Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Biogen
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
1. Patients (male or female) diagnosed with relapsing forms of MS.
2. Currently being treated with the same b-IFN (in accordance with FDA approved dosing and schedules) for 12 to 48 months inclusive.
3. All levels of disability
4. Age 18-65 years inclusive
5. Subjects must be willing to be followed for the 6-month study period.
You may not be if
1. Patients with prior b-IFN NAb test (whether positive or negative).
2. Patients who are currently being treated or have been treated within 6 months prior to screening with combination therapy (b-IFN plus any other immunosuppressant/immunomodulatory) other than IV steroids (either pulse or for a relapse).
3. Unwillingness or inability to comply with the requirements of this protocol including the presence of any condition (physical, mental, or social) that is likely to affect the subject's ability to comply with the study protocol.
4. Any other reasons that, in the opinion of the Investigator, the subject is determined to be unsuitable for enrollment into this study.
Clareo Health | A Serologic Study to Correlate Beta-IFN NAb Titers to Beta-IFN Induced Biomarker Response in Patients With Multiple Sclerosis
