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Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an acquired immune-mediated neuropathy affecting the peripheral nervous system, characterized by a progressive or relapsing clinical course. The condition is classified as acquired rather than heritable, with no causative gene variants or Mendelian inheritance patterns documented in this packet. Lewis-Sumner syndrome is documented as a recognized disease subtype in this packet.
Phenotypic data and characteristic clinical findings are not established in this packet's structured fields.
CIDP is an acquired inflammatory condition. No causative genes, molecular mechanism data, or Mendelian inheritance patterns are documented in this packet, consistent with its immune-mediated pathophysiology.
Specific diagnostic criteria and structured diagnostic methods are not established in this packet's fields.
Three FDA-approved therapies for CIDP carry active market status in this packet. Immune Globulin (Human) — marketed as Baygam and Gamastan S/D — holds BLA approval and currently maintains active market status; the approval date recorded in this packet (January 11, 2044) is anomalous and appears to reflect a data entry artifact rather than the actual historical approval date for this product. Efgartigimod alfa and hyaluronidase-qvfc (VYVGART HYTRULO) received BLA approval on June 20, 2023, and is currently marketed with active status. Immune Globulin Infusion 10% with Recombinant Human Hyaluronidase (Hyqvia) received BLA approval on September 12, 2014, and is currently marketed with active status.
54 trials found
Prognostic information is not established in this packet's structured fields.
Two clinical trials for CIDP are documented as recruiting in this packet. NCT06752356 is a Phase 3 study investigating intravenous immune globulin 10% KIg10 (QIVIGY) in subjects with CIDP, sponsored by Kedrion S.p.A., with planned initiation October 2026 and planned completion December 2027. NCT07032662 is a Phase 2 study of imeroprubart in adult participants with CIDP, sponsored by Immunovant Sciences GmbH, with enrollment begun March 2025 and planned completion May 2030.
Data assembled from 5 of 12 sources · Last updated Nov 3, 2026, 3:00 PM UTC
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European rare disease database
Genetic and Rare Diseases Info Center
AI-curated news mentioning chronic inflammatory demyelinating polyradiculoneuropathy
Updated Oct 22, 2026
New research identifies data-driven subtypes of chronic inflammatory demyelinating polyneuropathy (CIDP), challenging existing classification systems. This study highlights the clinical heterogeneity of CIDP, which may impact future diagnostic and treatment approaches.
A recent study discusses the use of matching-adjusted indirect treatment comparisons in chronic inflammatory demyelinating polyneuropathy (CIDP). The authors emphasize the need for improved methodologies to interpret current evidence and enhance future studies in this area.
A recent study identifies newly developing IgM anti-GD1a/GD1b ganglioside monoclonal gammopathy in a patient with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). This discovery may provide insights into the pathophysiology of CIDP and potential therapeutic targets.
Sanofi has discontinued its Phase 3 study for a complement inhibitor drug targeting chronic inflammatory demyelinating polyneuropathy due to underwhelming efficacy results. This decision reflects broader challenges within the drug class, impacting future development prospects.
A personal story highlights how a diagnosis of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) motivated the author to engage in advocacy efforts. The narrative emphasizes the importance of community support and awareness for rare diseases.