FAQ/Help |
Calendar |
Search |
Today's Posts |
07-24-2014, 04:51 PM | #1 | ||
|
|||
Magnate
|
http://iospress.metapress.com/conten...7/fulltext.pdf
this guy doesn't pull any punches. title: who dropped the ball on l-dopa by john palfeman i'm paraphrasing here, can' cut/paste. researchers basically bored by l-dopa? the following seems to apply to more advanced pd'ers suffering on/off. "the effort to produce a better delivered l-dopa failed, says henry ford hospital professor peter lewitt, because products were based on a lot of "half hearted pharmaceutical development, with poor design and not enough clinical research". he includes sinemet-cr, stalevo, dopamine agonists, mao-b inhibitors. Last edited by soccertese; 07-24-2014 at 05:13 PM. Reason: fixed link |
||
Reply With Quote |
"Thanks for this!" says: | Bogusia (07-25-2014), Conductor71 (07-24-2014), GerryW (07-25-2014), johnt (07-24-2014), lab rat (07-25-2014), lindylanka (07-25-2014), rainbow676 (07-24-2014), Tupelo3 (07-25-2014) |
07-24-2014, 08:26 PM | #2 | ||
|
|||
Senior Member
|
Yes, a "great essay".
Making levodopa work better for us is an attainable target. We can sit and hope for Big Pharma to deliver and likely wait years for something to get regulatory approval, and even then find that they charge such a high price that we can't afford it; or, we can work on the issue ourselves. On this forum we've discussed many possible approaches: - liquid levodopa, sipped frequently; - patches; - nasal sprays; - natural sources, e.g. fava beans; - grapefruit juice; - liposomes, etc. But all the time we stop short of running a clinical trial ourselves. Let's adopt a "can do" attitude NOW. John
__________________
Born 1955. Diagnosed PD 2005. Meds 2010-Nov 2016: Stalevo(75 mg) x 4, ropinirole xl 16 mg, rasagiline 1 mg Current meds: Stalevo(75 mg) x 5, ropinirole xl 8 mg, rasagiline 1 mg |
||
Reply With Quote |
"Thanks for this!" says: | Tupelo3 (07-25-2014) |
07-25-2014, 08:11 AM | #3 | ||
|
|||
Magnate
|
interesting he didn't comment on IMPAX LABS about to be released "improved" CR/IR combo.
|
||
Reply With Quote |
07-25-2014, 09:49 AM | #4 | ||
|
|||
Member
|
Quote:
As to Impax's Rytary, there has been little news regarding the FDA's follow up inspection. They have their quarterly earnings call on Aug. 6, maybe they'll give an update at that time. |
||
Reply With Quote |
"Thanks for this!" says: | lab rat (07-28-2014) |
07-25-2014, 10:47 AM | #5 | ||
|
|||
Magnate
|
i assume there's more money in other diseases especially if insurance companies continue to pay the astronomical prices for some of these new drugs, for example hepatitis C, cancer.
I assume when big pharma looks at pd, they see a disease where by the time they bring a new drug to market, there might be a "cure" of sorts or a less risky/cheaper DBS. it was assumed when i was diagnosed in late 2001 there would be a cure in 5 years. i wonder what the newly diagnosed are told by their neuros nowadays? rytary doesn't seem all that great, could be wrong. have to research DEPOMED and see if his optimism is justified. seems too good to be true, 1-2 pills/day. i know pd'ers on stalevo, requip, amantadine that are doing well 12+ years after diagnosis but the advantage of just 1 drug is obvious in any disease even if the cost was slightly more. let's hope for successful fetal and stem cell trials in 2015. keep exercising. |
||
Reply With Quote |
"Thanks for this!" says: | lab rat (07-28-2014) |
Reply |
|
|
Similar Threads | ||||
Thread | Forum | |||
new addition to Jon Palfreman’s Blog on pd, essay on pd diversity | Parkinson's Disease | |||
Haven't posted in a while - here's an update in essay form | Multiple Sclerosis | |||
Doc John? Perhaps this type of online site would be great for Patient/Advocates? | Parkinson's Disease | |||
My MS essay rough draft | The Stumble Inn |