Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 03-24-2008, 03:28 PM #11
Dan B Dan B is offline
New Member
 
Join Date: Mar 2008
Posts: 1
15 yr Member
Dan B Dan B is offline
New Member
 
Join Date: Mar 2008
Posts: 1
15 yr Member
Default Hi Peggy

75 programs!! do you have some suggestions of where to go and research the state of those programs. Just looked at the Prosavin, it seemed pretty exciting. I have a parent with Parkinson which is leaving pretty stressed out
Dan B is offline   Reply With QuoteReply With Quote

advertisement
Old 03-24-2008, 03:53 PM #12
pegleg's Avatar
pegleg pegleg is offline
Senior Member
 
Join Date: Sep 2006
Location: Tennessee
Posts: 1,213
15 yr Member
pegleg pegleg is offline
Senior Member
pegleg's Avatar
 
Join Date: Sep 2006
Location: Tennessee
Posts: 1,213
15 yr Member
Default Dan

that number (75) was taken from an article, but you can find a detailed status for most at our Pipeline Project website database at
www.pdpipeline.org
Peg
pegleg is offline   Reply With QuoteReply With Quote
Old 03-24-2008, 05:29 PM #13
paula_w paula_w is offline
In Remembrance
 
Join Date: Aug 2006
Location: Florida
Posts: 3,904
15 yr Member
paula_w paula_w is offline
In Remembrance
 
Join Date: Aug 2006
Location: Florida
Posts: 3,904
15 yr Member
Default duodopa

The FDA has been wrangling with Solvay over not having any placebo testing with duodopa. Solvay has finally agreed to do a phase III which will hopefully be in the U.S. this summer. I heard the same last year but this time it's closer to being true.

So to my knowledge, this problem is at least a year old, probably longer - I heard about it a year ago. Placebo testing for l-dopa because it involves a different delivery system. most of us with advanced PD know whether or not we can tolerate l-dopa and whether or not it works. But we have to have it tested with a placebo before it can be approved.

Does anyone know anyone outside the the U.S. who is on pump infused duodopa? If so, how is it at evening out ons and offs?

You can let me know sometime in the next year as they face delay after delay bringing it here.

paula
__________________
paula

"Time is not neutral for those who have pd or for those who will get it."
paula_w is offline   Reply With QuoteReply With Quote
Old 03-24-2008, 08:11 PM #14
Fiona Fiona is offline
Member
 
Join Date: Oct 2006
Posts: 492
15 yr Member
Fiona Fiona is offline
Member
 
Join Date: Oct 2006
Posts: 492
15 yr Member
Default

Word I heard on the gene therapy thing (which I guess would include ProSavin) is that they just don't know if the virus which bears the genetic material that is placed in the brain will at some unforseen future moment decide to mutate uncontrollably or unexpectedly.
Fiona is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
imark3000 (03-25-2008)
Old 03-25-2008, 05:45 AM #15
aftermathman aftermathman is offline
Member
 
Join Date: Sep 2006
Location: Evesham, England
Posts: 598
15 yr Member
aftermathman aftermathman is offline
Member
 
Join Date: Sep 2006
Location: Evesham, England
Posts: 598
15 yr Member
Default Fiona ...

you are right that gene therapy and the use of the AAV vector is new and as such may contain risk.

Not sure if things are quite as unknown as your reply suggests, at the moment, based on knowledge gathered, AAV is safe and well tolerated for the application of gene therapy in a number of products for PD.

IMHO gene therapy is no more risky or safe than any other ground breaking novel therapy.

Take care,
Neil.

Last edited by aftermathman; 03-25-2008 at 09:03 AM.
aftermathman is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
imark3000 (03-25-2008)
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
How far would you go for a cure?? MelodyL Social Chat 5 03-14-2008 03:36 PM
cure? maryfrances Parkinson's Disease 7 08-16-2007 10:10 PM
No Cure dealingwithtos Reflex Sympathetic Dystrophy (RSD and CRPS) 15 07-06-2007 05:37 PM
Cure helen totilo Community & Forum Feedback 2 02-01-2007 11:58 AM
Closer to cure for MS? pantos Multiple Sclerosis 1 11-04-2006 07:03 AM


All times are GMT -5. The time now is 04:57 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.