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Published on: February 28, 2021
[The use of rebif in the Moscow Municipal Multiple Sclerosis Center]
Abstract:
We summarized the 3-year experience of using beta-interferon 1a (44 mcg, subcutaneously) in the form of the preparation rebif in 141 patients including 120 patients with active remitting multiple sclerosis (RMS) and 21 patients with secondary progressive MS (SPMS). All patients were examined every three months. The significant decrease in the frequency of exacerbations per year was seen already during the first year of treatment. EDSS scores remained stable in 47.37% of all RMS cases and in 57.14% of all SPMS cases during the first year. A one point and more increase of EDSS was found only in 5.26% patients during three years of treatment. The drug was well tolerated during the long period, adverse effects were found in 16.31%, with a flu-like syndrome in the first place. Only 1.42% of patients refused treatment. All other patients were highly motivated and adherent to treatment.
Insights
Rebif (interferon beta-1a) significantly reduced multiple sclerosis exacerbations and maintained stable disability scores over three years in 141 patients. The treatment demonstrated good tolerability and high patient adherence.
Area of Science:
- Neuroscience
- Immunology
- Pharmacology
Context:
- Multiple Sclerosis (MS) is a chronic autoimmune disease affecting the central nervous system.
- Beta-interferons are a class of disease-modifying therapies used in MS treatment.
- Long-term treatment outcomes and patient adherence are crucial for managing MS.
Purpose:
- To evaluate the 3-year efficacy and tolerability of interferon beta-1a (Rebif) in patients with multiple sclerosis.
- To assess the impact of Rebif on exacerbation frequency and Expanded Disability Status Scale (EDSS) scores.
- To analyze patient adherence and adverse events associated with long-term Rebif treatment.
Summary:
- A 3-year study involved 141 patients with active relapsing-remitting MS (n=120) and secondary progressive MS (n=21) treated with interferon beta-1a (44 mcg, subcutaneously).
- Significant reductions in annual exacerbation frequency were observed within the first year of treatment.
- EDSS scores remained stable in 47.37% of relapsing-remitting MS and 57.14% of secondary progressive MS patients during the first year; only 5.26% experienced a one-point or greater EDSS increase over three years.
- The treatment was well-tolerated, with flu-like syndrome being the most common adverse effect (16.31%).
- High patient motivation and adherence were noted, with only 1.42% discontinuing treatment.
Impact:
- Interferon beta-1a (Rebif) demonstrates sustained efficacy in reducing MS relapses and stabilizing disability over three years.
- The findings support the long-term use of Rebif in managing both relapsing-remitting and secondary progressive MS.
- Good tolerability and high patient adherence contribute to the favorable long-term treatment profile of Rebif in MS care.
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