choroideremia

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Information
Disease name
choroideremia
Disease ID
DOID:9821
Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT04483440 Active, not recruiting Phase 1 Dose Escalation Study of Intravitreal 4D-110 in Patients With Choroideremia June 2, 2020 June 2027
NCT01603576 Completed N/A Pilot Study of a Suprachoroidal Retinal Prosthesis May 2012 August 2014
NCT01461213 Completed Phase 1/Phase 2 Gene Therapy for Blindness Caused by Choroideremia October 2011 October 2017
NCT01864486 Completed N/A Restoring Vision With the Intelligent Retinal Implant System (IRIS V1)in Patients With Retinal Dystrophy April 2013 October 13, 2017
NCT04795206 Completed Natural Disease Progression in Participants With Choroideremia August 26, 2020 August 10, 2021
NCT02671539 Completed Phase 2 THOR - Tübingen Choroideremia Gene Therapy Trial January 2016 February 2018
NCT03359551 Completed Natural History of the Progression of Choroideremia Study June 30, 2015 October 1, 2020
NCT03406416 Completed N/A Study of a Suprachoroidal Retinal Prosthesis February 13, 2018 December 18, 2020
NCT03496012 Completed Phase 3 Efficacy and Safety of BIIB111 for the Treatment of Choroideremia December 11, 2017 December 1, 2020
NCT03507686 Completed Phase 2 A Safety Study of Retinal Gene Therapy for Choroideremia With Administration of BIIB111 November 29, 2017 June 29, 2022
NCT04750785 Completed A Study to Assess Choroideremia (CHM) Health Outcomes December 15, 2020 September 27, 2021
NCT02077361 Completed Phase 1/Phase 2 An Open Label Clinical Trial of Retinal Gene Therapy for Choroideremia April 2015 May 16, 2022
NCT02341807 Completed Phase 1/Phase 2 Safety and Dose-escalation Study of AAV2-hCHM in Participants With CHM (Choroideremia) Gene Mutations January 15, 2015 October 12, 2022
NCT02407678 Completed Phase 2 REP1 Gene Replacement Therapy for Choroideremia August 16, 2016 July 23, 2021
NCT02553135 Completed Phase 2 Choroideremia Gene Therapy Clinical Trial September 2015 February 2018
NCT02670980 Completed N/A Compensation for Blindness With the Intelligent Retinal Implant System (IRIS V2) in Patients With Retinal Dystrophy January 2016 May 2019
NCT03584165 Enrolling by invitation Phase 3 Long-term Safety and Efficacy Follow-up of BIIB111 for the Treatment of Choroideremia and BIIB112 for the Treatment of X-Linked Retinitis Pigmentosa June 4, 2018 June 4, 2026
NCT05158049 Enrolling by invitation Longitudinal Study of a Bionic Eye December 9, 2021 December 9, 2026
NCT01866371 Recruiting High Resolution Retinal Imaging May 2013 December 2027
NCT05282953 Recruiting Phase 1/Phase 2 A Phase I/II Dose-escalating Study of the Safety, Tolerability and Efficacy of KIO-301 Administered Intravitreally to Patients With Retinitis Pigmentosa and Choroideremia (ABACUS) November 10, 2022 January 2025
NCT02435940 Recruiting Inherited Retinal Degenerative Disease Registry June 2014 June 2037
NCT05258032 Recruiting Structural and Functional Characterization of Rare Ocular Diseases November 24, 2021 November 24, 2025
NCT02994368 Terminated "Natural History" Study of Choroideremia December 2016 October 2021
NCT01654562 Terminated Phase 1/Phase 2 The Short-term Effects of Simvastatin on the Vision of Males Affected by Choroideremia December 2012 July 2013
NCT00427180 Unknown status N/A IRIS PILOT - Extended Pilot Study With a Retinal Implant System December 2006 December 2010
NCT05045703 Withdrawn N/A The Dark-Adapted Retinal Function Response in Choroideremia (DARC) Study May 2023 May 2024
Disase is a (Disease Ontology)
DOID:1417
Cross Reference ID (Disease Ontology)
GARD:6061
Cross Reference ID (Disease Ontology)
ICD10CM:H31.21
Cross Reference ID (Disease Ontology)
ICD9CM:363.55
Cross Reference ID (Disease Ontology)
MESH:D015794
Cross Reference ID (Disease Ontology)
MIM:303100
Cross Reference ID (Disease Ontology)
NCI:C34469
Cross Reference ID (Disease Ontology)
ORDO:180
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:75241009
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0008525
Exact Synonym (Disease Ontology)
progressive Choroidal Atrophy
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0001139
OrphaNumber from OrphaNet (Orphanet)
180
MeSH unique ID (MeSH (Medical Subject Headings))
D015794