About Hirudin
The most significant and extensively researched active constituent, 65–66 amino acids from the tiny molecules of protein, has been isolated together with leech and salivary glands (peptide). The most natural thrombin-specific inhibitor to date, hirudin has a substantial inhibitory impact on thrombin. Hirudin is an efficient anticoagulant, antithrombotic, and can prevent thrombin-catalyzed activation of coagulation factors and platelet responses as well as the further development of the blood stasis phenomenon, according to animal research and clinical trials. Additionally, it prevented thrombin from stimulating endothelial cells or causing fibroblasts to proliferate.
Attributes | Details |
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Study Period | 2017-2027 |
Base Year | 2021 |
Unit | Value (USD Million) |
Analyst at AMA Research estimates that United States Players will contribute the maximum growth to Global Hirudin market throughout the forecasted period. Established and emerging Players should take a closer view at their existing organizations and reinvent traditional business and operating models to adapt to the future.
Pfizer, Inc. (United States), Bayer Healthcare AG (Germany), Teva Pharmaceutical Industries Ltd. (Israel), Abbott India Limited (India), GlaxoSmithKline Plc. (United Kingdom), Sanofi S.A. (France), Boehringer Ingelheim (Germany), Aspen Holdings (South Africa), Bristol-Myers Squibb Company (United States), Mitsubishi Tanabe Pharma Corporation (Japan) and Eisai Inc. (Japan) are some of the key players that are part of study coverage.
Segmentation Overview
AMA Research has segmented the market of Global Hirudin market by Type (Natural Hirudin and Recombinant Hirudin) and Region.
On the basis of geography, the market of Hirudin has been segmented into South America (Brazil, Argentina, Rest of South America), Asia Pacific (China, Japan, India, South Korea, Taiwan, Australia, Rest of Asia-Pacific), Europe (Germany, France, Italy, United Kingdom, Netherlands, Rest of Europe), MEA (Middle East, Africa), North America (United States, Canada, Mexico). If we see Market by Disease Indication, the sub-segment i.e. Heparin-Induced Thrombocytopenia will boost the Hirudin market. Additionally, the rising demand from SMEs and various industry verticals gives enough cushion to market growth.
Hirudin Market Dynamics:
Attributes | Details |
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Growth Drivers | - Rising Number of Patients Suffering From Trauma
- Increasing Number of Thrombin Based Diseases
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Restraints | - Complete Dependence on Renal Function for Elimination
- Predominant Renal Excretion and Immunogenicity, Have Been Overcome Through Development Of The Hirudin Analogue, Bivalirudin
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Gaps & Opportunities | - Growing Number of Healthcare Facilities in Emerging Economies
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Market Leaders and their expansionary development strategies
In 2022, Eisai Co., Ltd. announced that Eisai has signed the Kigali Declaration made public at the Kigali Summit on Malaria and Neglected Tropical Diseases (NTDs) held on June 23, 2022 in Kigali, the capital of the Republic of Rwanda, and expressed Eisai's continued support for the eradication of NTDs in order to achieve a road map for NTDs 2021–2030 launched by the World Health Organization (WHO). Based on the philosophy of human health care (hhc), Eisai has identified the eradication of NTDs as a key area of attention and seeks to advance social welfare by reducing health disparities.
In 2022, Lecanemab is an investigational anti-amyloid beta (A) protofibril antibody for the treatment of mild cognitive impairment (MCI) caused by Alzheimer's disease (AD) and mild AD (collectively known as early AD), with confirmed amyloid pathology in the brain. Eisai Co., Ltd. and Biogen Inc. announced that the U.S. Food and Drug Administration (FDA) has accepted the Biologics License Application (BLA the Prescription Drug User Fee Act (PDUFA) action deadline for Eisai's application, which was finished in early May 2022, is January 6, 2023.
The Food and Drug Regulations require anyone intending to sell or distribute these products in Canada to obtain market authorization. The Biologics and Genetic Therapies Directorate (BGTD) is the section of Health Canada that is responsible for the regulatory oversight of these products. Sponsors are encouraged to set up a pre-submission meeting with BGTD to discuss regulatory requirements for obtaining a market authorization medicinal maggots or medicinal leeches.
About Approach
To evaluate and validate the market size various sources including primary and secondary analysis is utilized. AMA Research follows regulatory standards such as NAICS/SIC/ICB/TRCB, to have a better understanding of the market. The market study is conducted on basis of more than 200 companies dealing in the market regional as well as global areas with the purpose to understand the companies positioning regarding the market value, volume, and their market share for regional as well as global.
Further to bring relevance specific to any niche market we set and apply a number of criteria like Geographic Footprints, Regional Segments of Revenue, Operational Centres, etc. The next step is to finalize a team (In-House + Data Agencies) who then starts collecting C & D level executives and profiles, Industry experts, Opinion leaders, etc., and work towards appointment generation.
The primary research is performed by taking the interviews of executives of various companies dealing in the market as well as using the survey reports, research institute, and latest research reports. Meanwhile, the analyst team keeps preparing a set of questionnaires, and after getting the appointee list; the target audience is then tapped and segregated with various mediums and channels that are feasible for making connections that including email communication, telephonic, skype, LinkedIn Group & InMail, Community Forums, Community Forums, open Survey, SurveyMonkey, etc.