Clinical data | |
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Trade names | Spinraza |
Other names | IONIS-SMNRx, ISIS-SMNRx |
AHFS/Drugs.com | Monograph |
MedlinePlus | a617010 |
License data |
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Pregnancy category |
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Routes of administration | Intrathecal |
ATC code | |
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Pharmacokinetic data | |
Bioavailability | 100% (intrathecal) |
Protein binding | <25% (in CSF), >94% (in plasma)[6] |
Metabolism | Exonuclease (3'- and 5')-mediated hydrolysis |
Elimination half-life | 135–177 days (in CSF), 63–87 days (in plasma) |
Identifiers | |
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CAS Number | |
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Chemical and physical data | |
Formula | C234H323N61Na17O128P17S17[4] |
Molar mass | 7500.86 g·mol−1 |
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Nusinersen,[7] marketed as Spinraza,[4] is a medication used in treating spinal muscular atrophy (SMA), a rare neuromuscular disorder.[8][4] In December 2016, it became the first approved drug used in treating this disorder.
Since the condition it treats is so rare, Nusinersen has so-called "orphan drug" designation in the United States and the European Union.[9]
Spinraza FDA label
was invoked but never defined (see the help page).