Schnitzler syndrome

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Information
Disease name
Schnitzler syndrome
Disease ID
DOID:4371
Description
"A hypersensitivity reaction type IV disease that is characterized by chronic urticarial rash and monoclonal IgM gammopathy, has_symptom rash, intermittent fever, arthralgia, and lymphadenopathy." [url:https\://rarediseases.org/rare-diseases/schnitzler-syndrome/, url:https\://www.nomidalliance.org/schnitzler.php]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT00933296 Completed Schnitzler Syndrome: Clinical Study, Physiopathological and Search for Genetic Factors July 2009 September 2017
NCT01045772 Completed Phase 2 Safety and Tolerability of Rilonacept in Muckle-Wells Syndrome (MWS) or Schnitzler Syndrome (SchS) January 2009 September 2010
NCT01245127 Completed Phase 2 Ilaris (Canakinumab) in the Schnitzler Syndrome May 2011 May 2012
NCT01276522 Completed Phase 2 Efficacy and Safety of Canakinumab in Schnitzler Syndrome January 2011 December 2011
NCT01390350 Completed Phase 2 Ilaris® Effects in Schnitzler Syndrome (ILESCH) July 2011 May 2018
NCT04213274 Not yet recruiting Phase 2 Study of the Efficacy and Safety of RPH-104 in Adult Subjects With Schnitzler Syndrome May 2023 January 2024
NCT05200715 Recruiting AutoInflammatory Disease Alliance Registry (AIDA) August 6, 2020 August 6, 2030
NCT03595371 Terminated Phase 2 Pilot Study of Dapansutrile Capsules in Schnitzler's Syndrome May 15, 2018 May 29, 2018
Disase is a (Disease Ontology)
DOID:2916
Cross Reference ID (Disease Ontology)
GARD:12390
Cross Reference ID (Disease Ontology)
MESH:D019873
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:402415001
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0524988
OrphaNumber from OrphaNet (Orphanet)
37748
MeSH unique ID (MeSH (Medical Subject Headings))
D019873