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11-16-2010, 02:07 PM | #1 | |||
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Senior Member
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I am hoping this hasn't been posted already, but this bears repeating and may be of great interest in the development of new drugs/treatments.
The last really "new" drug approved for Parkinson's was Comtan -or generic name Entacapone in 1999. Rxlist.com says this: "Entacapone is an inhibitor of catechol-O-methyltransferase (COMT), used in the treatment of Parkinson's Disease as an adjunct to levodopa/carbidopa therapy. Azilect is another form of MAO-Inhibitor, so I didn't count it as new. And Parcopa is just a predissolved form of L-dopa, and Stalevo is a combination of L-dopa and Comtan. So unless I am wrong it has been a decade since an all new discovery in Parkinsoon's medications has been made. (noto counting DBS, also) Thus, I am excited about this effort announced in the Wall Street Journal! "Pfizer Inc. will announce Tuesday a collaboration with University of California, San Francisco, to spur the discovery of new medicines, in the latest instance of a drug maker tapping outside experts for research-and-development help." The collaboration tackles a particularly difficult stage of drug development—the translation of early scientific research into marketable treatments. That stage of R&D is often referred to as the "Valley of Death" because so many promising compounds fail to advance. Under the terms, Pfizer would pay up to $85 million over the next five years to help explore whether discoveries in UCSF labs could be turned into new biologic medicines. UCSF researchers will be able to draw upon Pfizer's drug-development know-how, such as its expertise. * * * UCSF researchers would be allowed to publish the results of their work, and the university would share with Pfizer ownership rights of any promising developments. Read full article here: http://online.wsj.com/article/SB1000...ist_smartbrief Should I be excited???? How can we as patients promote this effort? Peg |
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"Thanks for this!" says: | GregW1 (11-17-2010) |
11-16-2010, 05:15 PM | #2 | |||
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Member
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Hummmm, at the moment I don't know if excitement should be considered. Get me a chunk of hat $85 million and I'll think about it a bit.
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"You can't fight City Hall, but you can pee on the steps and run." --Gary North |
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11-17-2010, 08:30 AM | #3 | |||
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LOL You may be on to something there!
Peg |
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11-17-2010, 10:12 AM | #4 | ||
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Junior Member
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accck well,
i was diagnosed with parkinson's at 26 july 22, 1991. i just celebrated my 46th birthday in september. i maxed out all the prescribed doses in 12 hours, for sinemet, comtan and mirapex before i was medically retired in june 2000 at 36. i've walked through the shadow of death more than upon one occasion. the harley and tats just mean i don't always do what i'm told. give my kids and grand kids a small percentage of all that they can graduate from harvard or yale, mayhap, cure us. |
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"Thanks for this!" says: |
11-17-2010, 05:15 PM | #5 | ||
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The announced partnership continues to underscore that big pharma is working to rethink its strategies for funding innovation and building their pipelines. This is a big initiative (across many indications). Thought I would mention though that Pfizer is doing work in PD...programs they picked up in the Wyeth merger and have continued/expanded. Their continued work and support of our field is evident in their commitment to PPMI. They made a $4M pledge to the project...a great contribution and a great signal. So, a PD partnership too.
Debi |
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"Thanks for this!" says: |
11-17-2010, 07:05 PM | #6 | |||
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Senior Member
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Debi
This is music to my ears. It has been far too long since a really new medication has been created just for Parkinson's. Most all have been something to extend the life of levodopa/carbidopa, the gold standard of treatment for over 40 years. I am hopeful that the results of the PPMI study will turn this thinking around. Big pharma should take note how a change in treating Parkinson's has already resulted in a blockbuster - with Medtronics' debut of Deep Brain Stimulation (DBS). Another plus for Medtronics has also been that it has shown to be effective in some cases of dystonia and dyskinesia. So what can the PD community do to help endorse and support collaborative efforts like Pfizer and universities? The companies need to do human testing so WE NEED VOLUNTEERS FOR CLINICAL TRIALS! I know one such source of trial info specific to PD can be found at www.pdtrials.org Have you done your part? |
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"Thanks for this!" says: | jeanb (11-17-2010), tulip girl (11-17-2010) |
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