The MELAS Syndrome market reached a value of US$ 154.8 Million across the top 7 markets (US, EU4, UK, and Japan) in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 447.7 Million by 2034, exhibiting a growth rate (CAGR) of 10.14% 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$ 154.8 Million |
Market Forecast in 2034
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US$ 447.7 Million |
Market Growth Rate (2024-2034)
|
10.14% |
The MELAS syndrome market has been comprehensively analyzed in IMARC's new report titled "MELAS Syndrome Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". MELAS syndrome, an acronym for mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes, is a rare and complex mitochondrial disorder that affects multiple organ systems. It is primarily caused by mutations in mitochondrial DNA, leading to impaired energy production within cells. The hallmark symptoms of the ailment usually emerge during childhood or early adulthood. Patients often experience recurrent stroke-like episodes characterized by neurological indications, such as seizures, migraines, and focal neural deficits. Additionally, lactic acidosis, an accumulation of lactic acid in the bloodstream, may cause muscle weakness, fatigue, and metabolic disturbances. Several other common features include cognitive decline, hearing loss, and heart abnormalities. Diagnosing MELAS syndrome can be challenging due to its variable presentation and similarity to other conditions. The healthcare provider often relies on a combination of clinical history, physical examination, and specialized tests, such as genetic testing, to detect mutations in mitochondrial DNA. Brain imaging and muscle biopsies may also aid in confirming the diagnosis.
The growing prevalence of somatic mutations in the mitochondrial DNA, particularly in the MT-TL1 and MT-ND5 genes, which can result in disruption of cells and tissues is primarily driving the MELAS syndrome market. In addition to this, the increasing usage of effective medications, such as antioxidants, coenzyme Q10 supplements, L-arginine, etc., to manage the symptoms of the illness and improve mitochondrial function is also fostering a positive outlook for the market. These therapeutic agents aim to alleviate the severity of indications and enhance the overall quality of life for patients. Furthermore, the widespread adoption of physical and occupational therapies, which play a crucial role in managing the disease's debilitating effects by strengthening muscles, enhancing coordination, and improving gross motor skills, is further bolstering the market growth. Apart from this, the continuous advancements in gene therapy approach that hold promising potential for the prevention and treatment of complex and challenging disorders are acting as another significant growth-inducing factor. Additionally, the emerging popularity of innovative procedures, like mitochondrial replacement therapy, since it involves replacing defective mitochondrial genes with healthy donor DNA to correct the underlying genetic abnormalities responsible for the condition, is expected to drive the MELAS syndrome market during the forecast period.
IMARC Group's new report provides an exhaustive analysis of the MELAS syndrome market in the United States, EU4 (Germany, Spain, Italy, and France), 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 MELAS 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 MELAS syndrome market in any manner.
CY 6463, previously known as IW 6463, is an orally administered small molecule that stimulates soluble guanylate cyclase (sGC). Developed by Cyclerion Therapeutics, it serves as an sGC stimulator, functioning as a positive allosteric modulator to amplify the signaling of endogenous nitric oxide (NO). Cyclerion Therapeutics has outlined its intentions to proceed with a phase IIa trial for MELAS, utilizing CY-6463 as the investigational compound.
The development of the KL1333 project has reached the Phase I stage, aiming to establish its efficacy for the chronic oral treatment of primary mitochondrial disorders, particularly those within the MELAS-MIDD spectrum. KL1333 functions as a potent modulator of cellular NAD+ levels, essential for cell energy metabolism. Currently, patient studies are ongoing to assess KL1333, which has received orphan drug designation in both the United States and Europe.
Vatiquinone, under development for the treatment MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes), is an orally administered small molecule, it serves as 15-lipoxygenase inhibitors, Antioxidants and NQO1 modulators.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current MELAS syndrome marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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KH176 | Khondrion |
*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
MELAS Syndrome: Current Treatment Scenario, Marketed Drugs and Emerging Therapies