Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Bayer
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients with a first demyelinating event suggestive of MS, as well as patients with remittent recurrent MS (RRMS), secondary progressive MS (SPMS) and primary progressive MS (PPMS) will be able to join the study.
You may not be if
Pregnancy
Patients with a history of hypersensitivity to natural or recombinant interferon-beta, human albumin or to any of the excipients
Patients with a history of severe depressive disorders and/or suicidal ideation
Patient with decompensated liver disease
Patient with epilepsy not adequately controlled by treatment
