Investigation of Smoldering Inflammation in Multiple Sclerosis

Status: Recruiting
Location: See location...
Intervention Type: Radiation, Drug
Study Type: Observational
SUMMARY

The goal of this observational study is to learn about inflammation in those with relapsing remitting Multiple Sclerosis (MS). The main questions it aims to answer are: * How does abnormal neural inflammation compare to cellular and molecular inflammation in MS? * Once treated, why does abnormal inflammation persist?

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Male or female, any race

• Age ≥ 18 years

• Capable of providing written informed consent for volunteering to undergo research procedures

• Diagnosis of MS as established by the referring physician and confirmed by the Sponsor-Investigator. Only patients with active disease, defined as at least 1 enhancing lesion present in the preceding 6 months, will be enrolled

• Treatment naïve except for relapse-related treatments such as corticosteroids or plasmapheresis,

• Planned initiation, at the discretion of the referring physician, of a high efficacy DMT. High efficacy DMT will be defined to include ocrelizumab, natalizumab, or any MS treatment in the opinion of the Sponsor-Investigator to have similar efficacy as the named treatments

• Clinical labs, including at least a CBC and BMP, without significant abnormality as determined by the Sponsor-Investigator or designee, within the 3 months prior to enrollment

Locations
United States
Missouri
Barnes Jewish Center for Clinical Imaging Research
RECRUITING
St Louis
Contact Information
Primary
Matthew Brier, MD, PhD
brierm@wustl.edu
314-362-7666
Backup
Nicole Shelley, MA
nshelley@wustl.edu
314-680-1435
Time Frame
Start Date: 2024-06-19
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 25
Treatments
Participants
Adults with MS taking part in this study.
Related Therapeutic Areas
Sponsors
Leads: Washington University School of Medicine

This content was sourced from clinicaltrials.gov