Category Archives: Stem Cell Therapy

Sexual Health Health Home>>Sexual Health>>Health news Written by: QMI Agency May. 2, 2012

U.S. researchers are a step closer to launching human clinical trials of a stem cell therapy to fight HIV.

Scientists at the University of California Davis Health System have successfully transplanted anti-HIV stem cells into mice. They found the HIV-resistant cells thrived, and even renewed themselves, even when challenged with the HIV virus.

The immune systems in mice parallel those in humans, researchers said in a paper published in the May issue of the Journal of Virology.

"After we challenged transplanted mice with live HIV, we demonstrated that the cells with HIV-resistant genes were protected from infection and survived in the face of a viral challenge," lead author Joseph Anderson said in a release.

"Clinical trials could give us the critical information we need to determine whether our approach truly represents a functional cure for a terrible disease that has affected millions and millions of people," Pollard said.

The research team has submitted a grant application for human clinical trials and is currently seeking regulatory approval.

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Researchers see hope in stem cell HIV treatment

SAN DIEGO, CA--(Marketwire -05/03/12)- Regen BioPharma (Regen), Inc. a newly-formed subsidiary of Bio-Matrix Scientific Group, Inc. (BMSN.PK - News) (BMSN.PK - News), unveiled today its operational plan for its "Super-Incubator" stem cell company.

Month 1-2: Assembly of Team. Regen intends to assemble a team of world-class leaders in the spheres of Technology, Intellectual Property assessment, valuation and Clinical development. Regen will seek to compile a team of Physician-Scientists with experience in the area of clinical trials for regenerative medicine/stem cell products, Regulatory experts who have successfully taken products through the FDA and corresponding agencies internationally, and Biotech Entrepreneurs who have track records of excellence in business formation and value optimization.

Month 1-4: In-licensing of Intellectual Property. The Company having already assessed over 20,000 issued patents and having compiled a shortlist of 30 targets; Regen will seek to execute licensing deals on an initial core of 3 technologies. Regen focuses on issued patents that have already passed preclinical studies but are not under clinical development.

Month 3-6: Interaction with Regulatory Agencies. Regen intends to develop data packages for each of the technologies and initiate interaction with Regulatory Agencies such as the FDA for initiation of trials.

Month 6-18: Clinical Implementation. Regen intends to launch clinical trials with world-leading institutions to obtain human safety data and "signal" of therapeutic efficacy.

Month 18-24: Exit. It is intended that technologies "incubated" by Regen will be spun off either as separate companies, or sold to Large Pharma companies seeking to enhance their therapeutic pipeline.

"At present there exists a wealth of intellectual property that is 'collecting dust' in the corridors of Academia. Given the field of regenerative medicine and stem cell therapy is so young, and the business models are fuzzy at best in terms of valuation, we see this space as a unique opportunity for acceleration of clinical development/value optimization," said Bio-Matrix Chairman & CEO David Koos about its Regen BioPharma. "Valuations for stem cell companies that have passed the threshold of clinical safety, with signals of efficacy are astronomical. The $1.8 billion Mesoblast-Cephalon deal, as well as recent financings of private companies with as little as 3 patient data such as Promethera ($31 million) or Allocure with 16 patients ($23 million), is testimony to the extremely high valuations that are characteristic of this space."

About Bio-Matrix Scientific Group, Inc.:

Bio-Matrix Scientific Group, Inc. (BMSN.PK - News) is a biotechnology company focused on the development of regenerative medicine therapies and tools. The Company is specifically focused on human therapies that address unmet medical needs. Specifically, Bio-Matrix Scientific Group Inc. is looking to increase the quality of life through therapies involving stem cell treatments. These treatments are focused in areas relating to lung, heart, circulatory system and other internal organs.

Through Its wholly owned subsidiary, Regen BioPharma, it is the Company's goal to develop translational medicine platforms for the rapid commercialization of stem cell therapies. The Company is looking to use these translational medicine platforms to advance intellectual property licensed from entities, institutions and universities that show promise towards fulfilling the Company's goal of increased quality of life.

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Bio-Matrix Subsidiary "First in Class" Approach to Stem Cell Medicine

OLDSMAR, Fla., May 3, 2012 (GLOBE NEWSWIRE) -- via PRWEB - Cryo-Cell International, Inc. announced the appointment of Linda Kelley, Ph.D., as chief scientific officer. Dr. Kelley is responsible for overseeing Cryo-Cells state-of-the art laboratory, translational medicine initiatives and quality assurance program at its stem cell and cord blood banking facility in Oldsmar, Florida. She joins the company from the Dana Farber Cancer Institute at Harvard, where she was the director of the Connell OReilly Cell Manipulation Core Facility.

Dr. Kelley is an internationally recognized, cord blood stem cell scientist whose accomplishments have helped expand the scope of stem cell therapies from bone marrow transplantation to the treatment of heart, kidney, brain and other degenerative diseases. She was a member of the board of trustees of the Foundation for Accreditation of Cellular Therapy and chaired its Standards Committee. Dr. Kelley was one of 12 scientists selected by the Institute of Medicine of the National Academies of Science to serve on the panel that advised Congress on how to allocate $80 million in funding to optimally structure a national cord blood stem cell program.

While director of the Cell Therapy Facility at the University of Utah, she established that states first umbilical cord blood collection program that enabled families to donate their childrens cord blood to the national inventory. Dr. Kelley earned graduate and post-doctoral degrees in hematology and immunology at Vanderbilt University in Nashville, Tenn., where she also served as assistant professor in the Department of Medicine.

As a leader in our field, Cryo-Cell is delighted to have someone of Dr. Kelleys caliber directing our laboratory and translational medicine initiatives. Her expertise will ensure that we continue to exceed the industrys quality standards and maintain our tradition of offering clients the absolute best in cord blood, cord tissue, and menstrual stem cell cryopreservation services, said David Portnoy, chairman and co-CEO at Cryo-Cell. Under her guidance, Cryo-Cell will be propelled to the forefront of regenerative medicine.

Kelley replaces Julie Allickson, Ph.D., who is joining the Wake Forest Institute for Regenerative Medicine (WFIRM), where she will manage translational research. WFIRM is led by Anthony Atala, M.D., a Cryo-Cell board member and preeminent stem cell scientist.

The opportunity to work in a cutting-edge facility with a staff that is exceptionally well trained was very attractive to me, said Dr. Kelley. But equally important in my decision to join Cryo-Cell, was the commitment that co-CEOs David and Mark Portnoy have made to support the advancement of regenerative medicine through partnerships with Stanford University and private research facilities. Cryo-Cell is unique among stem cell cryopreservation firms in that regard.

About Cryo-Cell International, Inc. Cryo-Cell International, Inc. was founded in 1989. In 1992, it became the first private cord blood bank in the world to separate and store stem cells. Today, Cryo-Cell has over 240,000 clients worldwide from 87 countries. Cryo-Cell's mission is to provide clients with state-of-the-art stem cell cryopreservation services and support the advancement of regenerative medicine. Cryo-Cell operates in a facility that is compliant with Good Manufacturing Practice and Good Tissue Practice (cGMP/cGTP). It is ISO 9001:2008 certified and accredited by the American Association of Blood Banks. Cryo-Cell is a publicly traded company, OTC:QB Markets Group Symbol: CCEL. Expectant parents or healthcare professionals who wish to learn more about cord blood banking and cord blood banking prices may call 1-800-STOR-CELL (1-800-786-7235) or visit http://www.cryo-cell.com/.

Forward-Looking Statement Statements wherein the terms "believes", "intends", "projects", "anticipates", "expects", and similar expressions as used are intended to reflect "forward-looking statements" of the Company. The information contained herein is subject to various risks, uncertainties and other factors that could cause actual results to differ materially from the results anticipated in such forward-looking statements or paragraphs, many of which are outside the control of the Company. These uncertainties and other factors include the success of the Company's global expansion initiatives and product diversification, the Company's actual future ownership stake in future therapies emerging from its collaborative research partnerships, the success related to its IP portfolio, the Company's future competitive position in stem cell innovation, future success of its core business and the competitive impact of public cord blood banking on the Company's business, the Company's ability to minimize future costs to the Company related to R&D initiatives and collaborations and the success of such initiatives and collaborations, the success and enforceability of the Company's menstrual stem cell technology license agreements and umbilical cord blood license agreements and their ability to provide the Company with royalty fees, the ability of the reproductive tissue storage to generate new revenues for the Company and those risks and uncertainties contained in risk factors described in documents the Company files from time to time with the Securities and Exchange Commission, including the most recent Annual Report on Form 10-K, Quarterly Reports on Form 10-Q and any Current Reports on Form 8-K filed by the Company. The Company disclaims any obligations to subsequently revise any forward-looking statements to reflect events or circumstances after the date of such statements.

Contact: David Portnoy Cryo-Cell International, Inc. 813-749-2100 dportnoy(at)cryo-cell(dot)com

This article was originally distributed on PRWeb. For the original version including any supplementary images or video, visit http://www.prweb.com/releases/2012/5/prweb9469228.htm

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Cryo-Cell International Taps Leader in Stem Cell Therapy to Serve as Chief Scientific Officer

Sanford, FL (PRWEB) May 01, 2012

Veterinarians at Val-U-Vet are performing adipose stem cell therapy on dogs and cats suffering from arthritis, hip dysplasia and more. After treatment, severely arthritic pets experience substantial decrease in pain, and have significantly increased mobility.

These are not the controversial embryonic stem cells of the past. Adipose stem cells are harvested from a pets own fat tissue. According to MediVet, the patented technology provider, adipose stem cell treatment can actually reverse some degenerative diseases previously thought to be incurable. The documented before and after video footage of the patients is quite compelling.

All animals have billions of dormant stem cells in their bodies. Adipose tissue (fat) has the highest concentration of dormant stem cells. The treatment begins with the vet surgically removing a small amount of fat from the patient. The fat is then processed on-site with MediVets LED technology to awaken the hibernating stem cells.

The activated stem cells are injected back into the patient by the millions, where they go to work like heat-seeking missiles, repairing tissue. The stem cells also have an anti-inflammatory effect, which reduces the pets pain almost immediately stated Brandon Godwin, Marketing Director for Val-U-Vet.

Within 30 days of the procedure, the patients have significantly increased mobility and little or no pain in their knee and hip joints. In many cases the benefits remain throughout the rest of the pets life, but occasionally more injections are beneficial. Since the procedure is all natural and uses the pets own cells, there is no chance of bodily rejection.

Val-U-Vet has performed over 60 stem cell procedures in Central Florida. About 95% of our cases have shown lasting improvement and no longer need to take their daily pain medication. Our goal is to fix the problem, not mask the symptoms, said Godwin.

The results of the procedure are partially determined by the age and overall health of the pet. Stem cells taken from a young and healthy pet will typically be the most effective. The doctors at Val-U-Vet recommend banking a young pets potent stem cells in combination with their routine spay or neuter. The stem cells can be stored at sub-zero temperatures until they are needed.

There are two important tests that a pet must pass to qualify for the procedure. The pet is screened with blood work and full body x-rays to assure there is no cancer or active infections and that the pet is healthy enough to undergo anesthesia. Val-U-Vet offers a free consultation for any pet suffering from arthritis, hip dysplasia or ligament/cartilage damage. The all-inclusive cost of the same-day procedure is $1800, and they do offer payment plans.

For more information about the procedure, visit: http://www.valuvet.com/stem_cell_therapy.html

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Stem Cell Treatment Helps Pets with Arthritis and Hip Dysplasia

South San Francisco, CA (Marketwire) - VistaGen Therapeutics, Inc. (OTCBB:VSTA) (OTCQB:VSTA), a biotechnology company applying stem cell technology for drug rescue and cell therapy, has licensed breakthrough stem cell culture technology from the McEwen Centre for Regenerative Medicine located at the University Health Network (UHN) in Toronto, Canada.

VistaGen will be utilizing the licensed technology to develop hematopoietic precursor stem cells from human pluripotent stem cells, with the goal of developing drug screening and cell therapy applications for human blood system disorders. The breakthrough technology is included in a new United States patent application.

Hematopoietic precursor stem cells give rise to all red and white blood cells and platelets in the body. VistaGen will use the UHN invention to improve the cell culture methods used to efficiently produce hematopoietic stem cell populations.

"This technology dramatically advances our ability to produce and purify this important blood stem cell precursor for both in vitro drug screening and in vivo cell therapy applications," said H. Ralph Snodgrass, PhD, VistaGen's President and Chief Scientific Officer.

"In addition to defining new cell culture methods for our use, the technology describes the surface characteristics of stem cell-derived adult hematopoietic stem cells. Most groups study embryonic blood development from stem cells, but, for the first time, we are able to not only purify the stem cell-derived precursor of all adult hematopoietic cells, but also pinpoint the precise timing when adult blood cell differentiation takes place in these cultures," Snodgrass added. "It is our belief that these early cells will be the precursors of the ultimate adult, bone marrow-repopulating hematopoietic stem cells."

Bone marrow-derived hematopoietic stem cells are able to repopulate the blood and immune system when transplanted into patients prepared for bone marrow transplantation. These cells have important potential therapeutic applications for the restoration of healthy blood and immune systems in individuals undergoing transplantation therapies for cancer, organ grafts, HIV infections or for acquired or genetic blood and immune deficiencies.

About VistaGen Therapeutics VistaGen is a biotechnology company applying human pluripotent stem cell technology for drug rescue and cell therapy. 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 new chemical variants (Drug Rescue Variants) of once-promising small-molecule drug candidates. These are drug candidates discontinued due to heart toxicity after substantial development by pharmaceutical companies, the U.S. National Institutes of Health (NIH) or university laboratories. 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.

Additionally, VistaGen's small molecule drug candidate, AV-101, is in Phase 1b 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 approximately 1.8 million people in the U.S. alone. VistaGen is also exploring opportunities to leverage its current Phase 1 clinical program to enable additional Phase 2 clinical studies of AV-101 for epilepsy, Parkinson's disease and depression. To date, VistaGen has been awarded over $8.5 million from the NIH for development of AV-101.

Visit VistaGen athttp://www.VistaGen.com, follow VistaGen athttp://www.twitter.com/VistaGenor view VistaGen's Facebook page athttp://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 regulatory approvals, the issuance and protection of patents and other intellectual property, the success of VistaGen's ongoing clinical studies, including the safety and efficacy of its drug candidate, AV-101, the failure of future drug rescue and pilot preclinical cell therapy programs related to VistaGen's stem cell technology-based Human Clinical Trial in a Test Tube platform, its ability to enter into drug rescue collaborations, risks and uncertainties relating to the availability of substantial additional capital to support VistaGen's research, development and commercialization activities, and the success of its research, development, regulatory approval, marketing and distribution plans and strategies, including those plans and strategies related to AV-101 and any drug rescue variants identified and developed by VistaGen. 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 Licenses Breakthrough Stem Cell Culture Technology To Speed Development Of Drug Screening And Cell Therapy ...

Milwaukee, WI (PRWEB) May 02, 2012

Academic and industry leaders in gene and cell therapy will be featured at a Media Event in Philadelphia, PA on May 15, 2012, immediately preceding the 15th Annual Meeting of the American Society of Gene and Cell Therapy (ASGCT) on May 16-19, 2012. The event will focus on recent clinical developments in targeted biotherapeutics for various diseases.

Members of the media will also receive complimentary full-access registration to the ASGCT 15th Annual Meeting at the Pennsylvania Convention. To complete your registration to the Media Event and the Annual Meeting, please visit the ASGCT website.

2:00 pm 2:20 pm: Gene and cell-based immunotherapy for cancer Many cancers are known to acquire the ability to suppress anti-tumor immune responses in the host. The genetically modified cells developed and used in this clinical trial are designed to reawaken immune cells that have been suppressed by the leukemia and stimulate the generation of so-called memory T cells, which can provide ongoing protection against recurrence. Although long-term effectiveness of this novel treatment is not yet known, the doctors have found that months after infusion, the new cells had multiplied and continued their seek-and-destroy mission against cancerous cells throughout the patients bodies. The new paradigm provides a tumor-attack roadmap for the treatment of other cancers including lung, myeloma, ovarian cancer and melanoma.

Carl June, MD is currently the Director of Translational Research at the Abramson Cancer Center,, an Investigator of the Abramson Family Cancer Research Institute, and a tenured Professor of Pathology and Laboratory Medicine at the Perelman School of Medicine of the University of Pennsylvania.

2:20 pm 2:30 pm: Question and answer period

2:30 pm 2:50 pm: Gene therapy for hemophilia B Hemophilia B is an X-linked bleeding disorder caused by a deficiency of blood coagulation Factor IX, and patients need to be infused with the newly developed long-acting protein concentrates twice a month. Advances in gene therapy using intravenous infusion of an AAV vector expressing human Factor IX in a clinical trial on hemophilia patients have significantly improved circulation of Factor IX levels that transformed their disease from severe hemophilia to mild hemophilia. Other strategies are also under development that may confer the ability to correct the disease permanently by gene therapy.

Katherine High, MD is the William H. Bennett Professor of Pediatrics at the University of Pennsylvania School of Medicine, an Investigator of the Howard Hughes Medical Institute and Director of the Center for Cellular and Molecular Therapeutics at the Children Hospital of Philadelphia. Dr. High has pioneered safe and effective clinical translation of genetic therapies for inherited disorders including hemophilia B, and she is a Past President of the American Society of Gene and Cell Therapy.

2:50 3:00 pm: Question and answer period

3:00 pm 3:20 pm: Gene and cell-based therapy for severe combined immunodeficiency Severe combined immunodeficiency (ADA-SCID, a.k.a. bubble boy disease) is a rare disorder of immunity and without treatment; children affected with ADA-SCID will succumb to infections within the first two years of life. Over the past years >40 patients have been treated with gene-corrected hematopoietic stem cell transplantation, which has led to the regeneration of immune cells and the reconstitution of immune function in >70% of the patients. While hematopoietic stem cell transplantation from a matched donor remains the therapy of choice for ADA-SCID, the results obtained by the current clinical trials have indicated that gene and cell therapy should be considered as the first treatment option in the absence of a matched donor.

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A Media Event on Clinical Developments in Gene and Cell Therapy