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Trial record 1 of 1 for:    LGMD-501-NHS
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A Study of the Natural History of Participants With LGMD2E/R4, LGMD2D/R3, and LGMD2C/R5, ≥ 4 Years of Age, Who Are Managed in Routine Clinical Practice

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ClinicalTrials.gov Identifier: NCT04475926
Recruitment Status : Recruiting
First Posted : July 17, 2020
Last Update Posted : July 19, 2022
Sponsor:
Information provided by (Responsible Party):
Sarepta Therapeutics, Inc.

Brief Summary:
This study will follow participants who are screened and confirmed with a genetic diagnosis of Limb-girdle muscular dystrophy type 2E (LGMD2E/R4), Limb-girdle muscular dystrophy type 2D (LGMD2D/R3), or Limb-girdle muscular dystrophy type 2C (LGMD2C/R5). These enrolled participants will be followed to evaluate mobility and pulmonary function for up to 3 years after enrollment. Additional participant data will be collected from the time the individual began experiencing LGMD symptoms to the present.

Condition or disease
Limb-girdle Muscular Dystrophy

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Study Type : Observational
Estimated Enrollment : 90 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Journey: A Global, Multicenter, Longitudinal Study of the Natural History of Subjects With Limb Girdle Muscular Dystrophy (LGMD) Type 2E (LGMD2E/R4), Type 2D (LGMD2D/R3), and Type 2C (LGMD2C/R5)
Actual Study Start Date : April 22, 2021
Estimated Primary Completion Date : December 24, 2025
Estimated Study Completion Date : December 24, 2025


Group/Cohort
LGMD2E/R4 Cohort
Participants with LGMD2E/R4 will be enrolled in this cohort. Enrollment will be capped according to age as follows: 4 to 7 years age range, 8 to 16 years age range, and ≥17 years age range through the course of the study.
LGMD2D/R3 Cohort
Participants with LGMD2D/R3 will be enrolled in this cohort. Enrollment will be capped according to age as follows: 4 to 7 years age range, 8 to 16 years age range, and ≥17 years age range through the course of the study.
LGMD2C/R5 Cohort
Participants with LGMD2C/R5 will be enrolled in this cohort. Enrollment will be capped according to age as follows: 4 to 7 years age range, 8 to 16 years age range, and ≥17 years age range through the course of the study.



Primary Outcome Measures :
  1. North Star Assessment for Dysferlinopathy (NSAD) Total Score [ Time Frame: Baseline up to Month 36 ]
  2. Time to Rise from the Floor [ Time Frame: Baseline up to Month 36 ]
  3. Time of 10-Meter Walk/Run [10MWR] [ Time Frame: Baseline up to Month 36 ]
  4. Time to Ascend 4 Steps [ Time Frame: Baseline up to Month 36 ]
  5. Dimension of the Performance of the Upper Limb (PUL) [ Time Frame: Baseline up to Month 36 ]
  6. Timed Up and Go (TUG) [ Time Frame: Baseline up to Month 36 ]
  7. Time of 100-Meter Walk/Run (100MWR) [ Time Frame: Baseline up to Month 36 ]
  8. Pulmonary Function Test: Forced Vital Capacity (FVC) [ Time Frame: Baseline up to Month 36 ]


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Ages Eligible for Study:   4 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
The population for this study is ambulatory or non-ambulatory participants ≥ 4 years of age with confirmed genetic diagnosis of LGMD2E/R4, LGMD2D/R3, or LGMD2C/R5.
Criteria

Inclusion Criteria:

- Male or female participant ≥ 4 years of age with confirmed genetic diagnosis of LGMD2E/R4, LGMD2D/R3, or LGMD2C/R5.

Exclusion Criteria:

  • Demonstrates cognitive delay or impairment that could confound motor development, in the opinion of the Investigator.
  • Has a medical condition, in the opinion of the Investigator, that might compromise participants ability to comply with study requirements.
  • Is participating in other interventional study(ies) at the time of enrollment in this study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04475926


Contacts
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Contact: Sarepta Therapeutics Inc., For Clinical Trial Information, Select Option 4 1-888-SAREPTA (1-888-727-3782) SareptAlly@sarepta.com

Locations
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United States, Arizona
Barrow Neurological Institute Recruiting
Phoenix, Arizona, United States, 85013
Contact       bill.jacobsen@dignityhealth.org   
Principal Investigator: Bill Jacobsen, MD         
United States, Arkansas
Arkansas Children's Recruiting
Little Rock, Arkansas, United States, 72202
Contact    501-364-1850    AVeerapandiyan@uams.edu   
Principal Investigator: Aravindhan Veerapandiyan, MD         
United States, California
University of California, Davis Health Dept of PM&R Recruiting
Sacramento, California, United States, 95817
Principal Investigator: Craig McDonald, MD         
United States, Illinois
Anne & Robert H. Lurie Children's Hospital of Chicago Recruiting
Chicago, Illinois, United States, 60611
Contact    312-227-2201      
Principal Investigator: Vamshi Rao, MD         
United States, Ohio
Nationwide Children's Hospital Recruiting
Columbus, Ohio, United States, 43205
Contact    614-722-6881    Linda.Lowes@nationwidechildrens.org   
Principal Investigator: Linda Lowes, PT, PhD         
United States, Texas
University of Texas Southwestern Medical Center Recruiting
Dallas, Texas, United States, 75201
Contact    214-648-3111      
Principal Investigator: Diana Castro, MD         
United States, Virginia
Children's Hospital of the King's Daughters Recruiting
Norfolk, Virginia, United States, 23507
Principal Investigator: Crystal Proud, MD         
Canada, Ontario
Children's Hospital - London Health Science Centre Recruiting
London, Ontario, Canada, N6C 2R5
Contact    (519) 685-8332    Craig.Campbell@lhsc.on.ca   
Principal Investigator: Craig Campbell, MD         
Germany
Zentrum für Kinderheilkunde und Jugendmedizin Uniklinikum Giessen Marburg (UKGM), Standort Giessen Recruiting
Giessen, Hessen, Germany, 35392
Contact    +49 (0)641-985-56843    andreas.hahn@paediat.med.uni-giessen.de   
Principal Investigator: Andreas Hahn, MD         
Italy
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Recruiting
Milan, Italy, 20122
Contact    39-02-55033802    giacomo.comi@unimi.it   
Principal Investigator: Giacomo Comi, MD         
Turkey
Lokman Hekim Etlik Hastanesi Recruiting
Ankara, Turkey, 06100
Contact    90 532 234 12 26    htopalog@hacettepe.edu.tr   
Principal Investigator: Haluk Topaloglu, MD, Prof         
United Kingdom
UCL Institute of Child Health & Great Ormond Street Hospital for Children Recruiting
London, United Kingdom, WC1N 1EH
Principal Investigator: Giovanni Baranello, MD, PhD         
Institute of Genetic Medicine, International Centre for Life Recruiting
Newcastle Upon Tyne, United Kingdom, NE1 3BZ
Contact    0191 241 8652    Jordi.Diaz-Manera@newcastle.ac.uk   
Principal Investigator: Jordi Diaz-Manera, MD, PhD         
Sponsors and Collaborators
Sarepta Therapeutics, Inc.
Investigators
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Study Director: Medical Director Sarepta Therapeutics, Inc.
Additional Information:
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Responsible Party: Sarepta Therapeutics, Inc.
ClinicalTrials.gov Identifier: NCT04475926    
Other Study ID Numbers: SRP-LGMD-501-NHS
First Posted: July 17, 2020    Key Record Dates
Last Update Posted: July 19, 2022
Last Verified: July 2022
Keywords provided by Sarepta Therapeutics, Inc.:
North Star Assessment for Dysferlinopathy (NSAD)
Performance of Upper Limb (PUL)
Pulmonary function tests (PFTs)
Ambulatory
Non-Ambulatory
Limb-girdle
LGMD
sarcoglycanopathy
β -sarcoglycan
Muscular Dystrophy
α -sarcoglycan
γ -sarcoglycan
LGMD-2D/R3
LGMD-2E/R4
LGMD-2C/R5
Clinical Outcomes Assessment
Additional relevant MeSH terms:
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Muscular Dystrophies
Muscular Dystrophies, Limb-Girdle
Sarcoglycanopathies
Muscular Disorders, Atrophic
Muscular Diseases
Musculoskeletal Diseases
Neuromuscular Diseases
Nervous System Diseases
Genetic Diseases, Inborn
Respiration Disorders
Respiratory Tract Diseases
Cardiomyopathies
Heart Diseases
Cardiovascular Diseases