Category Archives: Stem Cell Treatment


Wells seeks injury cure before Olympics

Kiwi freeskier Jossi Wells is hoping stem cell treatment will provide him with a shot at contesting next year's Sochi Winter Olympics free of knee pain. 7 February 2013

Wanaka freeskier Jossi Wells sounds almost wistful when he talks about the possibility of competing pain-free.

Still only 22, Wells has lived and skied with patella tendinopathy - the same condition haunting top tennis player Rafael Nadal - for the last seven years.

"I haven't had a day since I was 15 that I don't have excruciating pain in my knees as soon as I bend them," he told NZ Newswire.

That hasn't stopped him from compiling an outstanding record in the demanding sport, including X Games silvers in halfpipe (2010) and slopestyle (2008), backed up by an X Games Big Air bronze in 2012.

Now, a year out from the 2014 Winter Olympics in the Russian city Sochi, Wells is juggling his training workload with accumulating qualification points for ski halfpipe and slopestyle for their Olympic debut.

Just as important, he's also looking at beginning stem cell treatment later this month in Melbourne which has the potential to help him compete without pain.

It's a heady thought.

"I can't wait ... it's going to be like I was 14 again and skiing every moment that I could.

"This stem cell stuff's pretty exciting, because it's kind of the first thing that's come around that could really help."

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Wells seeks injury cure before Olympics

VistaGen's Collaborators Identify Definitive Precursor for Adult Blood and the Immune System

SOUTH SAN FRANCISCO, CA--(Marketwire - Feb 7, 2013) - VistaGen Therapeutics, Inc. ( OTCQB : VSTA ), a biotechnology company applying stem cell technology for drug rescue, predictive toxicology and drug metabolism assays, today announced significant advancements in its stem cell technology licensed from the University Health Network (UHN) in Toronto, Canada. The advancements, which improve VistaGen's ability to develop new stem cell-based bioassay systems and potentially improved cell therapies for human blood system disorders, were reported in the December 2012 edition of Cell Reports, an open-access journal from Cell Press.

The exclusively licensed stem cell technology from UHN, which applies equally to both embryonic stem cells and induced pluripotent stem cells (iPS cells), enables the efficient production of mature hematopoietic (blood) precursor cells.These blood cell precursors give rise to red cells, granulocytes and immune cells (lymphocytes), which represent the majority of the blood cells found in the body.

"In collaboration with our long-term strategic partners at UHN, we continue to pioneer stem cell technology that promises to change the way we develop medicine and apply treatment," stated Shawn K. Singh, CEO of VistaGen. "In addition to creating new capabilities and in vitro assays for drug rescue and predictive toxicology, these advancements open the door to development of new treatments for bone marrow failure, anemia, viral diseases and other conditions that compromise the immune system."

"Due to only partial understanding of the timing and control of the development of definitive hematopoiesis in humans, scientists were previously limited in their ability to identify and produce, from human pluripotent stem cells, the important precursor for mature red and white cells of the blood," said H. Ralph Snodgrass, PhD, VistaGen's President and Chief Scientific Officer. "The identification and characterization of this important precursor provides a readily accessible pluripotent stem cell-derived target cell population that can be expanded and matured into the types of cells needed for novel in vitro assays and our drug rescue efforts, and enables improved technologies and approaches for future cell therapy collaborations."

Dr. Gordon Keller, Chairman of UHN's McEwen Centre for Regenerative Medicine in Toronto and co-founder of VistaGen, stated, "We've been working for many years studying in vitro differentiation of pluripotent stem cells trying to identify, and then expand, the first human cell capable of producing the adult blood and immune system. I believe that we now have a better understanding of this important transition from embryonic to adult hematopoiesis, and have the tools to develop improved methods to expand this cell in large numbers for both drug development and cell therapy applications."

About VistaGen Therapeutics VistaGen is a biotechnology company applying human pluripotent stem cell technology for drug rescue, predictive toxicology and drug metabolism screening. VistaGen's drug rescue activities combine its human pluripotent stem cell technology platform, Human Clinical Trials in a Test Tube, with modern medicinal chemistry to generate novel, safer chemical variants (Drug Rescue Variants) of once-promising small molecule drug candidates. These are drug candidates discontinued by pharmaceutical companies, the U.S. National Institutes of Health (NIH) or university laboratories, after substantial investment in discovery and development, due to heart or liver toxicity or metabolism issues. VistaGen uses its pluripotent stem cell technology to generate early indications, or predictions, of how humans will ultimately respond to new drug candidates before they are ever tested in humans, bringing human biology to the front end of the drug development process.

VistaGen's small molecule prodrug candidate, AV-101, has completed Phase 1 development for treatment of neuropathic pain. Neuropathic pain, a serious and chronic condition causing pain after an injury or disease of the peripheral or central nervous system, affects millions of people worldwide.

Visit VistaGen at http://www.VistaGen.com, follow VistaGen at http://www.twitter.com/VistaGen or view VistaGen's Facebook page at http://www.facebook.com/VistaGen.

Cautionary Statement Regarding Forward Looking Statements The statements in this press release that are not historical facts may constitute forward-looking statements that are based on current expectations and are subject to risks and uncertainties that could cause actual future results to differ materially from those expressed or implied by such statements. Those risks and uncertainties include, but are not limited to, risks related to the success of VistaGen's stem cell technology-based drug rescue, predictive toxicology and metabolism screening activities, further development of stem cell-based bioassay systems, and potentially improved cell therapies, for human blood system disorders or other diseases or conditions, clinical development and commercialization of AV-101 for neuropathic pain or any other disease or condition, its ability to enter into strategic predictive toxicology, metabolism screening, drug rescue and/or drug discovery, development and commercialization collaborations and/or licensing arrangements with respect to one or more drug rescue variants, cell therapies or AV-101, risks and uncertainties relating to the availability of substantial additional capital to support its research, drug rescue, development and commercialization activities, and the success of its research and development plans and strategies, including those plans and strategies related to any drug rescue variant or cell therapy identified and developed by VistaGen, or AV-101. These and other risks and uncertainties are identified and described in more detail in VistaGen's filings with the Securities and Exchange Commission (SEC). These filings are available on the SEC's website at http://www.sec.gov. VistaGen undertakes no obligation to publicly update or revise any forward-looking statements.

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VistaGen's Collaborators Identify Definitive Precursor for Adult Blood and the Immune System

Living to 100 with Anti-Aging and Rejuvenation Stem Cells Therapy

The state of the art Laboratory and clinic at World Stem Cells Clinic announces its latest in Stem Cell Treatments and procedures to rejuvenate the face, body, organs and increase the feeling of well being.

Lutz, Florida (PRWEB) February 07, 2013

The Stem Cell Treatment at World Stem Cells Clinic takes 5 days to complete as the treatments are comprehensive and designed to maximize the benefits and safety a patient derive from the process.

World Stem Cells, LLC worldstemcells.com will provide patient management service assisting the patient on their flight, hotel, provide transportation to and from the airport, transportation to and from your hotel to World Stem Cells Clinic, provide 24/7 communication and be the patients ombudsmen.

FACTS ABOUT AGING

The science shows each minute, our body is dying, this is a fact. Each minute that passes by our body has lost 300,000,000 cells. That means the cells that die in our body equals the population of the United States, each and every single minute. As we age less and less of those cells are replace and we slowly decay. Doctors have see people over a 100 that if cut nothing happens as there are no cells to close the wound.

Thus Aging is a result of progressive depletion of stem cells, so the introduction of new stem cells and adjunctive treatments has the potential of slowing down or reversing this process. Stem cells possess a unique anti-aging effect by regenerating and repairing organs, improving immune function, repair damaged by stress, and various toxins we are exposed to in our daily life.

Stem Cells often thought of as futuristic, controversial and unknown, are now providing the latest anti-Aging, rejuvenation and beauty secret.

THE SIGNS OF AGING

The signs of aging generally start at 40, earlier for those who have burned the candle at both ends , smokers, have been under stress or in contact with toxic sustenances and generally later for those who have had less stress, non smokers, exercised and eat properly but in the end we all will age. Some of the signs of aging are:

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Living to 100 with Anti-Aging and Rejuvenation Stem Cells Therapy

Stem-cell doctor Grekos should lose license, pay heavy fines, costs, state recommends

Photo by Allie Garza

Zannos Grekos

Bonita Springs cardiologist Zannos Grekos should lose his license because he committed medical malpractice in performing an unscientific stem cell procedure on a patient who died, according to new case filings.

State Department of Health attorneys also recommend that a judge fine Grekos the maximum $40,000 and order him to pay expenses to investigate and prosecute him, according to the states recommended order to the judge.

The state costs to date are $200,222, according to Department of Health spokeswoman Ashley Carr.

The case involves Grekos' unorthodox stem-cell therapy on 69-year-old Domenica Fitzgerald in 2010, who suffered a stroke and was taken off life support. She died April 4, 2010.

John Fitzgerald, the victim's husband, pointed out Wednesday that the three-year anniversary of his wife's death is approaching.

"I'm worn out," he said. "I want some closure. My family wants closure."

Still, he said the state's two prosecutors have worked hard, and he had been told that $200,000 had been spent so far on the case.

"I know the system is slow," he said. "It seems to be working."

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Stem-cell doctor Grekos should lose license, pay heavy fines, costs, state recommends

Stem cell discovery identifies potential obesity treatment

Nutrition and Fitness Health Home>>Nutrition and Fitness>>Health news Written by: QMI Agency Feb. 6, 2013 (SHUTTERSTOCK)

Scientists at the Ottawa Hospital Research Institute say they 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.

"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," Dr. Michael Rudnicki, a senior scientist at the Institute, said in a statement Tuesday.

The research team say mice that were injected with an agent to reduce a gene regulator called miR-133 produced more brown fat, were protected from obesity and had an improved ability to process glucose.

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Stem cell discovery identifies potential obesity treatment

Cutting-Edge Medical And Stem Cell Technology Available In The Philippines But DoH cites concerns

Department of Health Undersecretary Dr. Teodoro Herbosa recently urged the public seeking treatment using stem cell technology to only undergo procedure initiated by reputable hospitals in the country.

The highly advanced procedure of using stem cell technology has recently gained popularity due to success claims of scientists here and abroad. However, due to the increasing demand for this technology, USEC Herbosa expressed concern that some individuals needing treatment might end-up in bogus clinics usually offering lower fees. "Just to ensure safety, it will be best for patients to seek treatment only among reputable hospitals," Usec. Herbosa stated in an interview.

Incidentally, a leading global Filipino scientist in the field of genetics and microbiology stated that the Philippines is now one of the leading countries in the world, even a step ahead of Germany, in the field of health science. Presidential Awardee Dr. Samuel D. Bernal, a Filipino-American regenerative medicine expert, medical oncologist, molecular biologist, chemist and a lawyer, calls on Filipinos here and abroad to patronize the technology we have here in the country.

"Very few know about it, but we can already actually culture or clone a human heart in the Philippines," claimed by Dr. Bernal in a recent lecture he delivered recently at UST College of Medicine CME Auditorium before hundreds of University of Sto. Tomas scientists, professors, medical doctors and students.

During the lecture event, dubbed, "Future of Molecular Medicine," Dr. Bernal discussed the beauty, art and importance of molecular medicine in addressing modern-day health problems such as cancer.

Dr. Bernal also talked about the state-of-the-art laboratory he has set up at the Medical City in Ortigas. "We already have the technology, the facility, and numerous experts trained abroad to do the procedures we thought can be accessible only by going to other advanced countries. Our efforts generate jobs for medical experts here, tempted to leave the country to work abroad. We are proud to say patients from other countries choose us over other facilities from other countries because not only are we at par with their services but we are also much affordable compared to treatments done in Germany or Singapore," Dr. Bernal asserts.

The recipient of Presidential Awards for Filipino Individuals and Organizations Overseas conferred by President Benigno S. Aquino III and the Commission on Filipino Overseas (CFO), Dr. Bernal is an accomplished medical expert who finished his fellowship training in Cancer medicine and Cell Biology at Harvard Medical School not to mention his internship and residency in Internal Medicine at the Johns Hopkins Hospital. He returned to the country to put-up a facility on regenerative medicine, molecular medicine laboratory for tumor profiling for drug resistance and sensitivity, and a comprehensive stem cell bank which collects babies' umbilical cords for the family's future use in treatment using stem cell technology.

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Cutting-Edge Medical And Stem Cell Technology Available In The Philippines But DoH cites concerns

First Patient Begins Treatment in BrainStorm’s Phase IIa Trial for ALS

NEW YORK & PETACH TIKVAH, Israel--(BUSINESS WIRE)--

BrainStorm Cell Therapeutics (BCLI), a leading developer of adult stem cell technologies for neurodegenerative diseases, announced today that the first patient began treatment in the Companys Phase IIa dose-escalating clinical trial for ALS. The trial, which will evaluate the safety and preliminary efficacy of BrainStorms NurOwn stem cell therapy candidate, is being conducted at the Hadassah Medical Center in Jerusalem.

In the Phase IIa trial, three groups of four patients will receive combined intramuscular and intrathecal administration of NurOwn cells, in increasing doses. The first cohort of four patients is expected to complete treatment by the end of April 2013. The trial participants will be monitored for three to six months following transplantation.

We are excited to be treating the first patient in this trial, which will build on the excellent safety profile and encouraging positive results from our Phase I/II study, commented Alon Natanson, BrainStorms CEO.

This trial will provide valuable data not only on the safety of NurOwn in ALS patients, but also on the ability of different dosing levels to provide clinical benefit, added Prof. Dani Offen, the Companys Chief Scientific Advisor.

Israels Ministry of Health recently approved BrainStorms acceleration to a Phase IIa trial following the positive safety evaluation of the first 12 patients in the companys recent Phase I/II trial at Hadassah. A description of the trial can be found at: http://www.clinicaltrials.gov/ct2/show/NCT01777646?term=NCT01777646&rank=1.

About BrainStorm Cell Therapeutics, Inc.

BrainStorm Cell Therapeutics Inc. is a biotechnology company engaged in the development of first-of-its-kind adult stem cell therapies derived from autologous bone marrow cells for the treatment of neurodegenerative diseases. The Company holds the rights to develop and commercialize its NurOwn technology through an exclusive, worldwide licensing agreement with Ramot, the technology transfer company of Tel Aviv University. For more information, visit the companys website at http://www.brainstorm-cell.com.

Safe Harbor Statement

Statements in this announcement other than historical data and information constitute "forward-looking statements" and involve risks and uncertainties that could cause BrainStorm Cell Therapeutics Inc.'s actual results to differ materially from those stated or implied by such forward-looking statements. Terms and phrases such as may, should, would, could, will, expect, likely, believe, plan, estimate, predict, potential, and similar terms and phrases are intended to identify these forward-looking statements. The potential risks and uncertainties include, without limitation, risks associated with BrainStorm's limited operating history, history of losses; minimal working capital, dependence on its license to Ramot's technology; ability to adequately protect the technology; dependence on key executives and on its scientific consultants; ability to obtain required regulatory approvals; and other factors detailed in BrainStorm's annual report on Form 10-K and quarterly reports on Form 10-Q available at http://www.sec.gov. These factors should be considered carefully, and readers should not place undue reliance on BrainStorms forward-looking statements. The forward-looking statements contained in this press release are based on the beliefs, expectations and opinions of management as of the date of this press release. We do not assume any obligation to update forward-looking statements to reflect actual results or assumptions if circumstances or managements beliefs, expectations or opinions should change, unless otherwise required by law. Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee future results, levels of activity, performance or achievements.

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First Patient Begins Treatment in BrainStorm’s Phase IIa Trial for ALS

International Stem Cell Corporation Announces Positive Results From In Vivo Animal Study of Parkinson's Disease

CARLSBAD, CA--(Marketwire - Feb 4, 2013) - International Stem Cell Corporation ( OTCQB : ISCO ) (www.internationalstemcell.com) ("ISCO" or "the Company") a California-based biotechnology company, today announced positive 12-week results from its pre-clinical in vivo Parkinson's disease study. The primary goal of this behavioral study was to demonstrate the therapeutic benefits of neuronal cells derived from human parthenogenetic stem cell (hpSC) line in a rat model of Parkinson's disease (PD).

Parkinson's disease is a common neurodegenerative disorder caused by a progressive degeneration of dopamine-producing neurons resulting in gradual dysfunction of the motor system and can eventually lead to death. Pharmacological treatments are useful in the relatively early stage of the disease, but the continuous use of pro-dopaminergic medication eventually becomes ineffective and can cause some of the motor symptoms to worsen.

Our proprietary technology is based on a homogeneous population of neuronal cells (NCs) derived from homozygous hpSCs through a scalable and efficient method, developed by ISCO's R&D team. These parthenogenetically-derived NCs are cryopreservable and can become neurons once they are implanted into the brain. As such, they hold significant therapeutic potential not only because they can differentiate into dopamine-producing neurons, but also because these cells deliver trophic factors that may be able to provide a level of protection to existing neurons affected by the disease.

The animal model used in this study is the 6-OHDA lesioned rat, a well-established and validated model of PD which has been used extensively in the development and testing of drugs for the treatment of PD. The pharmacological induction of rotational behavior in rats is widely used to assess the effects of lesions and potential of cell therapy to effectively replace the dopaminergic system in the rat brain and thus serves as a model of PD. The experimental rats with unilateral dopamine (6-OHDA) lesions survived the inoculation of cells into the brain and signs of improvement in rotational behavior of these animals were clearly observed. Correlational analysis of rotation intensity demonstrated a difference between the drug effects in the control group vs. experimental (transplanted) group of animals. These interim results demonstrate that a single injection of hpSC-derived neuronal cells into the striatum of rats with induced PD symptoms can lead to a significant slowdown in the progression of the disease.

Dr. Ruslan Semechkin, Vice President - head of R&D, comments: "This is a very important result for our pre-clinical Parkinson's program. The initial in vivo results are very encouraging and show the therapeutic promise of hpSC-derived neuronal cells in the treatment of individuals with Parkinson's disease. Results from this behavioral study will be presented and discussed together with the results of non-human primate study before the end of the first quarter of 2013"

About International Stem Cell CorporationInternational Stem Cell Corporation is focused on the therapeutic applications of human parthenogenetic stem cells (hpSCs) and the development and commercialization of cell-based research and cosmetic products. ISCO's core technology, parthenogenesis, results in the creation of pluripotent human stem cells from unfertilized oocytes (eggs) hence avoiding ethical issues associated with the use or destruction of viable human embryos. ISCO scientists have created the first parthenogenetic, homozygous stem cell line that can be a source of therapeutic cells for hundreds of millions of individuals of differing genders, ages and racial background with minimal immune rejection after transplantation. hpSCs offer the potential to create the first true stem cell bank, UniStemCell. ISCO also produces and markets specialized cells and growth media for therapeutic research worldwide through its subsidiary Lifeline Cell Technology (www.lifelinecelltech.com), and stem cell-based skin care products through its subsidiary Lifeline Skin Care (www.lifelineskincare.com). More information is available at http://www.internationalstemcell.com.

To receive ongoing corporate communications via email, visit: http://www.b2i.us/irpass.asp?BzID=1468&to=ea&s=0

To like our Facebook page or follow us on Twitter for company updates and industry related news, visit: http://www.facebook.com/InternationalStemCellCorporation and http://www.twitter.com/intlstemcell

Safe harbor statement Statements pertaining to anticipated developments, the potential use of technologies to develop therapeutic products and other opportunities for the company and its subsidiaries, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management constitute forward-looking statements. Any statements that are not historical fact (including, but not limited to statements that contain words such as "will," "believes," "plans," "anticipates," "expects" or "estimates") should also be considered to be forward-looking statements. Forward-looking statements involve risks and uncertainties, including, without limitation, risks inherent in the development and/or commercialization of potential products and the management of collaborations, regulatory approvals, need and ability to obtain future capital, application of capital resources among competing uses, and maintenance of intellectual property rights. Actual results may differ materially from the results anticipated in these forward-looking statements and as such should be evaluated together with the many uncertainties that affect the company's business, particularly those mentioned in the cautionary statements found in the company's Securities and Exchange Commission filings. The company disclaims any intent or obligation to update forward-looking statements.

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International Stem Cell Corporation Announces Positive Results From In Vivo Animal Study of Parkinson's Disease

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