C/L works well for me …..when it works. I have a lot of problems with gut absorption. Not only does protein seem to be a problem, but just eating in general inhibits the medicine working well. I need to take simemet every 2-3 hours, so mealtimes are a nightmare. I’m very much hoping that the new subcutaneous pump (not the pump into the stomach) which I believe is just waiting FDA approval will be a godsend for me.
Does anyone have any info/thoughts on this new method of levadopa administration?
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saraoutwest
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Same with me. My GP dismisses my reports of symptoms returning within just a few minutes after I eat anything; within the 1 to two hour “window of nutrition…”. 😬
I am waiting for the subcutaneous pump as well. AbbVie is the manufacturer. My understanding is the clinical trials are complete and show both efficacy and safety. Users love it as it provides steadier uptake and completely avoids the digestive track. The FDA has not asked the company for further testing but has some issue with the pump itself. They are saying the release date could happen sooner but most likely summer of 2024.
I am so looking forward to it’s approval so I can get back to eating enough protein! I work out almost daily but because of my lack of protein it’s difficult some days. I’m in year 9 of being diagnosed. From what I’ve read, the FDA has pushed back with a couple questions but I can’t remember where I read it.
I know quite a bit about pumps but only 2 nd hand. Never heard of a levadopa pump. The NZ parkinson friends fb site has quite a few on the apomorph pump which is sub cutaneous. The levadopa infusion is different. It involves an op and a gastric tube. It was trialled in nz over 10 yrs ago and rejected. I’ll have to check what you refer to but i’m afraid Pharmac wont approve for years even if the US agency does.
There are two pharma companies with subq pumps in development. Both have gotten to phase 3 trials but only one has applied for approval. That is Abbvie. The other company is Neuroderm. I’ve been waiting for them for over four years now.
DIVE, currently in phase 2 testing by CHU Lille is the one I find interesting, although it's grindingly slow development even by normal PD standards. Well, it is La France (refer to Micky Flanagan for an evaluation of that nation by an Anglo saxon)
its a pump fitted below the skin, refilled every 7 to 14 days via a syringe which pumps dopamine, NOT levadopa direct into the substantia nigra. it does involve brain surgery but it is simpler than DBS
Projected clinical availability -2028 I believe . But good to have in the pipeline for then. (Meantime I'll replay the MF video)
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