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World Stem Cells, LLC. facilitates Stem Cell Treatments In Cancun at World Stem Cells Clinic

World Stem Cells, LLC facilitates Stem Cell Therapies at a state of the art clinic in beautiful Cancun. The clinic is staffed by top specialist in the field of stem cell implants and a new laboratory to support the stem cell treatments given.

Lutz, Florida (PRWEB) February 05, 2013

The laboratory http://worldstemcells.com/stem-cell-laboratory construction is complete and operations were transferred to our new facility. This facility provides Cancun, and patient around the world, a state of the art cGTP laboratory to support their stem cell treatments in a beautiful, and positive environment. The lab was designed and constructed to provide one ISO7 lab, one wet lab along with a treatment area. This will allow stem cell retrieval, testing, culturing, selection, counting, analyses and sorting along with cryopreservation, without removal from the lab. This all in house capability reduces the possibility of contamination and errors. Dr. M. Abblitt will operate the Lab under cGTP guidelines and use the state of the art facility to provide quality care to her stem cell transplant patients. Our strict adherence to these established guidelines and policies guarantees the highest quality of clinical care and stem cell treatment safety for you.

Our clinic and laboratory and clinic were designed, built and are operated under the stringent guidelines as established by The International Cellular Medical Society (ICMS) and the US Federal Drug Administrations Good Tissue Practice (cGTP)regulations for pharmaceutical, biologics and clinical laboratories. Working under the guidelines set forth by ICMS world stem cells, LLC ( http://worldstemcells.com/ ) provides stem cell treatment for ankylosing spondylitis, autism, cerebral palsy, charcot-marie-tooth disease (cmt), crohns diseases, copd, fuchs disease, guillain-barre syndrome, hashimotos thryroiditis, itp, kidney diseases, macular degeneration, lupus (sle), multiple sclerosis, pad, parkinsons disease, rheumatoid arthritis, scleroderma, stroke, ulcerative colitis

The laboratory and clinic will be engaged in private clinical trials, IRBs and joint studies with US companies, Mexican Educational Institutes, US universities and doctors to better understand the benefits and precaution to be taken in the stem cell treatment process.

Colleen Powers World Stem Cells, LLC (800)234-1693 Email Information

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World Stem Cells, LLC. facilitates Stem Cell Treatments In Cancun at World Stem Cells Clinic

Stem Cell Therapeutics Announces Agreement With Trillium Therapeutics Inc. for Merger

TORONTO, ONTARIO--(Marketwire - Feb 4, 2013) - Stem Cell Therapeutics Corp. (TSX VENTURE:SSS), a life sciences company developing stem cell-related technologies, today announced the execution of a Letter of Agreement with Trillium Therapeutics Inc. ("Trillium") of Toronto, under which Trillium would be merged into Stem Cell Therapeutics Corp. ("SCT") by way of a three-cornered amalgamation or plan of arrangement with a newly-created SCT subsidiary.

In addition, SCT announces that its Board of Directors has authorized the implementation of a share consolidation approved by its shareholders at the special meeting held on December 20, 2012 at a ratio of 1 post-consolidation common share for 10 pre-consolidation common shares.

Proposed Merger

Trillium specializes in immunotherapy and cancer stem cell research, with a particular focus on blocking the negative pathways that malignant cells exploit to suppress anti-tumor responses. Trillium is developing TTI-621, a novel SIRPaFc fusion protein that targets CD47, augmenting the ability of the immune system to destroy cancer stem cells. The project originated from leading researchers in the field, including Drs. John Dick and Jean Wang of the University Health Network and Dr. Jayne Danska of the Hospital for Sick Children, all of Toronto. TTI-621, which is expected to enter formal IND-enabling studies in the second quarter of 2013, is being developed initially as a treatment for acute myeloid leukemia (AML), with potential applications in other hematological and solid tumours. Trillium''s preclinical cancer immunotherapy pipeline also includes a fully human CD200-specific monoclonal antibody which is also ready to enter formal IND-enabling studies. In addition to its preclinical portfolio, Trillium is conducting a clinical trial in patients with interstitial cystitis, a chronic and painful bladder disease. Results from this trial are expected in mid-2013.

"The proposed merger of Trillium and SCT would create Canada''s only public company advancing cancer stem cell technologies," said David Allan, the Executive Chairman of SCT. "With a combined pipeline containing both TTI-621 and the Tigecycline small-molecule program, which SCT recently optioned from the University Health Network, the resulting entity will be well positioned as a global contender in the cancer stem cell field."

It is intended that all Trillium executives and staff will remain with the resulting entity. The current CEO of Trillium, Dr.Niclas Stiernholm, will become the CEO of SCT, Dr. Robert Uger, Chief Scientific Officer, Dr. Penka Petrova, Vice President, Drug Development and Mr. James Parsons, CFO. Upon closing of the transaction, Dr.Michael Moore, Trillium''s long-serving Chairman and veteran biotechnology executive, will join the Board of Directors of SCT. Following a career at the London Stock Exchange-listed biotechnology company, Xenova Group plc, in 2003 Dr. Moore was appointed Chief Executive Officer of then newly-formed Piramed Limited, which was sold to Roche five years later for $160million. As a result of these permanent management appointments the executive services provided by Drs. Albert Agro and Bev Incledon, as an interim measure through their company Concept 2 Clinic Inc., will cease as of closing of the proposed merger.

It is contemplated that the Board of SCT post-merger will consist of Mr. David Allan, Dr. James DeMesa, Dr. Henry Friesen, Mr. Dean Peterson, Dr. Calvin Stiller and Dr. Niclas Stiernholm, all current board members of the Corporation, together with Dr.Michael Moore.

"This transaction will allow the companies'' combined assets to gain access to the capital required for their proper development in order to transform them, over time, into valuable new treatments," commented Dr. Stiernholm. "My colleagues and I are excited about the upcoming creation of a much needed commercial vehicle for Canada''s world class cancer stem cell discoveries. Although a formidable challenge for a company of any size, by building on the strength of our own capabilities, our existing links to several of Ontario''s leading cancer research organizations, and our global industry network, we believe we have a real opportunity to make a difference in the future treatment of cancer."

Pursuant to the Letter of Agreement, the security holders of Trillium will receive, on closing of the transaction, an aggregate consideration of $2,850,000. This consideration is comprised of $1.2 million in cash and $1.65 million in SCT common shares, at a deemed price per share not lower than the post-consolidation Discounted Market Price (as per the policies of the TSXV) at the time of this announcement. SCT and Trillium intend to close the transaction in the first half of 2013, subject to customary closing conditions, including corporate and regulatory approvals, as well as securing the additional financing required to conclude the proposed merger and to advance the SCT development programs. The latter will be done through a public offering of securities for an amount of $2.5million to be priced based on market conditions. There can be no assurance that the proposed merger with Trillium will be completed as proposed, or at all.

The proposed merger is an arm''s-length transaction and will not result in a change of control of SCT or the creation of a new control person (as defined in TSX-V policies). All matters of the formation, negotiation and conclusion of the planned merger are being managed by a Special Committee of each of SCT and Trillium. Dr. Niclas Stiernholm, the CEO of Trillium, is a Director of SCT and in recognition of these relationships, the Trillium Board engaged an independent advisor, reporting directly to Trillium''s Special Committee, to explore this proposed merger and other transaction options. The principal securityholders of Trillium have indicated they will support the proposed merger.

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Stem Cell Therapeutics Announces Agreement With Trillium Therapeutics Inc. for Merger

Fighting fat with fat: Stem cell discovery identifies potential obesity treatment

Public release date: 5-Feb-2013 [ | E-mail | Share ]

Contact: Paddy Moore padmoore@ohri.ca 613-737-8899 x73687 Ottawa Hospital Research Institute

February 5, 2013OttawaOttawa scientists have discovered a trigger that turns muscle stem cells into brown fat, a form of good fat that could play a critical role in the fight against obesity. The findings from Dr. Michael Rudnicki's lab, based at the Ottawa Hospital Research Institute, were published today in the prestigious journal Cell Metabolism.

"This discovery significantly advances our ability to harness this good fat in the battle against bad fat and all the associated health risks that come with being overweight and obese," says Dr. Rudnicki, a senior scientist and director for the Regenerative Medicine Program and Sprott Centre for Stem Cell Research at the Ottawa Hospital Research Institute. He is also a Canada Research Chair in Molecular Genetics and professor in the Faculty of Medicine at the University of Ottawa.

Globally, obesity is the fifth leading risk for death, with an estimated 2.8 million people dying every year from the effects of being overweight or obese, according to the World Health Organization. The Public Health Agency of Canada estimates that 25% of Canadian adults are obese.

In 2007, Dr. Rudnicki led a team that was the first to prove the existence of adult skeletal muscle stem cells. In the paper published today, Dr. Rudnicki now shows (again for the first time) that these adult muscle stem cells not only have the ability to produce muscle fibres, but also to become brown fat. Brown fat is an energy-burning tissue that is important to the body's ability to keep warm and regulate temperature. In addition, more brown fat is associated with less obesity.

Perhaps more importantly, the paper identifies how adult muscle stem cells become brown fat. The key is a small gene regulator called microRNA-133, or miR-133. When miR-133 is present, the stem cells turn into muscle fibre; when reduced, the stem cells become brown fat.

Dr. Rudnicki's lab showed that adult mice injected with an agent to reduce miR-133, called an antisense oligonucleotide or ASO, produced more brown fat, were protected from obesity and had an improved ability to process glucose. In addition, the local injection into the hind leg muscle led to increased energy production throughout the bodyan effect observed after four months.

Using an ASO to treat disease by reducing the levels of specific microRNAs is a method that is already in human clinical trials. However, a potential treatment using miR-133 to combat obesity is still years away.

"While we are very excited by this breakthrough, we acknowledge that it's a first step," says Dr. Rudnicki. "There are still many questions to be answered, such as: Will it help adults who are already obese to lose weight? How should it be administered? How long do the effects last? Are there adverse effects we have not observed yet?"

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Fighting fat with fat: Stem cell discovery identifies potential obesity treatment

YaFarm Technologies, Inc. Announces It Has Signed a Definitive Agreement With The Integrative Stem Cell Institute

PITTSTON, ME--(Marketwire - Feb 5, 2013) - YaFarm Technologies, Inc. ( PINKSHEETS : YFRM ) (YaFarm, or the Company) is pleased to announce that it has signed a definitive agreement to acquire the Integrative Stem Cell Institute (the ISCI). The ISCI is a pioneer in the field of cell-based regenerative medicine. Combining a world-class medical facility with a state-of-the-art laboratory, the ISCI provides investigational treatments to patients as part of clinical studies, while providing long-term follow up to advance these promising therapies. The acquisition of the ISCI provides the Company with an entry into stem cell research and treatment. With the advent of regenerative medicine, clinics such as the ISCI have taken the years of scientific research and started to apply them to treatment of patients.

YaFarm Technologies President Brian Hermenze stated, "Since the 2012 Nobel Prize in Physiology or Medicine was awarded jointly to John B. Gurdon and Shinya Yamanaka for their work in stem cell research, we are very excited about the synergies this acquisition will bring to the Company. The ISCI has been providing point-of-care therapies to patients for over a year and operates at an internationally recognized medical facility accredited by both the Joint Commission and Accreditation Canada International. With a seasoned and successful management team in place, we believe we are creating an organization that has the capabilities to understand and support the many facets of the stem cell industry. We believe that there will be significant growth opportunities in stem cell research and treatment in the near future, and it is our intent to capitalize on them."

Juan Castillo, MD, founder of the ISCI, said, "Physicians from around the world have shown that cells may have a tremendous impact on such chronic and debilitating diseases as diabetes, Parkinson's disease and Chronic Obstructive Pulmonary Disease (COPD)." Dr. Castillo continued, "The ISCI provides quality patient care and a uniquely integrated medical community. Our patients, physicians and researchers work together to provide access to innovative, point-of-care, cell-based therapies, while evidencing the regenerative capabilities of cell medicine, and delivering on the promise of adult stem cell therapies."

In addition, the Company has received final approval from the Financial Industry Regulatory Authority (FINRA) for a 4 for 1 forward stock split.To receive the dividend the investor must be a registered shareholder of record on the Company's books on or before the record date of January 18, 2013. Shareholders who were not registered as of this date will not receive the dividend. Shares of YaFarm began trading ex-dividend on January 22, 2013.

YaFarm Technologies currently has 49,857,368 shares issued and outstanding. Of the issued and outstanding, the current public float is 17,908,975 and 31,948,393 shares are restricted.

About The Integrative Stem Cell Institute (ISCI)

The Integrative Stem Cell Institute (ISCI) is a premier provider of point-of-care, stem cell-based therapies for patients from around the world. With a state of the art laboratory housed within the Hospital Galenia in Cancun, Mexico, the ISCI combines the most advanced scientific application of stem cells with second to none medical care within the structure of adaptive clinical trials to effectively track long term outcomes and assure patient safety.

More information on The Integrative Stem Cell Institute is available on the company's website at http://www.iscelli.com

SAFE HARBOR STATEMENT

This press release may contain certain forward-looking statements and information, as defined within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, and is subject to the Safe Harbor created by those sections.Forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified.This material contains statements about expected future events and/or financial results that are forward-looking in nature and subject to risks and uncertainties. Future events and actual results could differ materially from those set forth in, contemplated by, or underlying the forward-looking statements. The risks and uncertainties to which forward looking statements are subject include, but are not limited to, the effect of government regulation, competition, adequate financing, and other material risks. Such forward-looking statements by definition involve risks, uncertainties and other factors, which may cause the actual results, performance, or achievements to be materially different from the statements made herein.

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YaFarm Technologies, Inc. Announces It Has Signed a Definitive Agreement With The Integrative Stem Cell Institute

YaFarm Technologies, Inc. Announces a Definitive Agreement With The Integrative Stem Cell Institute

PITTSTON, ME--(Marketwire - Feb 5, 2013) - YaFarm Technologies, Inc. ( PINKSHEETS : YFRM ) (YaFarm, or the Company) is pleased to announce that it has signed a definitive agreement to acquire the Integrative Stem Cell Institute (the ISCI). The ISCI is a pioneer in the field of cell-based regenerative medicine. Combining a world-class medical facility with a state-of-the-art laboratory, the ISCI provides investigational treatments to patients as part of clinical studies, while providing long-term follow up to advance these promising therapies. The acquisition of the ISCI provides the Company with an entre into stem cell research and treatment. With the advent of regenerative medicine, clinics such as the ISCI have taken the years of scientific research and started to apply them to treatment of patients.

YaFarm Technologies CEO Brian Hermenze stated, "Since the 2012 Nobel Prize in Physiology or Medicine was awarded jointly to John B. Gurdon and Shinya Yamanaka for their work in stem cell research, we are very excited about the synergies this acquisition will bring to the Company. The ISCI has been providing point-of-care therapies to patients for over a year and operates at an internationally recognized medical facility accredited by both the Joint Commission and Accreditation Canada International. With a seasoned and successful management team in place, we believe we are creating an organization that has the capabilities to understand and support the many facets of the stem cell industry. We believe that there will be significant growth opportunities in stem cell research and treatment in the near future, and it is our intent to capitalize on them."

Juan Castillo, MD, founder of the ISCI said, "Physicians from around the world have shown that cells may have a tremendous impact on such chronic and debilitating diseases as diabetes, Parkinson's disease and Chronic Obstructive Pulmonary Disease (COPD)." Dr. Castillo continued, "The ISCI provides quality patient care and a uniquely integrated medical community. Our patients, physicians and researchers work together to provide access to innovative, point-of-care, cell-based therapies, while evidencing the regenerative capabilities of cell medicine, and delivering on the promise of adult stem cell therapies."

In addition, the Company has received final approval from the Financial Industry Regulatory Authority (FINRA) for a 4 for 1 forward stock split.To receive the dividend the investor must be a registered shareholder of record on the Company's books on or before the record date of January 18, 2013. Shareholders who were not registered as of this date will not receive the dividend. Shares of YaFarm began trading ex-dividend on January 22, 2013.

YaFarm Technologies currently has 49,857,368 shares issued and outstanding. Of the issued and outstanding, the current public float is 17,908,975 and 31,948,393 shares are restricted.

About Integrative Stem Cell Institute (ISCI)The Integrative Stem Cell Institute (ISCI) is a premier provider of point-of-care, stem cell-based therapies for patients from around the world. With a state of the art laboratory housed within the Hospital Galenia in Cancun, Mexico, the ISCI combines the most advanced scientific application of stem cells with second to none medical care within the structure of adaptive clinical trials to effectively track long term outcomes and assure patient safety.

More information on The Integrative Stem Cell Institute is available on the company's website atwww.iscelli.com.

SAFE HARBOR STATEMENT

This press release may contain certain forward-looking statements and information, as defined within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, and is subject to the Safe Harbor created by those sections.Forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified.This material contains statements about expected future events and/or financial results that are forward-looking in nature and subject to risks and uncertainties. Future events and actual results could differ materially from those set forth in, contemplated by, or underlying the forward-looking statements. The risks and uncertainties to which forward looking statements are subject include, but are not limited to, the effect of government regulation, competition, adequate financing, and other material risks. Such forward-looking statements by definition involve risks, uncertainties and other factors, which may cause the actual results, performance, or achievements to be materially different from the statements made herein.

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YaFarm Technologies, Inc. Announces a Definitive Agreement With The Integrative Stem Cell Institute

Adult Stem Cells Regrow cut off Finger! – Video – Stem Cell Cafe

Feb 04

Adult Stem Cells Regrow cut off Finger! Some studies illustrated that adult stem cell having behaviour similar to embryonic stem cell, when it comes to having properties of differentiate into all types of living cells within the human body, source of the pluripotency adult stem cell comes from the bone marrow, clinical studies shown researchers have uses somatic cells treating all kind of degenerative disease with promising results, including using the patient's own adult stem cell serves as a DNA delivery vehicles to correct genetic defect at the cellular level, instead of the conventional approach by applying the re-engineered retrovirus for gene therapy applications. This video demonstrated the use of extra cellular matrix from pig bladder, this powder can instructed the adult stem cell to regrow the cut-off finger rather than stimulate the wounded site to seal the damaged area. Similar to the regeneration mechanism salamanders possess. But the human body need to have a constant supply of adult stem cell in order for the limb to regrow faster. I've discovered several nutritional herbal supplement, that helps support the natural release of adult stem cells from the bone marrow, the lists of supplements are listed below, all the supplement are scientifically proven from credible source, it has over thousands of sciencific studies documented. Clinicial research have conduct extensively on therapeutic application of adult stem cell. please come to my webpage for more detail Astragalus Root, Anti Aging

By: artnet1

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Adult Stem Cells Regrow cut off Finger! – Video – Stem Cell Cafe

Febe, a Scleroderma Patient, Starts New Life After Receiving a Stem Cell Treatment at World Stem Cells Clinic in Cancun

Febe's family was told by doctors there was nothing they could do and to take her home to die, says her emotional son as he relates her story. That all changed when they met Dr. Sylvia Abblitt at World Stem Cells Clinic and received a stem cell treatment.

Lutz, FL (PRWEB) February 02, 2013

In the case of Febe, she and her son related the story that Febe was near death with her only option being a feeding tube and oxygen and a slow deteriorate and then a painful death. She was isolated from her family and unable to join in family functions and events then Febe and son said they met an angel named Dr. Sylvia Abblitt at World Stem Cells Clinic and that was the start of a new life for Febe and her family. After the treatment she began to get stronger, had more energy, better skin texture, able to eat food, and her breathing became normal. Not only did it change her interactions with the family but she began to work full time and ran for Mexican congress and her son says she has more energy and act younger than him as he smiles at her. She now live a normal life working every day to meet or exceed her goals and the painful and tragic past is fading but is always present driving her to more accomplishments and understand of lifes value.

Scleroderma http://worldstemcells.com/stem-cell-therapy-scleroderma.html is a chronic systemic autoimmune disease (primarily of the skin -"derma") characterized by fibrosis (or hardening -"sclero"), vascular alterations, and auto antibodies. Scleroderma is a connective tissue disease that involves changes in the skin, blood vessels, muscles, and internal organs. It is a type of autoimmune disorder, a condition that occurs when the immune system mistakenly attacks and destroys healthy body tissue.

Although World Stems Clinic in Cancun has had great success in stem cell treatments of Scleroderma with their approach, which includes stimulation prior to collection, processing and expansion of the cell along with the use of growth factors together with an integrated medical approach to maximize the implantation potentials and optimize the potentials of making changes in the patients disease. Not all patients receive the dramatic life altering rejuvenation and outcome of Febe but may receive benefits that can increase their quality of life.

Our clinic and laboratory were designed, built and are operated under the stringent guidelines as established by The International Cellular Medical Society (ICMS) and the US Federal Drug Administrations Good Tissue Practice (cGTP)regulations for pharmaceutical, biologics and clinical laboratories. Our strict adherence to these established guidelines and policies guarantees the highest quality of clinical care and stem cell treatment safety for you.

At World Stem Cells Clinic we continually try to improve our patients outcomes with research and by creating new cells and protocols.

Colleen Powers World Stem Cells, LLC (800)234-1693 Email Information

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Febe, a Scleroderma Patient, Starts New Life After Receiving a Stem Cell Treatment at World Stem Cells Clinic in Cancun

CellTex Says It's Moving Its Stem Cell Business to Mexico

CellTex Therapeutics, the Houston company that opened one of the first commercial stem-cell labs in the country in 2011, then closed it after a warning from regulators last fall, issued surprising news this week. The company sent its patients a cheery e-mail saying that it is going to be working with doctors in Mexicoinstead of the U.S.to provide its unapproved treatment.

We are happy to report we are bringing this technology to Mexico, CellTex wrote in its note. We anticipate that we will be able to offer our stem cell therapy services to physicians in Mexico starting very soon! These winter-time trips to beautiful, sunny locations in Mexico to build these relationships have been an added benefit! The company declined to comment further.

CellTex, whose adventures I chronicled early in January, also said it is opening a new research lab in Houston (its original lab had been cited by the U.S. Food and Drug Administration for having major manufacturing problems) and hoped to begin clinical trials under FDA supervision. Looks like the showdown with the feds is over for now.

CellTex had been charging patients up to $30,000 for its treatments. First, a doctor would remove two teaspoons of fat from a patients abdomen. Then lab technicians would extract about 250,000 adult stem cells, multiply them in a medium, and freeze and store them in vials. Some time later a doctor would give the stem cells to the patient intravenously200 million stem cells a week for three weeks. Theres no word as to how much money new patients will have to pay to be treated in those beautiful sunny locations in Mexico.

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CellTex Says It's Moving Its Stem Cell Business to Mexico

FDA Challenges Stem Cell Companies As Patients Run Out Of Time

Scientists have seen promise in the potential of stem cells, but not everyone agrees stem cell replacement therapy is ready for prime time.

Americans seeking stem cell replacement therapy hope the process can heal them of myriad diseases, and a 2011 report by the Baker Institute estimated the industry could bring in $16 billion in revenue by 2020.

But the Food and Drug Administration has expressed concerns. The agency sued to stop treatments at a Regenerative Sciences clinic in Colorado and closed the lab of another company, Celltex Therapeutics, in Texas.

While patients in dire situations are willing to try the therapy (and pay the hefty costs), there's concern the research doesn't support broad practice just yet.

Running Out Of Options

SammyJo Wilkinson remembers the day 18 years ago when she suddenly couldn't stand. She was a young, ambitious computer programmer, launching an Internet startup.

Her doctor told her it was secondary progressive multiple sclerosis.

Now, at 48, Wilkinson is in a wheelchair. She's tried every available FDA-approved drug and two experimental therapies, including a two-year course of chemotherapy. Nothing worked.

Over time, she started researching adult stem cell replacement, but it was available only abroad. The U.S. opened its doors to the treatment two years ago.

Wilkinson had to see a doctor first, but then she paid Celltex $28,000 for stem cell replacement. In a nutshell, the company promises to remove good, healthy stem cells; store them; make more; and put them back into her body where they can help her heal.

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FDA Challenges Stem Cell Companies As Patients Run Out Of Time

ViaCyte's Role as a Leading Cell Therapy Company Bolstered with the Issuance of 20 Patents in 2012

SAN DIEGO, Jan. 31, 2013 /PRNewswire/ -- ViaCyte, Inc., a leading regenerative medicine company focused on developing new approaches to treat major diseases through the application of a stem cell-derived cell therapy, announced today that the Company was granted 20 patents worldwide in 2012, eight U.S. and twelve foreign. These patents bolster the Company's already strong proprietary position for its ground-breaking diabetes product, VC-01, as well as other applications of its broad technology platform.

(Logo: http://photos.prnewswire.com/prnh/20121026/LA00871LOGO-a)

VC-01 is a very promising, development-stage product that consists of pancreatic precursor cells (called PEC-01) derived from a proprietary human embryonic stem cell line and encapsulated in a proprietary, immune isolating medical device (the ENCAPTRA device). When implanted under the skin in suitable animal models, the cells further differentiate into insulin producing and other endocrine cells that regulate blood glucose in a manner similar or identical to a normal pancreas. If VC-01 performs in humans as it has in animal studies, it could effectively cure type 1 diabetics and be an important new therapy for insulin dependent type 2 diabetics.

ViaCyte's significant intellectual property portfolio now includes over 300 issued patents and pending applications related to the growth, directed differentiation and use of human pluripotent stem cells such as human embryonic stem cells and induced pluripotent stem cells. This portfolio includes 51 issued U.S. and foreign patents specifically directed to the Company's VC-01 product. In addition to the protection afforded by patents, the Company also relies on significant proprietary know-how to develop its product offerings.

Dr. Paul Laikind, ViaCyte's president and chief executive officer said, "Our comprehensive and growing intellectual property portfolio helps to establish us as a leading company in the cell therapy and regenerative medicine field. Although the Company's resources are currently fully committed to the rapid development of VC-01 as a potentially transformative treatment for patients with insulin-dependent diabetes, our platform technology has many other important applications."

In July and August of 2012, the Board of Patent Appeals and Interferences of the U.S. Patent and Trademark Office (the "Board") also issued two decisions favoring ViaCyte on motions filed in the patent interference proceedings between ViaCyte and Geron Corporation (Menlo Park, California). The interferences involved ViaCyte's U.S. Patent No. 7,510,876 ("876 Patent"), which is directed to human definitive endoderm cell cultures in vitro. The Board upheld the claims of ViaCyte's '876 Patent in its entirety over Geron's applications. In September 2012, Geron appealed this decision in the United States District Court for the Northern District of California.

About ViaCyteViaCyte, a private company that has emerged as a leader in the field of regenerative medicine, is currently focused on developing a novel cell therapy for the treatment of diabetes. The Company's lead product is based on the production of pancreatic progenitors derived from human pluripotent stem cells. These cells are implanted in a durable and retrievable encapsulation device. Once implanted and matured, these cells secrete insulin and other regulatory factors in response to blood glucose levels. ViaCyte's goal for this potentially transformative diabetes product is long term insulin independence without immune suppression, and without risk of hypoglycemia and other diabetes-related complications.

ViaCyte is headquartered in San Diego, California with additional operations in Athens, Georgia. The Company is funded in part by the California Institute for Regenerative Medicine (CIRM) and JDRF.

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ViaCyte's Role as a Leading Cell Therapy Company Bolstered with the Issuance of 20 Patents in 2012