Condition: Multiple Sclerosis · Sponsor: Northwestern University
The primary outcome measure is PIRA (progression independent of relapse activity), based primarily on clinical assessment, dichotomized as present or not. For Aim 1, the cohort, patient-derived disability status (PDDS) score, and ambulation score (self-reported) will be the primary endpoints of interest. For Aim 2, the clinical trial, PIRA will be measured pre-GLP-1 start and at study end (week 72). A composite score of disability, similar to the ORATORIO13 trial will be constructed including EDSS score, 25-foot timed walk, 9-hole peg test, and SDMT score.
This description comes directly from the study's public registry record.
Dylan Rice, BA · 240-362-4800 · dylan.rice@northwestern.edu
Caroline Gebczak, BS · 630-313-0470 · caroline.gebczak@northwestern.edu
Always discuss trial participation with your own doctor first.
| Northwestern Memorial Hospital | Chicago, Illinois, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07207148