X-Linked Hypophosphatemia (XLH) – Market Outlook, Epidemiology, Competitive Landscape, and Market Forecast Report – 2023 To 2033
X-linked
hypophosphatemia (XLH) is a hereditary disorder affecting phosphate metabolism.
It arises from mutations in the Phosphate Regulating Endopeptidase Homolog,
X-Linked (PHEX) gene. These mutations result in local and systemic effects,
encompassing impaired growth, bone pain, osteomalacia, bone deformities,
rickets, spontaneous dental abscesses, osteoarthritis, enthesopathy, hearing
issues, and muscular dysfunction. XLH patients exhibit elevated levels of
fibroblast growth factor 23 (FGF23). Diagnosis relies on a consistent medical
history, physical examination, radiological evidence of rickets, biochemical
tests, and a family history indicating the presence of XLH, whether through
multiple generations or sporadic occurrences. The differential diagnosis should
consider nutritional rickets, metaphyseal dysplasia, and other renal phosphate
wasting disorders. Fibroblast growth factor 23 (FGF23) is primarily produced by
osteocytes and osteoblasts, playing a crucial role in regulating phosphate
metabolism. Mutations in the PHEX gene, which is highly expressed in osteocytes
and osteoblasts, lead to elevated FGF23 levels. This occurs because abnormal
cleavage of FGF23 results in hypophosphatemia due to impaired phosphate
reabsorption in the renal proximal tubules (causing reduced NPT2a and 2c
transporter activity) and decreased phosphate absorption in the intestines (due
to decreased activity of 1α-hydroxylase, which reduces the renal synthesis of
1,25(OH)2D3).
·
A humanized monoclonal antibody for FGF23,
known as burosumab, has received approval for treating XLH in pediatric
patients aged one year and older. Crysvita® (burosumab) was approved by the FDA
and became available in the USA in March 2018. Additionally, it has gained
approval from the EMA for use in 28 countries.
Thelansis’s
“X-Linked Hypophosphatemia (XLH) Market Outlook, Epidemiology, Competitive
Landscape, and Market Forecast Report – 2023 To 2033" covers disease
overview, epidemiology, drug utilization, prescription share analysis,
competitive landscape, clinical practice, regulatory landscape, patient share,
market uptake, market forecast, and key market insights under the potential X-Linked
Hypophosphatemia (XLH) treatment modalities options for eight major markets
(USA, Germany, France, Italy, Spain, UK, Japan, and China).
KOLs insights of X-Linked
Hypophosphatemia (XLH) across 8 MM market from the centre of Excellence/
Public/ Private hospitals participated in the study. Insights around current
treatment landscape, epidemiology, clinical characteristics, future treatment
paradigm, and Unmet needs.
X-Linked
Hypophosphatemia (XLH) 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.
Thelansis Competitive Intelligence (CI) practice
has been established based on a deep understanding of the pharma/biotech
business environment to provide an optimized support system to all levels of
the decision-making process. It enables business leaders in forward-thinking
and proactive decision-making. Thelansis supports scientific and commercial
teams in seamless CI support by creating an AI/ ML-based technology-driven
platform that manages the data flow from primary and secondary sources.
Tags: X-Linked
Hypophosphatemia (XLH), X-Linked Hypophosphatemia (XLH) market outlook, X-Linked Hypophosphatemia (XLH) competitive landscape, X-Linked Hypophosphatemia
(XLH) market forecast, Thelansis, Primary market
research, KOL insights, Competitive Intelligence (CI)

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