epidermolysis bullosa

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Information
Disease name
epidermolysis bullosa
Disease ID
DOID:2730
Description
"A vesiculobullous skin disease that is characterized by formation of blisters with only minor skin trauma, which can cause widespread wounds, dehydration, electrolyte abnormalities, and severe infection, frequently develops_from mutations in connective tissue elements, including genes encoding keratin, collagen, and laminin." [url:https\://rarediseases.org/rare-diseases/epidermolysis-bullosa/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT04227106 Completed Phase 3 Phase 3, Open-label Clinical Trial of EB-101 for the Treatment of Recessive Dystrophic Epidermolysis Bullosa (RDEB) January 10, 2020 October 18, 2022
NCT00004791 Completed Study of the Nutritional, Metabolic, and Body Composition Profile in Children and Adolescents With Epidermolysis Bullosa August 1995
NCT00014729 Completed Phase 1 Phase I Study of Isotretinoin in Patients With Recessive Dystrophic Epidermolysis Bullosa October 2000 September 2002
NCT01033552 Completed Phase 1/Phase 2 Biochemical Correction of Severe EB by Allo HSCT and "Off-the-shelf" MSCs January 2010 August 12, 2021
NCT01263379 Completed Phase 1/Phase 2 Gene Transfer for Recessive Dystrophic Epidermolysis Bullosa October 5, 2010 March 9, 2022
NCT01716169 Completed N/A Treatment of Chronic and Non-Chronic Wounds in Patients With Recessive Dystrophic Epidermolysis Bullosa Using Helicoll Collagen Dressings Versus Standard of Care October 2012 November 2013
NCT02014376 Completed Phase 2 Study of Effectiveness and Safety of SD-101 in Participants With Epidermolysis Bullosa January 6, 2014 June 24, 2014
NCT02384460 Completed Phase 3 ESSENCE Study: Efficacy and Safety of SD-101 Cream in Participants With Epidermolysis Bullosa March 11, 2015 July 5, 2017
NCT02582775 Completed Phase 2 MT2015-20: Biochemical Correction of Severe EB by Allo HSCT and Serial Donor MSCs March 2016 July 26, 2023
NCT02654483 Completed Phase 2 Neurokinin-1 Receptor Antagonist for the Treatment of Itch in EB Patients August 31, 2016 July 27, 2018
NCT02670837 Completed N/A Study of Cellutome System for Treatment of Individual Lesions in EB Pts August 4, 2016 April 3, 2024
NCT02793960 Completed Phase 1 Topical BPM31510 3.0% Cream in Patients With Epidermolysis Bullosa August 10, 2016 August 26, 2019
NCT03068780 Completed Phase 3 Phase III Efficacy and Safety Study of Oleogel-S10 in Epidermolysis Bullosa March 29, 2017 May 27, 2022
NCT03158662 Completed Survey to Identify Burdens and Unmet Needs of Patients With Epidermolysis Bullosa April 2, 2017 June 30, 2017
NCT03389308 Completed Phase 2 Long Term Open-label Study Evaluating Safety of Diacerein 1% Ointment Topical Formulation in Subjects With Epidermolysis Bullosa Simplex December 1, 2017 April 17, 2020
NCT03730584 Completed N/A Evaluation of the Efficacy of ROPIVACAINE in Children and Young Adults With Hereditary Epidermolysis Bullosa February 27, 2017 November 28, 2019
NCT03836001 Completed Phase 2 A Neurokinin-1 Receptor Antagonist for the Treatment of Pruritus in Patients With Epidermolysis Bullosa April 18, 2019 June 24, 2022
NCT03928093 Completed Phase 3 Pregabalin Treatment for RDEB Pain and Itch August 7, 2019 February 1, 2024
NCT03942250 Completed N/A Uses of Irradiated Human Amniotic Membrane in the Treatment of Dystrophic Epidermolysis Bullosa Patients January 2017 February 2019
NCT04217538 Completed Observational Study of a Cohort of Patients With Hereditary Epidermolysis Bullosa January 4, 2017 December 11, 2019
NCT00004761 Completed Establishment of the National Epidermolysis Bullosa Registry September 1986
NCT04644627 Completed Phase 1/Phase 2 Topical Gentamicin Nonsense Suppression Therapy of EB December 1, 2020 May 1, 2022
NCT04853667 Completed Improve Adherence to Weak or Strong Opioid Analgesics at the Time of Care in Children With Hereditary Epidermolysis Bullosa April 29, 2021 May 20, 2021
NCT05378997 Completed Phase 1 Safety, Tolerability, and Pharmacokinetics of Ascending Topical Doses of TCP-25 Applied to Epidermal Suction Blister Wounds, Non-Healing Leg Ulcers and Patients With Dystrophic Epidermolysis Bullosa. April 7, 2022 March 16, 2024
NCT00380640 Completed Phase 2 The Efficacy of Trimethoprim in Wound Healing of Patients With Epidermolysis Bullosa September 2006 September 2007
NCT00825565 Completed Phase 2 Study of Alwextin® Cream in Treating Epidermolysis Bullosa February 2009 November 2010
NCT00987142 Completed Phase 2 Trial To Assess Efficacy Of A Chimeric Skin In Patients With Epidermolysys Bullosa December 2006 May 2010
NCT05533866 Enrolling by invitation Early Phase 1 Characterization of the Microbiome in Colonized Dystrophic and Junctional Epidermolysis Bullosa Wounds Before and After Use of APR-TD011 ® Spray Solution February 6, 2023 December 2024
NCT06330324 Enrolling by invitation Reproductive Options in Inherited Skin Diseases January 1, 2024 September 1, 2026
NCT06330350 Recruiting Qualitative Study in Patients With Genodermatoses and Healthcare Professionals on Reproductive Counselling January 1, 2024 December 31, 2025
NCT03269474 Recruiting Computational Drug Repurposing for All EBS Cases November 28, 2017 December 31, 2024
NCT05464381 Recruiting Phase 3 Allogeneic ABCB5-positive Dermal Mesenchymal Stromal Cells for Treatment of Epidermolysis Bullosa (Phase III, Cross-over) February 1, 2023 December 2025
NCT05725018 Recruiting Phase 3 EB-101 Treatment for New and Previously Treated Patients With Recessive Dystrophic Epidermolysis Bullosa (RDEB) April 2, 2023 December 1, 2024
NCT05838092 Recruiting Phase 3 Allogeneic ABCB5-positive Dermal Mesenchymal Stromal Cells for Treatment of Epidermolysis Bullosa (Phase III) October 18, 2023 December 1, 2025
NCT00311766 Terminated Phase 2 A Phase 2 Study on Effect of Thymosin Beta 4 on Wound Healing in Patients With Epidermolysis Bullosa February 2006 November 2012
NCT00478244 Terminated N/A Allogeneic Hematopoietic Stem Cell Transplant For Epidermolysis Bullosa April 2007 August 2011
NCT00881556 Terminated Early Phase 1 Allogeneic Stem Cell Transplantation (ALLOSCT) in Recessive Dystrophic Epidermolysis Bullosa (RDEB) August 20, 2009 September 2015
NCT01619670 Terminated Phase 4 A Observational Study to Evaluate Apligraf(R) in Nonhealing Wounds of Subjects With Epidermolysis Bullosa June 2012 January 2015
NCT01749306 Terminated Phase 3 A Study of the Efficacy and Safety of ABH001 in the Treatment of Patients With Epidermolysis Bullosa Who Have Wounds That Are Not Healing December 2012 November 2013
NCT02090283 Terminated Phase 2 Open-Label Extension Study to Evaluate the Safety of SD-101 Cream in Participants With Epidermolysis Bullosa March 26, 2014 September 14, 2018
NCT02670330 Terminated Phase 3 Open Label Extension Study to Evaluate the Long-term Safety of Zorblisa (SD-101-6.0) in Patients With Epidermolysis Bullosa June 9, 2015 September 3, 2018
NCT01340235 Unknown status Phase 3 Treatment of Dowling Maera Type of Epidermolysis Bullosa Simplex by Oral Erythromycin June 2011 June 2012
NCT05033574 Unknown status The State of Sexual Development in Children With Inherited Epidermolysis Bullosa December 8, 2020 June 1, 2023
NCT04213703 Unknown status A Pilot Study to Explore the Role of Gut Flora in Epidermolysis Bullosa March 2, 2020 July 2023
NCT05288478 Unknown status Phase 2 Dose-ranging Study of Dentoxol® Mouthrinse for Managing Oral Symptoms in People With Epidermolysis Bullosa. April 6, 2022 March 2023
NCT01454687 Withdrawn N/A Grafting of Epidermolysis Bullosa Wounds Using Cultured Revertant Autologous Keratinocytes October 2011
NCT00336154 Withdrawn Phase 4 Study to Evaluate the Efficacy of Tetracycline in Epidermolysis Bullosa
NCT04613102 Withdrawn Phase 2/Phase 3 The Efficacy and Safety of 3% Cannabidiol (CBD) Cream in Patients With Epidermolysis Bullosa: A Phase II/III Trial August 1, 2020 December 30, 2022
Disase is a (Disease Ontology)
DOID:2731
Cross Reference ID (Disease Ontology)
GARD:6359
Cross Reference ID (Disease Ontology)
ICD10CM:Q81
Cross Reference ID (Disease Ontology)
MESH:D004820
Cross Reference ID (Disease Ontology)
NCI:C67383
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:205580008
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0014527
Exact Synonym (Disease Ontology)
acantholysis bullosa
ICD10 preferred id (Insert disease from ICD10)
D0014098
ICD10 class code (Insert disease from ICD10)
Q81
MeSH unique ID (MeSH (Medical Subject Headings))
D004820