Drug data last refreshed 5h ago · AI intelligence enriched 1w ago
ENSPRYNG (satralizumab-mwge) is a humanized monoclonal antibody approved in 2020 for neuromyelitis optica spectrum disorder (NMOSD) in adults. It works by inhibiting IL-6-mediated signaling through binding to soluble and membrane-bound IL-6 receptors, reducing neuroinflammation. This rare disease therapy addresses a critical unmet need in a small but severely affected patient population.
Peak-stage biologic with modest Part D penetration (~1,551 claims in 2023) indicates mature commercial phase; specialist and MSL-heavy team structure typical for rare disease.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Study To Evaluate Pharmacokinetics, Efficacy, Safety, Tolerability, And Pharmacodynamics Of Satralizumab In Pediatric Patients With Aquaporin-4 Antibody Positive Neuromyelitis Optica Spectrum Disorder (NMOSD)
A Study to Assess the Efficacy and Safety of Satralizumab in Duchenne Muscular Dystrophy (DMD)
Satralizumab in Aneurysmal Subarachnoid Hemorrhage
A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Thyroid Eye Disease
Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Thyroid Eye Disease
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Upgrade to Pro — $25/moENSPRYNG offers specialized career opportunities in rare disease commercialization, requiring deep clinical expertise and payer navigation skills. Working on this product builds domain knowledge in neurology and immunology while developing specialized expertise in small-population market strategies—valuable for future rare disease roles across the industry.