Last reviewed · How we verify

Rebif®

EMD Serono · FDA-approved active Small molecule Quality 2/100

Rebif®, marketed by EMD Serono, is a well-established treatment in the multiple sclerosis (MS) market. The drug's key composition patent is set to expire in 2028, providing a period of market exclusivity and revenue stability. However, the primary risk lies in the increasing competition from newer therapies, which could erode Rebif's market share.

At a glance

Generic nameRebif®
Also known asinterferon-beta-1a, Interferon beta-1a, IFNβ-1b, Interferon beta 1a, Recombinant interferon beta-1a
SponsorEMD Serono
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results