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ACTIVE NOT RECRUITING Phase 4

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

NCT06637072 · View on ClinicalTrials.gov ↗

Study 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.

Interventions

  • BIOLOGICAL Efgartigimod PH20 SC

Study Locations (13)

Texas

  • National Neuromuscular Research Institute — Austin
  • Horizon Clinical Research: Gill Neuroscience — Cypress
  • Northwest Houston Neurology - Cypress — Cypress
  • Cedar Health Research - Dallas — Dallas

Florida

  • Neurology Associates PA — Maitland
  • Visionary Investigators Network — Miami

Tennessee

  • Erlanger Neuroscience Institute — Chattanooga
  • Vanderbilt University Medical Center — Nashville

District of Columbia

  • MedStar Washington Hospital Center — Washington D.C.

Illinois

  • Northwestern Memorial Hospital — Chicago

Louisiana

  • Velocity Clinical Research — Lafayette

Michigan

  • SRI International - ClinEdge — Plymouth

North Carolina

  • Velocity Clinical Research — Raleigh

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2024-12-10
Est. Completion 2026-02-23
Phase Phase 4

Sponsor

argenx

96 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06637072

The ClinicalTrials.gov registry entry for NCT06637072 describes a study currently listed as active not recruiting. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is argenx, which has 96 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Chronic Inflammatory Demyelinating Polyneuropathy appearing as the primary indexed condition, and to 1 intervention — of which Efgartigimod PH20 SC is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06637072 reports 13 study locations spanning 8 distinct geographic areas — top geographies include Texas, Florida, Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06637072 about?

NCT06637072 is a clinical study titled "A Study to Assess Adults With CIDP Transitioning From IVIg to Efgartigimod PH20 SC". 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.

What is the current status of trial NCT06637072?

This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 23 participants. The study started on 2024-12-10. Estimated completion is 2026-02-23.

What conditions does trial NCT06637072 study?

This clinical trial studies the following conditions: Chronic Inflammatory Demyelinating Polyneuropathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06637072?

The interventions under investigation include: Efgartigimod PH20 SC (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06637072?

This trial is sponsored by argenx, which has 96 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06637072 being conducted?

This trial has 13 study locations across District of Columbia, Florida, Illinois, Louisiana, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial