Well friends,
I am sitting here on 6 hours of pharmacokinetic monitoring after taking two white capsules that may or may not be Selnoflast!
This is part of the long awaited Phase 1B, (first in PWP).
My guess is that many may want to know how I feel. Fine. No different but that is expected.
Selnoflast is one of several new drugs that hope to address the problem of neuroinflamation, a NLRP3 inhibitor that is already in phase 1 trial for ulcerative colitis. I had a long PET scan last week to get baseline data on my current neuroinflamatory state. One endpoint is to compare that to scan data at the end of the study to see if there is measurable evidence of reduction in inflammation markers. They have also done a ton of blood draws, Lumbar puncture and the usual (and to me unsatisfying) UPDRS.
The trial is only 28 days so there is essentially zero potential for personal benefit in the near term but it KEEPS THIS WHOLE ENTERPRISE MOVING FORWARD. ( as flawed as it may be!)
It is an intense month with weekly neuro visits and two cross country trips for the scans. I was very nervous last week but doing better now. I have a bit of a phobia about being slid into tubes but during the MRI I kept thinking that if THIS vibration does not jiggle the neurons to a new state, nothing will. Flawed but it kept me going!
If there is anything dramatic I will post.
Onward!
CTime
PS my trial coordinator who was also my coordinator for Buntenetap said they expect a preliminary readout very soon!