This study will measure how adults with CIDP receiving IVIg treatment adjust to efgartigimod PH20 SC. The study duration for each participant will be approximately 17 to 19 weeks.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
23
Subcutaneous injection of efgartigimod PH20 SC
MedStar Washington Hospital Center
Washington D.C., District of Columbia, United States
Neurology Associates PA
Maitland, Florida, United States
Visionary Investigators Network
Miami, Florida, United States
Proportion of participants who begin treatment with efgartigimod PH20 SC within 1 week after stopping IVIg therapy and are still receiving efgartigimod PH20 SC at the end of the 12-week treatment period
Time frame: Up to 12 weeks
Changes from baseline in EQ-5D-5L scores over time
Time frame: Up to 12 weeks
Changes from baseline in TSQM-9 scores over time
Time frame: Up to 12 weeks
Changes from baseline in PGI-C scores over time
Time frame: Up to 12 weeks
Changes from baseline in PGI-S scores over time
Time frame: Up to 12 weeks
Incidence of (S)AEs
Time frame: Up to 16 weeks
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