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Recruiting Phase 3 Interventional

A Study to Assess Efficacy and Safety of Empasiprubart Versus IVIg in Adults With CIDP

ClinicalTrials.gov ID: NCT06920004

Public ClinicalTrials.gov record NCT06920004. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 11:06 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Randomized, Double-Blinded, Double-Dummy Study Evaluating the Efficacy and Safety of Intravenous Empasiprubart Versus Intravenous Immunoglobulin in Adults With Chronic Inflammatory Demyelinating Polyneuropathy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The main purpose of this study is to compare empasiprubart and IVIg for treating people with CIDP. This study consists of a Part A where participants will either receive empasiprubart and a placebo resembling IVIg, or IVIg and a placebo resembling empasiprubart for 24 weeks (6 months). Following Part A, participants will enter Part B in which all participants will receive empasiprubart for 96 weeks (24 months). More information can be found here: https://clinicaltrials.argenx.com/emvigorate

Study identification

NCT ID
NCT06920004
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
argenx
Industry
Enrollment
218 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 21, 2025
Primary completion
Aug 31, 2027
Completion
Aug 31, 2030
Last update posted
Aug 25, 2026

2025 – 2030

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35233 Recruiting
Samir Macwan, M.D., Inc. Rancho Mirage California 922701 Recruiting
Colorado Springs Neurological Associates Colorado Springs Colorado 80907 Recruiting
MedStar Washington Hospital Center Washington D.C. District of Columbia 20010 Recruiting
Homestead Associates in Research Inc Homestead Florida 33033 Recruiting
Visionary Investigators Network Miami Florida 33133 Recruiting
University of South Florida Tampa Florida 33616 Recruiting
Paradigm Health System Slidell Louisiana 70458 Recruiting
Erlanger Health System Columbia Maryland 21044 Recruiting
University of Michigan Hospital Ann Arbor Michigan 48109 Recruiting
Perelman Center for Advanced Medicine Philadelphia Pennsylvania 19104-5127 Recruiting
Jefferson Health Honickman Center Philadelphia Pennsylvania 19107 Recruiting
NeuroCarePlus Houston Texas 77094 Recruiting
National Neuromuscular Research Institute Irving Texas 75063 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 75 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06920004, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 25, 2026 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06920004 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →