California Stem Cell Agency Launches $30 Million Plan to Lure Industry


Just one week after the $3 billion California stem cell agency was sharply criticized for its failure to adequately support biotech firms, the agency formally kicked off a $30 million effort to engage industry more closely.

The initiative, in the works since the middle of last year, was heralded as the beginning of a "new era" for CIRM, which is moving to transform into cures the stem cell research it has funded over the last seven years. The agency has scheduled a webinar for April 25 for prospective applicants.

CIRM's press release, crafted by the agency's new PR/communications director, Kevin McCormack, yesterday quoted CIRM President Alan Trounson as saying,

"This initiative is a major new development in the progress towards providing new medical treatments for patients by engaging the most effective global industry partners."

Elona Baum, the agency's s general counsel and vice president of business development, said the program "represents a new era for CIRM."

Under the RFA, the agency will award up to $10 million each for three grants or loans. The program, however, is not limited to businesses. Non-profits may apply as well. Representatives from industry have complained about a strong tilt on the part of CIRM towards academic and non-profit research enterprises. The CIRM board is dominated by representatives from those two sectors.

The program grew out of recommendations in November 2010 from an "external review" panel put together by CIRM that said the agency needed to do better with business. The refrain was heard again directly from stem cell firms at last week's hearing by the Institute of Medicine on the stem cell agency's performance. According to CIRM's figures, businesses have received $54 million in grants and loans since 2005, the first year the CIRM board approved grants, out of a total of $1.3 billion.

Only one news outlet has written a story so far about the posting of the RFA and the press release, as far as can be determined.

Ron Leuty of the San Francisco Business Times said,

"The most likely candidates to attract industry funding would be CIRM’s 'disease team' grant winners, who face a deadline of 2014 to bring a project to the point of first-in-human clinical trials. CIRM has weighed options for pushing those projects — there are 13 of them now — deeper into the FDA approval process."

CIRM said in the RFA material,

"The intent of the initiative is to create incentives and processes that will: (i) enhance the likelihood that CIRM funded projects will obtain funding for Phase III clinical trials (e.g. follow-on financing), (ii) provide a source of co-funding in the earlier stages of clinical development, and (iii) enable CIRM funded projects to access expertise within pharmaceutical and large biotechnology partners in the areas of discovery, preclinical, regulatory, clinical trial design and manufacturing process development.

"This initiative requires applicants to show evidence of either having the financial capacity to move the project through development or of being able to attract the capital to do so. This may be evidenced by, for example, (i) significant investment by venture capital firms, large biotechnology or pharmaceutical companies and/or disease foundations; or (ii) a licensing and development agreement with a large biotechnology or pharmaceutical company or a commitment to enter into such an agreement executed prior to the disbursement of CIRM funding.

"The objective of the first call under this initiative, the Strategic Partnership I Awards, is to achieve, in 4 years or less, the completion of a clinical trial under an Investigational New Drug (IND) application filed with the Food and Drug Administration (FDA)."

CIRM has scheduled a webinar on the RFA for prospective applicants for next Wednesday, April 25. It is asking for registration and questions in advance.



(Editor's note: An earlier version of this article did not contain the sentence about businesses receiving $54 million out of $1.3 billion awarded by CIRM.)

Source:
http://californiastemcellreport.blogspot.com/feeds/posts/default?alt=rss

Study Compares Abdominal Aortic Aneurysm Repair Methods

(HealthDay News) -- A less-invasive method of abdominal aortic aneurysm (AAA) repair reduces the short-term risk of death, according to a new U.S. study.

The interim findings are from a nine-year multicenter trial comparing patient outcomes after endovascular and open surgical repair of AAA. The report included postoperative outcomes of up to two years (average 1.8 years of follow-up) for 881 patients, aged 49 or older, who had endovascular repair (444) or open repair (437).

Endovascular repair is performed through a catheter inserted into an artery. Open repair involves an abdominal incision. Of the 45,000 patients in the United States who undergo elective repair of an unruptured AAA each year, more than 1,400 die in the perioperative period -- the first 30 days after surgery or inpatient status. There's limited data available about whether short-term survival is better after endovascular repair compared to open repair. Read more...




Ayurtox for Body Detoxification

Source:
http://feeds.feedburner.com/integratedmedicine

Want to learn more about Parkinson's Disease?

Readmore: Local, News, Parkinson's Disease, Want to Learn more about Parkinson's Disease?, Parkinsons Conference, Crown Reef Resort, Parkinson's Conference at Crown Reef Resort

Parkinson's Disease affects nearly one million people in the United States.

A man who has the disorder and his mother put on a conference at the Crown Reef Resort Thursday to teach people about the disease.

Parkinson's involves the malfunction or death of nerve cells in the brain that produce a chemical that sends messages to part of the brain that controls movement.

The cause of Parkinson's in unknown and there is no cure. But there are treatment options like medication and surgery to manage symptoms.

"There is a lot of hope out there. There's a lot of new medications coming through the pipeline that will be helpful. We also encourage people to live their lives to the fullest everyday," says Karlin Schroeder with the Parkinsons Disease Foundation.

Clickhereto read more about Parkinson's Disease.

View original post here:
Want to learn more about Parkinson's Disease?

Want to learn more about Parkinson’s Disease?

Readmore: Local, News, Parkinson's Disease, Want to Learn more about Parkinson's Disease?, Parkinsons Conference, Crown Reef Resort, Parkinson's Conference at Crown Reef Resort

Parkinson's Disease affects nearly one million people in the United States.

A man who has the disorder and his mother put on a conference at the Crown Reef Resort Thursday to teach people about the disease.

Parkinson's involves the malfunction or death of nerve cells in the brain that produce a chemical that sends messages to part of the brain that controls movement.

The cause of Parkinson's in unknown and there is no cure. But there are treatment options like medication and surgery to manage symptoms.

"There is a lot of hope out there. There's a lot of new medications coming through the pipeline that will be helpful. We also encourage people to live their lives to the fullest everyday," says Karlin Schroeder with the Parkinsons Disease Foundation.

Clickhereto read more about Parkinson's Disease.

View original post here:
Want to learn more about Parkinson's Disease?

Sanofi and Michael J. Fox Foundation Collaborate on Potential New Treatment for Parkinson's Disease

- Fox Foundation to sponsor a clinical trial to study Sanofi compound -

PARIS , France , April 19, 2012 /CNW Telbec/ - Sanofi (EURONEXT: BSAC - News) (NYSE: SNY - News) announced today that it has entered into a collaboration with the Michael J. Fox Foundation (MJFF) to conduct a clinical trial to assess the safety and tolerability of AVE 8112, a Sanofi PDE4 inhibitor - phosphodiesterase type 4 inhibitor - in patients with Parkinson's disease (PD).

"AVE8112 has shown promising pro-cognitive activity in preclinical models that could be of interest to the under-addressed cognitive aspects of Parkinson's disease, an area of unmet need where a new treatment could make a tangible difference in patients' lives," said Todd Sherer , Ph.D., Chief Executive Officer of MJFF. "Groundbreaking collaborations with like-minded partners such as Sanofi are a hallmark of the Fox Foundation's approach and help us speed scientific advances with potential to improve the treatment of Parkinson's for patients today and in the future."

Under the terms of the collaboration, MJFF will sponsor a phase I b clinical trial to assess the safety and tolerability of AVE8112 in patients with Parkinson's disease. All data and results generated by the clinical trial will be owned by MJFF and shared with Sanofi. Further development plans will be based upon the results of the study.

"The Michael J. Fox Foundation has been a driving force in discovering and developing improved therapies for those living with Parkinson's disease. Through this research collaboration, together we will be able to study Sanofi's pharmaceutical compound for a possible new treatment for PD patients around the world," said Dr. Elias Zerhouni , President, Global R&D, Sanofi. "We hope to continue to develop relationships with private foundations like the Michael J. Fox Foundation to pool our resources and maximize the potential of our drug portfolio to address unmet medical needs."

The clinical trial will be conducted at clinical sites in the United States in Baltimore , MD, and Los Angeles , CA. Patient enrollment in the study is expected to begin later this year.

***

About Parkinson's Disease Over one million people in the US and an estimated 5 million people globally suffer from Parkinson's disease, a neurodegenerative disorder caused by the diminished production of dopamine, a key neurotransmitter, resulting in progressive impairment of motor function including tremors, rigidity and difficulty in moving. Another symptom of PD is cognitive dysfunction, such as difficulty planning, sequencing, initiating and sustaining behavior toward a goal. Estimates vary but some studies suggest a cognitive deficit may occur in up to 80% of people with Parkinson's. While there is a drug approved for the treatment of dementia in PD, there are currently no treatments available for patients who experience less severe cognitive impairments.

About Sanofi Sanofi, a global and diversified healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients' needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new Genzyme. Sanofi is listed in Paris (EURONEXT: BSAC - News) and in New York (NYSE: SNY - News).

About The Michael J. Fox Foundation for Parkinson's Research As the world's largest private funder of Parkinson's research, The Michael J. Fox Foundation is dedicated to accelerating a cure for Parkinson's disease and improved therapies for those living with the condition today. The Foundation pursues its goals through an aggressively funded, highly targeted research program coupled with active global engagement of scientists, Parkinson's patients, business leaders, clinical trial participants, donors and volunteers. In addition to funding more than $285 million in research to date, the Foundation has fundamentally altered the trajectory of progress toward a cure. Operating at the hub of worldwide Parkinson's research, the Foundation forges groundbreaking collaborations with industry leaders, academic scientists and government research funders; increases the flow of participants into Parkinson's disease clinical trials with its online tool, Fox Trial Finder; promotes Parkinson's awareness through high-profile advocacy, events and outreach; and coordinates the grassroots involvement of thousands of Team Fox members around the world. Now through December 31, 2012 , all new and increased giving to The Michael J. Fox Foundation, as well as gifts from donors who have not given since 2009 or earlier, will be matched on a dollar-for-dollar basis with the $50-million Brin Wojcicki Challenge, launched by Sergey Brin and Anne Wojcicki .

Read more:
Sanofi and Michael J. Fox Foundation Collaborate on Potential New Treatment for Parkinson's Disease

Sanofi and Michael J. Fox Foundation Collaborate on Potential New Treatment for Parkinson’s Disease

- Fox Foundation to sponsor a clinical trial to study Sanofi compound -

PARIS , France , April 19, 2012 /CNW Telbec/ - Sanofi (EURONEXT: BSAC - News) (NYSE: SNY - News) announced today that it has entered into a collaboration with the Michael J. Fox Foundation (MJFF) to conduct a clinical trial to assess the safety and tolerability of AVE 8112, a Sanofi PDE4 inhibitor - phosphodiesterase type 4 inhibitor - in patients with Parkinson's disease (PD).

"AVE8112 has shown promising pro-cognitive activity in preclinical models that could be of interest to the under-addressed cognitive aspects of Parkinson's disease, an area of unmet need where a new treatment could make a tangible difference in patients' lives," said Todd Sherer , Ph.D., Chief Executive Officer of MJFF. "Groundbreaking collaborations with like-minded partners such as Sanofi are a hallmark of the Fox Foundation's approach and help us speed scientific advances with potential to improve the treatment of Parkinson's for patients today and in the future."

Under the terms of the collaboration, MJFF will sponsor a phase I b clinical trial to assess the safety and tolerability of AVE8112 in patients with Parkinson's disease. All data and results generated by the clinical trial will be owned by MJFF and shared with Sanofi. Further development plans will be based upon the results of the study.

"The Michael J. Fox Foundation has been a driving force in discovering and developing improved therapies for those living with Parkinson's disease. Through this research collaboration, together we will be able to study Sanofi's pharmaceutical compound for a possible new treatment for PD patients around the world," said Dr. Elias Zerhouni , President, Global R&D, Sanofi. "We hope to continue to develop relationships with private foundations like the Michael J. Fox Foundation to pool our resources and maximize the potential of our drug portfolio to address unmet medical needs."

The clinical trial will be conducted at clinical sites in the United States in Baltimore , MD, and Los Angeles , CA. Patient enrollment in the study is expected to begin later this year.

***

About Parkinson's Disease Over one million people in the US and an estimated 5 million people globally suffer from Parkinson's disease, a neurodegenerative disorder caused by the diminished production of dopamine, a key neurotransmitter, resulting in progressive impairment of motor function including tremors, rigidity and difficulty in moving. Another symptom of PD is cognitive dysfunction, such as difficulty planning, sequencing, initiating and sustaining behavior toward a goal. Estimates vary but some studies suggest a cognitive deficit may occur in up to 80% of people with Parkinson's. While there is a drug approved for the treatment of dementia in PD, there are currently no treatments available for patients who experience less severe cognitive impairments.

About Sanofi Sanofi, a global and diversified healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients' needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new Genzyme. Sanofi is listed in Paris (EURONEXT: BSAC - News) and in New York (NYSE: SNY - News).

About The Michael J. Fox Foundation for Parkinson's Research As the world's largest private funder of Parkinson's research, The Michael J. Fox Foundation is dedicated to accelerating a cure for Parkinson's disease and improved therapies for those living with the condition today. The Foundation pursues its goals through an aggressively funded, highly targeted research program coupled with active global engagement of scientists, Parkinson's patients, business leaders, clinical trial participants, donors and volunteers. In addition to funding more than $285 million in research to date, the Foundation has fundamentally altered the trajectory of progress toward a cure. Operating at the hub of worldwide Parkinson's research, the Foundation forges groundbreaking collaborations with industry leaders, academic scientists and government research funders; increases the flow of participants into Parkinson's disease clinical trials with its online tool, Fox Trial Finder; promotes Parkinson's awareness through high-profile advocacy, events and outreach; and coordinates the grassroots involvement of thousands of Team Fox members around the world. Now through December 31, 2012 , all new and increased giving to The Michael J. Fox Foundation, as well as gifts from donors who have not given since 2009 or earlier, will be matched on a dollar-for-dollar basis with the $50-million Brin Wojcicki Challenge, launched by Sergey Brin and Anne Wojcicki .

Read more:
Sanofi and Michael J. Fox Foundation Collaborate on Potential New Treatment for Parkinson's Disease

19th century therapy for Parkinson's disease may help patients today

Public release date: 19-Apr-2012 [ | E-mail | Share ]

Contact: Deb Song deb_song@rush.edu 312-942-0588 Rush University Medical Center

(CHICAGO) In the 19th century, Jean-Martin Charcot, the celebrated neurologist, developed a "vibration chair," to relieve symptoms of Parkinson's disease. Charcot reported improvements in his patients, but he died shortly thereafter and a more complete evaluation of the therapy was never conducted. Now, a group of neurological researchers at Rush University Medical Center have replicated his work in a study to see if Charcot's observation holds true against modern scientific testing.

Results from the study indicate that while vibration therapy does significantly improve some symptoms of Parkinson's disease, the effect is due to placebo or other nonspecific factors, and not the vibration. The findings are published in the April issue of Journal of Parkinson's Disease.

"We attempted to mimic Charcot's protocol with modern equipment in order to confirm or refute an historical observation," explains lead investigator Christopher G. Goetz, MD, director of the Parkinson's disease and Movement Disorders Center at Rush. "Both the treated group and the control group improved similarly, suggesting other factors had an effect on Parkinson's disease motor function."

Charcot's patients told him that during long carriage rides or train journeys, uncomfortable or painful symptoms of Parkinson's disease seemed to disappear, and the relief lasted quite some time after the journey. He developed a chair that mimicked the continuous jerking of a carriage or train.

Goetz and his colleagues randomly assigned 23 patients to either a vibrating chair or the same chair without vibration. During the treatment sessions, both groups of study participants listened to a relaxation CD of nature sounds. Study participants underwent daily treatment for a month.

The patients in the vibration treatment group showed significant improvement in motor function after daily 30-minute treatments for four weeks. Although not as high, motor function scores for the no vibration group also improved significantly. Both groups showed similar and significant improvement in depression, anxiety, fatigue, and nighttime sleep and both groups reported similar high satisfaction with their treatment.

"Our results confirm Charcot's observation of improvement in Parkinson's disease symptomology with chronic vibration treatment, but we did not find the effect specific to vibration," said Goetz. "Instead, our data suggest that auditory sensory stimulation with relaxation in a lounge chair or simply the participation in a research protocol has equivalent benefit as vibration on motor function."

"While we can agree that our results may not change scientific thinking on treatment mechanisms, our results will allow clinicians to guide patients to at least one apparatus that is safe and associated with objective changes in parkinsonian impairment scores," said Goetz. "Charcot's advice to colleagues resonates as one places vibration therapy in the context of potential options for patients. 'It is no small gain to be able to relieve the sufferers of paralysis agitans.'"

The rest is here:
19th century therapy for Parkinson's disease may help patients today

19th century therapy for Parkinson’s disease may help patients today

Public release date: 19-Apr-2012 [ | E-mail | Share ]

Contact: Deb Song deb_song@rush.edu 312-942-0588 Rush University Medical Center

(CHICAGO) In the 19th century, Jean-Martin Charcot, the celebrated neurologist, developed a "vibration chair," to relieve symptoms of Parkinson's disease. Charcot reported improvements in his patients, but he died shortly thereafter and a more complete evaluation of the therapy was never conducted. Now, a group of neurological researchers at Rush University Medical Center have replicated his work in a study to see if Charcot's observation holds true against modern scientific testing.

Results from the study indicate that while vibration therapy does significantly improve some symptoms of Parkinson's disease, the effect is due to placebo or other nonspecific factors, and not the vibration. The findings are published in the April issue of Journal of Parkinson's Disease.

"We attempted to mimic Charcot's protocol with modern equipment in order to confirm or refute an historical observation," explains lead investigator Christopher G. Goetz, MD, director of the Parkinson's disease and Movement Disorders Center at Rush. "Both the treated group and the control group improved similarly, suggesting other factors had an effect on Parkinson's disease motor function."

Charcot's patients told him that during long carriage rides or train journeys, uncomfortable or painful symptoms of Parkinson's disease seemed to disappear, and the relief lasted quite some time after the journey. He developed a chair that mimicked the continuous jerking of a carriage or train.

Goetz and his colleagues randomly assigned 23 patients to either a vibrating chair or the same chair without vibration. During the treatment sessions, both groups of study participants listened to a relaxation CD of nature sounds. Study participants underwent daily treatment for a month.

The patients in the vibration treatment group showed significant improvement in motor function after daily 30-minute treatments for four weeks. Although not as high, motor function scores for the no vibration group also improved significantly. Both groups showed similar and significant improvement in depression, anxiety, fatigue, and nighttime sleep and both groups reported similar high satisfaction with their treatment.

"Our results confirm Charcot's observation of improvement in Parkinson's disease symptomology with chronic vibration treatment, but we did not find the effect specific to vibration," said Goetz. "Instead, our data suggest that auditory sensory stimulation with relaxation in a lounge chair or simply the participation in a research protocol has equivalent benefit as vibration on motor function."

"While we can agree that our results may not change scientific thinking on treatment mechanisms, our results will allow clinicians to guide patients to at least one apparatus that is safe and associated with objective changes in parkinsonian impairment scores," said Goetz. "Charcot's advice to colleagues resonates as one places vibration therapy in the context of potential options for patients. 'It is no small gain to be able to relieve the sufferers of paralysis agitans.'"

The rest is here:
19th century therapy for Parkinson's disease may help patients today

NI in Parkinson's research world first

Published Friday, 20 April 2012

Researchers from around the world are coming together to study Parkinson's (Getty)

The announcement was made at a special event at Queen's University, as part of Parkinson's Awareness Week.

Parkinson's UK says the research study will boost the chances of finding a cure to stop the devastating symptoms, including tremors, mood changes, movement difficulties, loss of smell and speech problems.

The charity is looking to recruit up to 3,000 sufferers throughout the UK, who are at an early stage of the condition, for the study called 'Tracking Parkinson's'.

The aim of the 1.6m study is to identify elusive biomarkers and develop simple tests, like blood tests, to diagnose the disease.

We could identify some of the problems and, moving forward, we could actually treat Parkinson's rather than the symptoms, and that would be a cure.

Kieran Breen, Director of Research and Innovation at Parkinson's UK

As part of the study, the responses to treatments for tremors, movement problems, anxiety, memory lapses and digestion problems will be closely monitored for up to five years.

"Studies like 'Tracking Parkinson's' could make a huge difference and help us to ultimately find a cure," said Dr Kieran Breen.

Read more here:
NI in Parkinson's research world first

NI in Parkinson’s research world first

Published Friday, 20 April 2012

Researchers from around the world are coming together to study Parkinson's (Getty)

The announcement was made at a special event at Queen's University, as part of Parkinson's Awareness Week.

Parkinson's UK says the research study will boost the chances of finding a cure to stop the devastating symptoms, including tremors, mood changes, movement difficulties, loss of smell and speech problems.

The charity is looking to recruit up to 3,000 sufferers throughout the UK, who are at an early stage of the condition, for the study called 'Tracking Parkinson's'.

The aim of the 1.6m study is to identify elusive biomarkers and develop simple tests, like blood tests, to diagnose the disease.

We could identify some of the problems and, moving forward, we could actually treat Parkinson's rather than the symptoms, and that would be a cure.

Kieran Breen, Director of Research and Innovation at Parkinson's UK

As part of the study, the responses to treatments for tremors, movement problems, anxiety, memory lapses and digestion problems will be closely monitored for up to five years.

"Studies like 'Tracking Parkinson's' could make a huge difference and help us to ultimately find a cure," said Dr Kieran Breen.

Read more here:
NI in Parkinson's research world first

Clinical Trial at Evergreen Healthcare Shows Intestinal Gel Reduces Symptoms of Advanced Parkinson's Disease

KIRKLAND, Wash., April 20, 2012 /PRNewswire/ -- A recent clinical trial conducted at Evergreen Healthcare shows that a new form of a common drug used to treat Parkinson's Disease greatly improves the quality of life for patients and reduces the affects of symptoms such as tremors, slowness, stiffness and difficulty walking.

Evergreen was the only site in the Pacific Northwest to hold the trial, which was led by Dr. C. Warren Olanow, a Fellow of the American Academy of Neurology and Professor of Neurology and Neuroscience at the Mount Sinai School of Medicine in New York.

The trial tested standard oral dosages of a Parkinson's drug against the newer levodopa-carbidopa intestinal gel (LCIG) and found that the intestinal treatments gave patients an average of two extra hours per day of reduced symptoms and improved movement.

"We have been involved in the trials since 2008," said Dr. Alida Griffith, principal investigator for the trial at Evergreen's Booth Gardner Parkinson's Care Center. "Levodopa is the 'gold standard' treatment for Parkinson's disease."

The intestinal gel contains levodopa and carbidopa, two drugs commonly prescribed for Parkinson's, and is infused through a portable pump connected to a tube implanted in the intestine.

In the three-month, double-blind trial, 71 participants were randomized to receive either the continuous infusion of LCIG and dummy pills or a dummy intestinal gel and pills that contained levodopa and carbidopa. At the start of the study, the average person had Parkinson's disease for about 11 years and experienced 6.6 hours of symptomatic behavior per day. A total of 93 percent of participants completed the study.

The results of the study are set to be presented as part of the Emerging Science program (formerly known as Late-Breaking Science) at the American Academy of Neurology's 64th Annual Meeting in New Orleans from April 21 to April 28, 2012.

The study was supported by Abbott.

Learn more about Parkinson's disease at http://www.aan.com/patients.

To learn more about the Evergreen Neuroscience Institute, visit http://www.evergreenhealthcare.org/parkinsons or call the Evergreen Healthline 425.899.3000.

Visit link:
Clinical Trial at Evergreen Healthcare Shows Intestinal Gel Reduces Symptoms of Advanced Parkinson's Disease

Clinical Trial at Evergreen Healthcare Shows Intestinal Gel Reduces Symptoms of Advanced Parkinson’s Disease

KIRKLAND, Wash., April 20, 2012 /PRNewswire/ -- A recent clinical trial conducted at Evergreen Healthcare shows that a new form of a common drug used to treat Parkinson's Disease greatly improves the quality of life for patients and reduces the affects of symptoms such as tremors, slowness, stiffness and difficulty walking.

Evergreen was the only site in the Pacific Northwest to hold the trial, which was led by Dr. C. Warren Olanow, a Fellow of the American Academy of Neurology and Professor of Neurology and Neuroscience at the Mount Sinai School of Medicine in New York.

The trial tested standard oral dosages of a Parkinson's drug against the newer levodopa-carbidopa intestinal gel (LCIG) and found that the intestinal treatments gave patients an average of two extra hours per day of reduced symptoms and improved movement.

"We have been involved in the trials since 2008," said Dr. Alida Griffith, principal investigator for the trial at Evergreen's Booth Gardner Parkinson's Care Center. "Levodopa is the 'gold standard' treatment for Parkinson's disease."

The intestinal gel contains levodopa and carbidopa, two drugs commonly prescribed for Parkinson's, and is infused through a portable pump connected to a tube implanted in the intestine.

In the three-month, double-blind trial, 71 participants were randomized to receive either the continuous infusion of LCIG and dummy pills or a dummy intestinal gel and pills that contained levodopa and carbidopa. At the start of the study, the average person had Parkinson's disease for about 11 years and experienced 6.6 hours of symptomatic behavior per day. A total of 93 percent of participants completed the study.

The results of the study are set to be presented as part of the Emerging Science program (formerly known as Late-Breaking Science) at the American Academy of Neurology's 64th Annual Meeting in New Orleans from April 21 to April 28, 2012.

The study was supported by Abbott.

Learn more about Parkinson's disease at http://www.aan.com/patients.

To learn more about the Evergreen Neuroscience Institute, visit http://www.evergreenhealthcare.org/parkinsons or call the Evergreen Healthline 425.899.3000.

Visit link:
Clinical Trial at Evergreen Healthcare Shows Intestinal Gel Reduces Symptoms of Advanced Parkinson's Disease

New Online Community Highlights that Living with Parkinson's Disease May Involve More Than Motionâ„¢

ATLANTA, April 20, 2012 /PRNewswire/ --To help people learn more about the full range of symptoms associated with Parkinson's disease, global biopharmaceutical company UCB, Inc., is launching a new online community -- Parkinson's More than Motion -- that provides a platform for people living with Parkinson's disease and their caregivers to interact and learn from others with the condition. Part of this launch is the debut of a new reality-style video series depicting real families living with the condition.

"My family and I are telling my story in the More than Motion community to encourage others to educate themselves about all symptoms of Parkinson's disease, so they can best manage the condition," said Jo-Ann Golec, who was diagnosed more than 15 years ago and has become an active Parkinson's disease advocate.

The Parkinson's More than Motion community includes a Facebook page where people can add their voices to the conversation, connect with experts, take quizzes and more:

One million Americans currently live with Parkinson's disease. Symptoms of Parkinson's disease are typically categorized as either affecting motor function or non-motor function. The cardinal motor symptoms include stiffness, tremors, slow movements and postural instability. In addition, the medical and research communities are starting to better understand the full spectrum of symptoms that can have a significant impact on a patient's life. These include:

In celebration of Parkinson's Awareness Month, which occurs each April in the U.S., Parkinson's More than Motion will travel to community events this month including the American Academy of Neurology's Brain Health Fair in New Orleans and the Parkinson's Unity Walk in New York City.

To learn more about Parkinson's More than Motion and to view the first installment of the video series, visit Facebook.com/ParkinsonsMorethanMotion.

More About Parkinson's Disease

Parkinson's disease is a chronic, progressive, neurological disease that occurs when certain cells in the brain stop producing enough of a chemical called dopamine. Dopamine plays several important roles in the body -- it helps regulate movement and it plays a role in cognitive and emotional function.

As dopamine levels fall, the cardinal motor symptoms (stiffness, tremors, slow movement, and postural instability) can progress, along with the underlying non-motor symptoms of Parkinson's disease, which are less well-recognized and may be under-treated. It is estimated that 60 percent of people with Parkinson's have two or more non-motor symptoms, and that 25 percent have four or more.

Parkinson's disease is the second most common neurological disorder affecting older people in the United States. Each year, between 50,000 and 60,000 new cases of Parkinson's disease are diagnosed in the U.S.; worldwide it is estimated that 7 to 10 million people have Parkinson's disease.

See the original post here:
New Online Community Highlights that Living with Parkinson's Disease May Involve More Than Motionâ„¢

New Online Community Highlights that Living with Parkinson’s Disease May Involve More Than Motionâ„¢

ATLANTA, April 20, 2012 /PRNewswire/ --To help people learn more about the full range of symptoms associated with Parkinson's disease, global biopharmaceutical company UCB, Inc., is launching a new online community -- Parkinson's More than Motion -- that provides a platform for people living with Parkinson's disease and their caregivers to interact and learn from others with the condition. Part of this launch is the debut of a new reality-style video series depicting real families living with the condition.

"My family and I are telling my story in the More than Motion community to encourage others to educate themselves about all symptoms of Parkinson's disease, so they can best manage the condition," said Jo-Ann Golec, who was diagnosed more than 15 years ago and has become an active Parkinson's disease advocate.

The Parkinson's More than Motion community includes a Facebook page where people can add their voices to the conversation, connect with experts, take quizzes and more:

One million Americans currently live with Parkinson's disease. Symptoms of Parkinson's disease are typically categorized as either affecting motor function or non-motor function. The cardinal motor symptoms include stiffness, tremors, slow movements and postural instability. In addition, the medical and research communities are starting to better understand the full spectrum of symptoms that can have a significant impact on a patient's life. These include:

In celebration of Parkinson's Awareness Month, which occurs each April in the U.S., Parkinson's More than Motion will travel to community events this month including the American Academy of Neurology's Brain Health Fair in New Orleans and the Parkinson's Unity Walk in New York City.

To learn more about Parkinson's More than Motion and to view the first installment of the video series, visit Facebook.com/ParkinsonsMorethanMotion.

More About Parkinson's Disease

Parkinson's disease is a chronic, progressive, neurological disease that occurs when certain cells in the brain stop producing enough of a chemical called dopamine. Dopamine plays several important roles in the body -- it helps regulate movement and it plays a role in cognitive and emotional function.

As dopamine levels fall, the cardinal motor symptoms (stiffness, tremors, slow movement, and postural instability) can progress, along with the underlying non-motor symptoms of Parkinson's disease, which are less well-recognized and may be under-treated. It is estimated that 60 percent of people with Parkinson's have two or more non-motor symptoms, and that 25 percent have four or more.

Parkinson's disease is the second most common neurological disorder affecting older people in the United States. Each year, between 50,000 and 60,000 new cases of Parkinson's disease are diagnosed in the U.S.; worldwide it is estimated that 7 to 10 million people have Parkinson's disease.

See the original post here:
New Online Community Highlights that Living with Parkinson's Disease May Involve More Than Motionâ„¢

New Neupro® Data in Parkinson's Disease and Restless Legs Syndrome to be Presented at the 64th American Academy of …

ATLANTA, April 20, 2012 /PRNewswire/ --Data examining the effect of Neupro (rotigotine transdermal system) in both Parkinson's disease and Restless Legs Syndrome (RLS) will be presented at the 64th American Academy of Neurology (AAN) Annual Meeting in New Orleans, LA, between April 21-28, 2012. Key data presentations will focus on post hoc analyses of pivotal and other studies of rotigotine transdermal system and are designed to investigate the impact of rotigotine transdermal system on the core symptoms of RLS and on the motor and underlying symptoms of Parkinson's disease such as depression, anxiety, anehdonia, fatigue and pain.

"These resultsaddto thebody of clinical evidencesupporting rotigotine transdermal system. The dataunderscore UCB's continuing commitment to discovering and developing therapies that address unmet medical needs for potentially debilitating central nervous system disorders," said Dr. James Zackheim, PhD, Senior Medical Director, Central Nervous System Business Unit, UCB, Inc.

Earlier this month, the U.S. Food and Drug Administration (FDA) approved Neupro (rotigotine transdermal system) for the treatment of the signs and symptoms of advanced stage idiopathic Parkinson's disease (PD) and as a treatment for moderate-to-severe primary RLS. Neupro was previously approved by the FDA for the signs and symptoms of early stage idiopathic PD. The FDA has also approved UCB's new formulation of Neupro.

Following is a guide to UCB-supported research featuring rotigotine transdermal system being presented during the AAN Annual Meeting. For more information please contact Andrea Levin at 404.483.7329 or Andrea.Levin@ucb.com.

Parkinson's disease abstracts

1. [P.06.088] Abstract Title: Rotigotine Transdermal System Improves Neuropsychiatric Features (Apathy, Anhedonia, Anxiety, and Depression) and Fatigue in Patients With Parkinson's Disease: A Post-hoc Analysis of Five Double-blind Placebo-controlled Studies Date/Time: Thursday, April 26, 20127:30 am 12:00 pm Session Info:Session P06: Assessment and Treatment of Parkinson's Disease

2. [P.06.085] Abstract Title: Rotigotine Transdermal System Improves Pain in Patients With Parkinson's Disease: A Post-hoc Analysis of Patients Reporting Pain in the RECOVER StudyDate/Time: Thursday, April 26, 20127:30 am 12:00 pm Session Info:Session P06: Assessment and Treatment of Parkinson's Disease

3. Abstract Title: An International Study to Investigate Rotigotine Dose Response (2-8 mg/24 h) on 'Off' Time in Patients With Advanced Stage Parkinson's Disease Date/Time: Wednesday, April 25, 2012 5:45 pm 7:00 pm

RLS abstracts

4. [P04.032] Abstract Title: Effects of 24-h Transdermal Delivery of Rotigotine on the Core Symptoms and Symptom Impact of Restless Legs Syndrome/Willis-Ekbom Disease: A Post-hoc Analysis of IRLS Single Item Data from a 6-month Placebo-controlled European StudyDate/Time:Wednesday, April 25, 20127:30 am 12:00 pm Session Info:Session P04: Movement Disorders: Restless Legs Syndrome, and Tardive Dyskinesia

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New Neupro® Data in Parkinson's Disease and Restless Legs Syndrome to be Presented at the 64th American Academy of ...

New Neupro® Data in Parkinson’s Disease and Restless Legs Syndrome to be Presented at the 64th American Academy of …

ATLANTA, April 20, 2012 /PRNewswire/ --Data examining the effect of Neupro (rotigotine transdermal system) in both Parkinson's disease and Restless Legs Syndrome (RLS) will be presented at the 64th American Academy of Neurology (AAN) Annual Meeting in New Orleans, LA, between April 21-28, 2012. Key data presentations will focus on post hoc analyses of pivotal and other studies of rotigotine transdermal system and are designed to investigate the impact of rotigotine transdermal system on the core symptoms of RLS and on the motor and underlying symptoms of Parkinson's disease such as depression, anxiety, anehdonia, fatigue and pain.

"These resultsaddto thebody of clinical evidencesupporting rotigotine transdermal system. The dataunderscore UCB's continuing commitment to discovering and developing therapies that address unmet medical needs for potentially debilitating central nervous system disorders," said Dr. James Zackheim, PhD, Senior Medical Director, Central Nervous System Business Unit, UCB, Inc.

Earlier this month, the U.S. Food and Drug Administration (FDA) approved Neupro (rotigotine transdermal system) for the treatment of the signs and symptoms of advanced stage idiopathic Parkinson's disease (PD) and as a treatment for moderate-to-severe primary RLS. Neupro was previously approved by the FDA for the signs and symptoms of early stage idiopathic PD. The FDA has also approved UCB's new formulation of Neupro.

Following is a guide to UCB-supported research featuring rotigotine transdermal system being presented during the AAN Annual Meeting. For more information please contact Andrea Levin at 404.483.7329 or Andrea.Levin@ucb.com.

Parkinson's disease abstracts

1. [P.06.088] Abstract Title: Rotigotine Transdermal System Improves Neuropsychiatric Features (Apathy, Anhedonia, Anxiety, and Depression) and Fatigue in Patients With Parkinson's Disease: A Post-hoc Analysis of Five Double-blind Placebo-controlled Studies Date/Time: Thursday, April 26, 20127:30 am 12:00 pm Session Info:Session P06: Assessment and Treatment of Parkinson's Disease

2. [P.06.085] Abstract Title: Rotigotine Transdermal System Improves Pain in Patients With Parkinson's Disease: A Post-hoc Analysis of Patients Reporting Pain in the RECOVER StudyDate/Time: Thursday, April 26, 20127:30 am 12:00 pm Session Info:Session P06: Assessment and Treatment of Parkinson's Disease

3. Abstract Title: An International Study to Investigate Rotigotine Dose Response (2-8 mg/24 h) on 'Off' Time in Patients With Advanced Stage Parkinson's Disease Date/Time: Wednesday, April 25, 2012 5:45 pm 7:00 pm

RLS abstracts

4. [P04.032] Abstract Title: Effects of 24-h Transdermal Delivery of Rotigotine on the Core Symptoms and Symptom Impact of Restless Legs Syndrome/Willis-Ekbom Disease: A Post-hoc Analysis of IRLS Single Item Data from a 6-month Placebo-controlled European StudyDate/Time:Wednesday, April 25, 20127:30 am 12:00 pm Session Info:Session P04: Movement Disorders: Restless Legs Syndrome, and Tardive Dyskinesia

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New Neupro® Data in Parkinson's Disease and Restless Legs Syndrome to be Presented at the 64th American Academy of ...

Swimming With Multiple Sclerosis: Top 5 Florida Swim Destinations

I have been swimming all over the state of Florida. I frequent the state of Florida in the summertime because this is the most exciting state to swim in. Where else can you enjoy a good relaxing swim with this many sea creatures? My swims in Florida have brought me face-to-face with dolphins, manatees, and barracudas. This is the reason I love to swim in Florida.

I also enjoy the white sandy beaches, and the perfectly clear waters that Florida has to offer.

This is the reason I want to share with you the 5 best locations to swim in Florida:

Destination number one

Our first stop for a good swim comes from the Miami Seaquarium. The Seaquarium offers a unique experience, which is the reason I put it first on my list. The Seaquarium allows people of all ages to interact with the dolphins. The Seaquarium educates you about the dolphins first. Then allows you to interact and swim with the dolphins.

This was not a free swim, though. It cost me about $200 for this swim. The most exciting part to me was the opportunity to go into the deeper end of the water and get a ride back. I was able to grab a hold of the fin on the dolphins back, and go for a quick ride. These animals sure can move. I have never been able to interact like I did this day with the dolphins. It made me forget that I even had multiple sclerosis, as it was the most memorable day I have ever had.

Destination number two

Crystal River, Fla., is my second stop to swim with the manatees. There are a lot of different trips you can take in Crystal River to go and swim with the manatees. I have to say that it is a special treat every time I get to swim with these beautiful creatures. The manatees are rather friendly animals for all the experiences I've had with them.

The reason I love to swim with the manatees is that while you are enjoying the water you do not have to try very hard to encounter one of these animals. I have noticed that as long as you are swimming in their vicinity they will come up to you. I have noticed when I swim with the manatees they seem to be as interested in me as I am in them. Being that at anytime my multiple sclerosis could get worse and put me in a wheelchair, I take every chance I can to enjoy these creatures.

Destination number three

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Swimming With Multiple Sclerosis: Top 5 Florida Swim Destinations

Clinical trial launches to see whether vitamin D helps treat multiple sclerosis

Public release date: 19-Apr-2012 [ | E-mail | Share ]

Contact: Arney Rosenblat arney.rosenblat@nmss.org 212-476-0436 National Multiple Sclerosis Society

New York Doctors at several centers across the U.S. are recruiting people who have multiple sclerosis (MS) to determine the effectiveness of high-dose vitamin D supplements for reducing MS disease activity. The vitamins would be added to standard therapy with glatiramer acetate (Copaxone, Teva Pharmaceutical Industries). The study, funded by the National Multiple Sclerosis Society, is being led by Ellen Mowry, MD, MCR, at Johns Hopkins University in Baltimore. Other cities with centers recruiting participants include Portland, St. Louis, and San Francisco, and additional centers are being established.

A number of genetic and environmental factors influence whether a person will get MS. These factors may also impact the severity of the disease. Mounting evidence has been pointing to a reduced level of vitamin D in the blood as a risk factor for developing MS. In lab mice, vitamin D can reduce the effects of EAE, an MS-like disease, and growing evidence suggests it is time to test whether vitamin D can provide benefits to people who have MS.

Investigators are seeking 172 clinical trial participants between the ages of 18 and 50, who have been diagnosed with the relapsing-remitting form of MS. More details on the enrollment criteria are available at: http://www.clinicaltrials.gov/ct2/show/NCT01490502.

Participants will begin standard Copaxone treatment daily and will be randomly assigned to take the current recommended daily allowance of vitamin D or a high dose. The primary goal of the study is to determine whether vitamin D can reduce the proportion of people who experience a relapse. Other outcomes being studied include relapse rates, quality of life, brain tissue volume, disability progression, and safety.

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About Multiple Sclerosis

Multiple sclerosis, an unpredictable, often disabling disease of the central nervous system, interrupts the flow of information within the brain, and between the brain and body. Every hour in the United States, someone is newly diagnosed with the disease. Symptoms range from numbness and tingling to blindness and paralysis. The progress, severity and specific symptoms of MS in any one person cannot yet be predicted, but advances in research and treatment are moving us closer to a world free of MS. Most people with MS are diagnosed between the ages of 20 and 50, with at least two to three times more women than men being diagnosed with the disease. MS affects more than 400,000 people in the U.S. and over 2.1 million worldwide.

About the National Multiple Sclerosis Society

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Clinical trial launches to see whether vitamin D helps treat multiple sclerosis

EMD Serono to Present New Data on Multiple Sclerosis at the American Academy of Neurology’s 64th Annual Meeting

ROCKLAND, Mass.--(BUSINESS WIRE)--

EMD Serono, Inc., a subsidiary of Merck KGaA, Darmstadt, Germany, announced today that new data from the companys multiple sclerosis (MS) portfolio will be presented at the American Academy of Neurologys 64th Annual Meeting, taking place from April 21 to 28, in New Orleans, Louisiana. The data presented will focus on Rebif (interferon beta-1a), an established therapy for relapsing forms of MS, and ONO-4641 (S1P receptor agonist), an investigational oral drug in Phase II for the treatment of relapsing-remitting MS, for which Merck KGaA signed a collaboration agreement with Ono Pharmaceuticals in October 2011.

Presentations to be made at the upcoming AAN meeting further improve our understanding of the clinical effects of Rebif and show Phase II results on our new investigational drug ONO-4641, said Dr. Annalisa Jenkins, Head of Global Drug Development and Medical at Merck Serono, a division of Merck KGaA, Darmstadt, Germany. We are committed to advancing multiple sclerosis care, research and outcomes in order to provide treatments for people living with this devastating disease.

The following abstracts have been accepted for presentation at the 64th AAN Annual Meeting:

Rebif(interferon beta-1a) Data blitz1presentation followed by a poster presentation - Efficacy of two dosing frequencies of subcutaneous interferon beta-1a on the risk of conversion from a first demyelinating event to multiple sclerosis and on MRI measures of disease: 3-year results of Phase III, double-blind, multicentre trials (REFLEX and REFLEXION) (presentation #014, Wednesday, April 25, 2012, 6:24 PM)* * The formulation used in these studies is currently not approved in the United States

Poster presentations - Subcutaneous interferon -1a in children and adolescents with multiple sclerosis: an international retrospective study of 307 patients (poster session P04.119, Wednesday, April 25, 2012)** - Disease characteristics, dosing, and outcomes of subcutaneous interferon -1a treatment differ between children and adolescents with multiple sclerosis (poster P04.120, Wednesday, April 25, 2012)** ** This retrospective cohort study examines both Rebif and the serum-free formulation of Rebif. The serum-free formulation of Rebif is currently not approved in the United States. - Association of Targeted Blood Biomarkers with Interferon Beta-1a Treatment Administration, Magnetic Resonance Imaging Activity, and Treatment Response (poster P02.089, Tuesday, April 24, 2012)

ONO-4641 (S1P receptor agonist) Data blitz1presentation followed by a poster presentation - A double-blind, placebo-controlled, Phase II, 26-week DreaMS trial of a selective S1P receptor agonist ONO-4641 in patients with Relapsing-Remitting Multiple Sclerosis (presentation #013, Wednesday, April 25, 2012, 6:21 PM)

1 A data blitz presentation is a 3 minute oral presentation included in a 45 minutes oral session.

About Multiple Sclerosis

Multiple sclerosis (MS) is a chronic, inflammatory condition of the central nervous system and is the most common, non-traumatic, disabling neurological disease in young adults. It is estimated that there are approximately 400,000 people in the United States living with MS.

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EMD Serono to Present New Data on Multiple Sclerosis at the American Academy of Neurology’s 64th Annual Meeting

Multiple Sclerosis and Baseball: Top 5 Tips to Staying in the Game

They say the boys of summer are baseball players. So I guess this would make me one of the girls of summer. All my life I grew up with boys around. I had one sister, and she also hung out with the boys. I was the competitive one; I did not care if it was against guys or girls. This may be the reason that in the summertime I played baseball with the boys.

I have been playing baseball for the last 20 years. I play competitively against the boys. I have always said if a boy can do it, so can I. I have a mean arm on me, and can play with the best of them. Since being diagnosed with multiple sclerosis, though, I can no longer bat. I cannot run as fast as I need to in order to be able to bat. This is the reason that we use a pinch hitter in my place.

I have compiled a list of ways that keep me in the game even with my multiple sclerosis:

Tip number one

I have to maintain a cool body temperature. In order to do this I drink plenty of water. I maintain enough water to keep me hydrated and cool. I wear bright colors in order to keep the sun rays off of me as well.

The reason that playing baseball is still important to me even with multiple sclerosis is that I want to show the boys I can still strike them out. This is something that I have always taken great pride in being able to do. I told myself that I would never give up playing baseball, unless I ended up in a wheelchair. Well, I have not ended up in a wheelchair, so I still look forward to striking the boys out.

Tip number two

I always stretch before every game. I always spend about 15 minutes warming up before a game because it loosens up the muscles. This allows me to stay in the game longer. It also means that I get to make the boys suffer. I can still throw a mean fastball as long as I'm warmed up. This is the reason I stick to warming up for 15 minutes.

Tip number three

Even though I'm still competitive on the mound, it does not mean I can overdo it. The saying "no pain, no gain" is a saying I do not listen to when it comes to my multiple sclerosis. I know I'm still in pretty good shape for somebody that has a disability like multiple sclerosis, but I know not to overdo it. The mentality of sitting out the game when my multiple sclerosis has the best of me is what has allowed me to endure 20 years of this sport.

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Multiple Sclerosis and Baseball: Top 5 Tips to Staying in the Game