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RecruitingCIDPImmunoglobulin DeficiencyChronic Inflammatory Demyelinating Polyneuropathy

IVIG vs SCIG in CIDP

Eligible age

18–65 yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

Current dosing practices for immunoglobulin G (IgG) may be inadequate in extreme body weight. The current study will evaluate the influence of body composition on intravenous and subcutaneous administration of immunoglobulin G in patients.

Sponsor: Rutgers, The State University of New Jersey

You may qualify if…

  • Patients aged \>18 years with a current diagnosis of CIDP (based on European Federation of Neurological sciences / Peripheral Nerve Society CIDP diagnostic criteria).
  • 1:1 conversion of IVIG to SCIG (weekly dose conversion) must fall within 0.2-to-0.4 mg/kg dose for SCIG.

You may not qualify if…

  • Patients receiving IVIG for indications other than CIDP will be excluded.
  • Patients with liver impairment (elevations in liver enzymes of greater than 3 times the upper limit of normal) or reduced renal function (CrCl \< 50 mL/min) will be excluded
  • Active malignancies
  • Diabetes
  • Myasthenia gravis
  • Immunodeficiency
  • Autoimmune disease

Where it's recruiting

New Jersey

New Brunswick

Source: ClinicalTrials.gov · NCT05584631 · last updated 2025-12-11