Johnson & Johnson reports positive results from Imaavy study

Scientist looking into microscope

Solskin

  • Johnson & Johnson (NYSE:JNJ) on Monday reported new findings from an indirect treatment comparison of its FcRn blocker, nipocalimab, marketed as Imaavy, for generalized myasthenia gravis in adults.
  • The analysis, which draws from a late-stage study, reveals that patients experienced similar relief from symptoms as early as Week 1.
  • Furthermore, Imaavy demonstrated sustained disease control, showing significant improvements in MG-ADLa scores compared to the Phase 3 results of other FcRn blockers at various points throughout a 24-week treatment period.
  • Imaavy is currently approved in the U.S. for use in both adult and pediatric patients aged 12 and older who test positive for either anti-acetylcholine receptor or anti-muscle-specific tyrosine kinase antibodies.

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