Treatment failing for Arroyo

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TREATMENT NOT WORKING. Gloria Macapagal-Arroyo is experiencing more intense pain and "numbness" in her neck. File photo

MANILA, Philippines - Former President Gloria Macapagal-Arroyo is not recovering from her spinal condition despite having undergone stem cell treatment and tried other remedies.

Arroyo is suffering numbness and shooting pain near her neck, she said on her official Twitter account @gmarroyo on Thursday, September 20.

The Pampanga Rep. added that her doctors have advised her to wear her neck brace for longer periods of time in order to cope with the pain, and a recent CT scan showed that her neck muscles have "atrophied" due to her spinal condition.

According to Arroyo, the pain was so intense that she was unable to attend a scheduled pictorial for the members of the House of Representatives and sent a file photo.

After the former President was granted bail by a Pasay City Court last July, she contacted alternative medicine doctor Antonia Park, who owns a wellness center in Tagaytay City, and this week Arroyo started searching for another specialist who can correct her spinal condition.

Arroyo still has physical therapy sessions 3 times a week at the Veterans Memorial Medical Center, where the Pampanga Rep. had spent 8 months in hospital arrest over electoral sabotage charges in connection with the 2007 midterm polls.

Dr. Roberto Anastacio, her physician at the Makati Medical Center, earlier said the treatment for Arroyos condition cannot be found in the Philippines.

However, the former President is prevented from traveling abroad by 3 hold departure orders issued by the courts in relation to electoral sabotage, plunder and graft cases filed against her. - Rappler.com

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Treatment failing for Arroyo

Embattled Bonita Springs doctor back in stem cell business

Dr. Zannos Grekos is back in the stem cell business in his Bonita Springs office even though state health-care regulators suspended his license in February.

Grekos, a cardiologist, is chief medical officer of a new company, Intercellular Sciences, which "follows in the footsteps" of his earlier practice called Regenocyte Therapeutics, according to Intercellular's website.

Intercellular operates at 9500 Bonita Beach Road where Regenocyte is located.

The new company website says all stem cell treatment is done in the Dominican Republic, which follows how Grekos was doing the therapy before he faced state sanctions for performing it in his Bonita Springs practice.

Staff at Intercellular Sciences could not be reached for comment.

The state health department is aware of Grekos involvement with Intercellular but cannot say whether serving as chief medical officer means he is actively practicing medicine against the suspension, health department spokeswoman Ashley Carr said.

Incorporation papers were submitted and filed May 15 for Intercellular with the state Division of Corporations, but Grekos is not listed as an agent or manager, the documents show.

The registered agent, Mike Calcaterra, of North Fort Myers, serves as president and chief operating officer of Intercellular. He could not be reached for comment.

Several years ago, Grekos' medical practice evolved into stem cell therapy, where patients would come to his practice in Bonita Springs for medical evaluation and a blood sample would get sent to a laboratory in Israel for cultivating the stem cells. The blood would then be sent to the Dominican Republic.

The patient would travel to the island nation and Grekos' physician partner there would inject the stem cells into the patient. The hope is the therapeutic healing abilities of the stem cells would help the patient buy more time against congestive heart failure, lung disease and other conditions where conventional treatment was no longer effective.

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Embattled Bonita Springs doctor back in stem cell business

Bonita Springs stem cell doctor back working again

BONITA SPRINGS, fla - A controversial stem cell doctor, who lost his medical license in March, is back in business.

Dr. Zannos Grekos is listed as the Chief Medical Officer on the website for Intercellular Sciences, a new company that is "following in the footsteps of Regenocyte," a stem cell company started by Grekos.

WINK News has not been able to confirm whether or not that means the stem cell doctor is practicing medicine at the new company.

In 2011, Grekos was ordered to stop practicing medicine after a cancer patient died following an unapproved stem cell treatment at Regenocyte.

Then, in March of 2012, the Health Department revoked Grekos medical license following the death of a second patient, Richard Poling. At that time, the Lee County Sheriff's Office raided Regenocyte.

We tracked down the phone number of Intercellular Sciences, Grekos new company. The answering machine message links Grekos' old company Regenocyte and Intercellular Sciences.

Despite all the trouble Grekos faces, many of his patients stand by him. "He gave me new life," says Peter Holler. "I can't say enough for him. He's so dedicated to his work and his patients and he doesn't deserve what he's going through."

Holler, like many of Grekos patients traveled out of the United States for his procedure. Holler went to the Dominican Republic four years ago. At the time, he said his heart was half dead.

He says now, he feels great and has since had regular checkups, but has not seen or spoken to Dr. Grekos since his license was revoked.

As for the new company, Holler believes it will get Grekos away from the Regenocyte name and give his doctor a fresh start.

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Bonita Springs stem cell doctor back working again

StemGenex to Launch Adult Stem Cell-Based Therapy to Relieve COPD Symptoms

LA JOLLA, Calif., Sept. 20, 2012 /PRNewswire/ -- New developments in regenerative medicine are bringing about exciting, novel approaches to create therapies for hard to treat diseases. Chronic obstructive pulmonary disease (COPD) is a hard to treat disorder that progressively blocks airflow in the lungs making it increasingly difficult for an individual to breathe, and is one of the leading illnesses in the US. Yet, current treatments for COPD can only try to limit the extent of damage to the lungs, and to bring some relief from symptoms. Novel treatments for COPD are urgently needed, and new applications with the use of adult stem cells may have much benefit. This is because adult stem cells have an ability to differentiate into many different types of cells, such as those required for healthy, functioning lung tissue. Also, adult stem cells can be isolated with ease from an individual's own fat tissue, and so adult stem cell therapy is not subject to the ethical or religious issues that trouble some other methods.

(Photo: http://photos.prnewswire.com/prnh/20120920/LA78252)

StemGenex, a US based company, is finding new avenues and methods for using adipose derived adult stem cells to help in diseases with limited treatment options. StemGenex has been working with scientists and physicians over the last 5 years to specifically advance adult stem cell treatment protocols, and the hope is that COPD adult stem cell therapy can help in alleviating COPD symptoms. Results from researchers working with adult stem cells have shown anti-inflammatory and immune modulatory effects, suggesting possible roles in treating COPD. Interestingly, recent studies in mice indicate the presence of stem cells in the lungs can regenerate damaged lung tissue which occurs through infection. Encouragingly, adult stem cell treatment studies in mice appear to have positive effects across a range of respiratory diseases, which includes COPD.

Taking these research findings into account and building on their own developments, StemGenex is about to submit a plan of using adult stem cell therapy for COPD treatment to an Institutional Review Board for review. This study could scientifically define any potential benefits of such clinical treatments. Rita Alexander, the President of StemGenex, says, "Chuck Liptak, a long-term COPD sufferer, eliminated his requirement for oxygen following a stem cell treatment. It's imperative that these results be scientifically quantified."

To find out more about stem cell treatments contact StemGenex. An experienced stem cell physician reviews the patient evaluation and a patient can have any questions or requests for more detailed information addressed by a patient advocate. StemGenex is based in La Jolla, California with treatment locations on the east and west coast.

Contact: La Jolla Cove Research Center 505 Coast Boulevard South La Jolla, CA 92037 858-459-STEM (7836) Contact@StemGenex.comhttp://www.StemGenex.com

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StemGenex to Launch Adult Stem Cell-Based Therapy to Relieve COPD Symptoms

NeoStem to Present at Noble Capital Markets' Life Sciences Exposition on September 24

NEW YORK, Sept. 19, 2012 (GLOBE NEWSWIRE) -- NeoStem, Inc. (NYSE MKT:NBS) ("NeoStem" or the "Company"), a rapidly emerging market leader in the fast growing cell therapy market, today announced that Company management has been invited to participate at BIOX, the Noble Financial Capital Markets' Life Sciences Exposition on Monday, September 24. Company management will make a webcasted company presentation and participate in a cell therapy panel.

Noble Financial Capital Markets Investor Conference - BIOX Life Sciences Exposition

For more information about the conference, please visit http://www.nobleresearch.com/BIOX.htm.

About NeoStem, Inc.

NeoStem, Inc. continues to develop and build on its core capabilities in cell therapy, capitalizing on the paradigm shift that we see occurring in medicine. In particular, we anticipate that cell therapy will have a significant role in the fight against chronic disease and in lessening the economic burden that these diseases pose to modern society. We are emerging as a technology and market leading company in this fast developing cell therapy market. Our multi-faceted business strategy combines a state-of-the-art contract development and manufacturing subsidiary, Progenitor Cell Therapy, LLC ("PCT"), with a medically important cell therapy product development program, enabling near and long-term revenue growth opportunities. We believe this expertise and existing research capabilities and collaborations will enable us to achieve our mission of becoming a premier cell therapy company.

Our contract development and manufacturing service business supports the development of proprietary cell therapy products. NeoStem's most clinically advanced therapeutic, AMR-001, is being developed at Amorcyte, LLC ("Amorcyte"), which we acquired in October 2011. Amorcyte is developing a cell therapy for the treatment of cardiovascular disease and is enrolling patients in a Phase 2 trial to investigate AMR-001's efficacy in preserving heart function after a heart attack. Athelos Corporation ("Athelos"), which is approximately 80%-owned by our subsidiary, PCT, is collaborating with Becton-Dickinson in the early clinical exploration of a T-cell therapy for autoimmune conditions. In addition, pre-clinical assets include our VSELTM Technology platform as well as our mesenchymal stem cell product candidate for regenerative medicine. Our service business and pipeline of proprietary cell therapy products work in concert, giving us a competitive advantage that we believe is unique to the biotechnology and pharmaceutical industries. Supported by an experienced scientific and business management team and a substantial intellectual property estate, we believe we are well positioned to succeed.

For more information on NeoStem, please visit http://www.neostem.com.

Forward-Looking Statements for NeoStem, Inc.

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements reflect management's current expectations, as of the date of this press release, and involve certain risks and uncertainties. Forward-looking statements include statements herein with respect to the successful execution of the Company's business strategy, including with respect to the Company's or its partners' successful development of AMR-001 and other cell therapeutics, the size of the market for such products, its competitive position in such markets, the Company's ability to successfully penetrate such markets and the market for its CDMO business, and the efficacy of protection from its patent portfolio, as well as the future of the cell therapeutics industry in general, including the rate at which such industry may grow. Forward looking statements also include statements with respect to satisfying all conditions to closing the disposition of Erye, including receipt of all necessary regulatory approvals in the PRC. The Company's actual results could differ materially from those anticipated in these forward- looking statements as a result of various factors, including but not limited to (i) the Company's ability to manage its business despite operating losses and cash outflows, (ii) its ability to obtain sufficient capital or strategic business arrangement to fund its operations, including the clinical trials for AMR-001, (iii) successful results of the Company's clinical trials of AMR-001 and other cellular therapeutic products that may be pursued, (iv) demand for and market acceptance of AMR-001 or other cell therapies if clinical trials are successful and the Company is permitted to market such products, (v) establishment of a large global market for cellular-based products, (vi) the impact of competitive products and pricing, (vii) the impact of future scientific and medical developments, (viii) the Company's ability to obtain appropriate governmental licenses and approvals and, in general, future actions of regulatory bodies, including the FDA and foreign counterparts, (ix) reimbursement and rebate policies of government agencies and private payers, (x) the Company's ability to protect its intellectual property, (xi) the company's ability to successfully divest its interest in Erye, and (xii) matters described under the "Risk Factors" in the Company's Annual Report on Form 10-K filed with the Securities and Exchange Commission on March 20, 2012 and in the Company's other periodic filings with the Securities and Exchange Commission, all of which are available on its website. The Company does not undertake to update its forward-looking statements. The Company's further development is highly dependent on future medical and research developments and market acceptance, which is outside its control.

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NeoStem to Present at Noble Capital Markets' Life Sciences Exposition on September 24

Stem cell therapy to lead DOT’s proposed ‘medical tourism’ plan

The Department of Tourism plans to add another reason for more visitors to come to the country through a soon-to-be drafted medical tourism plan, which highlights the relatively cheap yet world-class health services some of the countrys hospitals have to offer.

In this proposed plan, DOT Secretary Ramon Jimenez aims to get the countrys medical sector to put its best foot forward by highlighting stem cell therapy as well as other areas of specialization.

Medical tourism focuses on some very serious, important areas of healthcare that the world will travel for, Jimenez said during a forum on stem cell science conducted at the Medical City hospital in Pasig City on Tuesday evening.

Through promoting world-class medical services in the country, such as some of Philippine hospitals stem cell programs, Jimenez said the DOT aims to draw foreigners into the country who, in his words, yung sasakay sila ng eroplano, tatawid sila ng dagat.

(Foreigners) would obviously spend less if they sought care in their own country like the United States or (places in) Europe. So you really have to have a value that will mitigate the cost of that travel. Your service has to be superior, greater value for their money, Jimenez said.

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Stem cell therapy to lead DOT’s proposed ‘medical tourism’ plan

South Korean lawmakers one step from rigorous new system for stem cell Advancement: scientists, physicians and …

SEOUL, South Korea, Sept. 19, 2012 /PRNewswire/ -- Seung-Jo Yang, a Parliament member, prepared a bill proposing new law for the management and transplantation of stem cells. On September 17, the National Health and Welfare Committee referred the bill to the Conference for review. The previous 18th National Assembly proposed a similar stem cell bill when much of its term had already passed so it was not fully discussed until the period ended, disappointing many patients with rare diseases. The Bill was referred to the 19th National Assembly, though, which shows the willingness of South Korean leaders to meet the expectations that this new law will be passed coming from the medical community and patient groups throughout South Korea.

Dr. Jeong-Chan Ra, president of RNL BIO's stem cell technology institute said "This effort for new stem cell bill will advance the use and sophistication of autologous adult stem cell technology as a powerful solution for overcoming incurable diseases." Dr. Ra, whose pioneering efforts in Korean stem cell research are known worldwide, is equally known in Korea as an ardent advocate for governmental investment in regenerative medicine. Perhaps no scientist has pushed harder for rigorous standards for stem cell banking, which this proposal may at last bring to fruition.

In South Korea stem cell banks have not been operated under a specific legal structure, so development and progress has been limited. The proposed law suggests that the harvesting and preservation of stem cells must be controlled by national regulation, specifically a management system for stem cell harvesting, storage and implantation. Through this, stem cell experts expect growth in responsible stem cell research and faster, even safer development of therapeutics.

Additionally, the current Korean policy requires stem cell programs - regardless of whether there are available therapies for patients with any particular condition - to complete clinical trial phase III for market approval. Had such rules been in place, for example, for the treatment of H.I.V., tens of thousands of people would have died. Many treatments for those with incurable diseases have been approved without completion of Phase III including stem cell treatments in other nations, even for the treatment of HIV, which stem cells have now cured. The bill under consideration proposes that physicians can use their own stem cells to treat conditions under their discretion if those stem cells are properly expanded, managed, handled and provided to clinicians for them at or above the proposed standards, which is the best news patients with incurable diseases for which no existing cure is available by current medicine have had in a long time.

When the bill is passed, high standards will be established and the better methods will immediately be made obvious to both government and patients. Through this the stem cell community expects a leap in industrial growth, and a leap in the ethical adherence of physicians to do no harm to patients and to provide remedies where possible for the aid of their patients.

The Korean medical community also expects not only to see an influx of domestic patients but also many patients from other nations that lack standards for the growth of patients' own stem cells. South Korea, many economists predict, could become the Mecca for stem cell therapeutics.

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South Korean lawmakers one step from rigorous new system for stem cell Advancement: scientists, physicians and ...

Developments of Stem Cell Therapy and Regenerative Medicine

Queenstown Regenerative Medicine - http://www.queenstownRM.co.nz

Professor Richard Boyd and Dr Dan Bates Latest developments of Stem Cell Therapy and Regenerative Medicine

Queenstown Regenerative Medicine, in association with Monash University Immunology and Stem Cell Centre (MISCL), has the pleasure of requesting your attendance at an evening lecture by Prof Richard Boyd, Head of MISCL and Dr Dan Bates, Sports Medicine Physician from Melbourne AFL Club.

Professor Richard Boyd is a world leader in the research and development of potential uses of stem cells to treat disease in both human and animal. He is the Director of Australia's largest and most prestigious Stem Cell Laboratory and a recipient of numerous International Awards for unique research into how stem cells and the immune system develop and how they have their effects in the body.

Professor Boyd's talk will give an overall background to stem cells and the work going on around the world to put these cellular therapies and regenerative medicine into the clinic.

Doctor Dan Bates is a Sports Medicine Physician working with Professor Boyd in the development and use of cellular medicine applications in the field of Sports Medicine and musculoskeletal injuries. Dan is the current team doctor of the Melbourne AFL club and will speak on his experiences using Platelet Rich Plasma to treat musculoskeletal injuries and the opening of stem cell treatment centres in conjunction with MISCL in Australia.

This is a unique opportunity to get first- hand knowledge from some of the best people in the field. These talks will be aimed at the practical applications of how you can use these therapies currently, as well as giving an idea of what the near future holds.

Date: Friday 21 September 2012 Time: from 6 pm 7.30 pm Location: Heritage Hotel, 91 Fernhill Road, Queenstown (Icon Conference Room) Cost: Free of charge

Scoop Media

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Developments of Stem Cell Therapy and Regenerative Medicine

Gamida Cell Completes Enrollment for Phase I/II Study of Second Pipeline Product NiCord® for Hematological Malignancies

JERUSALEM--(BUSINESS WIRE)--

Gamida Cell, a leader in adult stem cell expansion technologies and products, announced today that it has completed enrollment for a Phase I/II clinical trial of NiCord, the companys second pipeline product.

NiCord is in development as an experimental treatment for a series of indications that potentially could be cured with a bone marrow transplantation including hematological malignancies (blood cancer), sickle cell disease, thalassemia, severe autoimmune diseases and metabolic diseases. The clinical trial announced today (clinicaltrials.gov identifier NCT01221857) is studying NiCord as an alternative investigational treatment for hematological malignancies (HM). A combined total of 11 patients were transplanted at Duke University Medical Center and at Loyola University Medical Center. Dr. Mitchell E. Horwitz of Duke University Medical Center is the principal investigator. Final results of the Phase I/II study are expected within 6 months. The company is also actively enrolling for a Phase I/II study of NiCord as an experimental treatment for sickle cell, a genetic blood disease (clinicaltrials.gov identifier NCT01590628).

NiCord is an expanded cell graft derived from an entire unit of umbilical cord blood enriched with stem cells. NiCord was developed based on Gamida Cells proprietary NAM technology. As the Phase I/II trial for HM is a first in man safety and efficacy study, for this stage, NiCord was transplanted with a second un-manipulated cord blood unit in a double cord blood configuration.

Dr. Tony Peled, chief scientific officer and vice president of research & development at Gamida Cell, said, Pre-clinical data demonstrated the uniqueness of NAM technology in not only decreasing the aging process but also preserving the characteristics and functions of ex vivo expanded stem cells (Experimental Hematology 2012;40:342355). Of significance, the Phase I/II clinical trial data have already shown that many of the patients in the study engrafted with the expanded cells of NiCord rather than with the second un-manipulated unit. This is the first time, in a situation where two units are transplanted, that the cultured stem cells demonstrated prompt and durable long-term engraftment (over one year) in the clinic. We look forward to sharing the complete results of this study in the coming months.

Dr. Yael Margolin, CEO of Gamida Cell, said, The clinical progress of the companys second pipeline product reaffirms Gamida Cells leadership role in the stem cell industry and the companys expertise in bone marrow transplantation. In the near future we plan to not only release the NiCord Phase I/II data but also the long awaited complete results of the Phase III study of StemEx, also for hematological malignancies, but clearly further ahead in development. The company remains on course with the development of StemEx and is considering strategic partners to develop its expanding pipeline of products and to bring StemEx to market.

About Gamida Cell

Gamida Cell is a world leader in stem cell population expansion technologies and stem cell therapy products for transplantation and regenerative medicine. The companys pipeline of stem cell therapy products are in development to treat a wide range of conditions including blood cancers, solid tumors, non-malignant hematological diseases such as hemoglobinopathies, neutropenia and acute radiation syndrome, autoimmune diseases and metabolic diseases as well as conditions that can be helped by regenerative medicine. Gamida Cells therapeutic candidates contain populations of adult stem cells, selected from non-controversial sources such as umbilical cord blood, bone marrow and peripheral blood, which are expanded in culture. Gamida Cells current shareholders include: Elbit Imaging (NASDAQ: EMITF), Clal Biotechnology Industries (TASE: CBI), Israel Healthcare Venture, Teva Pharmaceutical Industries (NADAQ:TEVA), Amgen, Denali Ventures and Auriga Ventures. For more information, please visit: http://www.gamida-cell.com.

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Gamida Cell Completes Enrollment for Phase I/II Study of Second Pipeline Product NiCord® for Hematological Malignancies

MEP fights European proposal to restrict stem cell research

Andrew Duff, MEP

Proposals to restrict stem cell research have been opposed by a Cambridge-based MEP.

Liberal Democrat Andrew Duff voted against a report in the European Parliament which he said would result in stricter requirements on voluntary and unpaid donations of tissues and cells for medical research.

Afterwards, he said: The report swings the debate on stem cell research in the wrong direction, allowing individual EU member states to stop important medical science in its tracks.

It is unhelpful to call for further restrictions on the donation of tissues and cells in the EU at a time when the number of patients in need of treatment based on stem cells is growing exponentially.

The report was drawn up by a Conservative MEP.

Mr Duff added: Cambridge is a world leader on life sciences. The European Parliaments restrictive conservative philosophy usually driven by ill-judged ethical motives puts our research centres at risk and could drive away high quality science abroad, for example to India.

Regenerative medicine relies on a steady supply of stem cells.

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MEP fights European proposal to restrict stem cell research