Stevens-Johnson syndrome

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Information
Disease name
Stevens-Johnson syndrome
Disease ID
DOID:0050426
Description
"A skin disease that is characterized by ulceration of less than 10 percent of the surface area of the body. The disease is often precipitated by the use of medications, such as antibiotics or antiepileptics, or onset of infection." [url:https\://en.wikipedia.org/wiki/Stevens%E2%80%93Johnson_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
NCT05520086 Active, not recruiting Phase 1/Phase 2 Clinical Trial to Evaluate Safety and Efficacy of Cell Therapy in Patients With Cicatricial Conjuntivitis. November 11, 2022 February 2024
NCT02149732 Available Clinical Trial on the Effect of Autologous Oral Mucosal Epithelial Sheet Transplantation May 2014 December 2016
NCT01696500 Completed Phase 3 Phase III Clinical Trial of NPB-01 in Patients With Stevens-Johnson Syndrome/ Toxic Epidermal Necrolysis Unresponsive to Corticosteroids. October 2012 June 2014
NCT00844038 Completed Stevens-Johnson Syndrome Antimicrobial August 2008 December 2008
NCT01488396 Completed Phase 4 Efficacy of 0.05% Cyclosporin Eye Drop in Stevens Johnson Syndrome Patient With Chronic Dry Eye February 2007 July 2009
NCT02945176 Completed N/A Safety and Performance Study of the ARGOS-IO System in Patients Undergoing Boston Keratoprosthesis Implantation March 2015 June 14, 2017
NCT06263140 Completed Vitamin D Levels in Non-immediate Drug Hypersensitivity Case-control Study May 30, 2021 February 1, 2022
NCT03585946 Not yet recruiting Outcomes in Stevens Johnsons Syndrome and Toxic Epidermal Necrolysis January 1, 2024 December 31, 2028
NCT03659227 Recruiting Drug Reactions Sampling (COLLECTIONTOXIDERMIES) September 26, 2018 September 25, 2028
NCT02987257 Recruiting Phase 3 NATIENS: Optimal Management and Mechanisms of SJS/TEN March 21, 2023 August 1, 2028
NCT02037347 Terminated Phase 1/Phase 2 Study to Evaluate the Use of Palifermin to Treat Toxic Epidermal Necrolysis October 2010 December 2014
NCT03046914 Unknown status N/A HLA-B*5801 Screening to Prevent Allopurinol-induced Severe Cutaneous Adverse Reaction February 24, 2016 November 30, 2017
NCT01122303 Unknown status Corneal Epitheliotropic Factors in Autologous Serum Eye Drops in Nonautoimmune and Stevens-Johnson Syndrome With Dry Eye December 2009 December 2010
NCT04313725 Unknown status N/A Evaluation of Tangible Boost for Patients With Stevens Johnson Syndrome, Sjogren's Syndrome, and Graft Vs Host Disease February 24, 2020 March 31, 2022
NCT05145959 Unknown status N/A Meibomian Gland Probing in the Sub-Acute Phase of Patients With Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis December 1, 2021 March 1, 2024
NCT05284929 Unknown status Human Leukocyte Antigen Class II (DRB1 and DQB1) Alleles and Haplotypes Frequencies in Patients With Pemphigus Vulgaris Among the Russian Population May 17, 2017 March 17, 2023
NCT02126020 Withdrawn Phase 1/Phase 2 Topical Infliximab in Autoimmune Eyes With Keratoprosthesis November 2014 April 3, 2017
NCT01256489 Withdrawn Phase 1/Phase 2 Infliximab to Improve Retention of the Boston Keratoprosthesis in Patients After Stevens Johnson Syndrome/ Toxic Epidermal Necrolysis (SJS/TENS) December 2010 January 2015
Disase is a (Disease Ontology)
DOID:37
Cross Reference ID (Disease Ontology)
EFO:0004276
Cross Reference ID (Disease Ontology)
GARD:7700
Cross Reference ID (Disease Ontology)
ICD10CM:L51.1
Cross Reference ID (Disease Ontology)
ICD9CM:695.13
Cross Reference ID (Disease Ontology)
MESH:D013262
Cross Reference ID (Disease Ontology)
NCI:C79484
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:73442001
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0038325
OrphaNumber from OrphaNet (Orphanet)
36426
MeSH unique ID (MeSH (Medical Subject Headings))
D013262