward-looking statements"). These forward-looking statements relate to, among other things, SCT''s objectives, goals, targets, strategies, intentions, plans, beliefs, estimates and outlook, and can, in some cases, be identified by the use of words such as "believe," "anticipate," "expect," "intend," "plan," "will," "may" and other similar expressions. In addition, any statements that refer to expectations, projections or other characterizations of future events or circumstances are forward-looking statements. These statements reflect management''s current beliefs and are based on information currently available to management. Certain material factors or assumptions are applied in making forward-looking statements, and actual results may differ materially from those expressed or implied in such statements. Important factors that could cause actual results to differ materially from these expectations include, among other things: uncertainties and risks related to, the availability of capital, changes in capital markets, uncertainties related to clinical trials and product development, rapid technological change, uncertainties related to forecasts, competition, potential product liability, unproven markets for technologies in development, the cost and supply of raw materials, management of growth, effects of payers'''' willingness to pay for products, risks related to regulatory matters and risks related to intellectual property matters. Additional information about these factors and about the material factors or assumptions underlying such forward-looking statements may be found in the body of this news release, as well as under the heading "Risk Factors" contained in SCT''s 2010 annual information form. SCT cautions that the foregoing list of important factors that may affect future results is not exhaustive.

When relying on SCT''s forward-looking statements to make decisions with respect to SCT, investors and others should carefully consider the foregoing factors and other uncertainties and potential events. Such forward-looking statements are based on a number of estimates and assumptions which may prove to be incorrect, including, but not limited to, assumptions regarding the availability of financing for research and development companies in addition to general business and economic conditions. These risks and uncertainties should be considered carefully and investors and others should not place undue reliance on the forward-looking statements. Although the forward-looking statements contained in this press release are based upon what management believes to be reasonable assumptions, SCT cannot provide assurance that actual results will be consistent with these forward-looking statements. SCT undertakes no obligation to update or revise any forward-looking statement.

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Stem Cell Therapeutics Announces Admission to Centre for Commercialization of Regenerative Medicine (CCRM) Consortium

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'Adequate guidelines for stem cell industry'

Posted: October 31, 2012 at 10:43 pm

KUALA LUMPUR (Oct 29): The Health Ministry has no intention of introducing a Stem Cell Act as the current guidelines are believed to be sufficient to regulate the research being carried out in this growing field.

Minister Datuk Seri Liow Tiong Lai said his ministry has taken the lead to regulate this field by producing four guidelines that provide framework for researchers, clinicians and companies involved in research, clinical trials as well as manufacturing of stem cells.

These four guidelines and standards cover haemopoietic stem cell therapy; cord blood banking and transplantation; stem cell transplantation; and stem cell research and therapy.

Liow stressed that these guidelines, which were introduced in December 2006, with a second edition in July 2009, serve as standards to which practitioners and scientists must abide to in order to ensure no harm is done to the patient.

As such, he said there was no need to table a Stem Cell Bill in Parliament to monitor research and transplants in this field.

Liow said the ministry set up a National Sub-Committee for Ethics in Stem Cell Research and Therapy (NSCERT) as an oversight body for all stem cell research in the country, and religious authorities were consulted while drafting the guidelines.

When asked, Liow said that a fatwa was issued by National Fatwa Council to allow researchers to use the excess embryos, produced through IVF, that have been stored by Muslim couples for research.

In addition, all the stem cell therapy must be tested before use on human body.

Liow also gave some statistics on stem cell transplants in the country.

In 2009, a total of 213 haemopoietic stem cell transplants were performed and registered in this country, with 87.7% performed in public or university hospitals. The Ampang Hospital is the largest centre for this type of transplant and currently, there are 11 such centres in Malaysia.

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'Adequate guidelines for stem cell industry'

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Liow: No plans for stem cell law at the moment

Posted: October 31, 2012 at 10:43 pm

Posted on October 30, 2012, Tuesday

KUALA LUMPUR: The Health Ministry did not have plans to introduce a stem cell Act at the moment, said the minister, Datuk Seri Liow Tiong Lai.

He said, the ministrys four guidelines on stem cell research sufficiently served as standards to which practitioners and scientists involved in stem cell research and therapy should adhere to, ensured patients were out of harms way.

The guidelines would provide a framework for researchers, clinicians and companies involved in research, clinical trials and manufacture of stem cells, he noted.

There is no stem cell act in this country. But the guidelines alone are sufficient to provide the grounds and ethical environment to carry out their work, Liow told reporters after launching the 1st National Stem Cell Congress here yesterday.

The four guidelines are National Standards For Haemopoietic Stem Cell Therapy, National Standards For Cord Blood Banking and Transplantation, National Standards For Stem Cell Transplantation and Guidelines On Stem Cell Research and Therapy.

Liow said: Before we came up with the guidelines, we formed a committee to discuss the details of the research. The committee also included Jakim and religious officials for their views.

He said the use of cell-based therapies should be done strictly under clinical trials.

Prior to the clinical trials, there must be sufficient evidence to show safety, quality and efficacy.

Meanwhile, Liow said stem cell therapy in Malaysia was developing well in government, as well as university hospitals, noting that the number of patients receiving bone marrow and stem cell transplantation for leukaemia and solid tumours was on the rise.

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New lab space for stem cell research

Posted: October 31, 2012 at 10:43 pm

SANTA BARBARA Biomedical research at UC Santa Barbara has catapulted to a position of leadership in the arena of stem cell biology, offering progress toward cures for vision diseases such as macular degeneration. Stem cell research has the potential to transform the practice of medicine, by replacing diseased tissue with healthy new cells. Interdisciplinary teams of UC Santa Barbara researchers including world-renowned faculty members recruited from the U.S. and Britain are leading the charge. The university's newly renovated lab space is critical to the mission.

The latest research holds the promise of developing stem cells from skin, called induced pluripotent stem cells, which could eventually replace the use of human embryonic stem cells. The hope is to find cures for diseases including macular degeneration, diabetic retinopathy and Alzheimer's.

Campus leaders, dignitaries, scientists, and engineers gathered at UC Santa Barbara on Friday (Oct. 26) to celebrate the completion of a dream: 10,000 square feet of renovated laboratory space devoted to stem cell research. This was the grand opening ceremony and ribbon-cutting in celebration of UC Santa Barbara's Center for Stem Cell Biology and Engineering, part of the Neuroscience Research Institute. The California Institute for Regenerative Medicine (CIRM) contributed to the renovation with a $3.2 million grant that was matched by $3.2 million from the university. The top-flight new laboratories are a magnet for attracting new talent.

Chancellor Henry T. Yang commented: "We think UCSB can make important contributions to stem cell research at the interface of biology, neuroscience, and engineering. The future is very bright as we continue to grow and add more top-notch researchers and faculty to this area. These new laboratories will make this possible."

Kenneth S. Kosik, physician and Harriman Chair in the Department of Molecular, Cellular, and Developmental Biology, and co-director of the Neuroscience Research Institute, remarked on this watershed moment in UCSB's stem cell research. "This is a momentous event," said Kosik. "It's a big milestone for UCSB to have come from a premier engineering institute to a place where we are doing world-class work in another entire area, in stem cell biology. With that triumph, that success, we are moving into world-class ranks here."

Leading stem cell biologist Dennis Clegg, center executive director of strategy, planning and operations, and co-principal director of the California Project to Cure Blindness, has directed the center since its inception, and also directed strategy for UC Santa Barbara's specific contribution to stem cell biology.

"We realized that we have a tremendous collection of expertise in bioengineering, basic molecular biology, and neuroscience," said Clegg. "Those groups together, working together collaborating across normal interdisciplinary lines make for a powerful combination of expertise. And we've been able to address some of the key problems in stem cell research, like how to deliver the cells, how to get the cells pure, how to monitor the cells after transplantation, using this combination of bioengineering and molecular biology.

"This has been a long process to complete this renovation for the stem cell center," Clegg said. "It started back in 2007, with our application to CIRM for a major facilities grant. It involved a large number of people on campus scientists, design and construction, administrators.

"We spent many hours figuring out how to come up with matching funds and how to raise money for the stem cell center. It really is a realization of our dream to expand stem cell research on campus. We think we have a lot more to offer. The trajectory is upward; we are really making progress. This will allow us to hire new people, new faculty, bring them in and collaborate with the group of stellar scientists that we've already assembled."

One of the new center directors, Peter Coffey, was hired with a CIRM recruitment grant earlier this year. Coffey, who holds the Garland Chair and is the center's executive director of translation, is considered a star in the world of stem cell science. While at the University College London, he started a group called the London Project to Cure Blindness, which will begin clinical trials early next year. Coffey hopes to bring a part of this project to California.

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Pedersen creates stem cell drug powerhouse

Posted: October 31, 2012 at 10:43 pm

A Cambridge University technology team that developed a way to generate liver cells from skin cells has formed a new company to supply stem cell products to the drug discovery and regenerative medicine sectors.

DefiniGEN is based on the research of Dr Ludovic Vallier, Dr Tamir Rashid and global stem cell guru Professor Roger Pedersen of the Anne McLaren Laboratory of Regenerative Medicine.

DefiniGEN is based in Cambridge and has been funded by a group led by Cambridge Enterprise, the Universitys commercialisation arm, along with members of Cambridge Angels and Cambridge Capital Group.

Prof Pedersen is one of the coveted brains of stem cell research. He moved to Cambridge to escape a puritan US approach to stem cell research and has resisted attempts to woo him back across the Atlantic.

The potential therapeutic applications of stem cells such as regenerating damaged tissues or organs have generated a great deal of interest over the past decade. While these types of applications are exciting, it is a long journey from lab to clinic.

The most immediate impact of stem cells on human health will most likely come from their use in the development of new drugs. The ability to generate stem cells by reprogramming cells from patients skin has revolutionised human stem cell research.

These cells, known as human induced pluripotent stem cells (hIPSC), can be differentiated into almost any cell type, allowing the opportunity to have a ready source of human cells for testing new therapies.

DefiniGEN has developed the technology to generate human liver cells (hepatocytes) in a highly reproducible and scalable manner for commercial use. This represents a major breakthrough in the costly and time-consuming process of developing new therapies.

The technology has also been used to effectively model a diverse range of inherited liver diseases and has the potential to accelerate the development of new therapies for these conditions.

The liver is the key organ for metabolising drugs and removing toxins from the body. Consequently, it is often affected by toxic compounds.

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No need for stem cell Act, says health minister

Posted: October 31, 2012 at 10:43 pm

KUALA LUMPUR: EXISTING guidelines on stem cell research are sufficient to regulate the industry and the Health Ministry sees no need for a stem cell Act for now.

Health Minister Datuk Seri Liow Tiong Lai said guidelines on stem cell research were clear and were drafted with the help of stakeholders, including religious bodies.

He said the ministry had produced four guidelines:

* National Guidelines for Haemopoietic Stem Cell Therapy;

* National Standards for Cord Blood Banking and Transplantation;

* National Standards for Stem Cell Transplantation; and

* Guidelines on Stem Cell Research and Therapy

"We hope researchers follow these guidelines. The ministry does not intend to introduce any Act yet," he said after officiating the First National Stem Cell Congress here yesterday.

Liow said guidelines would be enough to provide a sound and ethical environment for researchers to carry out work. He said the public should also be informed of stem cell services available and be aware that stem cell research here was encouraging.

"In 2009 alone, 213 haemopoitic stem cell transplants were performed and registered in the country," he said.

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California Stem Cell Agency First: Big Pharma Hook Up

Posted: October 28, 2012 at 8:00 am


BURLINGAME, Ca. – For the first
time, a Big Pharma company has hooked into the $3 billion California
stem cell agency, a move that the agency described as a “watershed”
in its efforts to commercialize stem cell research.

The involvement of GlaxoSmithKline
comes via a partnership with ViaCyte, Inc., of San Diego, Ca., in a
clinical trial, partially financed with a $10.1 million grant today
from the stem cell agency. The trial involves a human embryonic stem
cell product that has “the potential to essentially cure patients
with type 1 diabetes and provide a powerful new treatment for those
with type 2 disease,” ViaCyte said. Scientific reviewers for the agency, formally known as the California Institute for Regenerative Medicine(CIRM),  “characterized the goal of the proposed therapy as as the 'holy grail' of diabetes treatments.”
CIRM Director Jeff Sheehy, who is co
vice chair of the agency's grant review group, said the ViaCyte product
could be manufactured on a large scale and basically involves “taking
(small) pouches and popping them into patients.”
The stem cell agency's award triggered
arrangements between ViaCyte and Glaxo that will bring in financial
and other support from Glaxo. The exact amount of cash was not
disclosed. CIRM said Glaxo will “co-fund and, assuming success,
conduct the pivotal trial and commercialize the product.” Under the terms of the grant, Glaxo and ViaCyte will have to meet CIRM milestones in order to secure continued funding. 
Following board approval, Jason
Gardner
, head of the Glaxo stem cell unit, characterized the
arrangement as a partnership. He told the board that the company
intends to develop a “sustainable pipeline.”
Gardner credited CIRM President Alan
Trounson
with being instrumental in helping to put the arrangement
together, beginning with their first meeting three years ago.
Trounson said the deal will resonate not only in California but
throughout the world.
Paul Laikind, president of ViaCyte,
also addressed the board, stressing the importance of CIRM's
financial support for his company over past years. It has received
$26.3 million (not including the latest grant) from California taxpayers at a time when stem cell
funding was nearly dried up. He noted that small companies such as ViaCyte do not have the resources to carry a product through the
final stages of clinical trials and subsequent production. Gardner also said,

“When the commercial funding avenues
have become much more risk averse, CIRM support (has ensured) that
promising, innovative cell therapy technologies are fully explored.”

In comments to the California Stem Cell
Report,
Elona Baum, CIRM's general counsel and vice president for
business development, described the award as a “watershed” for
the eight-year-old agency, linking the agency with Big Phama for the
first time. Much of CIRM's current efforts are aimed at stimulating
financial commitments from large companies, which are necessary to
commercialize stem cell research.
Arrangements between Big Pharma and
small companies are not unusual and can vanish quickly. However, the
CIRM-ViaCyte-Glaxo deal sends a message to other Big Pharma companies
and smaller ones, perhaps clearing away concerns that have hindered
other deals that could involve the stem cell agency.
The stem cell agency is pushing hard to
fulfill the promises of the 2004 ballot campaign that created CIRM.
Voters were led to believe that stem cell cures were virtually around
the corner. None have been developed to date.

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Trounson Going Halftime in January and February

Posted: October 28, 2012 at 8:00 am


BURLINGAME, Ca. -- The president of the $3 billion California stem cell agency, Alan Trounson, will be working half-time while living in Australia during January and February of next year.

Trounson told the governing board of the agency of his plans at the beginning of its meeting here morning. He said he needs to spend more time with his family, which lives in Melbourne.

Trounson has an 11-year-old son with whom Trounson said he hasn't spend much time in the last 18 months.  Trounson said he intends to teach his son to surf. Trounson's daughter also will be getting married in February.

Meanwhile, directors are currently discussing approval of grants in its $20 million-plus strategic partnership round.

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Texas Science Flap Cited as California Stem Cell Agency Eyes its Own Processes

Posted: October 28, 2012 at 8:00 am


OAKLAND, Ca. – Meeting against a
backdrop from Texas that involves conflicts of interest and mass
resignations of grant reviewers, a task force of the $3 billion
California stem cell agency today began a partial examination of its
own grant approval process, specifically focusing on appeals by
rejected applicants.

The president of the California
organization, Alan Trounson, told the task force that it was dealing
with a “very serious matter” that in some ways is similar to what
happened in Texas. He said the science community is “very much
concerned.”
The situation in Texas involves the
five-year-old Cancer Prevention and Research Institute, which like
the California stem cell agency, formally known as the California
Institute of Regenerative Medicine (CIRM)
, has $3 billion of borrowed
money to use to finance research.
The chief scientific officer of the
Texas organization, Nobel laureate Alfred Gilman, resigned Oct. 12
during a flap about its attempts “to simultaneously support basic
research and nurture companies.”
Gilman's departure was triggered by a
$20 million award made without scientific review. Reviewer
resignations followed with letters that accused the Texas group of
“hucksterism” and dishonoring the peer review process. (Writer Monya Baker has a good overview today in Nature.)
The situation in Texas came to a head
AFTER the governing board of the California research group created
its task force. The problems in Texas are bigger and not identical to
those in California, which mainly involve the free-wheeling nature of the appeal process, not an entire lack of scientific review.
Nonetheless, this past summer, directors of the California agency for
the first time approved an award that was rejected twice by
reviewers. The award went to StemCells, Inc., of Newark, Ca., which
now has won $40 million, ranking the company No. 1 in
awards to business from CIRM.
Earlier this month, Los Angeles Times
business columnist Michael Hiltzik characterized the StemCells, Inc.,
award as “redolent of cronyism.”
Today's session of the CIRM task force
focused primarily on an aspect of the agency's appeals process that
CIRM labels as “extraordinary petitions.” They are letters which
rejected applicants use to challenge decisions by grant reviewers.
The researchers follow up with public appearances before the
governing board, often trailing squads of patients making emotional
appeals.
Both researchers and patients have a
right under state law to appear before the CIRM board to discuss any
matter. CIRM, however, is trying to come up with changes in the
appeal process that will make it clear to researchers on what the
grounds the board might overturn reviewers' decisions. The agency is
also defining those grounds narrowly and aiming at eliminating
appeals based on differences in scientific opinion.
At today's meeting, CIRM Director Jeff
Sheehy
, a patient advocate and co-vice chair of the grants review
group, said peer review is an “extraordinary way of analyzing
science, but it is not always perfect.” However, he also said that
“as a board we are not respecting input” from scientists and thus
allow the perception that we can be “persuaded against the judgment
of scientists.”
CIRM Director Oswald Steward, director
of the Reeve-Irvine Research Center at UC Irvine, agreed with a
suggestion by Sheehy that board must act with “discipline” when
faced with appeals by rejected applicants. Steward said, 

“The
process has gotten a little out of hand.”

It was a sentiment that drew no dissent
at today's 90-minute meeting.
Missing from today's meeting, which had
teleconference locations in San Francisco, Irvine, La Jolla and Palo
Alto, were any of the hundreds of California scientists whose
livelihoods are likely to be affected by changes in the grant
approval process. Also absent were California biotech businesses,
along with the only representative on the task force from CIRM's
scientific reviewers.
Our comment? When researchers and
businesses that have millions at stake fail to show up for key
sessions that set the terms on how they can get the money, it is a
sad commentary on their professional and business acumen.
Bert Lubin, a CIRM director and
chairman of the task force, indicated he would like to have two more
meetings of the task force prior to making recommendations to a full
board workshop in January with possible final action later that
month. Lubin, CEO of Children's Hospital in Oakland, said the matter
is “really important for the credibility of our whole
organization.”

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