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Base Year
Historical Year
Forecast Year
The polycythemia vera market size is expected to grow at a CAGR of 14% during the forecast period of 2024-2032. The market growth is likely to be driven by the advanced research and development activities to develop targeted therapies for patients.
Global Polycythemia Vera Market Report Summary | Description | Value |
Base Year | USD Million | 2023 |
Historical Period | USD Million | 2018-2023 |
Forecast Period | USD Million | 2024-2032 |
Market Size 2023 | USD Million | XX |
Market Size 2032 | USD Million | XX |
CAGR 2018-2023 | Percentage | XX% |
CAGR 2024-2032 | Percentage | 14.0% |
CAGR 2024-2032 - Market by Region | Asia Pacific | 16.1% |
CAGR 2024-2032 - Market by Country | India | 18.5% |
CAGR 2024-2032 - Market by Country | China | 15.5% |
CAGR 2024-2032 - Market by Type | Idelalisib | 16.0% |
CAGR 2024-2032 - Market by End User | Hospitals | 14.8% |
Market Share by Country 2023 | Germany | 4.5% |
Polycythemia vera is a type of rare blood cancer where the body produces a lot of red blood cells, leading to blood thickening and blood clot formation. Itchiness (especially after a warm bath or shower), numbness, a feeling of fullness or bloating due to enlarged spleen, unusual bleeding are some of the early symptoms. Polycythemia vera belongs to the BCR-ABL1–negative myeloproliferative neoplasms and poses an elevated risk of myelofibrosis progression and acute myeloid leukemia.
Polycythemia Vera Epidemiology
The polycythemia vera prevalence rate is around 22 cases per 100,000 people. It can affect all the ethnic groups, however, the incidence observed is slightly higher among Jewish patients of Eastern European descent than Asians or other Europeans. In United States, it affects around 0.6 to 1.6 per million people. The median age of being affected by the disease is around 60 years of age, with cases being slightly higher in males than females. In younger patients, polycythemia is expected to be higher in people with hemoglobinopathies and congenital cyanotic heart diseases. Consequently, there has been key focus on developing novel therapeutics to meet the high polycythemia vera market demand.
Growth in FDA Approvals for Delivering Quality Treatment
In September 2023, the FDA offered fast track designation to a new polycythemia vera treatment alternative called MWTX-003 (also known as DISC-3405). Developed by Disc Medicine Inc., it is an investigational anti-TMPRSS6 monoclonal antibody developed to increase hepcidin production and suppress serum iron. The rise in number of drugs under clinical trials is expected to boost the polycythemia vera market growth in the forecast period.
Increased Investigation in New Drug Formulas
A University of Birmingham -coordinated trial conducted in May 2023 revealed that Ruxolitinib, a drug that targets JAK2 gene, showed promising results in patients by controlling the blood count and reducing mutated JAK2 by 50%. When compared to existing therapies, Ruxolitinib led to fewer disease related events, slower disease progression and reduced spleen size effectively as well. As there is no permanent cure for the condition and associated, the research activity in new drugs is a key driver for enhanced polycythemia vera market share in upcoming years.
Advancements in Combination Therapies to Manage Treatment Resistance in Patients
Phlebotomy (blood withdrawal through a needle) has been conventionally used in patients. However, the treatment may differ based on a patient’s history of thrombosis and other dynamics. In the case of high-risk disease, cytoreductive therapy with either hydroxyurea or interferon alfa (IFN-α) may be applied to treat inflammation. Furthermore, the polycythemia vera market trend also involves rising technical advances in the biotechnological domain along with a deeper understanding of genetics. Understanding disease modification with respect to cytokine level modulations, along with hematologic, molecular, and histopathologic parameters and their association to clinical outcomes, is a major aspect of research.
Market Breakup by Type
Market Breakup by Population
Market Breakup by Treatment
Market Breakup by Route of Administration
Market Breakup by End User
Market Breakup by Region
CAGR 2024-2032 - Market by | Country |
India | 18.5% |
China | 15.5% |
UK | 12.8% |
USA | 12.5% |
Italy | 9.8% |
Canada | XX% |
Germany | XX% |
France | XX% |
Japan | 9.6% |
Australia | XX% |
Saudi Arabia | XX% |
Brazil | XX% |
Mexico | XX% |
In the forecast period, the United States is expected to dominate the polycythemia vera market. The market size can be attributed to a well-designed medical infrastructure, along with skilled healthcare professionals. The existence of prominent pharmaceutical and biotechnology companies also fosters market growth in the region.
With multiple mergers and acquisitions occurring in the region, Europe is a leading market for polycythemia vera. The presence of proactive authorities, such as the European Medicines Agency, plays a vital role in approving and labeling effective drugs for best possible outcomes in patients. Moreover, the well-structured medical and research infrastructure allows the development of new therapeutic approaches, significantly impacting the market positively. There is immense focus on spreading awareness of the condition via campaigns and programs.
Within the Asia Pacific, Japan is a major market with advanced technologies aiding better understanding the molecular and genetic basis of the disease. However, other emerging economies, such as India, China and South Korea are expected to observe notable polycythemia vera market growth in upcoming years. The growth in market size can be accredited to increasing improvements in the healthcare framework with the help of foreign fundings made in the region. The region is also witnessing a shift towards telemedicine and value-based care, which can play a critical role in fueling market growth.
In August 2023, Agios Pharmaceuticals, Inc., announced their worldwide license agreement with Alnylam Pharmaceuticals, Inc. to commercialise their latest preclinical siRNA targeting TMPRSS6. The potential treatment for polycythemia vera targets TMPRSS6, a key driver of red cell production in the body. The partnership aims to combine Agios’ scientific expertise in rare hematologic diseases with Alnylam’s siRNA platform. The agreement includes an upfront payment of USD 17.5 million to Alnylam and makes it eligible to receive up to USD 130 million in addition sales milestones and other tiered royalties. Similarly, various companies are expanding their research related activities with collaborations and acquisitions to devise improved therapeutics.
The key features of the polycythemia vera market report include patent analysis, grants analysis, clinical trials analysis, funding and investment analysis, partnerships, and collaborations analysis by the leading key players. The major companies in the market are as follows:
Kindly note that this only represents a partial list of companies, and the complete list has been provided in the report.
REPORT FEATURES | DETAILS |
Base Year | 2023 |
Historical Period | 2017-2023 |
Forecast Period | 2024-2032 |
Scope of the Report |
Historical and Forecast Trends, Industry Drivers and Constraints, Historical and Forecast Market Analysis by Segment:
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Breakup by Population |
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Breakup by Treatment |
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Breakup by Route of Administration |
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Breakup by End User |
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Breakup by Region |
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Market Dynamics |
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Companies Covered |
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*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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The market is anticipated to grow at a CAGR of 14% during the forecast period of 2024-2032, driven by the advanced research and development activities to develop targeted therapies for patients.
The market demand is driven by growing incidence of the condition, owing to increased genetic mutations in the population, along with rising competition between pharmaceutical companies to commercialise and develop innovative and effective solutions. Increased awareness initiatives via government, non-profit organisations and influential healthcare companies play a critical role to boost market demand as well.
The major market trend involves increasing frequency of drugs in clinical trials, developed to offer personalised treatment options to patients. One such drug is Ruxolitinib, created by the researchers at the University of Birmingham and led to slower progression of the disease.
Based on types, the market is divided into Dasatinib, Idelalisib, Givinostat, and M-009, among others.
Major end users include hospitals and clinics, among others.
It includes children as well as adults.
The major regions of the market include the United States, Japan, EU-4 which is segmented into Germany, France, Italy, Spain, and the United Kingdom.
Key players involved in the market are Novartis, Jakafi Ltd., Imago Biosciences, ANP Technologies, Miragen Therapeutics, AOP Orphan Pharmaceuticals AG, Incyte Corporation, PharmaEssentiaI, Promedior, Hoffman La Roche Ltd., Schering-Plough, Eli Lilly and Company, Otsuka America Pharmaceutical, Inc., Zydus Cadila and Gilead Sciences, Inc.
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United States (Head Office)
30 North Gould Street, Sheridan, WY 82801
+1-415-325-5166
Australia
63 Fiona Drive, Tamworth, NSW
+61 448 06 17 27
India
C130 Sector 2 Noida, Uttar Pradesh 201301
+91-858-608-1494
Philippines
40th Floor, PBCom Tower, 6795 Ayala Avenue Cor V.A Rufino St. Makati City, 1226.
+63 287899028, +63 967 048 3306
United Kingdom
6 Gardner Place, Becketts Close, Feltham TW14 0BX, Greater London
+44-753-713-2163
Vietnam
193/26/4 St.no.6, Ward Binh Hung Hoa, Binh Tan District, Ho Chi Minh City
+84865399124
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