Clin2
NCT05584631Possibly a fitRecruiting

Switching IVIG to weekly SCIG for CIDP treatment

CIDPImmunoglobulin DeficiencyChronic Inflammatory Demyelinating Polyneuropathy

Part of Blood & lymphatic, Brain & nervous system, Hormones & metabolism, Immune system & allergy clinical trials.

This Phase 1 study compares IVIG given through an IV versus SCIG given under the skin, for people with CIDP. It aims to find the right weekly SCIG dose based on your current IVIG dose, which could make treatment more convenient.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
20 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You are over 18 years old and have a confirmed CIDP diagnosis
  • You are already taking IVIG for CIDP (not for another condition)
  • Your weekly IVIG dose can be safely converted to a weekly SCIG dose in the study’s target range
  • Your liver function is not significantly elevated (no more than 3× the normal limit)
  • Your kidneys work well enough (creatinine clearance 50 mL/min or higher)
  • You do not have certain other conditions such as active cancer, diabetes, or immune-related disorders

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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