The 7 major beta thalassemia markets reached a value of US$ 340.3 Million in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 822.5 Million by 2034, exhibiting a growth rate (CAGR) of 8.35% 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$ 340.3 Million
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Market Forecast in 2034
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US$ 822.5 Million
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Market Growth Rate 2024-2034
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8.35% |
The beta thalassemia market has been comprehensively analyzed in IMARC’s new report titled “Beta Thalassemia Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034”. Beta thalassemia is an inherited blood disorder characterized by reduced levels of functional hemoglobin. It is primarily caused by mutations in the hemoglobin beta (HBB) gene. Beta thalassemia has three main forms – minor, intermediate, and major, and the symptoms depend on the severity of the disease. Beta thalassemia minor (beta thalassemia trait) is associated with mild anemia symptoms, such as fatigue, dizziness or weakness, frequent headaches, and pale skin. The most severe symptoms are associated with beta thalassemia major, which includes shortness of breath with exertion, heart palpitations, yellow skin, etc. The diagnosis of beta thalassemia relies on measuring red blood cell indices that reveal microcytic hypochromic anemia. A sample of the bone marrow may be taken to examine the number and shape of red blood cells. The diagnosis also includes hemoglobin analysis that reveals decreased amounts of HbA, increased amounts of hemoglobin F (HbF), as well as the clinical severity of anemia. Additionally, the hemoglobin electrophoresis test can help in identifying the specific type of thalassemia.
The increasing incidences of rare genetic blood disorders coupled with the escalating demand for novel treatment methods for reduced morbidity and improved quality of life are primarily driving the beta thalassemia market. In addition to this, the emerging popularity of bone marrow transplantation among beta thalassemia patients with available donors is further creating a positive outlook for the market. Moreover, the widespread adoption of oral iron chelators, such as deferiprone, which preferentially chelates the iron present in the heart to reduce the risk of beta thalassemia, is also bolstering the market growth. Apart from this, several key players are making extensive investments for an improved understanding of erythropoiesis, which will further lead to the development of new erythroid-stimulating factors effective in thalassemia. This, in turn, is acting as another significant growth-inducing factor. Additionally, numerous government bodies across the globe are introducing programs aimed at controlling the birth rate of thalassemia newborns through screening and diagnosis of populations with a high risk of beta thalassemia, thereby propelling the global market. Furthermore, the introduction of novel medications, such as hydroxyurea and L-glutamine, which help to reduce the symptoms of beta thalassemia by increasing the production of fetal hemoglobin, is expected to drive the global beta thalassemia market in the coming years.
IMARC Group’s new report provides an exhaustive analysis of the beta thalassemia market in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan. This includes treatment practices, in-market and pipeline drugs, the 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 beta thalassemia 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 beta thalassemia 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 Beta Thalassemia marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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Reblozyl (luspatercept-aamt) | Celgene |
Zynteglo | Bluebird bio |
Ferriprox | Chiesi Group |
VIT-2763 | Vifor Pharma |
CTX001 | CRISPR Therapeutics |
*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
Beta thalassemia: Current Treatment Scenario, Marketed Drugs and Emerging Therapies