To determine the effect of facilitated subcutaneous immunoglobulin (fSCIG; human immunoglobulin G 10% with recombinant human hyaluronidase) on patient-reported outcomes (PROs) in a Phase 3, randomized, placebo-controlled, double-blind, multicenter study (ADVANCE-CIDP 1; NCT02549170).
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Anderson‐Smits et al. (2024) studied this question.
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