Lysosomal Acid Lipase Deficiency Treatment Market, by Therapy Type, Drug Type, Disease Indication 2025

LYSOSOMAL ACID LIPASE
DEFICIENCY TREATMENT MARKET
Global Industry Insights, Trends, Outlook, and
Opportunity Analysis, 2017– 2025
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REPORT DESCRIPTION
Lysosomal Acid Lipase (LAL) Deficiency Treatment Market Overview
Lysosomal acid lipase (LAL) deficiency is a rare inherited condition in which the body is not able
to produce enough lysosomal acid lipase (LAL) enzyme, which is an important enzyme for
breakdown of fatty materials namely cholesteryl esters and triglycerides. This results in building
up of a large amount of fatty material in body organs, which include spleen, liver, and gut. The
deficiency of LAL causes two autosomal recessive disorders, Wolman disease (WD) and
Cholesteryl Ester Storage Disease (CESD). LAL deficiency is caused due to the genetic mutation in
LIPA gene, which results in decrease or loss of Lysosomal Acid Lipase (LAL) enzyme.
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FDA approval of innovative drugs is expected to fuel the growth of Lysosomal Acid Lipase (LAL)
Deficiency Treatment Market
The approval of innovative drugs by Food and Drug Administration (FDA) is expected to augment
the growth of market. In 2015 the U.S. Food and Drug Administration (FDA) approved Alexion
Pharmaceutical’s Kanuma(sebelipase alfa), an innovative enzyme replacement therapy (ERT).
Kanuma is first approved therapy that treats the underlying cause of the disease. It is the only
therapy for the treatment of LAL deficiency. As it is the only available therapy in market, kanuma
is expected to have a significant market growth in the near future. According to the National
Institute for Health and Care Excellence (NICE) 2016, around 50% of patients suffering from
lysosomal acid lipase (LAL) deficiency have chances of liver complications, which includes
cirrhosis or fibrosis and liver transplant
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REPORT DESCRIPTION
Lysosomal Acid Lipase (LAL) Deficiency Treatment Market Taxonomy
The global Lysosomal Acid Lipase (LAL) deficiency treatment market is segmented on the basis of
disease type, treatment type, and end user.
On the basis of disease type, the Lysosomal Acid Lipase (LAL) deficiency treatment market is
segmented into:
• Wolman Disease
• Cholesteryl Ester Storage Disease (CESD)
On the basis of treatment type, the Lysosomal Acid Lipase (LAL) deficiency treatment market is
segmented into:
• Liver Transplant
• Hematopoietic Stem Cell Transplant
On the basis of end users, the Lysosomal Acid Lipase (LAL) deficiency treatment market is segmented
into:
• Hospital
• Clinics
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REPORT DESCRIPTION
North America is expected to dominate market due to rapid novel innovations
Global market for the Lysosomal Acid Lipase (LAL) deficiency treatment market by Coherent
Market Insights is segmented into North America, Latin America, Europe, Asia Pacific, Middle
East, and Africa. North America is expected to dominate the lysosomal acid lipase (LAL)
deficiency treatment market attributed to rapid novel innovations, drug development, and
research. In 2015, FDA approved genetically modified organisms (GMO) chickens, for the
production of a recombinant human lysosomal acid lipase (LAL) protein in their eggs for the
treatment of lysosomal acid lipase (LAL) deficiency among Americans. Europe is expected to be
the second largest region for LAL deficiency treatment market. The Europe commission in 2015
granted marketing permission of Kanuma, for the treatment of LAL deficiency for patients of all
ages, which is expected to fuel the growth of kanuma in region.
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Rapid approval of therapy by FDA in various region, be an opportunities for companies
Ltd. In 2015, FDA approved Kanuma, an innovative enzyme replacement therapy (ERT) in the
U.S., Europe Union, and Japan, which is providing an opportunity to manufacturers for
exploring their business in the untapped market. Major players operating in global Lysosomal
Acid Lipase (LAL) Deficiency treatment market include Alexion Pharmaceutical Inc., Merck &
Co., Inc., Pfizer, Inc., and AstraZeneca plc. and Teva Pharmaceutical Industries.
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Lysosomal acid lipase (LAL) deficiency is a rare inherited condition in which the body is not able to produce enough lysosomal acid lipase (LAL) enzyme, which is an important enzyme for breakdown of fatty materials namely cholesteryl esters and triglycerides. This results in building up of a large amount of fatty material in body organs, which include spleen, liver, and gut. The deficiency of LAL causes two autosomal recessive disorders, Wolman disease (WD) and Cholesteryl Ester Storage Disease (CESD). LAL deficiency is caused due to the genetic mutation in LIPA gene, which results in decrease or loss of Lysosomal Acid Lipase (LAL) enzyme. Request to download and view Sample Report: https://www.coherentmarketinsights.com/insight/request-sample/904