POEMS syndrome

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Information
Disease name
POEMS syndrome
Disease ID
DOID:14039
Description
"A blood protein disease that is characterized by polyneuropathy, oranomegaly, endocrinopathy, monoclonal gammopathy, and skin changes, especially hyperpigmentation." [url:https\://rarediseases.info.nih.gov/diseases/7411/poems-syndrome]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT02921893 Active, not recruiting Early Phase 1 Ixazomib Citrate, Lenalidomide, and Dexamethasone in Treating Patients With POEMS Syndrome October 31, 2016 October 31, 2024
NCT04396496 Completed Phase 2 Treatment of POEMS Syndrome With Daratumumab September 22, 2020 October 16, 2023
NCT01639898 Completed Phase 2 POEMS Syndrome Treatment With Lenalidomide July 2012 July 2018
NCT01816620 Completed Phase 2 Study to Evaluate Lenalidomide Plus Dexamethasone in Patients With Newly Diagnosed POEMS Syndrome March 2014 April 2017
NCT02193698 Completed Phase 2 Efficacy and Safety of Lenalidomide as a Treatment for Recurrent or Refractory POEMS Syndrome Trial July 2014 April 2016
NCT06040567 Recruiting Polyneuropathy, Impairments and Physical Activity - The PolyImPAct Study September 23, 2023 December 31, 2026
NCT04561557 Recruiting Early Phase 1 Safety and Efficacy of CT103A Cells for Relapsed/Refractory Antibody-associated Inflammatory Diseases of the Nervous System September 22, 2020 May 31, 2027
NCT05263817 Recruiting Early Phase 1 A Clinical Study of CD19/BCMA CAR-T Cells in the Treatment of Refractory POEMS Syndrome, Amyloidosis, Autoimmune Hemolytic Anemia, and Vasculitis October 8, 2021 October 1, 2024
NCT05476458 Recruiting To Evaluate Efficacy of Red Dichromatic Imaging (RDI) in Achieving Hemostasis During POEM Using GF 1500 UGI Scope August 15, 2022 July 1, 2023
NCT00971685 Unknown status Phase 2 The Treatment of Lenalidomide in Patients With POEMS Syndrome July 2009 July 2011
Disase is a (Disease Ontology)
DOID:620
Cross Reference ID (Disease Ontology)
GARD:7411
Cross Reference ID (Disease Ontology)
MESH:D016878
Cross Reference ID (Disease Ontology)
NCI:C80303
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:79268002
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0085404
OrphaNumber from OrphaNet (Orphanet)
2905
MedGen concept unique identifier (MedGen Concept name)
C0085404
MedGen concept unique identifier (MedGen Concept name)
CN203035
MedGen unique identifier (MedGen Concept name)
39276
MedGen unique identifier (MedGen Concept name)
799584
MeSH unique ID (MeSH (Medical Subject Headings))
D016878