03/20/2026
Let’s talk safety. Visit ENSPRYNG at booth #2 during NANOS 2026. Read Important Safety Information
at bit.ly/4oXEbzz and Prescribing Information at bit.ly/ENSPRYPI.
ENSPRYNG is a prescription medicine used to treat neuromyelitis optica spectrum disorder (NMOSD) in adults who are aquaporin-4 (AQP4) antibody positive. It is not known if ENSPRYNG is safe and effective in children.
ENSPRYNG is a subcutaneous injection given every 4 weeks after taking 3 starting doses in the first month. After doctor approval and training, ENSPRYNG can be self-administered. Before and during treatment, your doctor may order tests and monitor you to ensure ENSPRYNG is still right for you.
If a starting dose is missed, take it immediately, and maintain the 2-week dosing interval from your new starting date until the first 3 doses are complete, then start ongoing doses every 4 weeks.
If an ongoing dose is missed, take it immediately, wait the 4-week interval from your new starting date, then continue with doses every 4 weeks. Talk to your doctor if you have questions on restarting treatment or if it’s been more than 8 weeks since your last dose.
ENSPRYNG, if unopened, can be removed from and returned to refrigeration. The total combined time out of refrigeration shouldn’t exceed 8 days above 86°F.
ENSPRYNG may cause serious side effects including: infections, increased liver enzymes, and low neutrophil counts. All required vaccinations should be completed before starting ENSPRYNG. Do not take ENSPRYNG if you are allergic to satralizumab-mwge or any of the ingredients in ENSPRYNG, have an active hepatitis B infection, or have active or untreated inactive (latent) TB.
These are not all the possible side effects of ENSPRYNG. Call your doctor for medical advice about side effects.