• Home
  • Topics
    • Health Insurance Coverage
    • Medicare
    • Medicaid and CHIP
    • Blue Cross Blue Shield
    • Health Insurance Companies
    • Prescription Drugs and Pharmacy
    • Healthcare Policy and Law
    • Hospitals and Health Systems
    • Healthcare Business
    • Health Technology and AI
    • Senior Care
    • Public Health and Research
  • Guides
    • All Health Insurance Guides
    • Choosing a Health Insurance Plan
    • Individual Health Insurance
    • Family Health Insurance
    • High Deductible Health Plans
    • Short-Term Health Insurance
    • Self-Employed Health Insurance
    • Student Health Insurance
    • Low Income Health Insurance
    • Health Sharing Plans
  • Insurance Company List
  • About Us

Health Plan News

Timely Health Plan News and Commentary

Health Plan News
Home Archives for Public Health and Research

Public Health and Research News

Public health is the work of protecting the health of entire populations rather than individual patients: tracking disease, preventing outbreaks, promoting vaccination and screening, and studying what actually improves health outcomes. Research findings and public health data also drive coverage decisions, because health plans and regulators rely on evidence when they decide which services, screenings and treatments to cover.

What We Cover

This section covers public health developments and medical research with consequences for patients and health plans. That includes infectious disease, including COVID-19 and influenza; chronic conditions such as diabetes, heart disease, obesity and cancer; Alzheimer's disease and dementia; mental health and substance use; maternal and child health; and studies on health care costs, outcomes and access. We report on guidance from the Centers for Disease Control and Prevention (CDC) and the National Institutes of Health (NIH), and on peer-reviewed research and survey data.

How We Report Research

A single study rarely settles a question. When we report research, we identify who conducted and funded it, how large it was, and whether the findings are preliminary. This content is news and general information; it is not medical advice, and readers should discuss treatment decisions with a licensed clinician.

Research and public health news connects to our other sections. Drug approvals and vaccine coverage appear in Prescription Drugs and Pharmacy, preventive services coverage appears in Health Insurance Coverage, public health policy appears in Healthcare Policy and Law, and research on aging appears in Senior Care.

The latest public health and research news appears below, newest first.

Miracle-Ear Marks American Diabetes Month(R) With Call to Action

Posted on October 20, 2010 Written by Editor

SOURCE: Miracle-Ear

Hearing Solutions Provider Has Joined the American Diabetes Association as a National Strategic Partner to Highlight Link Between Diabetes and Hearing Loss

PLYMOUTH, MN–(Marketwire – October 20, 2010) – November is American Diabetes Month® and Miracle-Ear is joining in a nationwide call to action to involve individuals and organizations in the movement to Stop Diabetes®. Over the next several months, Miracle-Ear will sponsor the American Diabetes Association‘s educational and fundraising events such as walks, bike tours and Association consumer EXPO events. This national strategic partnership will help emphasize the urgency of reducing the devastating impact — including hearing loss — of diabetes.

Today, nearly 24 million U.S. children and adults — nearly 8% of the population — have diabetes, and another 57 million individuals have prediabetes. If current trends continue, one out of every three American children born today will face a future with diabetes. For some high-risk populations, the risk is one in two. According to the American Diabetes Association, diabetes is a growing epidemic and is taking a devastating physical, emotional and financial toll on our country.

“Simple ‘awareness’ is not enough to change these statistics,” says Rebecca Younk, audiologist for Miracle-Ear. “What we need now is action. Individuals need to make the lifestyle, diet and exercise changes that can help prevent Type 2 diabetes; and we need increased education and outreach about symptoms that can help people seek early treatment before serious complications develop.”

Stop Diabetes is the movement to end the devastating toll that diabetes takes on the lives of millions of individuals and families across our nation. It will inspire and mobilize millions to take up the fight against diabetes.

Miracle-Ear is the first company in the hearing care industry to join the Association as a national strategic partner. Miracle-Ear will support the Stop Diabetes movement in order to shine a spotlight on the hearing-related risks of diabetes, as well as the Association’s education, prevention and treatment initiatives.

“Diabetes doubles your risk of developing a hearing loss,” Younk states. “Early diagnosis and treatment are critical in helping to minimize complications, including hearing loss. Since people with Type 2 diabetes frequently do not display any symptoms, hearing loss may be the first indicator that there may be a problem.”

To focus attention on diabetes and its link to hearing loss, throughout the month of November, all 1,200+ Miracle-Ear locations nationwide will donate $5 toward the Stop Diabetes movement for each Free Hearing Test they conduct — up to a maximum of $50,000. The test measures speech recognition in noise along with loudness discomfort levels; its purpose is to measure the degree of any possible hearing impairment.

“We hope that our involvement with the Stop Diabetes movement will inspire individuals to take meaningful action to Stop Diabetes,” said Younk. The Stop Diabetes movement identifies four primary options that everyone can take: Share your story to inspire others; Act by volunteering and raising funds in your community; Learn the facts about diabetes management, nutrition, lifestyle and prevention; and Give your time and your talents, along with your financial support, to support education, outreach, advocacy and critical research for a cure.

For more information on Miracle-Ear, please visit http://www.miracle-ear.com/. 

About Miracle-Ear
A trusted resource for hearing solutions for over 60 years, Miracle-Ear uses state-of-the-art technology to remove the barriers of hearing loss. The Plymouth, Minn.-based company specializes in customizable hearing solutions that feature discreet, comfortable products designed to meet each individual’s hearing loss needs. Free hearing tests and consultations are available at all of the company’s 1,200 locations across the U.S., many of which are in Sears stores. Franchise opportunities are available for those interested in running their own Miracle-Ear business with the support of a nationwide industry leader. 
For more information, visit www.miracle-ear.com.

Filed Under: Public Health and Research

The Patient Channel and dLife Partner to Increase Diabetes Education in U.S. Hospitals

Posted on October 20, 2010 Written by Editor

SOURCE: Interactivation Health Networks

WESTPORT, CT–(Marketwire – October 20, 2010) –  The Patient Channel, the largest U.S. hospital-based health and wellness TV channel, and dLife, the only multi-media network serving the diabetes community, have announced a strategic partnership that will significantly increase year-round diabetes education, wellness, and lifestyle programming for patients and caregivers in over 1,600 hospitals across the U.S. The partnership will help diabetes educators and patients by providing vital information at a critical time of need increase awareness and self-management, help decrease future hospital visits and encourage ongoing engagement at home.

As part of the agreement, 14 hours of dLifeTV‘s diabetes lifestyle programming will be added to The Patient Channel’s existing diabetes line-up. The partnership will begin in the fourth quarter of 2010 and advertisers will be offered special tie-in opportunities to commemorate American Diabetes Month in November. The Patient Channel’s existing topics of diabetes prevention, treatments, and avoiding complications will be supplemented with dLifeTV episodes profiling real people overcoming the challenges of living with diabetes, as well as interviews with celebrities living with diabetes such as The View co-host, Sherri Shepherd, and CBS newsman, Bob Schieffer. There will also be special programming on topics as varied as religion and diabetes, diabetes in the workplace, and the latest diabetes gadgets.

Patients will be encouraged to watch dLifeTV (Sundays at 7 p.m. ET, 4 p.m. PT on CNBC), as well as join dLife’s award-winning website, dLife.com, which has over one million visitors each month.

“Diabetes diagnosis often happens in the hospital, and inpatient stays are often caused by diabetes and its complications. For many of them it can be a time of profound fear, confusion and isolation. Not to mention a supreme teachable moment to improve their diabetes IQ going forward. We are delighted by our new partnership with The Patient Channel, which allows us to put dLifeTV in front of people with diabetes at such a critical time of need,” says Howard Steinberg, CEO and founder of dLife.

“The Patient Channel hospital footprint reaches 35 percent of hospitalized Americans with or at risk for diabetes,” says Dave Ross, COO of The Patient Channel. “This programming will help hospitals and diabetes educators to educate and improve the compliance of patients and families at the very time they are motivated and seeking information to manage their condition and lifestyle.” 

For a full list of the diabetes programming running on The Patient Channel, as well as other details about The Patient Channel’s educational offering and platform, visit www.thepatientchannel.com.

For additional resources on managing your or your patients’ diabetes lifestyle, please go to www.dLife.com.

About Interactivation Health Networks
The Patient Channel and the Newborn Channel are the most comprehensive in-hospital TV networks. Delivered directly to patient rooms and waiting areas, the Channels provide viewers with original, award-winning health programs and advertisers with the unique ability to integrate brand messaging with content that is compelling and endorsed by healthcare professionals. The Newborn Channel broadcasts baby care and postpartum programming for new parents, reaching 60% of new moms. The Patient Channel features both condition-specific and preventative health programming to empower and inform patients. The channels are currently available in over 2,700 hospitals nationwide. For more information, visit www.thenewbornchannel.com and www.thepatientchannel.com

About dLife – For Your Diabetes Life
dLife is the only multimedia network serving the diabetes community. Its award-winning media outlets include dLife.com, the leading online destination for diabetes information, inspiration, and connection, featuring more than 9,000 recipes, 400 videos, and 80,000 pages of content; dLifeTV, the only lifestyle TV series for people with diabetes, airing every Sunday on CNBC (7 p.m. ET, 4 p.m. PT); and other consumer and professional programs to inform, inspire and connect people with diabetes and those who care for them every day.

Filed Under: Hospitals and Health Systems, Public Health and Research

AVI BioPharma to Present Data on RNA-Based Duchenne Muscular Dystrophy and Influenza Drug Candidates at 6th Annual Meeting of the Oligonucleotide…

Posted on October 20, 2010 Written by Editor

SOURCE: AVI BioPharma, Inc.

BOTHELL, WA–(Marketwire – October 20, 2010) –  AVI BioPharma, Inc. (NASDAQ: AVII), a developer of RNA-based therapeutics, today announced the presentation of data from the Company’s Duchenne muscular dystrophy and influenza programs at the 6th Annual Meeting of the Oligonucleotide Therapeutics Society in Dana Point, Calif.

Peter Sazani, Executive Director, Preclinical Development at AVI, will present during the poster session at noon PDT on Friday, Oct. 22. The presentation, 063, is titled “Preliminary toxicological evaluation of AVI-7100, a phosphorodiamidate morpholino oligomer with selectively introduced positive charges (PMOplus™) targeted to a highly conserved region of Influenza A virus.” The presentation will feature preclinical data evaluating AVI-7100 for use in treating Influenza A.

Ryszard Kole, Ph.D., Senior Vice President of Discovery Research at AVI, will present during the oral abstract session, Splicing Applications, at 8 a.m. PDT on Saturday, Oct. 23. The presentation, 766, is titled “Oligonucleotide-Induced Skipping as Treatment for Duchenne Muscular Dystrophy: Development of AVI-4658.”

Both presentations will be posted on the AVI BioPharma Web site in the “Our Programs” section after their respective sessions are completed.

AVI-7100 is AVI’s lead therapeutic candidate for influenza virus infections. The investigational drug candidate employs AVI’s patented PMOplus™ technology that selectively introduces positive charges to its phosphorodiamidate morpholino oligomer (PMO) backbone to improve interaction between the drug and its target.

AVI-4658 is AVI’s lead investigational drug candidate in development as a systemically administered treatment for a substantial subgroup of patients with Duchenne muscular dystrophy (DMD), a genetic muscle wasting disease caused by failure to produce dystrophin.

About AVI BioPharma

AVI BioPharma is focused on the discovery and development of novel RNA-based therapeutics for rare and infectious diseases, as well as other select disease targets. Applying pioneering technologies developed and optimized by AVI, the Company is able to target a broad range of diseases and disorders through distinct RNA-based mechanisms of action. Unlike other RNA-based approaches, AVI’s technologies can be used to directly target both messenger RNA (mRNA) and precursor messenger RNA (pre-mRNA) to either down-regulate (inhibit) or up-regulate (promote) the expression of targeted genes or proteins. By leveraging our highly differentiated RNA antisense-based technology platform, AVI has built a pipeline of potentially transformative therapeutic agents, including one in the clinical development stage for the treatment of Duchenne muscular dystrophy. For more information, visit www.avibio.com. 

Filed Under: Health Technology and AI, Public Health and Research

Percée sur le marché américain : La solution québécoise Extenway en service dans une clinique externe du Memorial Sloan-Kettering Cancer Center…

Posted on October 19, 2010 Written by Editor

MONTRÉAL, QUÉBEC–(Marketwire – 19 oct. 2010) –

Note aux éditeurs : Une photo accompagnera ce communiqué de presse sur le site de Marketwire.

Quelques semaines à peine après la mise en service de sa solution à l’Hôpital juif de réadaptation de Laval au Québec, Solutions Extenway inc. (TSX CROISSANCE:EY) est heureuse d’annoncer que c’est maintenant au tour des patients du centre de traitement de chimiothérapie du Memorial Sloan-Kettering Cancer Center situé à Brooklyn, à New York, de profiter des avantages offerts par ses terminaux. Cette annonce marque la première phase du déploiement de la solution technologique Extenway en sol américain.

Une solution pour améliorer la qualité de vie des patients en milieu hospitalier

Les terminaux de chevet Extenway permettent aux patients de profiter à la fois d’un moyen de communication avec le personnel et leurs proches (vidéoconférence et service d’assistance), d’une plateforme de divertissement numérique (télé, jeux, lecteur MP3, radio et livres audio) et éducatif (capsules d’enseignement aux patients), ainsi que d’un environnement de bureautique (Internet, courriel, Microsoft Office, etc.).

« Notre solution permet aux patients de vivre une expérience plus positive durant leur traitement, a déclaré John McAllister, président et chef de la direction d’Extenway, une entreprise de Baie d’Urfé, dans la région de Montréal. Certains d’entre eux passent parfois de longues semaines en milieu hospitalier et les témoignages que nous avons reçus confirment que notre technologie améliore leur qualité de vie durant cette période. »

Les patients peuvent consulter les contenus proposés en utilisant l’écran tactile ou le clavier sans fil des terminaux. Dans le cas du Memorial Sloan-Kettering Cancer Center, il était très important d’offrir un environnement agréable et le moins « hospitalier » possible à ses patients. Le panneau d’installation mural des terminaux Extenway a été adapté afin que ces derniers puissent être fixés directement sur les chaises de traitement de chimiothérapie.

Une solution pour améliorer l’efficacité des services hospitaliers

La solution Extenway permet aussi de maximiser la communication entre le patient, les cliniciens et le personnel.

Les patients peuvent notamment consulter les menus et transmettre leurs sélections en ligne, ou encore contrôler la lumière et la température de leur chambre sans se déplacer. En étant plus autonomes, les patients permettent ainsi au personnel de se concentrer davantage sur les besoins médicaux.

Extenway tiendra sa prochaine assemblée annuelle et spéciale de ses actionnaires le 21 octobre à 11 h, au salon Musset du Centre Sheraton Montréal situé au 1201, boulevard René-Lévesque Ouest.

À propos de Solutions Extenway inc.

Solutions Extenway (TSX CROISSANCE:EY) (www.extenway.com) est un fournisseur de solutions technologiques d’information, de communication, de divertissement et d’éducation dans le domaine de la santé. Les terminaux Extenway offrent une vaste gamme de contenus et services intégrés dont la télévision, Internet, Microsoft Office, la vidéoconférence, la gestion de l’environnement des chambres des patients et la gestion des rendez-vous des patients. Basée à Baie d’Urfé, dans la région de Montréal au Canada, Extenway permet aux organisations d’optimiser la gestion et la coordination des interactions entre les partients et le personnel médical et administratif.

Clause libératoire et d’exonération

À l’exception des informations concernant les antécédents de l’entreprise ci-haut mentionnées, ce communiqué contient des déclarations futures qui impliquent des risques et des incertitudes. Les résultats réels peuvent être différents au niveau matériel. Les facteurs qui peuvent causer une différence incluent, mais ne sont pas limités à, l’acceptation des produits au niveau du marché, l’impact des produits compétitifs et technologies, la possibilité que certains produits portent atteinte aux brevets et autres propriétés intellectuelles de tierces parties, et aux coûts associés aux développements de produits. Solutions Extenway inc. ne procédera pas à la mise à jour de ces déclarations futures afin de refléter les événements ou circonstances après la date ci-haut mentionnée. Des informations plus détaillées sur les facteurs potentiels qui pourraient avoir une influence sur les résultats financiers sont incluses dans les documents fournies aux autorités canadiennes en valeurs mobilières.

Filed Under: Hospitals and Health Systems, Public Health and Research

Radient Pharmaceuticals and Gaur Diagno Launch Cancer Education and Screening Program in India

Posted on October 19, 2010 Written by Editor

SOURCE: Radient Pharmaceuticals Corporation

TUSTIN, CA–(Marketwire – October 19, 2010) –  Radient Pharmaceuticals Corporation (RPC) (NYSE Amex: RPC) and its exclusive India-based distribution partner Jaiva Technologies, Inc. (JTI) and Jaiva’s Indian subsidiary Gaur Diagno, Pvt Ltd (GDL) announced today the launch of a cancer education and screening program in India — a key international market where GDL is actively commercializing RPC’s Onko-Sure® in vitro diagnostic (IVD) cancer test. The goal of the program is to drive public education; raise market awareness; and offer Onko-Sure® as a commercialized cancer screening test that can potentially help stem the rising cancer epidemic in India.

According to the Cancer Foundation of India, cancer impacts up to 2.5 million people in India annually and the fight against cancer — in both the public and private healthcare sectors — is largely restricted to improving diagnostic and treatment facilities throughout the country. Because of this, it has become increasingly vital to enhance activities and programs that support cancer education and offer treatment options to potential and existing cancer patients. 

With the launch of its cancer education and screening program on behalf of RPC, GDL is taking an aggressive leadership role in India with two distinct launch strategies. The first comprises a widespread deployment of GDL’s mobile cancer screening laboratory units where Indian-based physicians and other medical staff travel to local towns to provide counseling and education, along with patient screening using RPC’s Onko-Sure® IVD cancer test. The second program is focused on Company collaboration with Indian government agencies to establish GDL-sponsored cancer screening and testing facilities directly on-site in government hospitals. Physician-referred general cancer screening will also be conducted at these hospitals and it is anticipated that RPC’s Onko-Sure® IVD cancer tests will be administered to patients contacted through the program. The goal of both strategies is to reduce the incidence of cancer in India, and through each program, patients will be provided with registered health cards that will track a patient’s health records for future reference and statistical analysis.

RPC’s projected Onko-Sure® IVD test kit purchase plan is focused primarily on the ramp-up of the government sponsored cancer testing program. RPC estimates test kit purchases to be approximately US$2 million in FY2011, and US$3 million in FY2012. These estimates are subject to change based on results of the 64-point questionnaire and these figures have the potential to increase if GDL’s results show more than 50% of the patients at high-risk when screened through the 64-point questionnaire.

According to Mr. Douglas MacLellan, Executive Chairman and CEO of RPC, “The introduction of GDL’s new cancer education and screening program in India is the next most important and major milestone in the commercialization of Onko-Sure® in India. GDL is taking a leadership role in providing a market with 2.5 million cancer patients with not only educational resources and support through this program, but also the potential of early disease detection and on-going monitoring though our USFDA approved Onko-Sure® IVD cancer test.”

According to Dr. Umesh Bhatia, CEO of JTI and GDL, “This government screening program is a breakthrough project and we believe a continuous and aggressive approach is necessary if we are to reduce the incidence of cancer in India. We anticipate this is just the beginning of additional large-scale screening programs we employ. GDL is committed to continuing all efforts to work with Indian government agencies with the ultimate goal of reducing cancer rates in this country.”

RPC’s Onko-Sure® IVD cancer test is a simple, non-invasive, patent-pending and regulatory-approved in vitro diagnostic (IVD) test used for the detection, screening, and monitoring of various types of cancer. The test enables physicians and healthcare professionals to effectively monitor and/or detect certain types of cancers by measuring the accumulation of Fibrin and Fibrinogen Degradation Products (FDP) in the blood. FDP levels rise dramatically with the progression of cancer. Onko-Sure® is approved by the US FDA for the monitoring of colorectal cancer and by Health Canada as a lung cancer detection and monitoring test. For more information visit www.onko-sure.com.

For additional information on Radient Pharmaceuticals, ADI and its portfolio of products visit the Company’s corporate website at www.Radient-Pharma.com. For Investor Relations information contact Kristine Szarkowitz at [email protected] or 1.206.310.5323.

About Radient Pharmaceuticals:
Headquartered in Tustin, California, Radient Pharmaceuticals is dedicated to saving lives and money for patients and global healthcare systems through the deployment of its Onko-Sure® In Vitro Diagnostic cancer test. The company’s focus is on the discovery, development and commercialization of unique high-value diagnostic tests that help physicians answer important clinical questions related to early disease detection; treatment strategy; and the monitoring of disease progression, prognosis, and diagnosis to ultimately improve patient outcomes. Radient Pharmaceutical’s current Onko-Sure® cancer test is used to guide decisions regarding patient treatment, which may include decisions to refer patients to specialists, perform additional testing, or assist in the selection of therapy. To learn more about our company, people and potentially life-saving cancer test, visit www.Radient-Pharma.com.

About Jaiva Technologies and Gaur Diagno:
Jaiva Technologies, headquartered in Houston, TX, and subsidiary Gaur Diagno, headquartered in New Delhi, India, are working to develop and license novel products for life-threatening diseases. Through science and innovation the company aims to develop novel therapies that will significantly impact and extend the quality of life for patients. Part of the company’s effort is large-scale screening of populations that result in meaningful and epidemiological slow-down of life threatening diseases, such as cancer. For further information visit www.gaurdiagno.com.

Forward Looking Statements:
Safe Harbor Statement under the Private Securities Litigation Reform Act of 1995: The statements contained in this document include certain predictions and projections that may be considered forward-looking statements under securities law. These statements involve a number of important risks and uncertainties that could cause actual results to differ materially including, but not limited to, the performance of joint venture partners, as well as other economic, competitive and technological factors involving the Company’s operations, markets, services, products, and prices. With respect to Radient Pharmaceuticals Corporation, except for the historical information contained herein, the matters discussed in this document are forward-looking statements involving risks and uncertainties that could cause actual results to differ materially from those in such forward-looking statements.

Radient Pharma Contact:
Kristine Szarkowitz
Director-Investor Relations
Email Contact
Tel: 206.310.5323

Click here to see all recent news from this company

Filed Under: Prescription Drugs and Pharmacy, Public Health and Research

MELA Sciences Announces MelaFind(R) Pivotal Data Published in Online Edition of Archives of Dermatology

Posted on October 19, 2010 Written by Editor

SOURCE: MELA Sciences

Peer-Reviewed Publication Also Includes Results of Pilot Reader Study

IRVINGTON, NY–(Marketwire – October 19, 2010) –  MELA Sciences, Inc. (NASDAQ: MELA) today announced that the results of the company’s MelaFind® pivotal trial and pilot reader study have been published in the online edition of the journal Archives of Dermatology. The paper will appear in the February 2011 print edition of the journal.

“We are extremely pleased to see the results of the MelaFind® pivotal trial reviewed by outside dermatology experts and published in this prestigious medical journal in the field of dermatology,” said Joseph V. Gulfo, MD, President and CEO of MELA Sciences. “We remain diligently focused on preparing for the November 18th panel meeting where these data will be presented to and discussed with the Food and Drug Administration’s advisors.”

The paper shows that MelaFind’s performance satisfied all primary and secondary sensitivity and specificity endpoints, as defined by the study protocol and a Protocol Agreement between MELA Sciences and the FDA. The Protocol Agreement calls for 95% lower confidence bound on sensitivity to be greater than 95% and for MelaFind® to be more specific than the study physicians at a p-value of less than 0.05. Since the measured values of sensitivity were very high, the “exact mid-P” statistical method was used to compute the 95% lower confidence bound. Specificity endpoints were based on relative performance of MelaFind® and investigators, with significance established at p-value less than 0.05.

In order to generate a comparison with dermatologists’ biopsy sensitivity to melanoma, MELA Sciences conducted a parallel pilot readers’ study with 39 other dermatologists who were blinded to the study results. Importantly, the average biopsy sensitivity of the readers was only 80%, and the inter-reader variability was high.

“The pilot reader study found that dermatologists do miss early melanomas,” study author Kenneth Gross, MD, said. “Only 20% of the melanomas in the pilot reader study would have been biopsied by all readers and different readers missed different melanomas. Thus, even though all lesions in the clinical trial were biopsied by the examining dermatologists, many of the melanomas would not have been biopsied by other dermatologists, underscoring the need for an objective tool to aid in the decision to biopsy. We believe that the results of the pivotal trial and the pilot reader study underscore the clinical utility of MelaFind® as an objective tool to aid clinicians in the detection of early melanoma.”

About MELA Sciences

MELA Sciences is a medical technology company focused on developing MelaFind®. MelaFind® is a non-invasive and objective multi-spectral computer vision system designed to aid physicians in the detection of early melanoma from among clinically atypical (those having one or more clinical or historical characteristics of melanoma, such as asymmetry, border irregularity, color variegation, diameter greater than 6 millimeters, evolving, patient concern, regression, and ugly duckling) cutaneous pigmented lesions that are non-ulcerated, not bleeding, and less than 2.2 centimeters in diameter, when a physician chooses to obtain additional information before making a final decision to biopsy to rule out melanoma.

The MelaFind® Pre-Market Approval (PMA) application was filed with the U.S. Food and Drug Administration (FDA) in June 2009 and is currently under review at the FDA. MELA Sciences cannot predict either the timing of the FDA’s decision on the PMA application or the outcome. FDA approval is required prior to marketing MelaFind® in the United States.

For more information on MELA Sciences, visit www.melasciences.com.

Safe Harbor

This press release includes “forward-looking statements” within the meaning of the Securities Litigation Reform Act of 1995. These statements include but are not limited to our plans, objectives, expectations and intentions and other statements that contain words such as “expects,” “contemplates,” “anticipates,” “plans,” “intends,” “believes” and variations of such words or similar expressions that predict or indicate future events or trends, or that do not relate to historical matters. These statements are based on our current beliefs or expectations and are inherently subject to significant uncertainties and changes in circumstances, many of which are beyond our control. There can be no assurance that our beliefs or expectations will be achieved. Actual results may differ materially from our beliefs or expectations due to economic, business, competitive, market and regulatory factors.

For further information contact:

For Investors:
David Carey
Lazar Partners, Ltd.
646-871-8485

For Media:
Hollister Hovey
Lazar Partners, Ltd.
646-871-8485

Filed Under: Public Health and Research

Bright Colors for Better Women’s Health

Posted on October 18, 2010 Written by Editor

SOURCE: Nutrilite

MISSION, KS–(Marketwire – October 18, 2010) – (Family Features) Only about a third of American women are meeting their fruit and vegetable intake recommendations, according to the Centers for Disease Control and Prevention. And that means they are likely missing out on potentially important breast and ovarian health benefits. Along with vitamins, minerals and fiber, fruits and vegetables contain a type of phytonutrient called carotenoids, which research suggests help support women’s health including breast and ovarian health. 

Based on a new report called America’s Phytonutrient Report: Women’s Health by Color, older women have total carotenoid intakes 20 percent greater than younger women after accounting for differences in caloric intake. Similar to the original America’s Phytonutrient Report: Quantifying the Gap which found that on average eight out of 10 American adults are falling short on phytonutrient consumption, the new report revealed a troubling shortfall, this time among women and carotenoids. America’s Phytonutrient Reports are released by The Nutrilite Health Institute, a worldwide collaboration of experts who are dedicated to helping people achieve optimal health — through research, education, and practical, personalized solutions. Nutrilite is the world’s leading brand of vitamin, mineral, and dietary supplements, based on 2008 sales.

Carotenoids are compounds that give fruits and vegetables their vibrant colors, which research suggests may offer breast, ovarian and other health benefits for women. Using NHANES energy-adjusted data to compare the diets of women 45 years and older with those younger, the report finds that many women of all ages lack carotenoid-rich foods in their diet, but the relative magnitude of the “carotenoid gap” is greater among women less than 45 years old as compared to older women.

“This points to a troubling phenomenon where younger women may be missing some of the benefits of consuming more carotenoid rich fruits and vegetables, and yet calorie for calorie, older women are eating more of these important nutrients,” said Keith Randolph, Ph.D., Technology Strategist for Nutrilite. 

Powering Up Produce
Choosing to increase the amount of the fruit and vegetables richest in carotenoids is important for long-term preventative health among women. While foods like spinach, tomatoes and carrots are certainly part of a healthy diet, there are opportunities for women to choose a wider variety of produce.

“It’s concerning that so many American women lack a variety of carotenoid-rich foods in their regular diets,” says Amy Hendel, Nutrilite’s Phytonutrient Coach. “By selecting the most carotenoid-rich produce choices, women can purposefully increase their carotenoid and phytonutrient intakes which can impact health significantly as they age.”

Hendel, a registered physician assistant and health/wellness expert, offers these easy substitutions to “power up” your plate and add new flavors to your meal plan:

Green: A serving of cooked kale provides triple the amount of lutein/zeaxanthin as a serving of raw spinach.
Red: A serving of guava delivers more than one and a half times the lycopene in a raw tomato.
Yellow/Orange:

  • A serving of sweet potatoes has nearly double the beta-carotene as a serving of carrots.
  • A serving of carrots delivers four times the amount of alpha-carotene as a serving of winter squash.
  • A serving of fresh papaya has roughly 10 times the beta-cryptoxanthin found in an orange.

Hendel adds, a good goal for most individuals is to consume 10 servings of fruits and vegetables daily, with an emphasis on quality, not just quantity. If this proves challenging, consider a natural, plant-based dietary supplement which includes phytonutrients such as carotenoids.

For more information about Nutrilite Nutritional Supplements and to get more practical tips, visit www.nutrilite.com/color.

Filed Under: Public Health and Research

UV Flu Technologies Selected for Second Profile in Influential UK-Based Public Service Review, as Outbreak of Legionnaires Disease Draws Renewed…

Posted on October 18, 2010 Written by Editor

SOURCE: UV Flu Technologies, Inc.

CENTERVILLE, MA–(Marketwire – October 18, 2010) –  UV Flu Technologies, Inc. (OTCBB: UVFT) (the “Company”) is pleased to announce that it has been selected as the only air purification medical device to be listed in the Infection Control Segment of the prestigious UK-based opinion and analysis industry publication “Public Service Review.” In this, our second appearance for 2010, the Company offers an informative profile within the magazine as well as a full page back cover advertisement.

The Public Service Review features contributors that include UK and foreign ministers, senior civil servants, experts and academics discussing the latest initiatives and projects along with case studies and comments on best practices affecting public sector initiatives worldwide.

“The spread of airborne bacteria and infectious diseases in the United Kingdom, in some areas, is reaching epidemic levels,” said Jack Lennon, President of UV Flu Technologies. “There is more than a 10% risk of becoming infected by HAI’s, or hospital associated infections, in many of the medical facilities in the United Kingdom, making Infection Control a much more visible issue than it is in this country. Being selected for inclusion by the ‘Review’ as the only laboratory tested device capable of killing these bacterial superbugs is a distinct honor.”

Mr. Lennon continued to say, “There is a great deal of attention in the UK, and in the United States, on the spread of MRSA, a bacteria resistant to antibiotics and estimated to kill tens of thousands of people every year, and in many instances affects people who have been in a medical facility. In fact, over the last 4 weeks an outbreak of Legionnaires Disease in South Wales garnered international attention as three deaths were reported, and a number of people were stricken. The world believed Legionnaires to no longer pose a threat, but experts believe it kills thousands of people yearly through improper diagnosis as pneumonia. The ViraTech UV-400 cost effectively and efficiently kills these airborne bacterial strains, and it was this that led to our inclusion in this particular issue.”

Further details regarding the Company’s business, financial reports and agreements are filed as part of the Company’s continuous public disclosure as a reporting issuer under the Securities Exchange Act of 1934 filed with the Securities and Exchange Commission’s (“SEC”) EDGAR database.

About UV Flu Technologies, Inc. (OTCBB: UVFT)
UV Flu Technologies is an innovative developer, manufacturer and distributor of bio technology products initially targeting the rapidly growing Indoor Air Quality (“IAQ”) industry sector. The Company manufactures the ViraTech UV-400, which utilizes high-intensity germicidal ultraviolet radiation (UV-C) inside a killing chamber that goes beyond filtration to destroy harmful airborne bacteria at rates exceeding 99.2% on a first-pass basis. The product also is highly effective in reducing odors and VOC’s, or Volatile Organic Compounds, such as acetone, benzene and formaldehyde. ViraTech UV-400 is a Class II medical device and is available without a prescription. 

Notice Regarding Forward-Looking Statements
This news release contains “forward-looking statements” as that term is defined in Section 27A of the United States Securities Act of 1933, as amended and Section 21E of the Securities Exchange Act of 1934, as amended. Statements in this press release which are not purely historical are forward-looking statements and include any statements regarding beliefs, plans, expectations or intentions regarding the future. Such forward-looking statements include, among other things, the development, costs and results of new business opportunities. Actual results could differ from those projected in any forward-looking statements due to numerous factors. Such factors include, among others, the inherent uncertainties associated with new projects and development stage companies. These forward-looking statements are made as of the date of this news release, and we assume no obligation to update the forward-looking statements, or to update the reasons why actual results could differ from those projected in the forward-looking statements. Although we believe that any beliefs, plans, expectations and intentions contained in this press release are reasonable, there can be no assurance that any such beliefs, plans, expectations or intentions will prove to be accurate. Investors should consult all of the information set forth herein and should also refer to the risk factors disclosure outlined in our annual report on Form 10-K for the most recent fiscal year, our quarterly reports on Form 10-Q and other periodic reports filed from time-to-time with the Securities and Exchange Commission.

ON BEHALF OF THE BOARD

UV Flu Technologies, Inc.
—————————–
John J. Lennon, President & CEO

Investor Information:
Geaux IR Services, Inc.
Toll-Free: 1-888-355-8838
[email protected]

Click here to see all recent news from this company

Filed Under: Public Health and Research

First U.S. Cancer Center Adds Trio of NitroSecurity Tools

Posted on October 14, 2010 Written by Editor

SOURCE: NitroSecurity, Inc.

Roswell Park Cancer Institute Selects NitroView for SIEM, Log Management and Database Monitoring

PORTSMOUTH, NH–(Marketwire – October 14, 2010) –  NitroSecurity, Inc., the leader in high-performance, content-aware security information and event management solutions (SIEM), today announced that Roswell Park Cancer Institute (RPCI) has selected the company’s integrated NitroView SIEM, log management and database monitoring solutions.

Founded in 1898, RPCI is the nation’s first cancer center, and the only upstate New York facility to hold the National Cancer Institute (NCI) designation of “comprehensive cancer center.” Accommodating approximately 200,000 outpatient visits annually, RPCI is a member of the prestigious National Comprehensive Cancer Network (NCCN). Its computing infrastructure comprises approximately 300 servers, 5,000 PCs and a host of tablets and smartphones.

For any healthcare organization, the security of personal health information (PHI) is of the highest priority. IT leadership at RPCI found that despite the Institute’s comprehensive infrastructure, security event and log information was not as rapidly discoverable and actionable as they desired — that data was often spread across disparate and disconnected systems. To remedy this, RPCI conducted an extensive search for a SIEM solution that would address those issues. The goal was to achieve greater visibility into and across data silos to more effectively and efficiently identify potential risks to PHI security.

“RPCI is a leader in cancer research, and leveraging innovative technology helps us achieve our mission: to understand, prevent and cure cancer,” said Edward Pardo, Senior IT Security Engineer at RPCI.

“e-Healthcare initiatives like electronic health records (EHR) and the relentlessly evolving cyberthreat landscape are accelerating the growth of both data and risk,” said Ken Levine, CEO of NitroSecurity. “Just as in the diagnosis of a patient, the ability to act rapidly based on comprehensive information is critical. That’s why marquee healthcare organizations around the country like RPCI have looked to partner with NitroSecurity more than any other SIEM vendor. We provide them with the greatest ability to secure their network environment and meet the letter of the law, without being distracted from their primary mission of saving lives.”

For more information on NitroView and other NitroSecurity offerings, please visit the company’s Web site at http://www.nitrosecurity.com.

About Roswell Park Cancer Institute
The mission of Roswell Park Cancer Institute (RPCI) is to understand, prevent and cure cancer. RPCI, founded in 1898, was one of the first cancer centers in the country to be named a National Cancer Institute-designated comprehensive cancer center and remains the only facility with this designation in Upstate New York. The Institute is a member of the prestigious National Comprehensive Cancer Network, an alliance of the nation’s leading cancer centers; maintains affiliate sites; and is a partner in national and international collaborative programs. For more information, visit RPCI’s website at http://www.roswellpark.org, call 1-877-ASK-RPCI (1-877-275-7724) or email [email protected].

About NitroSecurity
NitroSecurity develops high-performance security information and event management (SIEM) solutions that protect critical information and infrastructure. NitroSecurity solutions reduce risk exposure and increase network and information availability by removing the scalability and performance limitations of security information management. Utilizing the industry’s fastest analytical tools, NitroSecurity identifies, correlates and remediates threats in minutes instead of hours, allowing organizations to quickly mitigate risks to their information and infrastructure. NitroSecurity serves more than 500 organizations in the energy, healthcare, education, financial services, government, retail, hospitality and managed services industries. For more information, please visit http://www.nitrosecurity.com.

For more information:
Kevin Kosh
CHEN PR, Inc.
781-672-3111
Email Contact

Click here to see all recent news from this company

Filed Under: Health Technology and AI, Public Health and Research

DiaMedica Announces Positive Final Results in Type 1 Diabetes Study

Posted on October 14, 2010 Written by Editor

WINNIPEG, MANITOBA–(Marketwire – Oct. 14, 2010) – DiaMedica Inc., (TSX VENTURE:DMA) is pleased to announce positive final results from its previously announced type 1 diabetes study.

The study was designed to observe the potential protective and/or regenerative effects on beta cells (cells from the pancreas that produce insulin) in a widely accepted type 1 diabetes animal model. DiaMedica, in consultation with Dr. Maureen Gannon at Vanderbilt University, has confirmed that DM-99 can increase new beta cells by 1,277% (p<0.01) when administered to diseased animals compared to untreated diseased animals. Beta cell proliferation induced by DM-99 trended to be even greater than replication in non-diseased, untreated control animals.

The increased beta cell proliferation led to physiologically important improvements in the diabetic state. Improvements included the restoration of peak levels of plasma insulin to near normal levels (p<0.05) with positive trends of increase in the levels of both pancreatic and plasma insulin, which led to improved blood glucose clearance in a oral glucose tolerance test with DM-99 treatment. On July 8th, DiaMedica reported initial results of the study that included a 68% reduction in fasting blood glucose (p<0.05) with DM-99.

“These results are very provocative and would indicate that this compound offers both a level of protection of beta cells in a type 1 diabetes animal model as well as induces their proliferation,” stated Dr. Maureen Gannon, Associate professor of Medicine at Vanderbilt University, Division of Diabetes, Endocrinology and Metabolism. “Having a therapeutic compound that can either protect or proliferate beta cells is a key requirement for finding a cure for type 1 diabetes so that therapies involved in replacing or regenerating these cells can work long-term. DM-99 appears to be able to perform both of these functions.”

“The ability of DM-99 to significantly increase beta cell replication combined with our earlier data showing the ability of DM-99 to protect against a variety of autoimmune attacks may result in a first in class treatment for type I diabetes”, stated Mr. Rick Pauls, President and CEO of DiaMedica. “We are currently developing DM-199, a novel recombinant and humanized form of DM-99 for commercialization.”

About DiaMedica

DiaMedica is a biopharmaceutical company focused on developing drugs with the potential to be broadly applicable in treating large unmet diseases including diabetes, autoimmune disorders and neurological diseases by protecting and proliferating a variety of cells. Two of DiaMedica’s products have demonstrated human efficacy in lowering blood sugar levels in people diagnosed with Type 2 diabetes with an excellent safety profile. DiaMedica is listed on the TSX Venture Exchange under the trading symbol “DMA”.

Caution Regarding Forward-Looking Information

Certain statements contained in this press release constitute forward-looking information within the meaning of applicable Canadian provincial securities legislation (collectively, the “forward-looking statements“). These forward-looking statements relate to, among other things, DiaMedica’s objectives, goals, targets, strategies, intentions, plans, beliefs, estimates and outlook, and can, in some cases, be identified by the use of words such as “believe,” “anticipate,” “expect,” “intend,” “plan,” “will,” “may” and other similar expressions. In addition, any statements that refer to expectations, projections or other characterizations of future events or circumstances are forward-looking statements. Specifically, this press release contains forward-looking statements regarding matters such as, but not limited to, the anticipated use of proceeds from the Offering, management’s assessment of DiaMedica’s future plans, information with respect to the advancement of DiaMedica’s research and development programs, and DiaMedica’s other estimates and expectations. These statements reflect management’s current beliefs and are based on information currently available to management. Certain material factors or assumptions are applied in making forward-looking statements, and actual results may differ materially from those expressed or implied in such statements. Important factors that could cause actual results to differ materially from these expectations include, among other things: uncertainties and risks related to our research and development programs, the availability of additional financing, risks and uncertainties relating to the anticipated use of proceeds, changes in debt and equity markets, uncertainties related to clinical trials and product development, rapid technological change, uncertainties related to forecasts, competition, potential product liability, additional financing requirements and access to capital, unproven markets, the cost and supply of raw materials, management of growth, effects of insurers’ willingness to pay for products, risks related to regulatory matters and risks related to intellectual property matters.

Additional information about these factors and about the material factors or assumptions underlying such forward-looking statements may be found in the body of this news release, as well as under the heading “Risk Factors” contained in DiaMedica’s 2009 annual information form. DiaMedica cautions that the foregoing list of important factors that may affect future results is not exhaustive. When relying on DiaMedica’s forward-looking statements to make decisions with respect to DiaMedica, investors and others should carefully consider the foregoing factors and other uncertainties and potential events. Such forward-looking statements are based on a number of estimates and assumptions, which may prove to be incorrect, including, but not limited to, assumptions regarding the availability of additional financing for research and development companies, and general business and economic conditions. These risks and uncertainties should be considered carefully and investors and others should not place undue reliance on the forward-looking statements. Although the forward-looking statements contained in this press release are based upon what management believes to be reasonable assumptions, DiaMedica cannot provide assurance that actual results will be consistent with these forward-looking statements. DiaMedica undertakes no obligation to update or revise any forward-looking statement.

Filed Under: Public Health and Research

DentalPlans.com Supports the Fight Against Breast Cancer

Posted on October 13, 2010 Written by Editor

SOURCE: DentalPlans.com

Company to Donate a Portion of October Proceeds to Fund Life-Saving Research and Awareness Programs, Dentists Don Pink

PLANTATION, FL–(Marketwire – October 13, 2010) – For the second year in a row, DentalPlans.com, the top online source for affordable and easy-to-use alternatives to dental insurance, is proud to donate a portion of the firm’s October proceeds to support breast cancer research and awareness. DentalPlans.com is pleased to reaffirm their commitment to women’s health and fund groundbreaking research, education, screening and treatment during National Breast Cancer Awareness Month. 

“As a leader in discount dental plans, our company is fully committed to the well being of our nation’s oral health,” said Buddy Johnson, CEO of DentalPlans.com, Inc. “We are proud to extend our support to raise public awareness and fund life-saving research to ultimately cure this devastating disease.”

In further support of the company’s campaign, DentalPlans.com has provided select network dentists and their staff members with pink dental scrubs and badges inscribed with a pink ribbon and the word ‘hope.’ “Any small thing we can do to eradicate this disease is a huge step forward,” said Dr. Peter Krimsky, who is proudly setting aside the conventional blue scrubs to wear pink ones along with his staff. “We’re raising awareness and prompting our patients to think.”

Dr. Krimsky’s office sees wearing pink as making a difference, one that will one day contribute to the end of the disease. Others are adopting the same thinking and pink is popping up where one might least expect. This year, the National Football League has teamed with the American Cancer Society to feature players, coaches and referees wearing pink apparel in the name of awareness. 

According to the American Cancer Society, breast cancer is the second leading cause of cancer death in women, after lung cancer. One out of eight American women who live to be 85 years of age will develop breast cancer, a risk that was one out of 14 in 1960. Excluding cancers of the skin, breast cancer is the most common cancer diagnosed among U.S. women, accounting for more than 1 in 4 cancers.

Interviews with DentalPlans.com representatives, members and network dentists are available. For more information about DentalPlans.com and editorial inquiries, please contact Shamin Abas or Elizabeth Rose of Shamin Abas Public Relations at 561.366.1226, [email protected] or [email protected]. 

About DentalPlans.com (www.DentalPlans.com)
DentalPlans.com is dedicated to improving oral health nationwide by making quality dental care affordable and accessible to everyone. DentalPlans.com proudly offers the freedom to choose from an extensive selection of discount dental plans designed to save members money on their dental care needs. With more than 40 years of experience in the dental industry, their devoted team quickly transformed DentalPlans.com into a trusted industry leader and the largest online provider of discount dental plans. Since 1999, DentalPlans.com has offered great value and convenience with an extensive choice of money-saving discount dental plans in one user-friendly website.

Click here to see all recent news from this company

Filed Under: Public Health and Research

Radient Pharmaceuticals and Provista Life Sciences Announce New Blood Test for Lung Cancer

Posted on October 13, 2010 Written by Editor

SOURCE: Radient Pharmaceuticals Corporation

TUSTIN, CA–(Marketwire – October 13, 2010) – Provista Life Sciences and Radient Pharmaceuticals Corporation (RPC) (NYSE Amex: RPC) announced today the validation study results of a blood test for early detection of lung cancer and Provista’s plans to broadly introduce this new test to market.

The study completed the requisite analyses and data evaluation needed to validate Provista’s test, based on Radient Pharmaceutical Corporation’s antigens for fibrinogen degradation products (FDP), successfully detects lung cancer with a high degree of accuracy. The study included men and women between 20-76 years of age. The data generated in this final study proved consistent with previous findings and produced positive clinical performance marks of 87% sensitivity; 95% specificity; and an ROC Accuracy of 0.97. By industry standards the study proved very successful and will serve as the cornerstone to Provista’s efforts to introduce a new lung cancer detection assay branded LC Sentinel™ to market. Provista intends to introduce LC Sentinel™ as a CLIA Laboratory Developed Test (LDT) for use in high-risk lung cancer patient populations in the U.S. by the end of the fourth quarter 2010 through its standard clinical channels that include physicians, medical clinics and hospitals. The company expects to seek FDA registration for LC Sentinel™ in 2011.

According to Provista CEO William Gartner, “We are exceptionally pleased at the test results and will aggressively market and commercialize this important and potentially life-saving lung cancer test beginning in the fourth quarter 2010.” Gartner also expressed high praise for the quality of the RPC’s manufacturing facilities and chemicals indicating the Company is pleased to be an exclusive partner of RPC in the development of the test. In conjunction with today’s announcement, RPC and Provista also announced the two Companies will execute an exclusive lab partnership agreement where Provista Life Sciences will purchase RPC reagents exclusively for the development of LC Sentinel™.

The American Cancer Society’s estimates of the impact of lung cancer in the U.S. during 2009 include approximately 219,000 new cases (both non-small cell and small cell) and 159,000 deaths resulting from the disease, accounting for 28 percent of all cancer deaths. Lung cancer is the leading cause of cancer death among both men and women — 62% of those diagnosed in late stages die within 5 years. Provista estimates there are approximately 18 million high-risk patients who stand to benefit from the test’s US introduction. 

According to Mr. Douglas MacLellan, Executive Chairman and CEO of RPC, “The detection benefit observed in this study represents a meaningful additional to tests available today. We are very encouraged by the potential benefit of this test to patients who are facing the deadly threat of lung cancer. As previously announced, RPC is actively engaged in acquisition negotiations with Provista and with the success of the deal; we expect to combine both companies to achieve a leadership presence in the global cancer diagnostics market.”

On September 27, 2010 RPC signed an extension of its original agreement dated July 13, 2010 to merge with Provista Diagnostics Inc., making the agreement between Provista Diagnostics and Radient Pharmaceuticals effective through December 31, 2010. Both Companies have confirmed continued interest in the merger and to pursue completion of the deal within a timeframe that suits the needs of both Companies and shareholders.

For additional information on Radient Pharmaceuticals, ADI and its portfolio of products visit the Company’s corporate website at www.Radient-Pharma.com. For Investor Relations information contact Kristine Szarkowitz at [email protected] or 1.206.310.5323.

For additional information on Provista Diagnostics Inc and its diagnostic portfolio, visit the company’s website at www.ProvistaLS.com. For additional information contact Donald Weber, COO, or William Gartner, CEO, at 602.224.5500.

About Provista Life Sciences:
Provista Life Sciences is a biotechnology diagnostics development and Commercialization Company located in Phoenix, AZ, the Company provides the scientific and operating management resources to rapidly advance the development and introduction of novel diagnostics technologies into the domestic and global marketplace. For more information, visit the company’s Web site at www.ProvistaLS.com or call 1.602.224.5500.

About Radient Pharmaceuticals:
Headquartered in Tustin, California, Radient Pharmaceuticals is dedicated to saving lives and money for patients and global healthcare systems through the deployment of its Onko-Sure® In Vitro Diagnostic cancer test. The company’s focus is on the discovery, development and commercialization of unique high-value diagnostic tests that help physicians answer important clinical questions related to early disease detection; treatment strategy; and the monitoring of disease progression, prognosis, and diagnosis to ultimately improve patient outcomes. Radient Pharmaceutical’s current Onko-Sure® cancer testis used to guide decisions regarding patient treatment, which may include decisions to refer patients to specialists, perform additional testing, or assist in the selection of therapy. To learn more about our company, people and potentially life-saving cancer test, visit.

Forward Looking Statements:
Safe Harbor Statement under the Private Securities Litigation Reform Act of 1995: The statements contained in this document include certain predictions and projections that may be considered forward-looking statements under securities law. These statements involve a number of important risks and uncertainties that could cause actual results to differ materially including, but not limited to, the performance of joint venture partners, as well as other economic, competitive and technological factors involving the Company’s operations, markets, services, products, and prices. With respect to Radient Pharmaceuticals Corporation, except for the historical information contained herein, the matters discussed in this document are forward-looking statements involving risks and uncertainties that could cause actual results to differ materially from those in such forward-looking statements.

Radient Pharma Contact:
Kristine Szarkowitz
Director-Investor Relations
Email Contact
Tel: 206.310.5323

Click here to see all recent news from this company

Filed Under: Prescription Drugs and Pharmacy, Public Health and Research

Pizza Patron to Raise Money for St. Jude Children’s Research Hospital in October

Posted on October 12, 2010 Written by Editor

SOURCE: Pizza Patron

No Child Is Ever Turned Away for Medical Treatment Due to Lack of Ability to Pay

DALLAS, TX–(Marketwire – October 12, 2010) –  For the entire month of October, Pizza Patron will be raising funds in all its stores for the St. Jude Children’s Research Hospital.

Pizza Patron stores have St. Jude posters and counter top displays up that explain why and how to donate. St. Jude is a pediatric treatment and research facility in Memphis, Tennessee which treats children with cancer and other catastrophic diseases. Founded by entertainer Danny Thomas on the premise that “no child should die in the dawn of life,” the hospital is well-known for being the only pediatric cancer center in the country that won’t charge parents for any treatment not covered by their insurance plan. No child is ever turned away from St. Jude’s because of his or her family’s inability to pay.

“We were really amazed by the professionalism and support shown by St. Jude’s team. They visited every Pizza Patrón across the country personally, and provided training to our team members,” said Andrew Gamm, brand director for Pizza Patrón. “The response from our employees has been overwhelmingly positive; everyone is very excited to play a part in helping this amazing charity.”

Gamm explained that donations of any size can be given and the donation will be indicated on the receipt in a separate line item. One-hundred percent of the money raised will go to St. Jude’s. 

In 2010, St. Jude Children’s Research Hospital was named the number one children’s cancer hospital in the United States by U.S. News & World Report. Discoveries at St. Jude have changed how doctors treat children with cancer and other catastrophic illnesses. Since St. Jude was established, the survival rate for acute lymphoblastic leukemia, the most common type of childhood cancer, has increased from 4 percent in 1962 to 94 percent today. St. Jude has treated children from across the U.S. and from more than 70 countries. Doctors around the globe consult with St. Jude on their toughest cases. Additionally, St. Jude has an International Outreach Program to improve the survival rates of children with catastrophic illnesses worldwide through the transfer of knowledge, technology and organizational skills.

About Pizza Patrón
Pizza Patrón, America’s #1 Latin pizza brand, offers traditional pizza, wings and sides in its community based, Latin-influenced stores. Pizza Patrón was founded by restaurateur Antonio Swad in 1986, in Dallas, Texas, and today operates 100 dine-in and carry-out restaurants in seven states with 40 more under development. Pizza Patrón has franchise opportunities available in prime markets throughout the country offering a proven system for hard-working franchisee candidates. In 2007, the brand received international news coverage when it decided to accept Mexican Pesos at all of its locations, gaining over 500,000,000 media impressions worth over $30 million in the U.S. alone. The company’s medium AMIGO PIZZAS® start as low as $4 and X-Large LISTA-NOW READY™ pepperoni pizzas start as low as $6 all day, every day.

Website – www.pizzapatron.com
Facebook – http://www.facebook.com/pizzapatron
Twitter – http://www.twitter.com/pizzapatron
MySpace – http://www.myspace.com/mypizzapatron
YouTube – http://www.youtube.com/user/pizzapatroncorp

Contact:
Sandy Bell
Phone 972-934-2850 x106
Fax 972-934-2870
Email Contact

Click here to see all recent news from this company

Filed Under: Hospitals and Health Systems, Public Health and Research

There’s Just No Stopping the Pink Glove Dance

Posted on October 11, 2010 Written by Editor

SOURCE: Medline Industries, Inc.

Twelve New Video Versions Featuring Breast Cancer Survivors and Healthcare Workers Dancing From Coast to Coast Make Debut on YouTube

MUNDELEIN, IL–(Marketwire – October 11, 2010) –  The more than 4,000 healthcare workers and breast cancer survivors who danced in the Pink Glove Dance: The Sequel video are still working to raise awareness for breast cancer prevention — and maybe inspire more people to dance and support the cause. Medline Industries, Inc. — the makers of the pink gloves and creator of the dance videos — has just posted videos from each of the 12 healthcare facilities and breast cancer survivor groups that participated in the Pink Glove Dance sequel. The videos can be viewed at www.pinkglovedance.com.

“Our video involved doctors and nurses, employees, students, survivors and others from the IU Simon Cancer Center, the IU school of nursing and medicine, and Clarian Health,” said Michael Schug, communications specialist at the Indiana University Melvin and Bren Simon Cancer Center. “So, a lot of our people danced to help spread the word about breast cancer awareness. To let our dancers and community know about our custom video, we have done mass e-mailings, posted it on our Facebook pages, YouTube channels, and Flickr accounts. It’s definitely gone viral around here.” 

Linda Rumore, purchasing agent for Thibodaux Regional Medical Center in Thibodaux, Louisiana, and the coordinator of the shoot at the hospital said: “The video is such a morale booster for all of us throughout the hospital because it’s such a great cause. It’s like Christmas Eve here because everyone is so excited and honored to be involved in the video.”

The original Pink Glove Dance video was launched about a year ago with healthcare workers at Providence St. Vincent Medical Center in Portland, Oregon. Because of the overwhelming response from the video (now with more than 11.8 million views on YouTube), Medline went across the country and into Canada to film healthcare workers and breast cancer survivors dancing in pink gloves to raise awareness for breast cancer prevention. The result was The Pink Glove Dance: The Sequel, which was launched September 17, featuring workers from 11 hospitals, three nursing homes and breast cancer survivors in five different locations from the Golden Gate Bridge to New York’s Times Square and several points in between. (See list of participating facilities and locations at the end of this release.)

“I cannot begin to tell you what participating in the video does for someone like me — a survivor. After going through hell and back and being able to have fun, dance and share these moments, it’s amazing and it shows how Medline really cares and thinks about the people they are serving,” said Annette Rodriguez, a New York City resident and participant in the survivor shoot in Times Square. “Being in the video shows that we aren’t just pieces of meat being dealt with, we are people too. People aren’t noticing the lack of hair or how skinny or fat someone is getting from treatments. It made all of us feel beautiful and allowed us to just have fun, let loose.” 

Since the original video was released last November, the Pink Glove Dance has grown way beyond Medline’s efforts. In the past year, more than 80 pink glove videos have been posted on YouTube from around the world (including Germany, The Netherlands and Canada) featuring people dancing in pink gloves to support breast cancer awareness. Some of the more interesting videos feature the Penn State women’s basketball team, students in elementary schools, high school cheerleaders, grandmothers, and even cats and babies wearing pink gloves.

Medline originally developed the pink exam gloves and the Pink Glove Dance video as a way to spread awareness for breast cancer prevention.

“Breast cancer awareness and prevention is now the largest philanthropic cause in our company,” said Andy Mills, president of Medline. “The pink gloves are symbolic of healthcare workers’ connection with breast cancer patients. Prevention and early detection are among the most important ways you can fight breast cancer and that is why our campaign focuses on helping fund mammograms for women who cannot afford them.”

Medline donates $1 to the National Breast Cancer Foundation for every case sold of its pink gloves to help fund mammograms for underserved women. Medline has donated more than a half million dollars to provide education and free mammograms to those in need and continues to make contributions every year.

About Medline
As the nation’s largest privately held manufacturer and distributor of medical supplies, Medline is focused on helping to improve the quality of care for patients and residents. Breast cancer awareness is a natural extension of Medline’s corporate mission to help save lives through the early detection of breast cancer. (Visit www.medline.com/breast-cancer-awareness for details). Based in Mundelein, Ill., Medline manufactures and distributes more than 100,000 products to hospitals, extended care facilities, surgery centers, home care dealers and agencies, and other markets.

Who is in the sequel?
The sequel features more than 4000 healthcare workers and breast cancer survivors from 14 separate facilities in the U.S. and Canada (11 hospitals, 3 nursing homes and 5 separate breast cancer survivor shoots). Here is a list of participating locations:

Providence St. Vincent Medical Center
Portland, Oregon

University of Minnesota Medical Center, Fairview
Minneapolis, Minnesota

Indiana University Melvin and Bren Simon Cancer Center
Indianapolis, Indiana

Tallahassee Memorial Healthcare, Inc.
Tallahassee, Florida

Saint Michael’s Medical Center
Newark, New Jersey

The Medical Center of Plano
Plano, Texas

HCA Johnston?Willis Hospital
Richmond, Virginia

Scripps Memorial Hospital La Jolla
La Jolla, California

Sky Ridge Medical Center
Lone Tree, Colorado

Thibodaux Regional Medical Center
Thibodaux, Louisiana

Capital Health
Halifax, Nova Scotia

Burgess Square Healthcare and Rehab Centre
Westmont, Illinois

Isabella Geriatric Center
New York, New York

Lorien Health Systems
Maryland

Breast Cancer Survivor Sites
New York City
Chicago
San Francisco
Minneapolis
Portland

Medline Media Contacts:
John Marks
(847) 643-3309
Jerreau Beaudoin
(847) 643-3011

Filed Under: Hospitals and Health Systems, Public Health and Research

Diabetes Stops Here

Posted on October 11, 2010 Written by Editor

SOURCE: American Diabetes Association

The American Diabetes Association Launches Blog to Help Stop Diabetes®

ALEXANDRIA, VA–(Marketwire – October 11, 2010) – The American Diabetes Association launched its first official blog today to help put a face on a disease that kills more people each year than breast cancer and AIDS combined. The blog, called Diabetes Stops Here: Living with Diabetes; Inspired to Stop It, aims to document the Stop Diabetes® movement by reaching and engaging the 23.6 million Americans living with diabetes as well as the 57 million who are at risk for developing type 2 diabetes. 

Diabetes Stops Here will provide snap shots of the people who are committed to putting an end to this disease, from inspiring volunteer stories to moving staff experiences to celebrity stories about how to be successful while living with diabetes. The stories, interviews and news will be shared by the blog’s author, a staff member at the American Diabetes Association, who has lived with type 1 diabetes for nearly ten years. 

The Stop Diabetes movement was launched during American Diabetes Month® in November 2009 as a call to action for people to stand up against this disease and its devastating complications. The Association hopes to have one million people join the movement by the end of 2010.

“There have been so many touching moments in the movement to Stop Diabetes since we launched last year,” commented Larry Hausner, CEO, American Diabetes Association. “People have shared courageous stories of facing their diabetes head on, while others have shared their heart-breaking experiences of losing a loved one because of diabetes. The blog is a new way to raise our collective voices and tell people why we need to Stop Diabetes once and for all.” 

Some of the most vocal diabetes stories come from blogs and other social media platforms which create a broad online community of people who have diabetes or whose loved ones are living with the disease. “By means of this blog,” noted Hausner, “we hope to add our voice to this dialogue and further engage with those who may be well aware of the effects diabetes can have on their lives.”

Today’s first post is titled “Why ‘Stop Diabetes’?” can be found at www.diabetesstopshere.org. This initial post seeks to explain why the Stop Diabetes movement was created and its goal for engaging the public. “The goal of the Stop Diabetes movement is to grow to epic proportions, to be bigger than the disease itself,” the blog explains. “In short, it’s the answer to why the Association does the work that it does.”

The American Diabetes Association is leading the fight to stop diabetes and its deadly consequences and fighting for those affected by diabetes. The Association funds research to prevent, cure and manage diabetes; delivers services to hundreds of communities; provides objective and credible information; and gives voice to those denied their rights because of diabetes. Founded in 1940, our mission is to prevent and cure diabetes and to improve the lives of all people affected by diabetes. For more information please call the American Diabetes Association at 1-800-DIABETES (1-800-342-2383) or visit www.diabetes.org. Information from both these sources is available in English and Spanish.

Contact:
Dayle Kern
703-549-1500 ext. 2290

id=”nav_links”>

Filed Under: Public Health and Research

Spina Bifida Association Launches New Program and Asks You to Educate Yourself and Loved Ones During Spina Bifida Awareness Month

Posted on October 5, 2010 Written by Editor

SOURCE: Spina Bifida Association

Through Education SBA Hopes to Help More Families Learn About the Birth Defect

WASHINGTON, DC–(Marketwire – October 5, 2010) –  Did you know that birth defects occur in 7 out of every 10,000 live births in the U.S.? And Spina Bifida is the most common permanently disabling birth defect? In honor of October being Spina Bifida Awareness Month, the Spina Bifida Association is asking folks to take a few minutes today and get involved in the awareness month by educating loved ones.

The first question many have: What exactly is Spina Bifida? In short, Spina Bifida happens when the spinal column doesn’t close completely.

And how many births each day are affected? Well, it’s hard to believe, but eight births each day are affected by Spina Bifida or a similar birth defect of the brain and spine. If you think about it, there are currently over 65 million women in the U.S. who could become pregnant and each one of these ladies is at risk of having a baby born with Spina Bifida. So because Spina Bifida occurs during the first month of pregnancy (that’s even before most women know they’re pregnant!) it is that much more important to take proper precautions to help try to prevent it now. 

Okay. So what type of precautions can help in prevention, you may wonder?  
Although at this time there is no known cause of Spina Bifida, research has shown that if a woman takes 400 mcg of folic acid every day and before she becomes pregnant, she reduces her risk of having a baby with Spina Bifida or another neural tube defect by as much as 70%! That fact is reason enough to encourage women (and men) to get out there this month and spread awareness.

Families with a history of Spina Bifida should take extra dosages of folic acid prior to pregnancy. Hear one mom’s message: http://www.youtube.com/watch?v=qshRfegnGD4

And in honor of October’s Spina Bifida Awareness Month, SBA will also be launching some great new online resources, including:

  1. SB University (SBU) (www.sbuniversity.org), a new online educational program featuring taped sessions from the 2010 National Conference as well as monthly live seminars conducted by Spina Bifida medical professionals from around the country. During Awareness Month, SBU will debut new sessions each Monday.
  1. SBTween2Teen (www.sbtween2teen.org) a new Web site for tweens and teens with Spina Bifida. Complete with blogs, videos, real stories, fact sheets, and an Ask the Expert feature, the interactive site helps tweens and teens navigate the difficult road to adulthood. There is even a social networking component run through Facebook, allowing tweens and teens to interact with one another and build peer-to-peer relationships!
  1. Preparations, a new transition-focused Web site launching in late October allowing parents, caregivers, and clinicians to answer specific questions with regard to a child’s developmental milestones. This tool can even help young adults remedy some transitional challenges.

For even more information, tips and resource, you may visit: www.spinabifidaassociation.org
And be sure to join the Spina Bifida Association on Facebook: www.facebook.com/spina.bifida.learn

The Spina Bifida Association (SBA) serves adults and children who live with the challenges of Spina Bifida. Since 1973, SBA has been the only national voluntary health agency solely dedicated to enhancing the lives of those with Spina Bifida and those whose lives are touched by this challenging birth defect. Its tools are education, advocacy, research, and service. Through its network of chapters, SBA has a presence in more than 125 communities nationwide and touches thousands of people each year. For more information visit: www.spinabifidaassociation.org.

Media Contact
Amanda Darnley
[email protected]
800.621.3141 ext.15

id=”nav_links”>

Filed Under: Public Health and Research

Kauffman Foundation to Release a Host of Studies on Health Care Issues in the United States

Posted on October 4, 2010 Written by Editor

SOURCE: Ewing Marion Kauffman Foundation

Papers Range From Recommendations for Accelerating Drug Development to an Analysis of a New Health Care Reform Provision

KANSAS CITY, MO–(Marketwire – October 4, 2010) –  The Ewing Marion Kauffman Foundation will release several studies over the next month on various aspects of health care. Topics range from a call for a personalized health manifesto to employer-based health insurance effects on business creation and an analysis of the costs and benefits of the health care reform bill’s expanded comparative effectiveness research. Highlights of these studies are outlined below. Please contact us if you are interested in specific reports or would like advance copies.

  • The Personalized Health Manifesto. Billed as “an old-fashioned call to arms and action plan for a new age of health care,” the paper says there is a “new urgency for scientists to work together to focus on the whole human organism… and for society to absorb and implement scientific discoveries.” The Manifesto is an outgrowth of a larger study, and it calls on the life science community, policymakers, patients and society at large to take a list of actions to accelerate a transformation to personalized health.
  • Is Employer-based Health Insurance a Barrier to Entrepreneurship? This study asks whether employer-based health insurance has a negative effect on business creation by causing “job lock” in which workers may be reluctant to risk health coverage by leaving their jobs to start a company. The study examines the issue from several demographic factors, including gender and age, and raises concerns about how the bundling of health insurance and employment impacts business creation.
  • Promoting Comparative Effectiveness Research. This study addresses how to make the new health care reform law’s expansion of the comparative effectiveness research (CER) work best or to cause the least amount of harm. CER is research that attempts to analyze which treatment options are more effective than others in terms of quality and cost. A major focus of this study is on market-oriented, patient-centered approaches for disseminating and implementing CER to enhance health outcomes efficiently while preserving patient choice.
  • The New Role of Academia in Drug Development. The process for taking scientific discoveries from university labs to the market is stagnant and faces many obstacles. This paper outlines observations presented at a recent town hall meeting held at the Kauffman Foundation and presents recommendations for policymakers and thought leaders on how new collaboration models will benefit cancer cures and treatments. More information on the town hall meeting can be found here.

About the Kauffman Foundation
The Ewing Marion Kauffman Foundation is a private nonpartisan foundation that works to harness the power of entrepreneurship and innovation to grow economies and improve human welfare. Through its research and other initiatives, the Kauffman Foundation aims to open young people’s eyes to the possibility of entrepreneurship, promote entrepreneurship education, raise awareness of entrepreneurship-friendly policies, and find alternative pathways for the commercialization of new knowledge and technologies. In addition, the Foundation focuses on initiatives in the Kansas City region to advance students’ math and science skills, and improve the educational achievement of urban students, including the Ewing Marion Kauffman School, a college preparatory charter school for middle and high school students set to open in 2011. Founded by late entrepreneur and philanthropist Ewing Marion Kauffman, the Foundation is based in Kansas City, Mo. and has approximately $2 billion in assets. For more information, visit www.kauffman.org, and follow the Foundation on Twitter at @kauffmanfdn and Facebook.

Contacts:
Martin Maisonpierre
Edelman
212-704-8111
[email protected]

Barbara Pruitt
Kauffman Foundation
816-932-1288
[email protected]

Click here to see all recent news from this company

Filed Under: Public Health and Research

LIVESTRONG(R) Sponsors Global Day of Action Against Cancer

Posted on October 1, 2010 Written by Editor

SOURCE: LIVESTRONG

Supporters Host More Than 1,000 Events Around the World to Raise Cancer Awareness

AUSTIN, TX–(Marketwire – October 1, 2010) –  On Saturday, October 2nd, more than 1,000 events throughout the world will take place to mark LIVESTRONG Day, the annual global day of action to celebrate survivorship and work toward a world without cancer.

October 2 also marks the 14th anniversary of LIVESTRONG founder and chairman, cancer survivor and champion cyclist Lance Armstrong’s cancer diagnosis and the beginning of his life as a cancer advocate.

“The fight against cancer doesn’t happen in a lab,” said Armstrong. “It takes place in our homes and communities as families struggle to beat this disease. This year, cancer is projected to become the world’s leading cause of death, claiming more than eight million lives. On LIVESTRONG Day, communities throughout the world will unite to support those living with cancer and call for renewed action by our leaders to combat this global health crisis.” 

More than 1,000 events — from bike rides and “Wear Yellow” initiatives, to bake sales and beyond — will take place in all 50 U.S. states and across 57 countries on LIVESTRONG Day as individuals and communities stand unified in solidarity to raise awareness and funds for the fight against cancer. Events include:

  • A glow stick vigil on the Colorado Capitol steps in Denver where supporters will celebrate survivorship and remember lost loved ones
  • A group bike ride and cancer awareness event in Boston where participants will pedal to fight cancer
  • A 24-hour cycling event in Atlanta where cyclists will raise funds for cancer programs and research
  • A Texas/Oklahoma football game watching party at LIVESTRONG headquarters in Austin where LIVESTRONG staff will educate the community about its resources
  • A learning and awareness building event at an elementary school in Los Angeles where children will chalk up the playground and share their ideas about what it means to live strong

LIVESTRONG has also partnered with Nike to raise cancer awareness at the Red River Rivalry football game in Dallas featuring The University of Texas at Austin versus The University of Oklahoma. Fans will perform a cancer-focused card stunt sponsored by Nike during the game. The stunt will create a memorable experience for fans and help unite them in the fight against cancer.

LIVESTRONG and RadioShack are further raising cancer awareness on LIVESTRONG Day by enlisting the help of supporters through Facebook and Twitter. On October 2, for every person who adds the number “28” to their Facebook and Twitter profile pictures to support the 28 million cancer survivors around the world, RadioShack will donate $1 to LIVESTRONG up to $100,000.

RadioShack will also unveil a giant digital rendition of the “Team 28 Mosaic” in New York’s Times Square on LIVESTRONG Day for one day only. The mosaic is based on the iconic photograph of Lance taken at the final stage of the 2010 Tour de France. The Team 28 Mosaic is comprised of photos of all the Facebook and Twitter supporters who have tagged their profile photos with the Team 28 symbol (see #team28 or http://twb.ly/team-28 via Twitter). Video of the billboard at Times Square’s Military Island will be streamed live online during the day at http://team28.RadioShack.com, allowing supporters to view larger-than-life profile images on the digital mosaic as they are added.

Supporters are also encouraged to wear yellow, the universally recognized symbol of the fight against cancer, with Lance on LIVESTRONG Day to join in a global statement of strength and courage and show support for cancer survivors around the world. More than 7,000 people have already committed to wearing yellow on LIVESTRONG Day.

The impact of cancer around the globe is growing every day. The American Cancer Society and LIVESTRONG recently joined together to release a first-of-its-kind study on the economic cost of all causes of death globally, including cancer and other noncommunicable diseases and communicable diseases. The data from this study revealed that cancer has the most devastating economic impact of any cause of death in the world, costing the global economy nearly a trillion dollars a year.

LIVESTRONG Day is an opportunity for people from all walks of life to work toward the common goal of ensuring that cancer survivors around the world have the information, resources and support they need to live with strength and dignity.

“Today we have a powerful opportunity to change the way people think about cancer,” said Doug Ulman, LIVESTRONG President and CEO. “Every single person who joins the fight against cancer brings us closer to our goal of a world free from the disease.”

To learn more, visit www.LIVESTRONG.org.

About LIVESTRONG
Founded in 1997 by cancer survivor and champion cyclist Lance Armstrong and based in Austin, Texas, LIVESTRONG fights for the 28 million people around the world living with cancer today. LIVESTRONG connects individuals to the support they need, leverages funding and resources to spur innovation and engages communities and leaders to drive social change. Known for the iconic yellow wristband, LIVESTRONG‘s mission is to inspire and empower anyone affected by cancer.

Contact:
Rae Bazzarre
(512) 279-8367
[email protected]

Filed Under: Public Health and Research

Forbes Magazine Names Dr. Tom Tooma Leading U.S. Laser Eye Surgeon

Posted on October 1, 2010 Written by Editor

SOURCE: NVISION Laser Eye Centers

NEWPORT BEACH, CA–(Marketwire – October 1, 2010) –  NVISION Laser Eye Centers, formerly part of TLC Laser Eye Centers, announced today that Dr. Tom Tooma has been selected by Goldline Research as one of the leading Laser Eye Surgeons of the United States for 2010. The list of leading Laser Eye Surgeons of the United States was published this week in Forbes Magazine.

“It is a great honor to be selected by Goldline Research and to receive this distinction as one of only ten LASIK surgeons to be listed in Forbes Magazine in 2010,” said Dr. Tom Tooma, the Medical Director for NVISION Laser Eye Centers, formerly part of TLC Laser Eye Centers, and renowned eye surgeon who has performed more than 100,000 vision correction procedures.

“There are more than 10,000 laser eye surgeons in the United States. The practices that we selected provide outstanding patient care that exceeds the industry standard,” said Victoria Coryelle, Analyst, Goldline Research. “We believe that these practices are setting the benchmarks for patient service for the industry as a whole.”

Goldline Research, an independent, third-party research firm specializing in evaluating special services firms, undertook an extensive research process, including individual company interviews, qualitative analysis of company data and customer reference checks to determine high-quality patient care. Dr. Tom Tooma, NVISION Laser Eye Centers, was the only practice chosen in California due to his remarkable service and overall patient satisfaction in the industry.

About NVISION Laser Eye Centers
NVISION Laser Eye Centers, formerly part of TLC Laser Eye Centers, has eight locations throughout Southern California from San Diego to Camarillo. With more than 1,300 eye doctors who refer their patients and trust their own eyes to NVISION affiliate surgeons, we are the Eye Doctors’ #1 Choice, and serve the counties of San Diego, Los Angeles, Orange, Riverside, Ventura and San Bernardino. For more information, visit our new web site at www.NVISIONCenters.com or call 1-877-91NVISION (1-877-916-8474).

Contact:
Jennifer Heinly
J&J Consulting
949-716-9829 (w)
949-838-7335 (cell)
Email Contact

Click here to see all recent news from this company

Filed Under: Public Health and Research

New Mexico Scientific Laboratory Division Dedicates New State-of-the-Art Facility

Posted on October 1, 2010 Written by Editor

SOURCE: Association of Public Health Laboratories

SILVER SPRING, MD–(Marketwire – October 1, 2010) –  The Association of Public Health Laboratories (APHL) is proud to announce the dedication of the new comprehensive New Mexico public health laboratory. On September 29, 2010, the New Mexico Scientific Laboratory Division dedicated their beautiful, state-of-the-art facility which will double their space and greatly expand testing capabilities.

“This new laboratory is the crown jewel of state government,” said Arturo L. Jaramillo, cabinet secretary of the New Mexico General Services Department.

A LEED-certified green facility, this cutting edge laboratory boasts accreditations by numerous agencies. For the first time, the New Mexico public health laboratory will have onsite training facilities. Agreements have already been finalized with the Centers for Disease Control and Prevention to do Laboratory Response Network (LRN) training, the Food and Drug Administration for their dairy analyst training, and the University of New Mexico law school to teach new judges the scientific methods of DWI testing.

“It takes a special laboratory to help shape the future — a specially equipped facility staffed with highly qualified and trained experts, one like the laboratory here,” said APHL’s Executive Director, Scott Becker who attended the dedication. “Who knows — this new space could uncover the clues of some of our most pressing public health issues.”

This year marks the 90th anniversary of the New Mexico public health laboratory. From its origin in 1920 with one visionary employee in a one-room facility, the new building will house state-of-the-art clinical, environmental and forensic analytical services in support of public health across the state and nation.

Press tours of the new public health laboratory will take place on Friday, October 1, 2010.

The Association of Public Health Laboratories is a national non-profit located in Silver Spring, MD, that is dedicated to working with members to strengthen governmental laboratories with a public health mandate. By promoting effective programs and public policy, APHL strives to provide public health laboratories with the resources and infrastructure needed to protect the health of US residents and to prevent and control disease globally.

Contact:
Michelle M. Forman
Senior Media Specialist
240.485.2793
Email Contact

Click here to see all recent news from this company

Filed Under: Public Health and Research

GlobeImmune Announces Late-Breaker Oral Presentation of GI-5005 Prior Non-Responder Data at AASLD 2010 Meeting

Posted on October 1, 2010 Written by Editor

SOURCE: GlobeImmune, Inc.

Immunology Data Also to Be Presented in Poster Session

LOUISVILLE, CO–(Marketwire – October 1, 2010) –  GlobeImmune Inc. today announced that an abstract related to GI-5005, its Phase 2 investigational hepatitis C virus (HCV) product candidate, has been accepted for a late breaking oral presentation at the 61st Annual Meeting of the American Association for the Study of Liver Diseases (AASLD), which will take place October 29 through November 2, 2010, in Boston.

At the AASLD annual meeting, GlobeImmune will present end-of-study data, including sustained virologic response (SVR) rate from prior non-responders, from a Phase 2 clinical study investigating the safety and efficacy of GI-5005. The study compared GI-5005 plus peg-interferon (peg-IFN) and ribavirin, the current standard of care (SOC), versus SOC alone in patients with chronic type 1 hepatitis C infection. Prior non-responders were defined as those patients who did not achieve viral negativity by PCR after a minimum of 12 weeks of SOC. Patients that had achieved viral negativity by PCR during prior SOC but had relapsed during or after completion of SOC therapy were excluded from the study.

The abstract, titled “GI-5005 Therapeutic Vaccine Plus PEG-IFN/Ribavirin Improves Sustained Virologic Response Versus PEG-INF/Ribavirin in Prior Non-Responders With Genotype 1 Chronic HCV Infection,” is published online at the AASLD Web site.

Dr. Paul J. Pockros of Scripps Clinic is the lead author of the abstract that will be presented as part of a late breaker oral session beginning at 6 p.m. EDT on Monday, November 1, 2010 in the Hynes Auditorium. The presentation will include complete response and sustained virologic response rates for patients who received the GI-5005 plus SOC as well as SOC patients in the control arm of the study.

Additionally, Dr. John M. Vierling of Baylor College of Medicine will present a poster titled “GI-5005 Therapeutic Vaccine Improves Deficit in Cellular Immunity in IL28B Genotype T/T, Treatment-Naïve Patients with Chronic Hepatitis C Genotype 1 When Added to Standard of Care PEG-IFN-Alfa-2A/Ribavirin,” on Tuesday, November 2, 2010 in the Hynes Exhibit Hall C.

GI-5005 is a therapeutic vaccine candidate that the company believes generates HCV specific T-cell responses and improves virologic responses in patients with chronic hepatitis C infection. 

About GlobeImmune
GlobeImmune Inc. is a private company developing active immunotherapies called Tarmogens for the treatment of cancer and infectious diseases. Tarmogens generate activated killer T cells that are designed to locate and eliminate cancer cells and/or virally-infected cells. The Company’s lead product candidate, GI-5005, is a Tarmogen being developed for the treatment of chronic hepatitis C infection (HCV). GI-5005 is designed to complement both the current standard of care and emerging novel therapies for HCV. The Company’s lead oncology program, GI-4000, targets cancers caused by mutated versions of the Ras oncoprotein. GI-4000 is being investigated in clinical trials for the treatment of pancreas cancer as well as other cancers that contain mutated Ras, including non-small cell lung cancer and colorectal cancer. In May 2009, the Company announced a global partnership with Celgene focused on the discovery, development and commercialization of multiple product candidates for the treatment of cancer.

For additional information, please visit the company’s Web site at www.globeimmune.com.

This news release and the anticipated presentation contain forward-looking statements that involve risks and uncertainties, including statements relating to initiation and progress of the Company’s clinical trial programs and the results from the clinical trials. Actual results could differ materially from those projected and the Company cautions readers not to place undue reliance on the forward-looking statements contained in the release and anticipated presentation.

Filed Under: Hospitals and Health Systems, Public Health and Research

Discovery and Validation of 13 Diabetes Biomarkers to Be Commercialized

Posted on September 30, 2010 Written by Editor

SOURCE: Proteomics International

Findings Announced at the Human Proteome Organisation’s World Congress in Sydney, Australia

PERTH, AUSTRALIA–(Marketwire – September 29, 2010) –  After three years of collaborative research involving patients from The Busselton Health Study, drug discovery company Proteomics International announced the identification and analytical validation of 13 protein biomarkers for a significant complication of diabetes — diabetic nephropathy (kidney disease). In a presentation at the Human Proteome Organisation’s World Congress in Sydney, Australia, Dr. Richard Lipscombe, Managing Director of Proteomics International, revealed the findings that could benefit many of the 250 million people worldwide who have diabetes.

“Applying our uniquely accredited proteomics biomarker expertise to patient samples (plasma) from the Busselton Health Study and the Fremantle Diabetes Study allowed us to analyze three well characterized clinical cohorts of selected disease groups (adults who had Type II diabetes and diabetic nephropathy),” said Dr. Lipscombe. “The protein biomarkers that we found could now allow for the prediction of those patients who would progress to the development of kidney disease and provide new targets for drug therapies that prevent the onset of this serious complication.“

Proteomics International is actively seeking partners to further qualify and commercialize its patented diabetes biomarker portfolio.

The protein biomarker discovery and validation approach included the analysis of pooled plasma samples for differential protein expression, i.e. proteins that are found at different levels in the diabetic disease state relative to the normal diabetic state. Candidate biomarkers were identified from iTRAQ labelled samples by 2D-LC MALDI TOF/TOF mass spectrometry, an emerging technique in proteomics. This discovery phase identified 130-200 proteins per cohort and across all studies over 50 proteins showed significant differences in concentrations. Biomarker candidates were validated in a second approach using the advanced mass spectrometry technique Selected or Multiple Reaction Monitoring (SRM/MRM) to carry out concentration analysis on individual patient plasma samples. Statistical data analysis of the validation phase identified 13 putative protein biomarkers for diabetic nephropathy across the studies, including proteins involved in metabolism, inflammation and oxidative stress. The complexity of the diabetic kidney disease suggests that there would not necessarily be one biomarker but a set of biomarkers (signature) in varying degrees to characterize the diabetic nephropathy state. These biomarkers can be used as diagnostic tools or new drug targets.

About Proteomics International Pty Ltd
Proteomics International is both a drug discovery company and contract research service provider. Proteomics International combines the most advanced high throughput mass spectrometry instrumentation (MALDI TOF-TOF and LC-MS/MS) and a team of qualified scientists with proven expertise in protein and peptide chemistry. Proteomics International is the only company globally to achieve laboratory accreditation to International Standard ISO/IEC 17025:2005 for provision of proteomics services. The accreditation is a widely used benchmark for US Federal testing facilities and strengthens the company’s licensing position to deliver drug development data that is of the highest scientific integrity. The company has two focal research activities: new peptide drugs from venoms, and the discovery and use of biomarkers; both analyses build upon its proprietary transformative Bioven process.

Filed Under: Public Health and Research

Sunlight Research Analyzes Impact of iPSC Patent Activity on Stem Cell Research

Posted on September 28, 2010 Written by Editor

SOURCE: Sunlight Research, LLC

Live Webcast From World Stem Cell Summit in Detroit, Oct. 6, 2010, to Highlight Key Findings of Sunlight’s Induced Pluripotent Stem Cell Patent Report

MINNEAPOLIS, MN–(Marketwire – September 28, 2010) – Sunlight Research™ — The Source for Patent Analysis www.SunlightResearch.com, today announced the October 6, 2010 release of its Induced Pluripotent Stem Cell Patent Report analyzing this important stem cell technology segment. 

Stem cells have the remarkable potential to replace and rejuvenate injured, diseased and aging tissues. With the development of induced pluripotent stem cell (iPSC) technologies, differentiated cells with the exact genetic and immunological properties of a selected patient’s cells can be reprogrammed to be stem cells, thereby eliminating problems of immunological rejection and viral contamination.

“Induced pluripotent stem cells may be developed for treatment of a multitude of diseases, including cardiovascular and neurological conditions” says Robin A. Chadwick, PhD, JD, a patent attorney and lead author of Sunlight’s iPSC Patent Report. “In addition, iPSCs can end long waiting periods for organ transplants, and the use of immunosuppression drugs in transplant recipients. The process,” she explains, “could be as simple as mixing a few cells from a patient with a [patented] cocktail of biological molecules, letting the cells grow up, and then injecting them into the patient.”

Daniel A. Halpern, President of Sunlight Research, noted that “iPSCs represent a real game-changing technology, and one of the most exciting segments of the rapidly growing stem cell market.” The overall global stem cell market is projected to reach $2.6 billion by 2012, and to exceed $5.1 billion by 2014, according to estimates by Business Insights, a market research firm. Other estimates show considerably larger global market forecasts. “The gold rush is on,” Mr. Halpern added, “and many businesses and research institutions are staking claims to various aspects of iPSC technology, as evidenced by patent filings and issuances. Our mission is to shed light on these boundary-setting activities so that all stakeholders can make better decisions.” 

Webinar October 6, 2010
The webinar, which will be webcast live from the World Stem Cell Summit in Detroit, is scheduled for 12:00pm EDT on Wednesday, October 6, 2010 and will highlight key findings of Sunlight’s comprehensive claims-level analysis of the iPSC patent landscape, including issued patents and pending patent applications. Registration and report details are available online at iPSC Patent Report.

About Sunlight Research, LLC
Sunlight Research™ is the premier source for up-to-date Reports, Webinars and Educational Events concerning Patent Claims Coverage, Intellectual Property Market Research, Non-Practicing Entity (“Troll”) Patent Reports and Interactive Freedom-To-Operate databases. Sunlight provides timely, in-depth and actionable patent analyses that are easily accessible and cost effective. A key feature of many Sunlight reports is an interactive freedom-to-operate tool, which allows customers to rapidly test various product designs for infringement against relevant patents. Sample reports are available at www.SunlightResearch.com

Register Today
iPSC Patent Report.

About the World Stem Cell Summit
The summit will attract more than 1,000 attendees from 30 nations, 60 exhibitors and more than 200 endorsing organizations and media partners. The largest and most comprehensive multi-track stem cell conference, the Summit features more than 150 international speakers and 50 hours of in-depth science, business and society presentations. www.worldstemcellsummit.com.

Keywords: Induced Pluripotent Stem Cells, iPSCs, stem cell patent, biotech, biotechnology, world stem cell summit, claims, transplants

Sunlight Research, LLC.
900 2nd Avenue S., #490
Minneapolis, MN 55402 U.S.A.
Email Contact
612-977-1713 -extension #3

Click here to see all recent news from this company

Filed Under: Public Health and Research

Radient Pharmaceuticals Signs 5-Year Exclusive Distribution Agreement for Its Onko-Sure Cancer Test in Vietnam, Cambodia, and Laos

Posted on September 28, 2010 Written by Editor

SOURCE: Radient Pharmaceuticals Corporation

TUSTIN, CA–(Marketwire – September 28, 2010) –  Through its subsidiary AMDL Diagnostics Inc., Radient Pharmaceuticals Corporation (NYSE Amex: RPC), a US-based company specializing in the research, development, and international commercialization of In Vitro Diagnostic (IVD) cancer tests, announced today it has entered into an exclusive 5-year full-service distribution agreement with Phu Gia Trading Co. Ltd. to expand the Company’s Onko-Sure™ IVD cancer test into the Vietnam, Laos, and Cambodia healthcare markets.

Phu Gia has committed to purchase a minimum of 2,425 Onko-Sure™ kits over the duration of the agreement.  Phu Gia Trading Co. Ltd. will represent RPC while obtaining regulatory clearances and providing marketing, sales, and distribution services for Onko-Sure in diagnostic centers and clinical labs throughout the designated territory. Marketing, sales and distribution services include developing product localization strategies; representing Radient Pharmaceuticals and its Onko-Sure IVD cancer test at relevant healthcare conferences and events; and ensuring all relevant product marketing materials are available in local languages. The Phu Gia customer service team will also be responsible for responding to customer inquiries and technical questions. Phu Gia will work directly with the Vietnam Ministry of Health and other government officials to secure approvals and regulatory clearances.   

“Our full-service distribution partnership with Radient allows us to work closely with top diagnostic centers and clinical labs in Vietnam, and reach healthcare professionals across the designated territories of Vietnam, Cambodia and Laos. Cancer continues to be one of our gravest healthcare challenges and Onko-Sure offers a valuable new tool for cancer detection and cancer treatment monitoring,” commented Jack Nguyen, President, Phu Gia. “We plan to commit extensive outreach resources to oncology thought leaders along with automating the Onko-Sure test at top labs — including the Ho Chi Minh Diagnostic Centre, to increase cancer testing across our region.”

“With a significant cancer challenge, Asia continues to show an increased demand for cancer diagnostic products like Onko-Sure,” commented Mr. Douglas MacLellan, Executive Chairman and CEO of RPC. “Phu Gia becomes our third distribution partner for Onko-Sure in the rapidly expanding Asia healthcare market, and we feel confident in our ability to gain strong market share throughout the region as we establish long-term agreements with well positioned partners like Phu Gia.”

Onko?Sure is a simple, non?invasive, patent?pending and regulatory?approved in vitro diagnostic test that enables physicians and their patients to effectively monitor and/or detect certain types of cancers by measuring the accumulation of specific breakdown products in the blood called Fibrin and Fibrinogen Degradation Products (FDP). FDP levels rise dramatically with the progression of cancer. Onko?Sure is approved by the US FDA for the monitoring of colorectal cancer and by Health Canada for lung cancer detection and treatment monitoring. 

RPC Contact Information:
For additional information on Radient Pharmaceuticals, ADI and its portfolio of products visit the Company’s corporate website at www.radient-pharma.com. For Investor Relations information contact Kristine Szarkowitz at [email protected] or 1.206.310.5323.

About Radient Pharmaceuticals:
Headquartered in Tustin, California, Radient Pharmaceuticals is dedicated to saving lives and money for patients and global healthcare systems through the deployment of our Onko Sure™ In Vitro Diagnostic cancer test. Our focus is on the discovery, development and commercialization of unique high-value diagnostic tests that help physicians answer important clinical questions related to early disease detection; treatment strategy; and the monitoring of disease progression, prognosis, and diagnosis to ultimately improve outcomes for patients. Radient Pharmaceutical’s current Onko-Sure™ cancer test is used to guide decisions regarding patient treatment, which may include decisions to refer patients to specialists, perform additional testing, or assist in the selection of therapy. To learn more about our company, people and potentially life-saving cancer test, visit www.radient-pharma.com. 

Forward Looking Statements:
Safe Harbor Statement under the Private Securities Litigation Reform Act of 1995: The statements contained in this document include certain predictions and projections that may be considered forward-looking statements under securities law. These statements involve a number of important risks and uncertainties that could cause actual results to differ materially including, but not limited to, the performance of joint venture partners, as well as other economic, competitive and technological factors involving the Company’s operations, markets, services, products, and prices. With respect to Radient Pharmaceuticals Corporation, except for the historical information contained herein, the matters discussed in this document are forward-looking statements involving risks and uncertainties that could cause actual results to differ materially from those in such forward-looking statements.

Contact:
Kristine Szarkowitz
Director-Investor Relations
Email Contact
(Tel : ) 206.310.5323

Click here to see all recent news from this company

Filed Under: Prescription Drugs and Pharmacy, Public Health and Research

American Diabetes Association Announces Second Annual John Pipe Voices For Change Award Winners

Posted on September 24, 2010 Written by Editor

SOURCE: American Diabetes Association

Recipients Celebrated for Their Achievements in Diabetes Treatment and Prevention

SIOUX FALLS, SD–(Marketwire – September 24, 2010) –  The American Diabetes Association, the nation’s leading voluntary health organization in the fight against diabetes, announces several leading Special Diabetes Program for Indians (SDPI) grantees presented with the John Pipe Voices For Change Award in recognition of their effective diabetes treatment and prevention services in American Indian and Alaskan Native communities. The awards were presented at the National Indian Health Board’s 27th Annual Consumer Conference on Wednesday, September 22nd in Sioux Falls, South Dakota. 

“At nearly 17%, Alaska Natives have the highest age-adjusted prevalence of diabetes among all U.S. racial and ethnic groups,” said Gale Marshall, Chair of the American Diabetes Association’s Awakening the Spirit Native American initiative. “The John Pipe Voices For Change awards give us the opportunity to honor selected programs for their outstanding achievements in the delivery of diabetes prevention and treatment services in tribal communities. By showcasing these programs we are also acknowledging over 450 SDPI programs and their valuable efforts to stop diabetes.”

The name of these awards was changed to honor long-time diabetes supporter John Pipe of Wolf Point, Montana, who passed away earlier this year. Pipe was a dedicated diabetes advocate and served as a member of the Awakening the Spirit Subcommittee. His longstanding advocacy efforts reached from his local community to Washington, DC and impacted countless tribal communities. 

The 2010 John Pipe Voices For Change Award recognizes SDPI programs that have excelled in the following categories: Advocacy, Outcomes, and Innovation.

Advocacy Award:
Hualapai Healthy Heart Program
Peach Springs, Arizona
The Hualapai Healthy Heart Program is an SDPI funded demonstration project designed to reduce cardiovascular disease, the most compelling complication of diabetes among their participants. They have engaged their greater community in a variety of successful advocacy efforts having a local, regional and national impact.

Outcomes Award:
Bristol Bay Area Health Corporation (BBAHC)
Dillingham, Arkansas
BBAHC Diabetes Prevention/Lifestyle Change Program provides a comprehensive array of programs in effort to prevent diabetes or diabetes related complications spanning 34 villages within the Bristol Bay region. Programs work on improving individuals’ rates of diabetes, nutrition and exercise education, as well as lowering blood pressure.

Innovation Award:
Tuba City Diabetes Treatment and Prevention
Tuba City, Arizona
The Department of Diabetes Treatment and Prevention Services at the Tuba City Regional Health Care Corporation (TCRHCC) has employed innovative approaches that have resulted in community wide collaborations to effectively provide diabetes prevention and treatment services.

Honorable Mentions:

Advocacy Honorable Mention:

  • Native American Rehabilitation Association of the Northwest (NARA) Diabetes Treatment & Prevention Program (Portland, Oregon)
  • Cow Creek Health & Wellness Center (Roseburg, Oregon)

Outcomes Honorable Mentions:

  • SDPI Diabetes Prevention Program Warm Springs Health and Wellness Center Indian Health Services (Warm Springs, Oregon)
  • American Indian Health and Family Services (AIHFS) Diabetes Program (Detroit, Michigan) 

Innovation Honorable Mention:

  • Chickasaw Nation Division of Health (Ada, Oklahoma)

The SDPI continues to give Indian health programs and tribal communities the resources and tools they need to both prevent and treat diabetes. It funds more than 450 community directed programs, offering local tribes and health programs the opportunity to set priorities that meet the needs of the community, whether it be prevention activities or treatment. For over a decade Congress has provided funding for the SDPI and the American Diabetes Association has played an integral part in promoting this important program. The Association will continue to work for strong support of SDPI.

The American Diabetes Association is leading the fight to stop diabetes and its deadly consequences and fighting for those affected by diabetes. The Association funds research to prevent, cure and manage diabetes; delivers services to hundreds of communities; provides objective and credible information; and gives voice to those denied their rights because of diabetes. Founded in 1940, our mission is to prevent and cure diabetes and to improve the lives of all people affected by diabetes. For more information please call the American Diabetes Association at 1-800-DIABETES (1-800-342-2383) or visit www.diabetes.org. Information from both these sources is available in English and Spanish.

Contact:
Colleen Fogarty
[email protected]

id=”nav_links”>

Filed Under: Healthcare Business, Public Health and Research

MMRGlobal Prevails in Biotech Assets Case With Lymphoma Research Foundation

Posted on September 24, 2010 Written by Editor

SOURCE: MMRGlobal, Inc.

LOS ANGELES, CA–(Marketwire – September 24, 2010) –  MMRGlobal, Inc. (OTCBB: MMRF) (MMR) announced today that it has successfully opposed a Summary Judgment Motion brought by the Lymphoma Research Foundation (LRF) as part of its efforts to protect a portion of the Company’s intellectual property, which it previously disclosed on May 3, 2010.

The Company acquired the biotech assets from its reverse merger with Favrille, Inc., a San Diego biotech company, in January 2009. Over the past year, MMR identified a collection of these biotech assets, which include biotech samples that were in the possession of the Lymphoma Research Foundation. They do not include other pre-merger biotech assets, including the Company’s anti-CD20 monoclonal antibodies, results of clinical trials data, patents and other intellectual property.

According to declarations filed on behalf of MMR, the Company understands that the biotech samples could have a value as high as $1.376 million. However, based on other information currently maintained by the Company, the samples could have a far greater value, depending on the extent and depth of the clinical data collected at trial initiation, the extent and depth of the clinical data collected during patient follow-up, whether follow-up tissue samples are available, and whether accompanying whole blood or serum is available from patients from trial enrollment or during trial progression.

Robert H. Lorsch, Chairman and CEO of MMRGlobal, said, “We are pleased by this early ruling. When combined with clinical data from the Company’s vaccine research into the causes and potential treatment of B-Cell Non-Hodgkin’s Lymphoma, including data from patient follow-ups which the Company has, the value could be significant.”

The Company understands its intellectual properties may also be of value in a possible reinterpretation of the pre-merger Favrille vaccine trials and that the IP may also unlock ways to create other “custom-made” cancer vaccines and be valuable in discovering additional opportunities in cancer research. The Company hopes to enter into licensing agreements with biopharmaceutical companies, academic institutions, research organizations and others regarding the use of its assets.

About MMRGlobal, Inc.
MMR Global, Inc., through its wholly-owned operating subsidiary, MyMedicalRecords, Inc. (“MMR”), provides secure and easy-to-use online Personal Health Records (“PHRs”) and electronic safe deposit box storage solutions, serving consumers, healthcare professionals, employers, insurance companies, financial institutions, and professional organizations and affinity groups. MyMedicalRecords enables individuals and families to access their medical records and other important documents, such as birth certificates, passports, insurance policies and wills, anytime from anywhere using the Internet. The MyMedicalRecords Personal Health Record is built on proprietary, patented technologies to allow documents, images and voicemail messages to be transmitted and stored in the system using a variety of methods, including fax, phone, or file upload without relying on any specific electronic medical record platform to populate a user’s account. The Company’s professional offering, MMRPro, is designed to give physicians’ offices an easy and cost-effective solution to digitizing paper-based medical records and sharing them with patients in real time through an integrated patient portal. MMR is an Independent Software Vendor Partner with Kodak to deliver an integrated turnkey EMR solution for healthcare professionals. MMR is also an integrated service provider on Google Health. To learn more about MMR Global, Inc. and its products, visit www.mmrglobal.com.

Forward-Looking Statements
Statements in this press release that are not strictly historical in nature constitute “forward-looking statements.” Such statements include, but are not limited to, statements regarding MMRGlobal, Inc.’s assets including but not limited to its primary Health IT businesses, samples and data from vaccine and clinical trials, and anti-CD20 antibody assets. Such forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause actual results to be materially different from historical results or from any results expressed or implied by such forward-looking statements. These factors include, but are not limited to, risks and uncertainties related to the development and approval of biotechnology/biopharmaceutical product candidates and Health IT products and additional risks discussed in the Company’s filings with the Securities and Exchange Commission. All subsequent written and oral forward-looking statements attributable to the Company (or any person acting on the Company’s behalf) are qualified by the cautionary statements in this notice. MMRGlobal, Inc. is providing this information as of the date of this release and, except as required by law, does not undertake any obligation to update any forward-looking statements contained in this release as a result of new information.

CONTACT:

Michael Selsman
Public Communications Co.
(310) 553-5732
[email protected]

Click here to see all recent news from this company

Filed Under: Prescription Drugs and Pharmacy, Public Health and Research

Lance Armstrong Applauds Efforts to Ensure Affordable Health Care for Children

Posted on September 23, 2010 Written by Editor

SOURCE: LIVESTRONG

Armstrong Joined by American Cancer Society CEO John Seffrin at Special Visit to Children’s National Medical Center

WASHINGTON, DC–(Marketwire – September 23, 2010) –  Today, Lance Armstrong, LIVESTRONG(R) founder and chairman, cancer survivor and champion cyclist, made a surprise visit to the pediatric oncology unit at Children’s National Medical Center. He was joined by John R. Seffrin, PhD, chief executive officer of the American Cancer Society, to meet with hospital administrators, doctors and young patients and their families.

Today marks the six month anniversary of the Affordable Care Act. Starting today, several critical provisions of the law begin to take effect. Under the new law, healthcare plan providers cannot discriminate against children with pre-existing conditions. More than nine million children in the United States are currently living without health insurance. Up to 72,000 uninsured children with pre-existing conditions could gain coverage as a result of the new reform.

“Parents already feel the weight of the world on their shoulders when a child is diagnosed with cancer,” said Armstrong. “Insurance and health costs shouldn’t serve as a barrier to receiving quality, timely treatment. I’m hopeful that this reform will save lives and improve the quality of life for the more than 270,000 childhood cancer survivors currently living in the United States.”

“The Affordable Care Act is providing critical protections that are expanding access to lifesaving health care to children and adults with cancer or at risk of cancer,” said Seffrin. “Important provisions taking effect today prohibit health plans from denying coverage to children up to age 19 with pre-existing conditions such as cancer, and enable dependent children to remain on their parent’s insurance policy up to age 26.”

“With advances and breakthroughs in therapy, approximately 75% of children with cancer are cured of their disease. Nevertheless, cancer remains the leading cause of non-accidental death in children in the United States and many survivors suffer from chronic conditions that result from their treatment. Children’s National Medical Center is proud to be a leader in the search for novel treatments that will increase cure rates while decreasing adverse effects,” said Jeffrey S. Dome, MD, PhD; Chief, Division of Oncology; Center for Cancer and Blood Disorders; Children’s National Medical Center.

Armstrong’s visit also falls during National Childhood Cancer Awareness Month, a time to increase awareness and encourage support for the children and families affected by the disease. Cancer is currently the leading cause of death by disease among U.S. children between infancy and age 15, and it is estimated that 10,730 new cases of pediatric cancer were diagnosed in children 0-14 years of age in 2009. Two-thirds of childhood cancer survivors face at least one chronic health condition later in life and one quarter of survivors face a late effect from treatment that is severe or life threatening.

LIVESTRONG, the organization Armstrong established to support fellow cancer survivors and their families, offers a multitude of resources to help pediatric cancer survivors and their families manage the long-term effects of childhood cancers. The organization recently helped establish the LIVESTRONG Childhood Cancer Survivorship Center at Dell Children’s Medical Center in Austin, Texas. The Center aims to improve the health and well-being of childhood cancer survivors by promoting adherence to a schedule of follow-up appointments; providing referrals to specialists; offering psychosocial support groups; transitioning patients to adult care when they are ready; and educating patients, parents and healthcare professionals about the long-term effects of cancer treatment.

LIVESTRONG SurvivorCare also offers specialized resources that focus on the needs of cancer survivors, including children. The free resource, available in English and Spanish, provides survivors and their families with emotional support; individual counseling; financial and legal advice, including finding assistance for the uninsured or underinsured; and matching to clinical trials.

About LIVESTRONG
Founded in 1997 by cancer survivor and champion cyclist Lance Armstrong and based in Austin, Texas, LIVESTRONG fights for the 28 million people around the world living with cancer today. LIVESTRONG connects individuals to the support they need, leverages funding and resources to spur innovation and engages communities and leaders to drive social change. Known for the iconic yellow wristband, LIVESTRONG‘s mission is to inspire and empower anyone affected by cancer. For more information, visit www.LIVESTRONG.org.

About Children’s National Medical Center
Children’s National Medical Center in Washington, DC, has been serving the nation’s children since 1870. Home to Children’s Research Institute and the Sheikh Zayed Institute for Pediatric Surgical Innovation, Children’s National is consistently ranked among the top pediatric hospitals by U.S. News & World Report and the Leapfrog Group. With 283 beds, more than 1,330 nurses, 550 physicians, and seven regional outpatient centers, Children’s National is the only exclusive provider of pediatric care in the Washington metropolitan area. Children’s National has been recognized by the American Nurses Credentialing Center as a Magnet® designated hospital, the highest level of recognition for nursing excellence that a medical center can achieve. For more information, visit www.ChildrensNational.org.

Contact:
Rae Bazzarre
(512) 279-8367
[email protected]

Filed Under: Health Insurance Coverage, Public Health and Research

Symetis Reports on Its Trans-Apical ACURATE TA(TM) First-in-Man Clinical Study

Posted on September 23, 2010 Written by Editor

SOURCE: Symetis

LAUSANNE, SWITZERLAND–(Marketwire – September 23, 2010) –  

  • 40 patients enrollment completion
  • Positive preliminary results

Symetis SA, a private Swiss company developing new transcatheter aortic valve implantation (TAVI) systems, announced today the completion of patient enrollment in its ACURATE TA™ first-in-man (FIM) clinical study and positive preliminary results. ACURATE TA™ is a self-aligning nitinol stent valve designed for optimal trans-apical delivery, providing the physician with unmatched positioning tolerance and ease of use.

Details of the study
The study — the largest 2nd generation TAVI FIM study ever conducted — was conducted at 5 sites in Germany: Leipzig Herzzentrum, Kerckhoff-Klinik Bad Nauheim, Freiburg UniversitätsSpital, Westdeutsches Herzzentrum Essen and Universitäres Herzzentrum Hamburg. Forty (40) patients with severe aortic stenosis were recruited and treated with ACURATE TA™. The average age of treated patients was 83 years with a mean Logistic EuroScore of 21.5% and STS Score of 9.0%.

Results
Successful valve implantation with the ACURATE TA™ occurred in 38 patients (95.0%). One patient received a valve-in-valve using a commercially available transapical valve and one patient was converted to sAVR. Only one patient required a new pacemaker post-implant. 30-day mortality was 12.5% including 3 deaths from non-valve-related respiratory complications. Comprehensive 30-day results will be presented at the Dallas / Leipzig International Valve conference in December 2010.

Dr. Joërg Kempfert of Leipzig Herzzentrum commented: “The ACURATE TA™ is truly intuitive, easy to use, reliable and covers the full spectrum of severe aortic stenosis. We look forward to the Pilot study to confirm the excellent results obtained in this comprehensive FIM study.”

Laura Brenton, VP Clinical / Regulatory Affairs, added: “The ease of use of the ACURATE TA™ was acknowledged by all physicians participating in the study. Additionally, the learning curve was significantly shorter than that of competitive systems. Furthermore, the robust size of the FIM allows for comparison of its initial data to published statistics from competitors suggesting comparable or improved initial outcomes.”

Jacques R. Essinger, CEO of Symetis, added: “ACURATE™ TA is the second generation TAVI system with the largest clinical experience to date. We are building on this competitive advantage by soon beginning a pilot clinical study, a major step toward achieving European compliance and the CE mark.”

About Symetis
Symetis SA (www.symetis.com) is a private Swiss company developing innovative, minimally invasive heart valve replacement solutions. Symetis’s Acurate TA™ system, based on proprietary geometry and delivery technology, is in clinical trials and is well positioned to target the ca. $2 billion transcatheter aortic valve implantation (TAVI) market. The company is financed by leading European venture capital firms including Truffle Capital, Novartis Venture Fund, Aravis Venture, Wellington Partners, Vinci Capital, Banexi Venture and BiomedInvest.

For further information, please contact:
Dr. Jacques R. Essinger
CEO
Symetis SA
Tel: +41 21 651 01 60
Email: Email Contact

US Media
Michelle Linn
Linnden Communications
508-362-3087
Email Contact

Filed Under: Hospitals and Health Systems, Public Health and Research

Media Alert: An Important Update on Stem Cell Research in Toronto

Posted on September 22, 2010 Written by Editor

TORONTO, ONTARIO–(Marketwire – Sept. 22, 2010) –

Attention: Health and Science Reporters, Assignment and Photo Editors. 

On September 23 2010, media are invited to an in-depth briefing with senior scientists on current stem cell research activity at the McEwen Centre for Regenerative Medicine. McEwen Centre Director, Dr. Gordon Keller will discuss eight “Accelerated Discoveries.” These are research initiatives that include a new project that will push the frontier forward for patients suffering from heart disease, the number one killer in the western world. 

Research at the McEwen Centre also holds important implications for diabetes, lung disease, diseases of the blood as well as neurodegenerative disease.

Please join us to learn more about this exciting research field. The tour will include an opportunity to interview senior scientists and gain new understanding of the latest developments in this cutting edge research. You are also invited to attend a Public Symposium on The Stem Cell Healthcare Revolution which follows the tour at 1:30 p.m. to 3:30 p.m.

Telephone interviews with senior scientists, the McEwens, and patient advocates can be arranged in advance.

Filed Under: Public Health and Research, Senior Care

UV Flu Technologies UV-400 Air Purifier Fights Superbugs and Bacteria

Posted on September 22, 2010 Written by Editor

SOURCE: UV Flu Technologies, Inc.

CENTERVILLE, MA–(Marketwire – September 22, 2010) –  UV Flu Technologies, Inc. (OTCBB: UVFT) (the “Company”) announced today that in response to recent outbreaks of drug resistant superbugs such as NDM-1, and persistent occurrences of highly contagious strains of bacteria such as MRSA, the Company is implementing a national campaign to inform the public how its ViraTech UV-400 indoor air purifier significantly helps reduce exposure risks.

Dr. Wladyslaw Jan Kowalski, PE, Phd, a world leading expert on the bacteria killing efficacy of ultraviolet light, recently commented on the UV-400: “Ultraviolet germicidal irradiation (UVGI) destroys bacteria by damaging the nucleic acids and thereby preventing reproduction. Multidrug-resistant microbes (superbugs) may have resistance to antibiotics but they remain as susceptible to ultraviolet radiation as any normal bacteria variant. The number of multidrug resistant microbes has been increasing, apparently due to overuse of antibiotics and other factors, and is expected to pose a serious challenge to health care facilities in the future as treatment options diminish.”

Dr. Kowalski further added, “The ViraTech UV-400 model air cleaner has a demonstrated ability to disinfect air and inactivate a wide range of bacterial pathogens including Staphylococcus aureus (MRSA), Pseudomonas, and Klebsiella as has been conclusively demonstrated in independent laboratory tests. The UV-400 produces a germicidal UV exposure dose of 41 J/m2, as independently verified by biodosimetric testing, which is sufficient to reduce pathogenic bacterial populations by at least 99%. This disinfection rate will apply regardless of the multidrug resistance of bacteria such as those that may contain the NDM-1 enzyme (the superbug gene). The ViraTech UV-400 unit provides a viable option for health care facilities struggling to cope with the growing problem of multidrug resistant organisms and this technology can serve as an adjunct to existing infection management procedures and disinfection protocols wherever the potential exists for microorganisms to spread by the airborne route.”

“Our Company receives reports from around the world on an almost daily basis about the growing problems connected with the spread of these increasingly drug resistant bacterial strains,” said Jack Lennon, President of UV Flu Technologies. “Antibiotics have become so pervasive in today’s medical therapies, that not only are they becoming less effective, but their overuse is increasingly being considered as part of the problem. Drug-resistant superbugs have now been found in 20 states, as well as worldwide, and when they hit the critically ill, they can be fatal 30-60% of the time. In one recent incident at an infant ward at the University College Hospital in London, 15 babies in the unit were found to be carrying several types of bacteria, including 13 who had bacterial superbugs resistant to treatment. Of four babies seriously infected, one survived.”

“So that the public can participate in actions to help reduce the spread of these strains, the Company has committed to advertising, including television and other media in order to educate consumers and to offer help where needed,” said Mr. Lennon. “We are looking to develop a plan to offer our UV-400 indoor air quality units either free or at significantly discounted costs to those schools and hospitals that suffer from serious outbreaks. We hope to partner with institutions which are genuinely interested in working with us in order to develop an action plan for their facilities. For those with respiratory problems or weakened immune systems, hospital or institution acquired bacterial infections can prove deadly. We believe our product delivers an immediate, effective and proven ability to kill at least 99% of airborne bacteria thereby reducing the risk of infection.”

Further details regarding the Company’s business, financial reports and agreements are filed as part of the Company’s continuous public disclosure as a reporting issuer under the Securities Exchange Act of 1934 filed with the Securities and Exchange Commission’s (“SEC”) EDGAR database.

About UV Flu Technologies, Inc. (OTCBB: UVFT)
UV Flu Technologies is an innovative developer, manufacturer and distributor of bio technology products initially targeting the rapidly growing Indoor Air Quality (“IAQ”) industry sector. The Company manufactures the ViraTech UV-400, which utilizes high-intensity germicidal ultraviolet radiation (UV-C) inside a killing chamber that goes beyond filtration to destroy harmful airborne bacteria at rates exceeding 99.2% on a first-pass basis. VIRATECH UV-400 is a Class II medical device and is available without a prescription. 

Notice Regarding Forward-Looking Statements
This news release contains “forward-looking statements” as that term is defined in Section 27A of the United States Securities Act of 1933, as amended and Section 21E of the Securities Exchange Act of 1934, as amended. Statements in this press release which are not purely historical are forward-looking statements and include any statements regarding beliefs, plans, expectations or intentions regarding the future. Such forward-looking statements include, among other things, the development, costs and results of new business opportunities. Actual results could differ from those projected in any forward-looking statements due to numerous factors. Such factors include, among others, the inherent uncertainties associated with new projects and development stage companies. These forward-looking statements are made as of the date of this news release, and we assume no obligation to update the forward-looking statements, or to update the reasons why actual results could differ from those projected in the forward-looking statements. Although we believe that any beliefs, plans, expectations and intentions contained in this press release are reasonable, there can be no assurance that any such beliefs, plans, expectations or intentions will prove to be accurate. Investors should consult all of the information set forth herein and should also refer to the risk factors disclosure outlined in our annual report on Form 10-K for the most recent fiscal year, our quarterly reports on Form 10-Q and other periodic reports filed from time-to-time with the Securities and Exchange Commission.

ON BEHALF OF THE BOARD

UV Flu Technologies, Inc.
—————————–
John J. Lennon, President & CEO

Investor Information:
Geaux IR Services, Inc.
Toll-Free: 1-888-355-8838
Email Contact

Click here to see all recent news from this company

Filed Under: Public Health and Research

  • « Previous Page
  • 1
  • 2
  • 3
  • 4
  • 5
  • 6
  • …
  • 8
  • Next Page »

Search Our Site

Categories

  • Blue Cross Blue Shield
  • Health Insurance Companies
  • Health Insurance Coverage
  • Health Technology and AI
  • Healthcare Business
  • Healthcare Policy and Law
  • Hospitals and Health Systems
  • Medicaid and CHIP
  • Medicare
  • Prescription Drugs and Pharmacy
  • Public Health and Research
  • Senior Care

Entity Map

Disclaimer

All content on Health Plan News and information provided on this website is for informational purposes only and is not intended as a substitute for advice from your physician or other healthcare professional. You should not use the information on this site for diagnosis or treatment of any health problem or for prescription of any medication or other treatment. Always consult with a healthcare professional before starting any diet, exercise, or supplementation program, before taking any medication, or if you have or suspect you might have a health problem.

Copyright © 2026 - Privacy Policy - Terms of Use - Disclaimer