The 7 major Waldenstrom macroglobulinemia markets reached a value of US$ 152.1 Million in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 234.2 Million by 2034, exhibiting a growth rate (CAGR) of 4% 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$ 152.1 Million |
Market Forecast in 2034
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US$ 234.2 Million |
Market Growth Rate (2024-2034)
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4% |
The Waldenstrom macroglobulinemia market has been comprehensively analyzed in IMARC's new report titled "Waldenstrom Macroglobulinemia Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". Waldenstrom macroglobulinemia refers to a rare form of cancer that belongs to a group of disorders known as lymphoproliferative neoplasms. It is characterized by the overproduction of a specific type of abnormal white blood cell called lymphoplasmacytic cells, which accumulate in the bone marrow and produce monoclonal immunoglobulin M (IgM) protein. The most common symptoms associated with the illness include fatigue, weakness, enlarged lymph nodes and spleen, anemia, bleeding problems, easy bruising, nosebleeds, etc. Individuals suffering from this ailment may also experience indications related to high levels of IgM, such as thickened blood or hyperviscosity. The diagnosis of Waldenstrom macroglobulinemia involves several steps, including medical history evaluation, physical examination, laboratory tests, and imaging studies. A bone marrow biopsy is also crucial to detect characteristic findings and confirm the presence of abnormal lymphocytes in patients. The healthcare provider may further perform numerous other diagnostic procedures and tests, like a complete blood count, a computed tomography scan, serum protein electrophoresis, etc., to validate the underlying cause as well as evaluate the extent and spread of the disease.
The increasing cases of inherited disorders resulting from genetic mutations, which cause uncontrolled growth and accumulation of lymphoplasmacytic cells, are primarily driving the Waldenstrom macroglobulinemia market. In addition to this, the growing geriatric population, who are susceptible to various physiological changes and impaired immune system functioning, is creating a positive outlook for the market. Moreover, the widespread adoption of chemotherapy regimens, including bendamustine, cyclophosphamide, fludarabine, etc., to alleviate disease symptoms by reducing the proliferation of cancerous cells and decreasing the production of abnormal proteins is further bolstering the market growth. Apart from this, the escalating application of plasmapheresis procedures, since they help to lower the concentration of IgM, thereby enhancing blood flow and preventing complications related to high serum viscosity, is acting as another significant growth-inducing factor. Additionally, the emerging popularity of interferon-alpha therapy to treat the disorder owing to its several associated benefits, such as stimulating the immune system, inhibiting cell growth, and improving disease control, is expected to drive the Waldenstrom macroglobulinemia market during the forecast period.
IMARC Group's new report provides an exhaustive analysis of the Waldenstrom macroglobulinemia 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 Waldenstrom macroglobulinemia and also represents the largest market for its treatment. Furthermore, the current treatment practice/algorithm, market drivers, challenges, opportunities, reimbursement scenario, 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 Waldenstrom macroglobulinemia market in any manner.
Imbruvica (Ibrutinib) is a once-daily oral medicine co-developed and commercialized by Janssen Biotech, Inc. and Pharmacyclics LLC, an AbbVie company. IMBRUVICA inhibits the Bruton's tyrosine kinase (BTK) protein, which is required for normal and aberrant B cells, including certain cancer cells, to grow and spread. By inhibiting BTK, IMBRUVICA could potentially transfer abnormal B cells out of their nourishing surroundings and prevent their proliferation.
APG-2575 is a novel, orally administered Bcl-2‒selective inhibitor being developed by Ascentage Pharma. APG-2575 is intended to treat a number of hematologic malignancies by selectively inhibiting Bcl-2, restoring the normal apoptotic mechanism in malignant cells.
Acalabrutinib is a highly selective, powerful, covalent inhibitor of BTK that has shown minimal off-target activity in pre-clinical testing. This prospective new drug is being developed for the treatment of certain B-cell and other malignancies. The acalabrutinib development program involves both monotherapy and combination therapy methods in Waldenstrom macroglobulinemia.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current Waldenstrom macroglobulinemia marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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Brukinsa (Zanubrutinib) | BeiGene |
Imbruvica (Ibrutinib) | Janssen/Pharmacyclics |
Ulocuplumab | Bristol-Myers Squibb |
APG2575 | Ascentage Pharma |
Acalabrutinib | Acerta Pharma/AstraZeneca |
Pirtobrutinib | Eli Lilly and Company |
Daratumumab | Janssen Biotech |
*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
Waldenstrom Macroglobulinemia: Current Treatment Scenario, Marketed Drugs and Emerging Therapies