drugset / Trial / NCT06637072

A Study to Assess Adults With CIDP Transitioning From IVIg to Efgartigimod PH20 SC

NCT06637072

Phase 4 Completed 23 enrolled argenx
NaSingle-groupOpen-labelTreatment

Summary

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.

Timeline

Start
2024-12-10
Primary completion
2026-02-19
Completion
2026-02-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Efgartigimod Alfa Protein / enzyme biologic Subcutaneous