ARGX-117-2401
Brief description of study
Double-blind, double-dummy study in adults with CIDP. Patients will be randomized to receive either investigational ARGX-117 and IVIG-placebo OR active standard-of-care IVIG and ARGX-117-placebo. Blood/urine collection, patient-reported outcomes, physician efficacy assessments, ECGs, AEs/ConMeds, and suicidality assessments will be performed.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Medical Research
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Age: 99 years or below
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Gender: All
TBD
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