Multiple Sclerosis (MS) Clinical Trials

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Ocrevus Zunovo for Patients With Multiple Sclerosis: Mixed Methods on Barriers and Facilitators to Use and Retention

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

Ocrevus Zunovo implementation, feasibility, acceptability, patient satisfaction, treatment persistence, and impact on MS disease outcomes will be analyzed in this mixed methods study. This study will incorporate clinical data and questionnaire results from MS patients who take Ocrevus Zunovo as well as qualitative interviews with MS patients, family members, and other individuals involved in Ocrevus Zunovo treatment. The purpose of this study is to synthesize implementation strategies that improve patient access to high-efficacy MS therapies in real-world settings.

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

• Age of 18 years or older

• Resident of the USA

• Seen at Northwestern Medicine

• Meets diagnostic criteria (2024) for MS, either RMS or PPMS

• Diagnosis of MS (G35) on file by a neurologist

• Wants to start or restart a DMT for MS

• Willing to be in a 12-month follow up study

Locations
United States
Illinois
Northwestern Memorial Hospital
RECRUITING
Chicago
Contact Information
Primary
Dylan Rice, B.A.
dylan.rice@northwestern.edu
312-503-5298
Backup
Audrey Chang, B.A.
audrey.chang@northwestern.edu
312-503-8639
Time Frame
Start Date: 2026-06-12
Estimated Completion Date: 2028-12
Participants
Target number of participants: 150
Treatments
Clinical Arm
All enrolled OZ-treated MS participants will have at least one clinical inpatient visit at Northwestern Medicine.
Interview Arm
Interviews (with record taking) will take up to 2 hours to discuss barriers and facilitators to the administration of OZ.
Related Therapeutic Areas
Sponsors
Collaborators: Genentech, Inc.
Leads: Northwestern University

This content was sourced from clinicaltrials.gov

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