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Home > MS Treatment > MS Treatment Options > TYSABRI® (natalizumab)

TYSABRI®

(natalizumab)

  • TYSABRI is a prescription medicine approved for adult patients with relapsing forms of MS to slow the worsening of physical disability that is common in patients with MS and decrease the number of flare-ups (relapses). Because TYSABRI increases the risk of progressive multifocal leukoencephalopathy (PML), a rare brain infection that usually causes death or severe disability, TYSABRI is generally recommended for patients that have not been helped enough by, or cannot tolerate another treatment for MS. TYSABRI does not cure MS and has not been studied for longer than two years or in patients with chronic progressive MS.

View Clinical Benefits

Dosing regimen:

  • TYSABRI is administered by infusion at an infusion center or a specially equipped doctor's office. It is given once every 4 weeks.
  • In order to receive TYSABRI, you must be enrolled in the TOUCH® Prescribing Program, a restricted distribution program focused on safety.
Clinical Benefits

TYSABRI® (natalizumab) Clinical Benefits

Reduced flare-ups

At the end of a 2-year study, TYSABRI reduced how often flare-ups occurred by 67% compared with placebo. The average number of flare-ups a patient had each year was 0.22 for TYSABRI and 0.67 for placebo.

  • Of the patients who took TYSABRI in the 2-year study, more than 6 out of 10 had no flare-ups at all (67% of people taking TYSABRI had no flare-ups at the end of the 2-year study, compared with 41% of people taking placebo)

Slowed disability progression

In the same 2-year study, TYSABRI slowed the worsening of physical disability that is common in patients with MS. TYSABRI reduced the chance a person’s physical disability would worsen by 42% compared with placebo.

  • 17% of people taking TYSABRI had their physical disability worsen, while 29% of people taking a placebo had their physical disability worsen
    • Of people who took TYSABRI in the 2-year study, more than 8 out of 10 had no physical disability progression (83% of people taking TYSABRI had no physical disability progression at the end of the 2-year study, compared with 71% of people taking placebo)
  • Reduce the number of new active lesions
    • In a 2-year study, 9 out of 10 people taking TYSABRI had no new lesions that show new disease activity* (97% of people taking TYSABRI had no new lesions that showed disease activity, compared with 72% of people taking placebo*)

*Changes in MRI often do not relate to how your MS is progressing.

Please see full TYSABRI Prescribing Information, including Boxed Warning and TYSABRI Patient Medication Guide.

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Important Safety Information

 

Please see full TYSABRI Prescribing Information, including Boxed Warning and TYSABRI Patient Medication Guide.



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