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RECRUITING

Real-World Efgartigimod Effectiveness in CIDP: A Prospective Study

NCT07264426 · View on ClinicalTrials.gov ↗

Study 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.

Interventions

  • BIOLOGICAL Efgartigimod PH20 SC

Study Locations (19)

Other

  • Jüdisches Krankenhaus Berlin — Berlin
  • Universitätsklinikum Düsseldorf — Düsseldorf
  • Universitätsklinikum Frankfurt — Frankfurt
  • UKGM - Universitätsklinikum Gießen und Marburg GmbH — Giessen
  • Universitätsmedizin Göttingen — Göttingen
  • Universitätsklinikum Hamburg Eppendorf — Hamburg
  • Neurologie Neuer Wall - Dr.Bredow & Partner — Hamburg
  • Medizinische Hochschule Hannover — Hanover
  • Universitatsklinikum des Saarlandes — Homburg
  • Universitätsklinikum Magdeburg A.ö.R. — Magdeburg
  • Universitätsklinikum Mannheim — Mannheim
  • Universitätsklinikum Gießen und Marburg GmbH - Standort Marburg — Marburg
  • Mühlenkreiskliniken - Johannes Wesling Klinikum Minden — Minden
  • Friedrich-Baur-Institute München — München
  • Immanuel Klinik Rüdersdorf — Rüdersdorf
  • Diakonie-Klinikum Schwäbisch Hall gGmbH — Schwäbisch Hall
  • Universitätsklinikum Tübingen — Tübingen
  • Universitätsklinikum Ulm — Ulm

North Carolina

  • PPD Virtual — Wilmington

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2025-08-11
Est. Completion 2029-10

Sponsor

argenx

96 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07264426

The ClinicalTrials.gov registry entry for NCT07264426 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 200 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 3 conditions, with CIDP 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: NCT07264426 reports 19 study locations spanning 2 distinct geographic areas — top geographies include Other, North Carolina. 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 NCT07264426 about?

NCT07264426 is a clinical study titled "Real-World Efgartigimod Effectiveness in CIDP: A Prospective Study". 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...

What is the current status of trial NCT07264426?

This trial is currently recruiting. The enrollment target is 200 participants. The study started on 2025-08-11. Estimated completion is 2029-10.

What conditions does trial NCT07264426 study?

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

What interventions are being tested in trial NCT07264426?

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 NCT07264426?

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 NCT07264426 being conducted?

This trial has 19 study locations across North Carolina. 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