08/02/2026
Guillain-Barré syndrome strikes suddenly — the immune system attacks
the body's own nerves, causing rapid muscle weakness that can leave
patients unable to walk or even breathe unaided. For decades, the only
options have been IVIg or plasma exchange, both slow, intensive, and
only partially effective for many patients.
Now, a drug called tanruprubart (also known as ANX005) could become
the first targeted, disease-modifying therapy ever approved for GBS.
It's a first-in-class C1q monoclonal antibody, meaning it blocks a
single immune protein, C1q, shutting down the specific complement-
driven inflammatory pathway that damages nerves — delivered in one
30 mg/kg intravenous infusion, rather than repeated treatments over
several days.
In Phase 3 trials, patients treated with tanruprubart recovered faster
and more completely than those on standard care. The drug has already
received Fast Track and Orphan Drug status from regulators in both the
US and Europe, and Annexon, the company developing it, has now filed
its formal approval application with the European Medicines Agency.
Source: Annexon, Inc. / New Scientist (2026)