Category Archives: Stem Cell Treatment


Hair Loss Treatment – Video


Hair Loss Treatment
At each cell division in your hair follicles on your scalp , the frequencies encoded in this video along with the subliminal and supraliminal progamming will cause those new cells to become or take on the attributes of embryonic stem cells, and also increase the concentration of human growth hormone, in your scalp all working towards stimulating and pushing for hair recovery, thickening and full growth. The end product should be you with a full head of hair. Effective and cost free. You can look at it as often as you wish for faster results. All sounds and images are the copyright of sapienmedicine.com (formerly projectvampire)From:projectvampireTVViews:1 2ratingsTime:10:02More inScience Technology

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Hair Loss Treatment - Video

DOH to issue guidelines on stem cell treatment in Philippines

By: Philippine News Agency November 11, 2012 8:29 AM

Stem cell tray. FILE PHOTO FROM AGENCE FRANCE-PRESSE/GETTY IMAGES

InterAksyon.com The online news portal of TV5

MANILA - The Department of Health (DOH) is expected to come up with the guidelines on the practice of stem cell treatment in the Philippines by the end of the month.

According to DOH Secretary Enrique Ona, the consultative working task force has already been convened to formulate recommendations on how to handle the growing popularity of stem cell technology among Filipinos.

Ona said that at present, stem cell therapy is still considered as an investigational intervention and there is still no scientific evidence about its efficacy, safety and quality.

Stem cell research employs both autologous (from same person) or allogenic (from another organism like animal or another human cell or tissue sample) method. Because there are many steps in the preparation of this lab and invasive procedure, there is therefore need to have a regulatory framework to protect Filipino citizens, he said.

Ona ordered the creation of the task force after observing the growing number of healthcare facilities that offer stem cell services. He was also concerned about the possible use of aborted fetuses or human embryos for the procedures.

The task force is composed of Food and Drug Administration acting director Dr. Kenneth Hartigan-Go, Philippine Council for Health Research and Development director Dr. Jaime Montoya, and scientists from the University of the Philippines National Institute of Health and Marine Science.

It will come up with regulatory framework covering five fundamental areas, namely: sources of raw stem cell materials; observance of good laboratory practices in the preparation of the tissue and the cells; credentialing of scientists involved in the technology; monitoring of marketing claims; and regulation or accreditation of facilities.

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DOH to issue guidelines on stem cell treatment in Philippines

First Pediatric Sickle Cell Disease Patient Receives NiCord® Stem Cell Transplantation in Gamida Cell Pilot Study at …

JERUSALEM--(BUSINESS WIRE)--

Gamida Cell Ltd., a world leader in stem cell population expansion technologies and stem cell therapy products for transplantation and regenerative medicine, announced today that the first patient, enrolled in its pilot study of NiCord as an investigational treatment for sickle cell disease (SCD), has been transplanted at Duke University in North Carolina.

Gamida Cell CEO Dr. Yael Margolin said, The NiCord study is a first step in broadening Gamida Cells pipeline of cell therapies to treat patients who suffer from severe non-malignant diseases with a very large unmet clinical need.

SCD is a group of inherited red blood cell disorders where red blood cells become hard and sticky and look like a C-shaped farm tool called a sickle. According to statistics, SCD affects 90,000 to 100,000 in the US alone, mainly African-Americans and Hispanic-Americans. Symptoms range in type and severity. SCD can be fatal and to date, the only cure for SCD is stem cell transplantation from a family related matched donor.

Dr. Margolin continued, Sickle cell disease can be cured with a successful bone marrow transplantation, especially from a family related fully matched donor. Most patients do not pursue this option, since they do not have the suitable donor. NiCord is intended to reverse this situation and provide a readily available cure.

NiCord is an expanded cell graft derived from an entire unit of umbilical cord blood and enriched with stem cells. NiCord was developed based on Gamida Cells proprietary NAM technology.

The official name of the study is Allogeneic Stem Cell Transplantation of NiCord, Umbilical Cord Blood-Derived Ex Vivo Expanded Stem and Progenitor Cells, in Combination With a Second, Unmanipulated Cord Blood Unit in Patients With Sickle Cell Disease. http://www.clinicaltrials.gov/ct2/show/NCT01590628?term=nicord&rank=1. A total of 10 patients, ages 2 21, will be enrolled in the NiCord study, a single center, single arm trial evaluating the safety and efficacy of transplanting NiCord together with a second un-manipulated cord blood unit in patients with SCD following myeloablative therapy. The study will also assess transplant-related mortality, event-free survival and overall survival at 100, 180 and 365 days, respectively.

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 (EMITF), Clal Biotechnology Industries (CBI.TA), Israel Healthcare Venture, Teva Pharmaceutical Industries (TEVA), Amgen, Denali Ventures and Auriga Ventures. For more information, please visit: http://www.gamida-cell.com.

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First Pediatric Sickle Cell Disease Patient Receives NiCord® Stem Cell Transplantation in Gamida Cell Pilot Study at ...

Jerry discusses his stem cell treatment for his arthritic shoulder by Dr Harry Adelson – Video


Jerry discusses his stem cell treatment for his arthritic shoulder by Dr Harry Adelson
Jerry discusses his stem cell treatment for his arthritic shoulder and torn rotator cuff by Dr Harry AdelsonFrom:Harry AdelsonViews:0 0ratingsTime:00:41More inScience Technology

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Jerry discusses his stem cell treatment for his arthritic shoulder by Dr Harry Adelson - Video

cryo cell | Umbilical Cord Blood Banking Could Be an Investment in Our Future Health – Video


cryo cell | Umbilical Cord Blood Banking Could Be an Investment in Our Future Health
http://www.cordbloodrecommendation.com They were first used to regenerate healthy blood and immune cells for cancer patients. The treatment that has to be provided for leukemia should be such, that it would increase the amount of White Blood cells in the blood stream. Human umbilical cord blood cells are very rich in stem cells and progenitor cells which make them the perfect place to take cells from and then store them in a cord blood bank or a stem cells bank. This procedure can likewise diagnose disorders like malformations of fetus, fetal infection such as toxoplasmosis or rubella, fetal platelet count inside mum, fetal anaemia, and isoimmunisation to name a few. To make a long story short, the Adult Stem Cells did the trick. If the amount is less, the collected cord blood is used for scientific researches. Within an hour of receiving the stem cell treatment, she was able to turn her head and partially lift her arms. If there is any complication during delivery, the entire idea is abandoned. It is always wise to preserve this waste blood of the baby which is otherwise thrown away. The placenta and umbilical cord is often discarded along with the hospital #39;s medical waste. It is a simple and safe procedure for the mother and the baby, and is done by the doctor or the nurse. These cells have a unique capability of ""adjusting in any environment inside the body"". This is still new methodology but holds great promise for the future of regenerative therapies. This enables stem ...From:myc0kyViews:0 0ratingsTime:01:18More inScience Technology

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cryo cell | Umbilical Cord Blood Banking Could Be an Investment in Our Future Health - Video

Biotech Bits – Pluristem's science by press release?

Pluristem Therapeutics is taking heat for its failure to disclose the death of a child treated on a compassionate use basis with its experimental placental stem cell treatment.

Paul Knoepfler, a stem cell scientist and prolific stemblogger, bluntly criticizes Pluristem for what a bioethicist he interviewed called "science-by-press-release" in touting the apparent benefit of the treatment as life-saving, but failing to follow up.

In its defense, Israel-based Pluristem said it didn't know that the child had died until later, because the doctor and family didn't tell the company. Its statement also said Pluristem maintains a culture of transparency. And indications were that the treatment had improved the child's physical condition.

The bioethicist, associate professor Leigh Turner of the University of Minnesota Center for Bioethics, told Knoepfler that wasn't a good excuse:

"Transparency is important, but it appears that the company is being transparent about dramatic improvements in health of individuals receiving Pluristems PLX Cells while failing to issue press release disclosing case of a child who died after undergoing this experimental intervention."

In other words, if you're going to mention something favorable to your product, it's only ethical to mention the unfavorable. Once Pluristem had given favorable coverage to this compassionate-use case, the publicly traded company had an obligation to monitor the child's progress and tell the public of any future developments. Even if Pluristem was legally in the right (because the death apparently was not caused by the stem cell treatment), ethically it was wrong.

Knoepfler concluded by urging biotech companies working on stem cell treatments to keep this lesson in mind, and to be scrupulous in searching for and disclosing adverse events:

"Part of what is so disappointing about this case to me is that the PLX therapy might have real promise as a drug, promise that has been at least temporarily clouded by actions by the company. I hope the case does indeed provide lessons to all interested parties including other biotech companies working on stem cell treatments."

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Biotech Bits - Pluristem's science by press release?

International Stem Cell Corp Announces Third Quarter 2012 Financial Results

CARLSBAD, CA--(Marketwire - Nov 9, 2012) - International Stem Cell Corporation ( OTCQB : ISCO ) (www.internationalstemcell.com) ("ISCO" or "the Company") a California-based biotechnology company focused on therapeutic and research products, today announced financial results for the three months ended September 30, 2012.

Three Months Ended September 30, 2012

Revenue for the three months ended September 30, 2012 totaled $1.19 million compared to $0.84 million for the same period in 2011.Sales for Lifeline Skin Care (LSC) and Lifeline Cell Technology (LCT) increased by 46% and 37%, respectively. LSC and LCT accounted for 44% and 56% of total revenue in the three months ended September 30, 2012 compared to 43% and 57%, respectively, for the same period of 2011.

Research and development (R&D) expenses were $0.90 million for the three months ended September 30, 2012, compared to $1.13 million for the same period in 2011. The decrease was due primarily to lower stock-based compensation expense, lower personnel-related spending and lower consulting expenses, partially offset by higher stem cell line research and testing expenses and higher laboratory expenses associated with our Parkinson's disease program.

The Company continues to invest in its sales and marketing infrastructure. Marketing expenses for the three months ended September 30, 2012 were $0.48 million, compared to $0.37 million for the same period in 2011. The increase was primarily driven by investments to promote and build awareness of the Lifeline Skin Care brand and branded products. General and administrative expenses were $1.57 million, down 26% compared to the same period in 2011, as a result of ongoing operational efficiency initiatives.

Cash and cash equivalents totaled $2.38 million at September 30, 2012 compared to $1.34 million as of December 31, 2011 due primarily to two financing transactions totaling approximately $7.03 million completed in the first three months of 2012.

"We have made excellent progress in our therapeutic development programs, being able to start our non-human primate study in our Parkinson's disease program earlier than anticipated, and we remain on track to publish the results in the first half of next year," stated Dr. Andrey Semechkin, ISCO's CEO and Co-Chairman. "In addition, our results for the third quarter reflect good progress by LSC and LCT both in terms of growing sales and implementing their strategies. Particularly pleasing is LSC's continued revenue growth as they aim to diversify their sales channels, and LCT's strong quarter on quarter performance. General and administrative expenses continued to decrease reflecting our increased focus on cost containment.Looking ahead to next year, we anticipate our R&D expenses to increase further as we expand our pharmacology and safety studies and our Parkinson's program moves closer to IND filing in early 2014."

Q3 2012 Highlights:

Conference Call and Webcast Details:

Date: Friday, November 9, 2012 Time: 11:00 a.m. Eastern Time

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International Stem Cell Corp Announces Third Quarter 2012 Financial Results