Annexon, Inc.
Approval AI-extracted
tanruprubart
Guillain-Barré Syndrome (GBS)
Date
TBD
Approval decision · Date TBD estimated
What's at stake A final FDA approval decision on tanruprubart for Guillain-Barré Syndrome (GBS) is expected Date TBD.
“Tanruprubart: Potential to be the first targeted and fast-acting therapy for GBS, a leading cause of neuromuscular paralysis impacting 150,000 people annually worldwide.”

Provenance

1 source on file.

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