Clinical Trials Directory

Trials / Completed

CompletedNCT03981289

Defining Clinical Endpoints in Limb Girdle Muscular Dystrophy (LGMD)

GRASP-LGMD: Defining Clinical Endpoints in LGMD

Status
Completed
Phase
Study type
Observational
Enrollment
116 (actual)
Sponsor
Virginia Commonwealth University · Academic / Other
Sex
All
Age
4 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Limb Girdle Muscular Dystrophy comprise a group of disorders made up of over 30 mutations which share a common phenotype of progressive weakness of the shoulder and hip girdle muscles. While the individual genetic mutations are rare, as a cohort, LGMDs are one of the four most common muscular dystrophies. The overall goal of project 1 is to define the key phenotypes as measured by standard clinical outcome assessments (COAs) for limb girdle muscular dystrophies (LGMD) to hasten therapeutic development.

Detailed description

The genetic heterogeneity has been a barrier to broad natural history efforts, with prior investigations often limited to single gene mutations. Much attention is paid to the variability within individual mutations (e.g. distal presentations), as opposed to defining the best strategy for measuring change in overall LGMD disease burden. This presents a major dilemma for LGMD rare disease research: how to balance diverse genes leading to overlapping phenotypes, versus variants in the same gene leading to divergent phenotypes. What is clear, is as a group, LGMDs are chronic and progressive leading to significant lifetime morbidity and represent a large unmet clinical need. Recent developments in the investigator's genetic understanding of LGMD and molecular approaches to therapy have led to proposed gene replacement therapies for at least three of the LGMD mutations. Several of these gene replacement therapies are currently in pre-clinical/phase 1 testing, leading to an urgent need for natural history data. In addition, non-specific therapies which target muscle mass or function are being tested in other muscular dystrophies and may prove beneficial for LGMD.

Conditions

Timeline

Start date
2019-06-14
Primary completion
2025-06-30
Completion
2025-06-30
First posted
2019-06-10
Last updated
2026-02-27

Locations

10 sites across 2 countries: United States, United Kingdom

Source: ClinicalTrials.gov record NCT03981289. Inclusion in this directory is not an endorsement.