Research organizations help

Can someone tell me me what organizations/foundations are actually doing research on TN? The only one I’m familiar with is facial pain association. And as I sit here in the midst of a horrible relapse, I think about how much I want for us all to have more options.

There is a new drug in the works directly targeting TN. It’s in the clinical trials stage. It was originally started in the UK, I believe but was sold to an American company. it has been mentioned on this site before. I don’t recall the specifics.

Please, if anyone knows the name of this new drug, do share the name.
Thank you.


Do a search on this site for “Promising new drug” and it should show the discussion.

I hope this helps.