The 7 major sanfilippo syndrome markets reached a value of US$ 1.7 Billion in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 2.5 Billion by 2034, exhibiting a growth rate (CAGR) of 3.53% during 2024-2034.
Report Attribute
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Key Statistics
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Base Year |
2023
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Forecast Years | 2024-2034 |
Historical Years |
2018-2023
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Market Size in 2023
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US$ 1.7 Billion |
Market Forecast in 2034
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US$ 2.5 Billion |
Market Growth Rate (2024-2034)
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3.53% |
The Sanfilippo syndrome market has been comprehensively analyzed in IMARC’s new report titled “Sanfilippo Syndrome Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034”. Sanfilippo syndrome, commonly known as mucopolysaccharidosis type III (MPS III), is caused by a single gene abnormality. It is a hereditary metabolic disorder in which the body is unable to effectively break down long chains of sugar molecules known as mucopolysaccharides or glycosaminoglycans (GAGs). As GAGs accumulate, they cause damage to the cells in which they are stored, resulting in the gradual degeneration of the central nervous system. Sanfilippo syndrome is divided into four subcategories based on its genetic cause: IIIA, IIIB, IIIC, and IIID. The symptoms of Sanfilippo syndrome are not noticeable in newborns at birth and begin to emerge as the children grow. Some of the common symptoms include behavioral problems, communication issues such as delayed speech, sleep disorders, developmental delays, intellectual incapacity, seizures, muscle abnormalities, mildly coarse facial characteristics, an enlarged head and tongue, hernia, and some autistic signs. As the child ages, other symptoms, including hearing and vision impairment, arthritis, recurrent respiratory infections, chronic diarrhea, and organ enlargements, such as those of the liver and spleen, may appear. The doctor does a regular physical examination of the patient to diagnose this indication. Aside from this, additional tests are necessary to identify the condition correctly. These generally include a urine test to determine the number of GAGs and specific molecules, genetic testing, which needs a blood or saliva sample, and a blood enzyme test to validate the results. To identify Sanfilippo syndrome, clinicians may also undertake additional newborn screening on infants.
The increasing prevalence of inherited neurodegenerative lysosomal storage disorders is primarily driving the global Sanfilippo syndrome market. In addition to this, the widespread adoption of enzyme replacement therapy that assists in replacing or generating the missing or deficient enzyme in the body due to which Sanfilippo syndrome occurs is also creating a positive outlook for the market. Moreover, several key players are making extensive investments in conducting clinical trials to encourage the development of advanced medications and novel therapeutics that aid in slowing disease progression while trying to prevent complications. This, in turn, is further acting as a significant growth-inducing factor. Apart from this, the increasing number of specialty clinics owing to the escalating need for specialist care of a higher degree for the treatment and management of the disease is also bolstering the market growth. Additionally, the rising consumer awareness towards Sanfilippo syndrome, which has resulted in the formation of several support organizations aiming to raise funds for the treatment, is further augmenting the global market. Besides this, the introduction of favorable guidelines by various regulatory bodies to facilitate faster approvals of pipeline drugs and clinical trials that encourage the entry of new medications is expected to drive the Sanfilippo syndrome market in the coming years.
IMARC Group’s new report provides an exhaustive analysis of the Sanfilippo syndrome market in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan. This includes treatment practices, in-market, and pipeline drugs, share of individual therapies, market performance across the seven major markets, market performance of key companies and their drugs, etc. The report also provides the current and future patient pool across the seven major markets. According to the report the United States has the largest patient pool for sanfilippo syndrome and also represents the largest market for its treatment. Furthermore, the current treatment practice/algorithm, market drivers, challenges, opportunities, reimbursement scenario and unmet medical needs, etc. have also been provided in the report. This report is a must-read for manufacturers, investors, business strategists, researchers, consultants, and all those who have any kind of stake or are planning to foray into the sanfilippo syndrome market in any manner.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current sanfilippo syndrome marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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Trehalose | Seelos Therapeutics |
Olenasufligene Relduparvovec | Lysogene |
Tralesinidase Alpha | BioMarin Pharmaceutical |
DNL126 | Denali |
UX 111 | Abeona Therapeutics; Ultragenyx Pharmaceutical |
*Kindly note that the drugs in the above table only represent a partial list of marketed/pipeline drugs, and the complete list has been provided in the report.
Market Insights
Epidemiology Insights
Sanfilippo Syndrome: Current Treatment Scenario, Marketed Drugs and Emerging Therapies