Real-World Efgartigimod Effectiveness in CIDP: A Prospective Study

Status: Recruiting
Location: See all (13) locations...
Intervention Type: Biological
Study Type: Observational
SUMMARY

The aims of this study are to assess the real-world effectiveness of efgartigimod in treating chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), describe the treatment journey of participants with CIDP, and assess the utilization of health care services among adult participants with CIDP who initiate treatment with efgartigimod. As this is a noninterventional study, treatment choices and decisions will be left to the discretion of participants and their physicians, according to the standard of care. Each participant will be prospectively followed for up to 2 years from the date of initial administration of efgartigimod.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Aged ≥18 years at time of providing informed consent

• Diagnosed with CIDP

• Planned to be receiving efgartigimod treatment within the CIDP treatment label of efgartigimod in the participant's respective country

• Efgartigimod treatment-naïve at time of screening

Locations
United States
North Carolina
PPD Virtual
RECRUITING
Wilmington
Other Locations
Germany
Universitätsklinikum Düsseldorf
RECRUITING
Düsseldorf
Universitätsmedizin Göttingen
RECRUITING
Göttingen
Neurologie Neuer Wall - Dr.Bredow & Partner
RECRUITING
Hamburg
Medizinische Hochschule Hannover
RECRUITING
Hanover
Universitätsklinikum Magdeburg A.ö.R.
RECRUITING
Magdeburg
Universitätsklinikum Mannheim
RECRUITING
Mannheim
Mühlenkreiskliniken - Johannes Wesling Klinikum Minden
RECRUITING
Minden
Friedrich-Baur-Institute München
RECRUITING
München
Immanuel Klinik Rüdersdorf
RECRUITING
Rudersdorf
Diakonie-Klinikum Schwäbisch Hall gGmbH
RECRUITING
Schwäbisch Hall
Universitätsklinikum Tübingen
RECRUITING
Tübingen
Universitätsklinikum Ulm
RECRUITING
Ulm
Contact Information
Primary
Sabine Coppieters, MD
clinicaltrials@argenx.com
857-350-4834
Time Frame
Start Date: 2025-08-11
Estimated Completion Date: 2029-10
Participants
Target number of participants: 200
Sponsors
Leads: argenx

This content was sourced from clinicaltrials.gov