Participants are eligible to be included in the study only if all of the following criteria apply:
Neurologist-confirmed diagnosis of CIDP found in the medical record, with the last neurologist visit prior to enrollment containing no information that suggests this diagnosis was reversed
Active use of at least one of the following CIDP treatments for three months or longer, with no evidence of discontinuation of this therapy as of the last neurologist visit prior to enrollment
* immunoglobulin
* corticosteroids, with the exception of prednisone (or equivalent) monotherapy at 10mg or less per day
* plasma exchange
* efgartigimod alfa
* azathioprine
* mycophenolate mofetil
* cyclosporine
* rituximab
* methotrexate
Signed informed consent
Residual impairment, disability, or neurological deficits at enrollment, as defined by a raw I-RODS score of 44 or below
You may not be if
Participants are excluded from the study if any of the following criteria apply:
Evidence of participation in any interventional clinical trial with an investigational drug at the time of enrollment
Hyperreflexia (increased reflexes) recorded in the medical record during a neurological exam the year before enrollment and after CIDP diagnosis
Aged under 18 at the time of enrollment
The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.
