The 7 major alpha-1 antitrypsin deficiency markets reached a value of US$ 1.4 Million in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 3.9 Million by 2034, exhibiting a growth rate (CAGR) of 9.83% during 2024-2034.
Report Attribute
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Key Statistics
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---|---|
Base Year |
2023
|
Forecast Years | 2024-2034 |
Historical Years |
2018-2023
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Market Size in 2023
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US$ 1.4 Million |
Market Forecast in 2034
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US$ 3.9 Million |
Market Growth Rate (2024-2034)
|
9.83% |
The alpha-1 antitrypsin deficiency market has been comprehensively analyzed in IMARC's new report titled "Alpha-1 Antitrypsin Deficiency Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". Alpha-1 antitrypsin deficiency (AATD) refers to a genetic disorder characterized by decreased levels or malfunctioning of the alpha-1 antitrypsin protein, which leads to a higher risk of developing lung and liver diseases. The most common manifestation is lung disorder, which can include chronic obstructive pulmonary disease (COPD), emphysema, chronic bronchitis, etc. Individuals with AATD may experience various symptoms, such as shortness of breath, wheezing, coughing, recurring respiratory infections, etc. In some cases, the ailment can also affect the liver, leading to liver diseases characterized by jaundice, fatigue, and abdominal swelling. The diagnosis of alpha-1 antitrypsin deficiency typically consists of a combination of clinical evaluation, laboratory investigations, and genetic analysis. Numerous laboratory tests, such as alpha-1 antitrypsin protein level measurement and protease inhibitor activity assays, can provide initial indications of deficiency. A confirmatory diagnosis includes genetic testing to identify mutations in the SERPINA1 gene, which encodes the alpha-1 antitrypsin protein. Additionally, various other procedures, such as lung function tests, imaging studies, liver function tests, etc., may be performed to assess the extent of lung or liver involvement.
The rising cases of genetic mutations that result in the production of abnormal protein variants, thereby leading to an imbalance of protease enzymes in the body, are primarily driving the alpha-1 antitrypsin deficiency market. Apart from this, the widespread adoption of augmentation therapy, which involves regular intravenous infusions of purified alpha-1 antitrypsin protein, to protect the lungs from damage caused by an imbalance of protease enzymes, is acting as another significant growth-inducing factor. Additionally, the increasing utilization of pulmonary rehabilitation programs involving exercises and breathing techniques for improving lung function, developing physical endurance, and optimizing overall respiratory health is also augmenting the market growth. Moreover, several key players are making significant investments in R&D activities to introduce disease-modifying therapies that focus on reducing the accumulation of misfolded alpha-1 antitrypsin protein within cells and enhancing the clearance of abnormal protein aggregates. This, in turn, is creating a positive outlook for the market. Besides this, the emerging popularity of expanded genetic panels since they allow the identification of rare or novel mutations in addition to the commonly screened mutations, thereby improving the accuracy of genetic diagnosis, is expected to drive the alpha-1 antitrypsin deficiency market in the coming years.
IMARC Group's new report provides an exhaustive analysis of the alpha-1 antitrypsin deficiency 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 alpha-1 antitrypsin deficiency 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 alpha-1 antitrypsin deficiency 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 alpha-1 antitrypsin deficiency marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
---|---|
Prolastin C Liquid (Alpha 1 antitrypsin modified process) | Grifols |
Aralast (Alpha-1 antitrypsin) | Kamada |
Respreeza (Alpha-1 antitrypsin) | CSL Behring |
ARO AAT | Arrowhead Pharmaceuticals/Takeda Pharmaceuticals USA |
INBRX 101 | Inhibrx |
VX-864 | Vertex Pharmaceuticals |
Belcesiran | Dicerna Pharmaceuticals |
*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
Alpha-1 Antitrypsin Deficiency: Current Treatment Scenario, Marketed Drugs and Emerging Therapies