Any experience with Kynmobi?: Has anyone... - Cure Parkinson's

Cure Parkinson's

25,550 members26,870 posts

Any experience with Kynmobi?

desertbush profile image
5 Replies

Has anyone had experience with a new drug called Kynmobi? It purports to be an effective way to treat off times quickly - improvement in motor symptoms at 15 minutes and lasting through 90 minutes. It uses a film put under the tongue so the agent is absorbed through the mouth rather than a pill that takes time to go through the digestive system.

Written by
desertbush profile image
desertbush
To view profiles and participate in discussions please or .
5 Replies
Godiv profile image
Godiv

Hi desert,This probably isn’t very helpful, but my doctor almost prescribed it for me. But she opted instead for an inhaler system that does the same thing. I think she said the inhaler is a little faster. Sorry I don’t know anything about the film, but it sounded really interesting and easy to me. More so than the inhaler which you have to load with two capsules apparently before you breathe it in.

desertbush profile image
desertbush in reply to Godiv

Thanks for your reply. We tried an inhaler, Inbrija, but my wife couldn't use it. You inhale a very fine "dust" and she felt like she was choking. That's why the use of a film would be better.

Godiv profile image
Godiv in reply to desertbush

Oh OK thank you. I can understand why she would feel that way. I probably will too. I hope the film works for her. It just sounds so much easier. The pharmacy company just called me tonight and they were describing the process of getting the inhaler ready. Good grief! Nothing you could do discreetly.

Cropseyville profile image
Cropseyville

I tried Kynmobi. A nurse starts you on 10 mg, under your tongue like you said. She takes your blood pressure, heart rate and monitors your nausea (had to take antinausea pills for 3 days before they titrated the dose of Kynmobi). Then you wait for 2 hours and they give you 15 mg, same protocol, up to 30 mg. I made it to 25 with absolutely no change in my freeze but had tachycardia. It was a two day, grueling procedure and I was so disappointed. It just did not work for me.

desertbush profile image
desertbush in reply to Cropseyville

Thank you for giving your experience. Very disappointing result. You always hope for some good news with this disease.

You may also like...

Any experience with Thiamine [B1] holiday?

for a long time, have you ever had Thiamine holiday? If yes please share your experience. How long...

Titrating down on Sinemet experience

titrating down ½ pill at a time for months noticing improvement when I took the equivalent of 2...

Anyone have any experience with Celastrol?

Dopaminergic Neuronal Death of Parkinson's Disease through Activating Mitophagy...

Does Anyone With Parkinson's Experience Panic Attacks?

and again it's AFTER the fact so she has to go through all the distress. Also then it makes her...

Anyone experience a wearing off cough/shortness of breath?

not unwell. When the side effects of a drug could be the same as a symptom your Dr is likely to...