FDA approves first drug for spinal muscular
atrophy
New therapy addresses unmet medical need for
rare disease
The
U.S. Food and Drug Administration today approved Spinraza (nusinersen), the
first drug approved to treat children and adults with spinal muscular atrophy
(SMA), a rare and often fatal genetic disease affecting muscle strength and
movement. Spinraza is an injection administered into the fluid surrounding the
spinal cord.
Read more.
###
|