https://en.m.wikipedia.org/wiki/Iclepertin
This is Wiki on it.Assume it is patented.
When I was in NY, I didn’t have to pay anything for any medications. I was on Medicaid.
It is terrible that you are expected to pay 1000 dollars per month for what is a pretty disabling condition.
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How’s it going now?
I’m also on the trial. I thought I was on the placebo for part A, and I just started part B. I’m not feeling anything atm.
I have a feeling I’m on it but the benefits are pretty modest. The doctor leading the trial told me that that was pretty much par for the course. It’s not a particularly potent med.
Kinda of a bummer to know it’s not particularly potent. I guess I’ll have to wait some weeks to see if there are some changes