Randomized Open-label Trial to Compare Efficacy and Tolerance of Corticosteroids and IVIg (PRNC)

This is an interventional treatment trial for Demyelinating Polyneuropathy focused on measuring chronic inflammatory demyelinating polyneuropathy, immunoglobulin, prednisone Read More

Inclusion Criteria:

• Man or woman between 18 and 80, Weight ≤ 100 kg,

CIDP diagnosis:

• stable or deteriorated state (no spontaneous improvement),
• with the following features:
• motor or sensory and motor deficits, and reduced or abolished tendon reflexes,
• progressive or relapsing evolution,
• global symmetric disability in more than one limb,
• disease course installation over at least 2 months,
• cerebrospinal fluid with ≤10/µL white blood cells and > 0.5 g/L protein rate (non compulsory examination),
• electrophysiological or histological signs of demyelinization,
• INCAT disability score ≥ 2 in arms or ≥ 1 in legs

Exclusion Criteria:

• Severe electrophysiological axonal damage,
• Pure motor syndrome,
• Spontaneous improvement,
• Associated systemic disease that could be the cause of neuropathy,
• Severe cardiac insufficiency,
• Cardiac arrhythmia,
• Severe cardiopulmonary pathology,
• Inflammatory syndrome,
• Severe physical disease which can interfere with the trial,
• Patient in a strict salt-free diet,
• A clinically significant abnormal biological result,
• Positive serology in one of the following tests: HIV1, HIV2, A-B-C hepatitis, Hbs antigen, Lyme disease,
• IgA complete deficiency,
• History of anaphylactic reaction during previous IVIg infusion,
• Hypogammaglobulinemia (IgG < 3g/L),
• Creatinine clearance < 80 mL/min,
• Evolutive gastroduodenal ulcer, diabetes, serious infectious condition, evolutive virus disease (hepatite, herpes, varicella, zona), psychotic states not controlled by treatment, veinous or arterial thrombosis, non controlled high blood pressure, osteoporosis,
• Patient previously treated by corticosteroids, IVIg, plasma exchanges or any other immunosuppressive agent within 3 months before inclusion, except for azathioprine and mycophenolate mofetil which were tolerated in the case of the dose being unmodified within 3 months and kept unchanged during the trial,
• Experienced failure with a IVIG or prednisone prior treatment,
• Hypersensitivity to any components of the 2 treatments,
• Unsigned informed consent,
• Ongoing or planned pregnancy (mandatory pregnancy test at the screening visit), breastfeeding, effective contraception for over 3 months for women of childbearing age.