Limb-Girdle Muscular Dystrophy Type 2 – Market outlook, Epidemiology, Competitive Landscape, and Market Forecast Report – 2020 To 2030
Limb-Girdle Muscular Dystrophy Type 2 (LGMD2A, LGMD2B, LGMD2C, LGMD2D, LGMD2E, LGMD2F, LGMD2G, LGMD2I, LGMD2J, LGMD2L, Others (LGMD2H, LGMD2K, LGMD2M-Z)) includes forms of autosomal recessive characterized by progressive weakness of the muscles of the pelvic girdle, legs, arms, and shoulders. Progression of muscle weakness may be slow or rapid and may vary even among individuals in the same family. Intelligence is normal. The age of onset ranges from subgroup to subgroup. Overall, the beginning is more common in childhood, but it may occur in adulthood. Diagnosis of LGMD2A is complicated by phenotypic variability, lack of precise protein analysis, and absence of mutational hot spots in the CAPN3 gene. Children between the ages of 8-and 15 may range from 2-to 40 years of age. Most cases are characterized by muscle .weakness affecting the hip-girdle area, although the hip adductor muscles may be spared.
The prevalence of Limb-girdle muscular
dystrophy type 2 varies from 47 to 53 cases per million in the USA.
The competitive
landscape of Limb-Girdle Muscular Dystrophy Type 2 includes country-specific
approved and pipeline therapies. Any asset/product-specific designation or
review and Accelerated Approval are tracked and supplemented with analyst
commentary.
KOLs insights of Limb-Girdle
Muscular Dystrophy Type 2 across 8 MM market from the center of Excellence/
Public/ Private hospitals participated in the study. Insights around current
treatment landscape, epidemiology, clinical characteristics, future treatment
paradigm, and Unmet needs.
Limb-Girdle
Muscular Dystrophy Type 2 Market
Forecast: Patient Based Forecast Model (MS. Excel Based Automated
Dashboard), which Data Inputs with sourcing, Market Event, and Product Event,
Country specific Forecast Model, Market uptake and patient share uptake,
Attribute Analysis, Analog Analysis, Disease burden, and pricing scenario,
Summary, and Insights.
S. No Asset Company Stage
1 ATA-100 Atamyo
Therapeutics Phase 1
2 Deflazacort PTC
Therapeutics Phase 3
3 LION-101 Asklepios
Biopharmaceutical, Inc. Phase 2
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