REBIF (interferon beta-1a) by Biogen is mechanism(s) by which rebif (interferon beta-1a) exerts its therapeutic effects in patients with multiple sclerosis is unknown. First approved in 2002.
Drug data last refreshed 9h ago · AI intelligence enriched 1w ago
REBIF is interferon beta-1a, a biologic immunomodulator approved in 2002 for multiple sclerosis (MS). It is administered via subcutaneous injection and modulates immune responses, though the precise mechanism in MS remains incompletely understood. This is a foundational disease-modifying therapy in MS with decades of real-world clinical data.
Product is in terminal lifecycle with modest Part D spend ($131M); commercial teams are likely managing decline and preparing for patent cliff rather than growth initiatives.
mechanism(s) by which REBIF (interferon beta-1a) exerts its therapeutic effects in patients with multiple sclerosis is unknown.
Interferon beta
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Study to Investigate Pregnancy Outcomes in Female Participants Exposed to Subcutaneous (SC) Peginterferon Beta-1a and Intramuscular (IM) Interferon Beta-1a Reported in a German Participant Support Program
A Study to Evaluate the Safety, Tolerability, and Efficacy of BIIB017 (Peginterferon Beta-1a) in Pediatric Participants for the Treatment of Relapsing-Remitting Multiple Sclerosis
Study to Evaluate the Efficacy and Safety of Dimethyl Fumarate (Tecfidera) and Peginterferon Beta-1a (Plegridy) for the Treatment of Relapsing-Remitting Multiple Sclerosis in Pediatric Participants
Efficacy and Safety of Peginterferon Beta-1a (CinnaGen) in Participants With Relapsing Remitting Multiple Sclerosis
Pharmacokinetics and Pharmacodynamics of CinnoVex (Interferon Beta-1a) Compared to Avonex (Interferon Beta-1a)
Worked on REBIF at Biogen? Share your interview experience or compensation data (+7 days Pro)
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
Upgrade to Pro to access Medicare Part D spending data and other premium pharma intelligence.
Upgrade to Pro — $25/mo$131M Medicare spend — this is a commercially significant brand
REBIF roles (248 linked positions) skew heavily toward senior commercial and external affairs leadership, reflecting mature product lifecycle management and stakeholder education. Career growth is constrained by product decline; roles emphasize protecting remaining market share, provider relationships, and transition planning rather than expansion.
248 open roles linked to this drug