Becker muscular dystrophy

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Information
Disease name
Becker muscular dystrophy
Disease ID
DOID:9883
Description
"A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21." [url:https\://www.ncbi.nlm.nih.gov/pubmed/19461958, url:https\://www.omim.org/entry/300376]
Disease area statistics
Chromosome band
Gene symbol Chromosome Start Stop The number of variant
DMD X 31,119,222 33,211,549 10
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT01081080 Completed Cardiac Magnetic Resonance in Children With Muscular Dystrophy April 2010 October 2011
NCT00104078 Completed Phase 1/Phase 2 Study Evaluating MYO-029 in Adult Muscular Dystrophy February 2005 January 2007
NCT00592553 Completed Phase 2 Phase 2B Study of PTC124 (Ataluren) in Duchenne/Becker Muscular Dystrophy (DMD/BMD) February 29, 2008 December 31, 2009
NCT00873782 Completed Phase 1 Safety Study of Transvenous Limb Perfusion in Human Muscular Dystrophy March 2009 February 2014
NCT00893334 Completed Evaluation of Limb-Girdle Muscular Dystrophy April 2009 December 2013
NCT01066455 Completed Cardiac Outcome Measures in Children With Muscular Dystrophy January 2010 May 2012
NCT01070511 Completed Phase 4 Tadalafil in Becker Muscular Dystrophy January 2010 December 2012
NCT00005574 Completed Phase 1 Gentamicin Treatment of Muscular Dystrophy February 2000 January 2001
NCT01126697 Completed Phase 2/Phase 3 Clinical Trial of Coenzyme Q10 and Lisinopril in Muscular Dystrophies February 2010 December 2017
NCT01350154 Completed Phase 2 Effect of Modulating the nNOS System on Cardiac, Muscular and Cognitive Function in Becker Muscular Dystrophy Patients November 2011 April 2013
NCT01519349 Completed Phase 1 Follistatin Gene Transfer to Patients With Becker Muscular Dystrophy and Sporadic Inclusion Body Myositis January 2012 October 2017
NCT01540604 Completed Phase 2 CRD007 for the Treatment of Duchenne Muscular Dystrophy, Becker Muscular Dystrophy and Symptomatic Carriers
NCT01557400 Completed Phase 3 Study of Ataluren for Previously Treated Participants With Nonsense Mutation Duchenne/Becker Muscular Dystrophy (nmDBMD) in Europe, Israel, Australia, and Canada May 20, 2012 January 19, 2018
NCT01856868 Completed Phase 1/Phase 2 Use of (-)-Epicatechin in the Treatment of Becker Muscular Dystrophy (Pilot Study) May 2013 September 2018
NCT02147639 Completed Phase 2/Phase 3 Effects of Sodium Nitrate on Blood Flow in Becker Muscular Dystrophy October 2013 May 2014
NCT02165358 Completed Muscle MRI in Becker Muscular Dystrophy and in Limb-girdle Muscular Dystrophy Type 2I June 2014 January 2015
NCT02434627 Completed Phase 1 Sodium Nitrate for Muscular Dystrophy June 2015 April 2018
NCT02847975 Completed Phase 1 Sodium Nitrate to Improve Blood Flow October 2013 December 2014
NCT03236662 Completed Phase 2 (-)- Epicatechin Becker Muscular Dystrophy November 2016 December 2017
NCT03238235 Completed Phase 2 Clinical Study to Evaluate the Efficacy and Safety of Givinostat in Ambulant Patients With Becker Muscular Dystrophy December 12, 2017 March 19, 2021
NCT04054375 Completed Phase 2 Weekly Steroids in Muscular Dystrophy July 1, 2019 March 1, 2022
NCT04349566 Completed Fast Troponin as a Biomarker to Assess Exercise-induced Muscle Damage in Muscle Diseases June 1, 2020 December 20, 2021
NCT04386304 Completed Phase 1 Safety and Biomarker Response to (+)-Epicatechin in Becker Muscular Dystrophy July 13, 2020 March 1, 2022
NCT04585464 Completed Phase 1 A Study to Assess Safety, Tolerability, and PK of EDG-5506 in Healthy Volunteers and Becker Muscular Dystrophy Adults October 12, 2020 December 27, 2021
NCT05160415 Completed Phase 1 A Study of EDG-5506 in Adult Males With Becker Muscular Dystrophy December 28, 2021 March 1, 2024
NCT06066580 Enrolling by invitation Phase 2 Open-Label Extension of EDG-5506 in Participants With Becker Muscular Dystrophy November 2, 2023 March 2028
NCT06363526 Not yet recruiting N/A Effectiveness of 5-week Digital Respiratory Practice in a Group of Children With Duchenne Muscular Dystrophy and Becker Muscular Dystrophy. May 5, 2024 November 30, 2024
NCT05715957 Not yet recruiting Follow-up Study on Female Carriers With DMD Gene Variants March 1, 2023 August 1, 2025
NCT03057002 Recruiting UTSW HP [13-C] Pyruvate Injection in HCM May 1, 2018 November 8, 2024
NCT05257473 Recruiting Defining Endpoints in Becker Muscular Dystrophy April 13, 2022 May 2026
NCT05291091 Recruiting Phase 2 Phase 2 Study of EDG-5506 in Becker Muscular Dystrophy (GRAND CANYON) July 6, 2022 June 2026
NCT05409079 Recruiting N/A Schulze Muscular Dystrophy Ability Clinical Study May 26, 2022 June 30, 2023
NCT06378203 Recruiting N/A Rehabilitation in Muscular Dystrophies From the Hospital Facility to the Home: Pilot Project [RIMUDI] December 15, 2023 April 15, 2025
NCT05166109 Recruiting Phase 2 A Study to Assess Vamorolone in Becker Muscular Dystrophy (BMD) July 7, 2022 January 31, 2025
NCT02972580 Recruiting Characterization of Clinical Skeletal and Cardiac Impairment in Carriers of DMD and BMD June 2016 December 2025
NCT01484678 Recruiting Magnetic Resonance Imaging and Biomarkers for Muscular Dystrophy September 1, 2020 August 31, 2025
NCT04583917 Recruiting Brain Involvement in Dystrophinopathies Part 1 March 30, 2021 December 2023
NCT04668716 Recruiting Brain Involvement in Dystrophinopathies Part 2 October 11, 2021 May 2024
NCT02069756 Recruiting The Duchenne Registry October 2007 October 2047
NCT04972604 Recruiting CureDuchenne Link®: A Resource for Research July 9, 2021 July 9, 2031
NCT05019625 Recruiting Biomarker Development for Muscular Dystrophies February 20, 2015 June 2027
NCT01168908 Terminated Phase 2 Revatio for Heart Disease in Duchenne Muscular Dystrophy and Becker Muscular Dystrophy September 2010 January 2014
NCT01009294 Terminated Phase 2 Study of Ataluren (PTC124) in Nonambulatory Participants With Nonsense-Mutation-Mediated Duchenne/Becker Muscular Dystrophy (nmDMD/BMD) January 13, 2010 March 23, 2010
NCT00847379 Terminated Phase 2 Phase 2B Extension Study of Ataluren (PTC124) in Duchenne/Becker Muscular Dystrophy (DMD/BMD) January 31, 2009 May 24, 2010
NCT02109692 Unknown status N/A Evaluation of Muscle miRNA as Biomarkers in Dystrophinopathies May 19, 2014 November 2019
NCT01539772 Unknown status Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping April 2012 August 2018
NCT00819845 Unknown status Phase 4 Ramipril Versus Carvedilol in Duchenne and Becker Patients December 2008 December 2016
Disase is a (Disease Ontology)
DOID:9884
Cross Reference ID (Disease Ontology)
GARD:5900
Cross Reference ID (Disease Ontology)
MIM:300376
Cross Reference ID (Disease Ontology)
ORDO:98895
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:111501005
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0699741
Exact Synonym (Disease Ontology)
benign congenital myopathy
Exact Synonym (Disease Ontology)
Benign pseudohypertrophic muscular dystrophy
OrphaNumber from OrphaNet (Orphanet)
98895
MedGen concept unique identifier (MedGen Concept name)
C0917713
MedGen unique identifier (MedGen Concept name)
182959