The goal of this clinical trial is to evaluating the efficacy and safety of efgartigimod in the treatment of Guillain-Barré Syndrome and exploring the immunological mechanisms of efgartigimod therapy in Guillain-Barré Syndrome. The main questions it aims to answer are: Will efgartigimod improve the symptoms of participants? What medical problems do participants have when using efgartigimod? Participants will: On day 1 and day 5 of the treatment period, drug A was administered intravenously. Keep a diary of their symptoms
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
efgartigimod 20 mg/kg was administered via intravenous infusion on day 1 and day 5 of the treatment period only.
Guillain-Barré Syndrome Disability Scale (GBS-DS)
The mean time to first achieve a GBS-DS score of ≤1 within 12 weeks.
Time frame: 12 weeks.
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