Stargardt disease

Search with Google Search with Bing
Information
Disease name
Stargardt disease
Disease ID
DOID:0050817
Description
"An age related macular degeneration that is characterized by progressive vision loss usually to the point of legal blindness." [url:http\://en.wikipedia.org/wiki/Stargardt_disease]
Disease area statistics
Chromosome band
Gene symbol Chromosome Start Stop The number of variant
ABCA4 1 93,992,834 94,121,148 6
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT04909398 Completed N/A Pupil Dynamics and Color Vision for the Detection of Eye Diseases March 22, 2018 May 22, 2019
NCT05417126 Completed Phase 2 Safety and Effects of a Single Intravitreal Injection of vMCO-010 Optogenetic Therapy in Subjects With Stargardt Disease July 5, 2022 September 28, 2023
NCT02410122 Completed The Natural History of the Progression of Atrophy Secondary to Stargardt Disease Type 4: PROM1-Related Macular Dystrophy December 2014 March 2018
NCT05904444 Completed N/A The Effect of Duration Between Sessions on Microperimetric Biofeedback Training in Patients With Maculopathies August 15, 2018 April 30, 2023
NCT02230228 Completed Phase 1 Phase 1 Safety Study of ALK-001 in Healthy Volunteers April 2014 February 2015
NCT03772665 Completed Phase 3 Safety and Efficacy of Emixustat in Stargardt Disease January 7, 2019 June 23, 2022
NCT01977846 Completed A Natural History of the Progression of Stargardt Disease: Retrospective and Prospective Studies August 2013 February 2017
NCT05266014 Completed Phase 1/Phase 2 This is a Dose-finding Study Followed by 2-year Extension Study to Evaluate Safety and Tolerability of Tinlarebant in Adolescent Subjects With Stargardt Disease March 12, 2021 August 15, 2023
NCT06377150 Completed Stargardt Disease in Childhood April 1, 2022 March 31, 2024
NCT02255981 Completed N/A Efficacy of Acupuncture in Macular Diseases March 2013 November 2016
NCT03033108 Completed Phase 2 Pharmacodynamic Study of Emixustat Hydrochloride in Subjects With Macular Atrophy Secondary to Stargardt Disease January 2017 December 2017
NCT06048185 Enrolling by invitation Non-interventional Long Term Follow-up Study of Participants Previously Enrolled in the STARLIGHT Study October 19, 2023 July 2027
NCT04239625 Enrolling by invitation Phase 2 Open-Label Extension: Tolerability and Effects of ALK-001 on Stargardt Disease (TEASE) December 20, 2019 December 2026
NCT06319872 Not yet recruiting Phase 1 The Effects of Disulfiram (Antabuse®) on Visual Acuity in Patients With Retinal Degeneration April 15, 2024 April 15, 2025
NCT06445322 Recruiting Prescreening Study to Identify Potential Participants for ACDN-01 Clinical Trials May 30, 2024 August 31, 2030
NCT02402660 Recruiting Phase 2 Phase 2 Tolerability and Effects of ALK-001 on Stargardt Disease August 2015 March 2025
NCT02435940 Recruiting Inherited Retinal Degenerative Disease Registry June 2014 June 2037
NCT03011541 Recruiting N/A Stem Cell Ophthalmology Treatment Study II January 2016 July 31, 2026
NCT04545736 Recruiting Phase 1/Phase 2 Oral Metformin for Treatment of ABCA4 Retinopathy November 23, 2020 August 31, 2027
NCT05674058 Recruiting Function and Imaging Assessments for G1961E-associated Stargardt Disease November 1, 2022 October 31, 2025
NCT05956626 Recruiting Phase 1/Phase 2 Study to Assess the Safety and Efficacy of OCU410ST for Stargardt Disease August 25, 2023 October 28, 2025
NCT06435000 Recruiting An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 Gene March 29, 2024 February 2027
NCT01676766 Terminated Novel Quantification Methods for Fluorescence to Detect Progression in Stargardt Disease September 2012 October 2016
NCT02875704 Terminated Oxidative Stress In Stargardt Disease, Age Related Macular Degeneration and Diabetic Retinopathy January 3, 2017 September 22, 2022
Disase is a (Disease Ontology)
DOID:10871
Cross Reference ID (Disease Ontology)
GARD:181
Cross Reference ID (Disease Ontology)
MESH:D000080362
Cross Reference ID (Disease Ontology)
MIM:248200
Cross Reference ID (Disease Ontology)
MIM:600110
Cross Reference ID (Disease Ontology)
MIM:603786
Exact Synonym (Disease Ontology)
STARGARDT DISEASE 1
OrphaNumber from OrphaNet (Orphanet)
827