Avandia Search Engine Blog

Information on the Avandia Search Engine which indexes selected sites that offer medical and legal information on the diabetic drug Avandia which was found to cause heart attacks and other heart-related health problems.

Wednesday, May 28, 2008

$250 Million Damages in Boston Scientific Patent Case Awarded To Medtronic

Medtronic Awarded $250 Million Damages in Patent Case against Boston Scientific

Federal jury in Marshall, Texas, finds that Boston Scientific Corporation infringed three patents owned by Medtronic

MINNEAPOLIS-- May 27, 2008 --Medtronic, Inc. (NYSE: MDT) today announced that a federal jury found that Boston Scientific Corporation has infringed three patents owned by Medtronic, and awarded Medtronic $250 million in damages.

Medtronic sued Boston Scientific in 2006 asserting that Boston's Taxus Express2, Express2, Liberte, Maverick, Maverick2, and Quantum Maverick products infringed the Fitzmaurice and Anderson catheter patents owned by Medtronic. The trial began on Friday, May 16, 2008.

The Fitzmaurice patents cover angioplasty catheters with narrowed distal ends, which improve the deliverability of angioplasty catheters. The Anderson patent covers semicompliant angioplasty balloons. The Anderson balloons provide sufficient strength to withstand repeated inflations allowing custom vessel sizing.

About Medtronic

Medtronic, Inc. (www.medtronic.com), headquartered in Minneapolis, is the global leader in medical technology - alleviating pain, restoring health, and extending life for millions of people around the world.

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's Annual Report on Form 10-K for the year ended April 27, 2007. Actual results may differ materially from anticipated results.

Contacts


Medtronic, Inc.
Public Relations
Marybeth Thorsgaard, 763-505-2644
or
Investor Relations
Jeff Warren, 763-505-2696

Tuesday, May 27, 2008

Johns Hopkins Health Alerts Offers Heart-Smart Advice For Rheumatoid Arthritis

Rheumatoid Arthritis and Your Heart: Johns Hopkins Health Alerts Offers Heart-Smart Advice

Johns Hopkins Health Alerts reports on the latest findings on the causes of rheumatoid arthritis, and how it can affect your heart, leading to increased risk of heart attack and stroke, and thus decreased life expectancy.

New York, NY  - March 18, 2008 -- In a recent issue of The Johns Hopkins Arthritis Bulletin, Johns Hopkins specialists reported on the latest research regarding the link between rheumatoid arthritis and heart health.

With rheumatoid arthritis, the inflammation that damages joints also takes a toll on the heart. Johns Hopkins specialists offer bottom line advice on how to adopt a heart-healthy lifestyle to combat the effects of rheumatoid arthritis (RA) and its accompanying inflammation.

BEING HEART-SMART WITH RA
People with rheumatoid arthritis understandably focus on caring for their joints. But their most serious health risk involves their heart.

Compared to the general population, rheumatoid arthritis patients have a significantly increased risk of heart attack and stroke, and a shorter life expectancy.

RA AND YOUR HEART: THE RISKS
Here are some of the findings from recent studies about the link between rheumatoid arthritis and heart disease:

* Heart attacks are twice as common among women with rheumatoid arthritis as among those without the disease.
* Atherosclerosis ("hardening of the arteries") starts early and progresses more rapidly in people with rheumatoid arthritis.
* Carotid artery blockages (a risk factor for stroke) are three times more common in people with rheumatoid arthritis than in people without the disease (44% vs. 15%).
* Cardiovascular events, such as heart attack and stroke, occur about 10 years earlier in people with rheumatoid arthritis.
* Mortality is higher among rheumatoid arthritis patients after a first heart attack.
* Blood vessel damage is often already apparent at the time of rheumatoid arthritis diagnosis.
* Heart attacks in rheumatoid arthritis patients are more likely to be silent or to occur without the typical symptoms, and they more often result in sudden cardiac death.
* Congestive heart failure (weakening of the heart's pumping ability) is more common among people with rheumatoid arthritis.
Researchers have identified several links between rheumatoid arthritis and cardiovascular disease. Inflammation is believed to be the most important of these.

THE ROLE OF INFLAMMATION IN ATHEROSCLEROSIS
Cardiologists now understand that inflammation plays a crucial role in the onset of atherosclerosis. They believe that an injury to the inner lining of the arteries (the endothelium) triggers an immune response, sending immune system cells rushing to repair the damage.

THE EFFECTS OF CHRONIC INFLAMMATION ON YOUR ARTERIES
But in chronic inflammatory states such as rheumatoid arthritis, the immune response doesn't shut off after the injury heals. The accumulating immune system cells attract deposits of cholesterol, blood platelets, cellular debris, and calcium, which clump together to form plaque.

As plaque deposits grow, they restrict blood flow through the artery. If the plaque ruptures, clots can break away and travel to the heart or brain, where they may cause a heart attack or a stroke.

BOTTOM LINE ADVICE: WHAT CAN YOU DO TO STAY HEART-SMART EVEN IF YOU HAVE RHEUMATOID ARTHRITIS
The relationship between rheumatoid arthritis and the heart is complex, and rheumatologists still have a great deal to learn about how to reduce the risk of cardiovascular disease among people who have rheumatoid arthritis.

For now, it's important to do everything possible to reduce the traditional risk factors for heart disease and stroke:
smoking, obesity, a sedentary lifestyle, high blood pressure, high cholesterol, and diabetes.

Getting regular exercise and losing extra pounds (even a 5-10% weight reduction is beneficial) will help your joints as well as your heart. Monitor your blood pressure and have your cholesterol levels checked regularly.

Also, ask your physician about the possibility of taking a low-dose aspirin each day to reduce your risk of cardiovascular disease.

In addition, the cholesterol-lowering medications known as statins--atorvastatin (Lipitor) and others--not only help the heart, but also have modest beneficial effects on rheumatoid arthritis-related inflammation. If your doctor hasn't already suggested a statin drug for your heart health, you might ask about it.

This information is exceprted from The Johns Hopkins Arthritis Bulletin:
Johns Hopkins Arthritis Bulletin

Johns Hopkins Health Alerts publishes free email newsletters on arthritis at:
Johns Hopkins Arthritis Health Alerts

And on heart health at:
Johns Hopkins Heart Health Alerts

For the latest research on Heart Health and Heart Attack Prevention, see the new 2008 Johns Hopkins White Paper: Heart Attack Prevention at: Johns Hopkins White Paper Heart Attack Prevention

To get a copy of the free special report "Johns Hopkins 7 Keys to Reduce Cholesterol," please visit:
Johns Hopkins 7 Keys to Reduce Cholesterol

Press Contact: JOAN MULLALLY
Company Name: Johns Hopkins Health Alerts
Phone: 917-640-4362
Website:
http://www.johnshopkinshealthalerts.com

Monday, May 26, 2008

Should Mesothelioma Victims Call A Mesothelioma Victims Center?

Mesothelioma Victims Should Call Americas Watchdog's Mesothelioma Victims Center

If you are a victim of Mesothelioma or a family member friend of a victim Americas Watchdog is there for you. Americas Watchdog has created the Mesothelioma Victims Center as a free service to victims or family members of victims, of a rare form of cancer called Mesothelioma. Americas Watchdog has initiated this very complete free service because there was literally nothing close to this type of service in the United States and because this type of service is sorely needed by Mesothelioma victims and their families. The Mesothelioma Victims Center was created to assist victims & their families in every way possible

April 21, 2008 -- Americas Watchdog has created the most wonderful service for victims or family members of victims of Mesothelioma. Until a family member was diagnosed with Mesothelioma, Americas Watchdog had never heard of this disease or knew much about it. Mesothelioma is a rare and lethal form of cancer. Mesothelioma is caused by exposure to asbestos. The group never realized that there was no safety net for victims, to get help from the government. They did not know how difficult it might be to get veterans benefits or social security benefits. Americas Watchdog also discovered that it is critical for victims of this lethal disease to get proper legal representation. They have designed the Mesothelioma Victims Center to be the national advocacy center for the victims and family members of Mesothelioma.Their service is free. The web site is located at http://MesotheliomaVictimsCenter.com.

Their services include:
* Assisting the victims obtain Social Security permanent disability payments
* If the victim is a veteran and was exposed to asbestos during military duty, we will work with the victim and his/her family in obtaining veterans disability and health care benefits.
* We will assist the family in getting the best possible
health care options
* We will assist the victim in
getting legal representation.
* We will assist the victim and their family in getting counseling on a wide variety of topics that arise from this
disease.
A victim of Mesothelioma or their family can call the group any time at 866-714-6466.

Who Can Get Mesothelioma? Individuals exposed to asbestos. As Follows
* Individuals who served in the US Navy. Especially Navy personnel who served in or around naval ship engine rooms.
* Members of the US Army, Air Force, Marines, or Coast Guard.
* Naval ship yard workers
* Ship yard workers
* Automotive repair specialists
* Construction workers
* Plumbers
* Demolition contractors
 
 
Because no other group is providing this full range of services and because victims and their families need assistance in these areas, Americas Watchdog is doing this at no charge because its the right thing to do. Americas Watchdog's Mesothelioma Victims Center web site is located at Http://MesotheliomaVictimsCenter.Com . Any one wishing more information can call the Mesothelioma Victims Center anytime at 866-714-6466.

Americas Watchdog and its Mesothelioma Victims Center are all about taking care of precious souls in need and corporate responsibility.

Press Contact: THOMAS MARTIN
Company Name: Americas Watchdog
Phone: 866-714-6466
Website:
Http://MesotheliomaVictimsCenter.Com

Thursday, May 22, 2008

Consumers Take Control of Health Insurance Costs With Health Insurance Agency's Help

North Carolina Health Insurance Agency Help Consumers Take Control of Health Insurance Cost

Business, Economy, Finances, Banking & Insurance

Press release from: nchealthbenefits.com
PR Agency: Adviatech Corp

21.05.2008 - (openPR) - Many North Carolina health insurance consumers would love to lower their premiums, but are frightened by the idea of higher deductibles leading to financial problems in the event of an accident or illness. It can seem pointless to save money on premiums each month when those savings can be wiped out by one medical event.
For consumers in this situation, McLeod Insurance Agency, LLC., is pleased to offer access to Blue Cross and Blue Shield of North Carolina (R)'s BlueOptions Health Savings Account (SM) Over three million consumers nationwide have already taken advantage of programs like this one, which couples a low-premium, high-deductible health insurance plan with a tax-free savings account.

These health savings accounts offer insurance consumers tax deductions based on their yearly contributions to their medical savings account(up to $2900 yearly for individuals and $5800 yearly for families), tax-free investment earnings, and tax-free withdrawals for medical expenses. BlueOptions HA'S (SM) also enable families and individuals to grow savings that can be used to cover procedures and preventive measures that are sometimes neglected by typical health insurance policies. Two additional benefits conferred by HSAs are the liberty to choose where and whom to visit for medical procedures, and the portability of a health insurance plan that follows the insured from job to job, plan to plan, and state to state.
Consumers taking advantage of BlueOptions HSAs (SM) enjoy many of the same benefits associated with a traditional health insurance plan: prescription coverage, child coverage, preventive care, and a nationwide network of qualified providers. Those who choose BlueOptions (SM) have the added bonus of tax-advantaged payments and withdrawals and the relief of greatly reduced premiums (up to 50% in many cases).

BlueOptions HSAs (SM) are also available for business environments, enabling large businesses the freedom to cut costs and small businesses the potential to offer employer-paid health insurance for the first time.
To lean more visit: www.nchealthbenefits.com

Adviatech Corp., PR for nchealthbenefits.com
9280 Bay Plaza Blvd Suite 706
Tampa, FL 33619
1.813.600.3017

NChealthbenefits.com offers health insurance in North Carolina. Their preferred North Carolina Health Insurance provider is Blue Cross and Blue Shield of North Carolina (R).
http://openpr.de/news/45118/North-Carolina-Health-Insurance
-Agency-Help-Consumers-Take-Control-of-Health-Insurance-Cost.html

Wednesday, May 21, 2008

Mesothelioma Blog Reports on Man Fired for Reporting Asbestos Cleanup

LegalView Mesothelioma Blog Reports on Whistleblower Who Was Allegedly Fired for Reporting Improper Asbestos Cleanup to Authorities

LegalView recently updated its mesothelioma blog to include reports of a whistleblower being fired after he reported improper asbestos cleanup. The worker who refused to sign off on the demolition of the school was dismissed from his job duties permanently after he reported the improper procedure cleanup to officials.

Denver, CO  -  April 18, 2008 -- LegalView, the number one resource for everything legal on the Web, recently updated its mesothelioma blog with news of the firing of an alleged whistleblower who attempted to report improper asbestos cleanup of a local high school. The city worker was part of a crew that was to demolition an old schoolhouse. The worker allegedly told city managers that the schoolhouse was filled with asbestos and would be hazardous if improper asbestos removal procedures were not followed. However, after the worker refused to sign off on the demolition and spoke out, he was fired, according to reports.

Asbestos is a hazardous chemical that is often found in insulation of many older buildings including government buildings, offices, homes, apartments, universities and schools. It is derived of vermiculite, which was heavily mined early on in the 20th century throughout the world. Asbestos was revered for its qualities of being cost efficient and its ability to insulate sufficiently without catching on fire as easily as other insulations. However, it was discovered that breathing in asbestos fibers and dust caused a deadly form of lung cancer to develop. Additionally, areas that currently contain asbestos must follow strict procedures and methods from the Environmental Protection Agency (EPA) for removal, otherwise asbestos fibers will likely be released into the air and contaminate surrounding areas and individuals. Those who feel they have been previously exposed to asbestos fibers should contact a mesothelioma lawyer for immediate assistance on building a case.

Mesothelioma cancer can take years to develop and is incurable. It is often misdiagnosed, as symptoms of mesothelioma cancer are similar to many other illnesses. Individuals who have contracted mesothelioma should speak with an experienced medical attorney and receive a consultation on a potential mesothelioma lawsuit. To learn more about this recent mesothelioma blog posting as well as additional up-to-date news, reports and information on recent mesothelioma jury verdicts, visit http://mesothelioma.legalview.com/.

In addition to the extensive mesothelioma information portal, LegalView offers information on an assortment of other legal issues that may disrupt the lives of millions of Americans. Information on issues such as pharmaceutical investigations, including the latest Singulair recall, preventable conditions like Erb's Palsy, diseases, illnesses, accidents, chemical exposure, employment discrimination, etc.

LegalView even provides news on the most recent traumatic brain injury treatments, available through LegalView's Web site. Also on the brain injury site, readers can find information on what may be involved with filing a brain injury lawsuit.

On the Singulair practice area, readers will be able to access the latest news on the prescription drug, which had been under investigation by the U.S. Food and Drug Administration (FDA) after reports began to surface about Singulair side effects that can allegedly include moodiness, suicidal behaviors and thoughts.

Additionally, using the Erb's Palsy information portal will provide victims and their families insight into the cause of their condition as well as opportunities for developing an Erb's Palsy lawsuit for potential monetary compensation to help pay for costly medical bills commonly associated with this condition. Erb's Palsy can be a debilitating condition and is usually preventable. It is associated with birth-canal complications that have occurred when an infant's shoulders or head became lodged, causing damage to the nerve system controlling arm movement. While Erb's Palsy often can clear on its own through time, many individuals still require physical therapy and many will need surgery to fix their condition. Those who suffer from this disease are advised to use LegalView's site to easily be referred to a qualified Erb's Palsy lawyer.

About LegalView:
LegalView.com is a public service brought to you by Legal WebTV Network, LLC, a Limited Liability Corporation created by a group of the nation's most highly respected law firms: Anapol Schwartz; Brent Coon and Associates; Burg Simpson; Cohen, Placitella and Roth; James F. Humphreys and Associates; Lopez McHugh; and Thornton and Naumes. For more information on the accomplishments and track records of LegalView.com's superior sponsoring law firms and to get in touch with LegalView attorneys, visit LegalView at
www.LegalView.com.

Press Contact: Katie Kelley
Company Name: LegalView
Phone: 720-771-3246
Website:
http://mesothelioma.legalview.com

Sunday, May 18, 2008

Center to Assist All Victims of Mesothelioma

Mesothelioma Victims Center to Assist All Victims of Mesothelioma

Americas Watchdog has created the Mesothelioma Victims Center as a free service to victims or family members of victims, of a rare form of cancer called Mesothelioma. Americas Watchdog has initiated this very complete free service because there was literally nothing close to this type of service in the United States and because this type of service is sorely needed by Mesothelioma victims and their families. The Mesothelioma Victims Center was created to assist victims & their families in every way possible.

April 16, 2008 -- Americas Watchdog has just opened its Mesothelioma Victims Center, as a way to assist and protect victims of a rare form of cancer called Mesothelioma. The service is free to Mesothelioma victims or their families.

Until a family member was diagnosed with Mesothelioma, Americas Watchdog had never heard of this disease or knew much about it. Mesothelioma is a rare and lethal form of cancer. Mesothelioma is caused by exposure to asbestos. The group never realized that there was no safety net for victims, to get help from the government. They did not know how difficult it might be to get veterans benefits or social security benefits. Americas Watchdog also discovered that it is critical for victims of this lethal disease to get proper legal representation. They have designed the Mesothelioma Victims Center to be the national advocacy center for the victims and family members of Mesothelioma.Their service is free.

Their services include:
* Assisting the victims obtain Social Security permanent disability payments
* If the victim is a veteran and was exposed to asbestos during military duty, we will work with the victim and his/her family in obtaining veterans disability and health care benefits.
* We will assist the family in getting the best possible health care options
* We will assist the victim in getting legal representation.
* We will assist the victim and their family in getting counseling on a wide variety of topics that arise from this disease. A victim of Mesothelioma or their family can call the group any time at 866-714-6466.

Who Can Get Mesothelioma?

* Individuals who served in the US Navy. Especially Navy personnel who served in or around naval ship engine rooms.
* Members of the US Army, Air Force, Marines, or Coast Guard.
* Naval shop yard workers
* Ship yard workers
* Automotive repair specialists
* Construction workers
* Plumbers
* Demolition contractors

Because no other group is providing this full range of services and because victims and their families need assistance in these areas, Americas Watchdog is doing this at no charge because its the right thing to do. Americas Watchdog's Mesothelioma Victims Center web site is located at Http://MesotheliomaVictimsCenter.Com . Any one wishing more information can call the Mesothelioma Victims Center anytime at 866-714-6466.

Americas Watchdog and its Mesothelioma Victims Center are all about taking care of precious souls in need and corporate responsibility.

Press Contact: THOMAS MARTIN
Company Name: Americas Watchdog
Phone: 866-714-6466
Website:
http://MesotheliomaVictimsCenter.Com

Personal Injury Law Firm Makes General Motors Settles Auto Defect Case

General Motors Settles Auto Defect Case -- California Personal Injury Law Firm Bisnar Chase Wins Settlement

General Motors Corporation agreed to an out-of-court settlement of an automobile defect claim brought by a California teenager who was a passenger in a GMC Yukon accident. The California personal injury law firm of Bisnar Chase represented Michael Samardzich of Diamond Bar in the settlement reached in Los Angeles County for a "Confidential" amount, CASE No. BC 363661, Superior Court of California, County of Los Angeles, Central District.

Los Angeles, CA  -  March 7, 2008 -- General Motors Corporation agreed to an out-of-court settlement of an automobile defect claim brought by a California teenager who was a passenger in a GMC Yukon accident. The California personal injury law firm of Bisnar Chase represented Michael Samardzich of Diamond Bar in the settlement reached in Los Angeles County for a "Confidential" amount, CASE No. BC 363661, Superior Court of California, County of Los Angeles, Central District.

On July 7, 2006, Samardzich was a passenger in a GMC Yukon driven by Vincent Ibarra. Traveling westbound on Golden Springs Drive in Los Angeles County, Ibarra made a left turn at the intersection of Diamond Bar Boulevard. At the same time, Steven Jinseon Kang was operating a vehicle proceeding eastbound on Golden Springs Drive and hit the GMC truck on the right passenger's side.

The impact shattered the side passenger window of the GMC Yukon. Glass shards pierced and ruptured Samardzich's left eye, permanently blinding him. Samardzich was properly restrained at the time of the accident, the police report showed.

"Had General Motors used laminated glass instead of the less-expensive tempered glass, the side passenger window of the GMC truck would not have shattered and would not have caused permanent and serious personal injury to Samardzich," says John Bisnar, founder and partner of Bisnar Chase.

"This settlement was an appropriate resolution to Mr. Samardzich's claim against General Motors," says John Bisnar, founder and partner of Bisnar Chase. "Both sides took into consideration the costs and risks associated with taking the case to trial and settled for an amount greater than General Motors wanted to pay and less than my client demanded. It is Mr. Samardzich's hope that his lawsuit helps encourage General Motors to build safer vehicles and thereby prevents others from suffering a similar injury."

About Bisnar Chase:
Bisnar Chase is a California personal injury law firm that represents people who have been very seriously injured because of an accident, a defective product or negligence. Most of their accident and defective product cases are auto-related. They include cases against negligent drivers who have caused serious traffic accidents and against auto companies like Ford and General Motors that have manufactured defective vehicles. For more information, visit: www.auto-defect-attorneys.com,
www.bisnar-chase.com and www.californiainjuryblog.com

Press Contact: John Bisnar
Company Name: Bisnar Chase
Phone: 949-752-2999
Website:
www.auto-defect-attorneys.com

Thursday, May 15, 2008

Sudden Cardiac Arrest Risk Stratification Trials Unveiled

Major Sudden Cardiac Arrest Risk Stratification Trials Unveiled

Medtronic-Supported Research Efforts Commencing to Better Determine Which At-Risk Patients - Inside and Outside of Currently Indicated Populations - May Benefit Most from ICD Therapy


MINNEAPOLIS & SAN FRANCISCO-- May 14, 2008 --Medtronic, Inc. (NYSE: MDT), along with several partners, today announced details of several major clinical trials aimed at developing and validating new and innovative risk stratification tools to predict which post-myocardial infarction (MI, or heart attack) patients are at greatest risk of Sudden Cardiac Arrest (SCA). Medtronic's industry-leading research efforts aim to further advance the base of clinical evidence for implanted cardiac device therapies to ensure those patients at greatest risk of SCA are protected.

"We are on the cusp of new discoveries in clinical cardiology. These trials will utilize advanced innovations in technology and research, spanning novel diagnostics to genomics," said David M. Steinhaus, M.D., vice president and medical director of the Cardiac Rhythm Disease Management business at Medtronic. "Medtronic is proud to have partnered with leading researchers worldwide to apply these scientific innovations in an effort to better understand which patients may benefit from implantable medical therapies."

About Medtronic-Supported Risk Stratification Research Trials

    * VEST / PREDICTS (The Vest Prevention of Early Sudden Death Trial / The Prediction of ICD Therapies Study), is a multicenter, randomized controlled trial designed to test a strategy to reduce the early post-MI sudden cardiac arrest risk, followed by an observational cohort study to develop and validate a tool to determine which patients will benefit most from an ICD two months post-MI.

The VEST portion of the study will test the hypothesis that a non-invasive, wearable automatic defibrillator vest will reduce overall mortality in the first 60 days following an MI in patients with LVEF ?35 percent. The PREDICTS portion of the study aims to develop and validate a tool that predicts the occurrence of spontaneous "treatable" ventricular arrhythmias up to five years post-MI, and identify high-risk patients in whom an ICD would be most cost-effective. Study participants will receive either an ICD or Medtronic Reveal® DX insertable cardiac monitor (ICM) to ascertain data on ICD-treatable arrhythmic events.

VEST / PREDICTS is part of a National Institutes of Health (NIH) grant awarded to the University of California-San Francisco (UCSF) and is co-funded by Medtronic, GE Healthcare, and Zoll. It will involve up to 60 centers and more than 4,500 patients in the United States, Canada and Europe.

"The VEST / PREDICTS study is intended to address the two key deficiencies in our current post-MI treatment strategy, which include 1) the untreated high sudden death rate in the early post-MI period and 2) the non-specific nature of ejection fraction to predict spontaneous ventricular arrhythmias and ICD shocks," said Jeff Olgin, M.D., principal investigator for VEST / PREDICTS, and chief of cardiac electrophysiology and professor of medicine at UCSF. "This important study will define a clear pathway to identify those patients who benefit most from ICDs."

    * The objective of Medtronic's GAME (Genetic Arrhythmia Markers for Early Detection) trial is to determine if genetic markers can be used to identify individuals with an increased susceptibility to SCA. Involving 1,000 patients at more than 30 sites in the 48 contiguous United States, GAME will study cardiac events retrospectively to potentially develop a genetic risk scoring system to determine which patients would benefit from an ICD. The first patient enrollment in GAME recently took place at Arkansas Cardiology Clinic in Little Rock, Ark.

"We are about to enter a new era of medicine, one in which so much will eventually be individualized, including prevention and therapy," said Eric Topol, M.D., principal investigator of the GAME trial and chief academic officer at Scripps Health in San Diego. "Genomics has already had a major impact on the treatment of cancer and many other diseases. Now we're looking at genomics of patients with arrhythmias as a way to more precisely treat this important type of heart disease."

    * Also underway is the Medtronic-supported DISCOVERY (Diagnostic Data Influence on Disease Management and Relation of Genetic Polymorphisms to Ventricular Tachyarrhythmias in ICD Patients) trial, involving nearly 1,300 patients at approximately 80 centers in Europe. DISCOVERY is a non-randomized, prospective, multicenter study and is composed of two parts. The first is double-blinded and collects data on genetic polymorphisms and potential prognostic of ventricular and atrial tachyarrhythmias. The second part evaluates the influence of dual chamber ICD-based diagnostic information on long-term patient management and treatment.

Further, Medtronic is committed to ongoing study of Microvolt T-Wave Alternans (MTWA) and other risk markers that will further advance the understanding of how to better identify patients at risk for SCA. MTWA is being studied in the MASTER trial, of which data has previously been presented at the American Heart Association's Scientific Sessions 2007 and American College of Cardiology's Scientific Sessions 2008, and will be presented at Heart Rhythm 2008, the Heart Rhythm Society's 29th Annual Scientific Sessions. Medtronic will continue to explore the potential of MTWA, as evidenced in these aforementioned risk stratification studies.

About Medtronic

Medtronic, Inc. (www.medtronic.com), headquartered in Minneapolis, is the global leader in medical technology - alleviating pain, restoring health, and extending life for millions of people around the world.

Notes to editors: To arrange interviews on VEST/PREDICTS with representatives from the University of California-San Francisco, please contact Corinna Kaarlela at 415-476-2557; or GE, contact Corey Miller at 414-469-5499 (cell) or Corey.Miller@ge.com

VEST/PREDICTS disclaimer: The information stated above was prepared by Medtronic Inc. to report research strategies and reflects solely the opinion of Medtronic. Nothing in this statement shall be construed to imply any support or endorsement of Medtronic or any of its products by the Regents of the University of California, its officers, agents and employees.

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's Annual Report on Form 10-K for the year ended April 27, 2007. Actual results may differ materially from anticipated results.

Contacts

Medtronic, Inc.
Public Relations:
Tracy McNulty, 763-526-2492
On-site at HRS: 612-819-2190
or
Investor Relations:
Jeff Warren, 763-505-2696
On-site at HRS: 612-819-7630

Tuesday, May 13, 2008

Oral Cancer Now Covered under Specialty Benefits Dental Plans

`Early Warning' for Oral Cancer Now Covered under UnitedHealthcare Specialty Benefits Dental Plans

Coverage Applies to New Screening Test Used by Dentists

GOLDEN VALLEY, Minn.-- May 13, 2008 --UnitedHealthcare Specialty Benefits now provides coverage under all of its insured dental plans for a new oral cancer screening test for potential abnormalities inside the mouth, including premalignant lesions and oral cancer.

The test, which uses light-contrast technology, can improve a dentist's ability to identify, evaluate and monitor lesions that are difficult to see using visual inspection under conventional lighting.

"Evidence shows that dentists can serve as a valuable 'early warning' system for patients who have signs of oral cancer," said Dr. Michael Weitzner, vice president of clinical product development for UnitedHealthcare Specialty Benefits dental unit.

More than 34,000 Americans will be diagnosed with oral or pharyngeal cancer this year. The death rate associated with this cancer is particularly high - not because it is hard to discover or diagnose, but due to the cancer being routinely discovered late in its development. Studies confirm that survival does correlate with stage, making early diagnosis and treatment optimal for this disease and may have a positive impact on an individual's medical costs (Journal of the American Dental Association, Vol. 132, Nov. 2001).

By covering this type of oral cancer screening, UnitedHealthcare Specialty Benefits dental unit is renewing its longstanding commitment to early detection of oral cancer. In addition to oral cancer screening, UnitedHealthcare Specialty Benefits dental plans have covered brush biopsies since 2005 when the American Dental Association first introduced a current dental terminology (CDT) code for the procedure. Screening is covered once a year for individuals, starting at age 30. UnitedHealthcare Specialty Benefits' focus on wellness continues to build programs and plan enhancements that promote individuals' ability to better manage their overall health as well as their future medical and dental costs.

About UnitedHealthcare Specialty Benefits

UnitedHealthcare Specialty Benefits offers a broad array of specialty benefits, including vision, dental, group and voluntary insurance, worksite individual insurance and non-insurance programs. UnitedHealthcare Specialty Benefits is a business unit of OptumHealth, the health and wellness unit of UnitedHealth Group, Inc. (NYSE:UNH). More information about OptumHealth can be found at www.optumhealth.com/.

Contacts

OptumHealth
Ann Fleischauer, Director, External Communications
763-797-2652

Monday, May 12, 2008

Practice-Changing Clinical Data Anticipated By Medtronic

Medtronic Anticipates 'Practice-Changing' Clinical Data for Interventional Cardiologists at EuroPCR

ENDEAVOR II Four-Year Results, Updated ENDEAVOR Pooled Safety Analysis, One-Year Results from E-Five Registry and TAPAS Trial - All Feature on Meeting's Scientific Program

MINNEAPOLIS-- May 12, 2008 --Medtronic, Inc. (NYSE:MDT), today announced plans for the release of new clinical data on the Endeavor® Zotarolimus-Eluting Coronary Stent System and the Export® Aspiration Catheter at EuroPCR in Barcelona this week, May 13-16.

"New data from the ENDEAVOR clinical program and the TAPAS trial have the potential to be practice-changing for interventional cardiology," said Prof. Anthony Gershlick of University Hospitals of Leicester in the UK. "As the evidence from this clinical research continues to build, it shows more and more definitively the advantages of the Endeavor drug-eluting stent for a broad range of patients with coronary artery disease and of thrombus aspiration with the Export Aspiration Catheter for a specific group of patients suffering myocardial infarction."

A summary of the data presentations related to Medtronic's product portfolio for interventional cardiology at EuroPCR follows:

    * On Tuesday, May 13, the late-breaking clinical trials session from 15:30 - 18:30 in Room 1 includes presentations by:

- Dr. Jean Fajadet (at approximately 15:45) of the four-year results from ENDEAVOR II, a prospective, randomized, multicenter, controlled trial that compared the Endeavor drug-eluting stent to the Driver bare-metal stent.
                                                        
- Prof. Bart de Smet (at approximately 16:30) of one-year results from TAPAS, a single-center trial designed to evaluate the effect of thrombus aspiration preceding percutaneous coronary intervention by using the Export Aspiration Catheter in patients with acute myocardial infarction.

    * On Thursday, May 15, the Medtronic-sponsored symposium titled "Patients and Stents: Learning and Progress," 5:00 - 6:30 pm in Room 1, features presentations by:

- Prof. Martin Rothman on the one-year results of 8,300 patients in E-Five, an international registry that investigated the performance of the Endeavor drug-eluting stent in routine clinical practice.
                                                        
- Prof. Ian Meredith on the updated ENDEAVOR pooled safety analysis, which includes 2,132 Endeavor patients (from ENDEAVOR I, II, II continued access, III and IV) - 678 of whom have now been followed for four years, 1,271 for three years, 1,290 for two and 2,093 patients for one year.

All times are local to Barcelona. Room numbers are for The Forum CCIB Convention Center, the venue for EuroPCR.

"The data we're presenting this week at EuroPCR illustrate the depth of innovation within the CardioVascular business at Medtronic and the growing breadth of our offering to interventional cardiologists," said Scott Ward, senior vice president of Medtronic and president of the CardioVascular business. "We are particularly excited to share the long-term results from the ENDEAVOR clinical program, which continue to illustrate significant performance advantages for patients and physicians, positioning Medtronic for market leadership in coronary stents."

In addition to attending these data presentations and other educational and scientific sessions, EuroPCR participants are encouraged to visit the Medtronic exhibit (booth #D04), which will feature highlights of the company's current and future cardiovascular innovations, including the:

    * Endeavor and Endeavor Resolute Zotarolimus-Eluting Coronary Stent Systems
    * Sprinter Legend Balloon Catheter
    * Export XT Aspiration Catheter
    * Defender Embolic Protection Filter
    * Complete SE (Self-Expanding) Peripheral Stent
    * Assurant Cobalt Balloon-Expandable Iliac Stent
    * Melody Transcatheter Pulmonic Heart Valve

Information on Medtronic's programs designed to foster "Innovation through Collaboration" in the fields of educational development (Academia) and clinical science (Scientia) will also be available at EuroPCR.

"As the trend of closer collaboration across medical specialties continues, our CardioVascular business is uniquely positioned to forge the partnerships necessary to find novel solutions to unmet patient needs," Ward added. "As the theme of our EuroPCR exhibit, 'Better Together,' suggests, we know from decades of experience the profound power of collaboration with the clinical community in the service of patients with chronic diseases."

About Medtronic

Medtronic, Inc. (www.medtronic.com), headquartered in Minneapolis, is the global leader in medical technology - alleviating pain, restoring health, and extending life for millions of people around the world.

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's Annual Report on Form 10-K for the year ended April 27, 2007. Actual results may differ materially from anticipated results.

Contacts

Medtronic, Inc.
Joe McGrath, 707-591-7367 (Public Relations)
Jeff Warren, 763-505-2696 (Investor Relations)

Friday, May 9, 2008

South African Ban on Mesothelioma-Causing Asbestos

LegalView Updates Mesothelioma Blog Readers with News of South African Ban on Mesothelioma-Causing Asbestos

LegalView, on its mesothelioma blog, recently reported an asbestos ban on the use, manufacture and processing of the cancer-causing contaminant. Asbestos was mined for decades in South Africa and since the 1960s mesothelioma cancer and related illnesses have been associated with inhalation of the deadly fibers.

Denver, CO  -  April 11, 2008 -- LegalView.com recently reported on its mesothelioma blog the ban of asbestos in South Africa. The Environmental Affairs and Tourism Minister there announced the ban with regards to the use, manufacture and processing of asbestos, which causes a deadly form of lung cancer known as mesothelioma. The South African ban marks the latest addition to a worldwide effort to ban the mineral. Currently, approximately 50 countries around the globe have prohibited the production of the contaminant. For years, asbestos was mined in the area and, according to news reports, accounted for 3 percent of the value of all of the area's minerals. To learn more about how to locate mesothelioma attorneys in your area, which may be able to provide consultation on the effects of asbestos exposure.

Asbestos, which is derived from vermiculite - the mineral mined throughout the world and the source of asbestos, was widely used in a variety of construction projects such as the main source of installation in millions of homes, apartments, schools, universities, and business and government buildings worldwide. Individuals who have been exposed to asbestos should not only speak with a medical professional immediately, but should consider finding a mesothelioma lawyer as well.

Often it isn't until years after initial exposure to asbestos that individuals begin to notice symptoms of the inhaled asbestos fibers; the end result is usually an incurable lung cancer. Victims of this cancer in need of a mesothelioma attorney should utilize LegalView's referral service to connect them with any of the many mesothelioma lawyers available through the mesothelioma information portal. Here, an individual can be referred to an experienced mesothelioma attorney who will have important information on the legal implications of exposure to asbestos.

In addition to mesothelioma, LegalView also provides information portals on topics such as traumatic brain injury (TBI), Singulair side effects and the Baxter Heparin recall. TBIs adversely affect millions of Americans each year and thousands of these cases go unreported even though the effects may be severe. TBI side effects range from memory loss to poor motor and social skills to paralysis. Individuals who have been injured in a traumatic brain injury should use the LegalView TBI information portal to locate an attorney as well as to learn about the latest TBI treatments.

On the Singulair practice area, readers will learn of the latest U.S. Food and Drug Administration (FDA) investigation into the allergy symptom drug. The investigation stems from patient reports that there may be some Singulair side effects that are causing an increased risk of suicidal thoughts among patients.

Learn the latest updates on the FDA's investigation into the Baxter Heparin recall, which was spurred by a rash of allergic reactions among patients who had previously received the drug during surgical procedures. Most recently, the FDA discovered that a Chinese manufacturing plant was responsible for a tainted batch of Baxter Heparin. The drug is a blood thinner used to decrease the risk of deadly blood clots during surgical procedures such as heart surgery.

About LegalView:

LegalView.com is a public service brought to you by Legal WebTV Network, LLC, a Limited Liability Corporation created by a group of the nation's most highly respected law firms: Anapol Schwartz; Brent Coon and Associates; Burg Simpson; Cohen, Placitella and Roth; James F. Humphreys and Associates; Lopez McHugh; and Thornton and Naumes. For more information on the accomplishments and track records of LegalView.com's superior sponsoring law firms and to get in touch with LegalView attorneys, visit LegalView at
www.LegalView.com.

Press Contact: Katie Kelley
Company Name: LegalView
Phone: 720-771-3246
Website:
http://mesothelioma.legalview.com

Tuesday, May 6, 2008

Costs For Pharmacy and Over-The-Counter Drugs Reduced

Target Reduces Costs on Pharmacy and Over-The-Counter Drug Offerings

MINNEAPOLIS-- May 05, 2008 --As part of its ongoing commitment to provide exceptional value to guests and consistent with prior practices, Target (NYSE:TGT) will reduce prices on its prescription and over-the-counter drug offerings, remaining competitively priced with Wal*Mart.

"We understand the economic challenges our guests are facing and remain committed, as always, to meeting their health and wellness needs at a great value," said Kathee Tesija, executive vice president, merchandising.

The program includes an expanded assortment of $4 prescription drugs, 90-day supply of these medications for $10 and over-the-counter medications for $4 or less.

More information regarding eligible drugs soon will be available online at Target.com/pharmacy and in local Target pharmacies.

About Target

Minneapolis-based Target serves guests at 1,613 stores in 47 states nationwide by delivering today's best retail trends at affordable prices. Target is committed to providing guests with great design through innovative products, in-store experiences and community partnerships. Whether visiting a Target store or shopping online at Target.com, guests enjoy a fun and convenient shopping experience with access to thousands of unique and highly differentiated items. Target (NYSE:TGT) gives more than $3 million a week to its local communities through grants and special programs. Since opening its first store in 1962, Target has partnered with nonprofit organizations, guests and team members to help meet community needs.

Contacts

Target Corporation
Target Communications (media), 612-696-3400
or
John Hulbert (investors), 612-761-6627

Monday, May 5, 2008

Anti-counterfeit Drug Analyzer Provides Real-time Analysis

Briefcase-sized Portable Anti-counterfeit Drug Analyzer Provides Real-time Analysis Anywhere, Anytime

ASD Inc. introduces the RxSpec® 700Z -- a powerful new weapon in the Pharmaceutical Industry's war on counterfeit drugs. User-friendly system provides non-destructive, on-the-spot lab quality analysis for field agents from industry, government, and law enforcement world-wide.

Boulder, CO - May 1, 2008 --- ASD Inc. introduces the RxSpec® 700Z anti-counterfeit drug analyzer (
http://www.asdi.com/products-rxspec700z.asp), a lightweight fully-portable lab-quality system contained in a rugged aluminum briefcase. For the first time in history, field agents from industry, government, and law enforcement have the ability to test drugs on the spot, anywhere, anytime, to determine whether the actual pill, rather than the packaging, is authentic or counterfeit. With a much wider spectral range than other market offerings, the system simultaneously analyzes, in mere seconds, all components of the pharmaceutical in question, rather than the active ingredient only -- and because the test is non-destructive, the sample is unaltered and preserved. The system operates on either battery or wall power, and weighs a little less than 23 pounds (10.4 kg). The RxSpec 700Z is the realization of several years of extensive research and development, eight patents, and ASD's solid track record of building drug identification technology.

Counterfeiting and theft within the pharmaceutical industry supply chain range from conservative estimates of $30 billion to more than $50 billion in annual losses to corporations, according to market studies by organizations such as IMS Health and the U.S. Food and Drug Administration (FDA). Additionally, while the extent of pharmaceutical counterfeiting varies among different regions in the world, there is consensus among regulatory bodies that the problem is an extremely dangerous and escalating threat to the health and safety of the world's population. In 2003 the FDA established the Counterfeit Drug Task Force as a new initiative to combat this growing problem. ASD has answered this call to action with the RxSpec® 700Z anti-counterfeit drug analyzer.

"Field agents will find the easy-to-use interface of the RxSpec 700Z quick and intuitive," said Tom Brown, ASD Vice President of Sales and Channel Management. "And because the test takes only a few seconds, the agents will now be able to act more quickly when they have discovered a counterfeit."

ASD will be showing the RxSpec 700Z at the following 2008 events: The Fourth Global Forum on Pharmaceutical AntiCounterfeiting (
http://www.pharma-anticounterfeiting.info/) in Washington DC, June 4-6; Combating Counterfeit Medicines Symposium (http://www.jpag.org/Programme0608.pdf) in London, UK, June 12; Bio International Convention (http://www.bio2008.org/) in San Diego, California, June 17-20; 2008 AAPS National Biotechnology Conference (http://www.aapspharmaceutica.com/meetings/biotec/bt08/index.asp) in Toronto, Canada, June 22-25.

About ASD

ASD Inc. is unsurpassed in solving some of the world's most challenging materials measurement problems. We collaborate with industrial professionals, analytical researchers, and remote sensing scientists to provide the most reliable, high-performance analytical instrumentation solutions for real-world applications. Established in 1990 and based in Boulder, Colorado, USA, ASD Inc. has customers world-wide.

For more information, please contact Amanda Griffin, ASD Marketing Communications Manager, 2555 55th Street, Suite 100, Boulder, CO, 80301 USA; 303/444-6522, 303/444-6825 (fax); mktg @ asdi.com; www.asdi.com.

Contact Information
Amanda Griffin
ASD Inc
http://www.asdi.com
303.444.6522 +129

Deep Brain Stimulation Study Offers Hope for Severe Depression Patients

Results of Brodmann Area 25 Deep Brain Stimulation Pilot Study Offer Hope for Patients with Severe Depression

Study findings presented today at American Psychiatric Association Annual Meeting


ST. PAUL, Minn.-- May 05, 2008 --St. Jude Medical, Inc. (NYSE:STJ) today announced pilot study results from the first multi-center study investigating deep brain stimulation (DBS) of Brodmann Area 25 for major depressive disorder.

Results of the study, which were presented today at the American Psychiatric Association (APA) meeting in Washington, D.C., found that 6 months after the procedure, 56 percent of the patients experienced at least a 40 percent decrease in depressive symptoms. Patient's symptoms were measured using a standardized test called the Hamilton Rating Scale for Depression.

Results were presented by Sidney Kennedy, M.D., psychiatrist-in-chief with the University Health Network in Toronto. "Severe depression destroys a person's ability to be productive and have a normal quality of life," said Dr. Kennedy. "The results from this study are very promising, and we are hopeful that our research will lead to a therapy that can help these patients."

Prior to beginning the study, all patients were classified as having severe depression after multiple treatments - such as medications, psychotherapy and electroconvulsive therapy - had failed to provide sustained relief from depression. Each study patient had tried a minimum of 12 depression medications over his or her lifetime.

DBS was targeted at an area of the brain known as Brodmann Area 25, which appears to become overactive when people are profoundly sad and depressed. Conducted at three leading Canadian academic medical centers, the study expands and supports the groundbreaking research of Helen Mayberg, M.D., and Andres Lozano, M.D., which was published in Neuron in March 2005.

On average, the 20 study participants had suffered from depression for more than 20 years; they were disabled and unable to work at the time of enrollment. The study also found that:

    * At their most recent psychiatric evaluation, 78 percent of the patients experienced at least a 40 percent decrease in depressive symptoms.
    * Three of the study patients are considered to be in remission.
    * Eight patients have re-engaged in life activities such as work, school, relationships and travel.

In the study, DBS was delivered through the St. Jude Medical Libra® Deep Brain Stimulation System, which delivers mild electrical current from a device implanted near the collarbone; the device is connected to small electrical leads placed at specific targets in the brain.

"These results are important as they help establish the body of evidence that will continue to move depression research forward," said Chris Chavez, president of the St. Jude Medical ANS Division. "We are committed to leading the development of products that can make life better for patients suffering from this debilitating condition."

Based on the results of this research, St. Jude Medical announced the BROADENT (BROdmann Area 25 DEep brain Neuromodulation) study in February 2008, to further investigate the use of DBS for major depressive disorder. A controlled, multi-center, blinded clinical study, BROADEN is being conducted in the U.S. under an Investigational Device Exemption (IDE) from the U.S. Food and Drug Administration (FDA).

St. Jude Medical owns the intellectual property rights and has various patents issued and pending for the use of neurostimulation at Brodmann Area 25. For more information about this clinical trial, call toll-free 866-787-4332 or visit www.BROADENstudy.com.

According to the National Advisory Mental Health Council, of the 21 million adult Americans who suffer from depression, approximately 4 million live with severe depression that does not respond to medications, psychotherapy and, in certain cases, electroconvulsive therapy.

About St. Jude Medical

St. Jude Medical is dedicated to making life better for cardiac, neurological and chronic pain patients worldwide through excellence in medical device technology and services. The Company has five major focus areas that include: cardiac rhythm management, atrial fibrillation, cardiac surgery, cardiology and neuromodulation. Headquartered in St. Paul, Minn., St. Jude Medical employs more than 12,000 people worldwide. For more information, please visit www.sjm.com.

About the ANS Division of St. Jude Medical

The ANS Division (Advanced Neuromodulation Systems) became a part of St. Jude Medical in 2005. The ANS Division is an innovative technology leader dedicated to the design, development, manufacturing and marketing of implantable neuromodulation systems to improve the quality of life for people suffering from disabling chronic pain and other nervous system disorders (www.ans-medical.com).

Forward-Looking Statements

This news release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that involve risks and uncertainties. Such forward-looking statements include the expectations, plans and prospects for the Company, including potential clinical successes, anticipated regulatory approvals and future product launches, and projected revenues, margins, earnings, and market shares. The statements made by the Company are based upon management's current expectations and are subject to certain risks and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. These risks and uncertainties include market conditions and other factors beyond the Company's control and the risk factors and other cautionary statements described in the Company's filings with the SEC, including those described in the Company's Annual Report on Form 10-K filed on February 27, 2008 (see Item 1A on pages 13-20, and page 20 of Exhibit 13 to the Company's Form 10-K). The Company does not intend to update these statements and undertakes no duty to any person to provide any such update under any circumstance.

Contacts

St. Jude Medical, Inc.
Investor Relations:
Angela Craig, 651-481-7789
or
Media Relations:
Kathleen Janasz, 651-415-7042
Mobile: 612-743-8995
or
Denise Landry, 972-309-8085

Thursday, May 1, 2008

Infectious Disease Research Institute Collaborates With 3M On Vaccine Adjuvants

3M Collaborates with Infectious Disease Research Institute on Vaccine Adjuvants

ST. PAUL, Minn.-- May 01, 2008 --3M Drug Delivery Systems announces the signing of a non-exclusive license agreement with the Infectious Disease Research Institute (IDRI) in support of vaccine research for humanitarian efforts in developing countries. Under the agreement, 3M will donate its patented toll-like receptor (TLR) immune response modifier compounds.

3M's patented TLR immune response modifier compounds, which may be useful as vaccine adjuvants, will be used by IDRI to research new vaccines. Vaccine adjuvants are known to help boost the effectiveness of a vaccine.

"IDRI's vaccine platform has the potential to prevent and treat a number of important diseases in the developing world. By providing our vaccine adjuvant compounds to their vaccines, we are providing a cost-effective way for IDRI to conduct vaccine research," said Dr. Mark Tomai, PhD, Vaccine Business Development, 3M Drug Delivery Systems. "This will help them and us learn more about the potential effectiveness of our vaccine adjuvants. We anticipate this collaboration with IDRI to be the first in many deals around our TLR vaccine adjuvant portfolio."

3M's TLR compounds, also called TLR7 and TLR8 agonists, are small organically synthesized molecules that offer flexibility in formulating and route of delivery, and ease in manufacturing, unlike most other TLR agonists, which are much larger and not as easy to manufacture.

"IDRI's access to a 3M compound provides us with a very important tool for our efforts to develop adjuvants to be used in vaccines for diseases of global impact," says Steve Reed, IDRI's Founder and Head of Research. "We are very pleased that 3M has demonstrated this confidence in our organization-and are confident that IDRI's access to the 3M technology will improve our vaccine research and development."

"Our toll-like receptor agonist platform is a major part of our vaccine offering that also includes our Microstructured Transdermal System(a) for needle-free delivery of vaccines. We are at the start of a positive relationship that pairs our unique technology with a critical global need. We look forward to working with IDRI on its vaccine research," said Dr. Steven Wick, Technical Director, 3M Drug Delivery Systems.

About 3M Drug Delivery Systems Immune Response Modifiers

3M Drug Delivery Systems has a portfolio of patent protected toll-like receptor TLR7 and TLR8 agonists that have shown promise as vaccine adjuvants. There are a variety of assets in the portfolio that can be used topically, admixed or in conjugatable form. The lead candidate, resiquimod (TLR7/8 agonist) has shown promising results in a number of animal models and has an extensive toxicology and clinical data package to support further development as a vaccine adjuvant. In addition, 3M offers other TLR7 and TLR8 agonists, some of which can be attached to various proteins that enhance vaccine efficacy in a number of models. As small molecules, 3M's TLR7 and TLR8 agonists offer unique advantages over other TLR agonists with regards to delivery and manufacturing. 3M is actively seeking partners to license these assets on a non-exclusive basis. For more information, or to contact Dr. Tomai, go to www.3m.com/dds.

In addition, 3M Drug Delivery Systems has a variety of immune response modifier compounds that may be useful in oncology and dermatology.

About 3M

A recognized leader in research and development, 3M produces thousands of innovative products for dozens of diverse markets. 3M's core strength is applying its more than 40 distinct technology platforms - often in combination - to a wide array of customer needs. With $24 billion in sales, 3M employs 75,000 people worldwide and has operations in more than 60 countries.

About IDRI

IDRI is a non-profit organization committed to developing technologies to treat "neglected" diseases that place a significant burden on those living in the developing world. IDRI achieves its mission by working closely with industry, universities, and hospitals in developed and developing countries, government and private funding agencies, the Bill and Melinda Gates Foundation as well as the World Health Organization. For more information, go to www.idri.org.

(a)3M Microstructured Transdermal System (MTS) is a state-of-the-art solid microneedle system for transcutaneous or intra-dermal drug delivery. MTS bypasses the barrier properties of the stratum corneum and provides a means to deliver a wide variety of molecules that ordinarily would not penetrate the skin, including vaccines. MTS enhances the efficacy of vaccines by targeting the antigen presenting cells within the skin, thereby improving delivery efficiency and reducing dose requirements. MTS is a painless, easy-to-use system with the potential to greatly improve the delivery of vaccines.
Contacts

3M
Stephanie Sanderson, 651-733-8588
sjsanderson@mmm.com


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