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Old 12-11-2008, 08:37 AM   #1
cutekill
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Default Gene Therapy Grant is Larger than Initially Proposed!

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as a result of ffb’s generous donors, the gene therapy grant with cihr is larger than initially proposed! we anticipateministerial approval on a 2nd team grant on adult retinal stem cells in january. This is excellent news forcanadian gene therapy research and the hope it brings to canadians.cures really are in sight! Have a peaceful holiday season. Sharon.



$3 million towards gene therapy


to treat retinal degenerative diseases


toronto, december 9, 2008 – the foundation fighting blindness – canada (ffb) is partnering with the canadian institutes of health research (cihr) in a five-year grant that will fund an ambitious research project to develop innovative gene therapies for a number of degenerative retinal diseases.

this is a milestone in the charity’s 34 year history. It involves five research teams, four at prominent universities in canada and one in the u.s. It’s also the first time that the cihr is partnering with a health charity on a grant to develop therapies for degenerative eye diseases. The partnership will provide a much needed boost to eye research, which still receives significantly less funding in canada than other major disease areas such as diabetes or cancer.

“this is a huge milestone for the foundation fighting blindness and represents a historic shift in the type of vision research being funded,” said sharon colle, president and ceo, ffb-canada. “we’re taking the knowledge generated through decades of research into causes of these diseases, and are now applying it to the development of long awaited therapies.”

the five research teams involved will provide various specialized skills required for the success in this research project. The project will be led by dr. Robert molday, a molecular and cell biologist from the university of british columbia. The team’s other experts in gene therapy are dr. Jim hu from the university of toronto, and dr. Bill hauswirth from the university of florida. Dr. Marinko sarunic of simon fraser university will be responsible for the retinal imaging component of the project. As the team’s clinician-scientist, dr. Robert koenekoop will oversee the visual function testing and the gene analyses, first in animals and then in humans with a variety of retinal degenerations.

the strategy is to replace the defective gene with a “new healthy gene” in specific animal models for retinal degenerative diseases with the aim of slowing photoreceptor loss and partially restoring vision. Success in these animal models would lead to future human clinical trials.

"the application of gene therapy for three retinal degenerative diseases will be investigated: Stargardt macular dystrophy, leber congenital amaurosis (lca), and retinitis pigmentosa," dr. Molday explains. “the recent success in gene therapy for rpe65 has been highly conclusive for lca; we believe that we can learn from this and advance even more quickly this time.”

rpe65 mutations are one cause of leber congenital amaurosis. Three independent research teams have very recently shown that injecting a healthy version of that gene to young adults can partially restore their vision.

canadian institutes of health research (cihr)
cihr is the government of canada's agency responsible for funding health research in canada. Nine projects were awarded grants through the cihr program entitled “regenerative medicine and nanomedicine – emerging team grants – july 2008.” all of these projects hold great hope for medical applications in the fields of nanotechnology, stem cells, tissue engineering and rehabilitative sciences. To receive a grant, a team must show a multidisciplinary commitment to addressing problems in regenerative medicine. The long-term goal of this program is to develop innovative treatments that are scientifically based and socially validated.

the foundation fighting blindness (ffb) is canada's largest private contributor of vision research, thanks to its generous donors and long-time annual fundraisers, comic vision & ride for sight. Since its inception in 1974 the ffb has funded dozens of research discoveries to identify the causes of genetic forms of blindness at universities and hospitals across canada. Today, these discoveries have helped bring scientists to this very exciting time in vision research, translating knowledge into treatments to restore the gift of sight. For more information please visit: www.ffb.ca, or email: info@ffb.ca, or call 1-800-461-3331.


sharon colle
president and ceo
the foundation fighting blindness
890 yonge street, 12th floor
toronto, on, m4w 3p4

tel 416.360.4200 toll 1.800.461.3331
fax 416.360.0060 email scolle@ffb.ca

www.ffb.ca
www.rideforsight.com
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Old 12-12-2008, 11:14 AM   #2
The Last Boyscout
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Smile Re: Gene Therapy Grant is Larger than Initially Proposed!

That's awesome news. Glad to hear. Just adds a little more incentive to the drive for a cure.

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Old 12-15-2008, 07:00 PM   #3
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Default Re: Gene Therapy Grant is Larger than Initially Proposed!

Yippeeeeeeeeeeeeeee

That is such great news. We are very excited because if they do find a cure our family will benefit from all the hardwork. So keep fundraising and think of Meghan when you do

Katie
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