市場調查報告書
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1401859
2030 年藥物基因組學市場預測:按配銷通路、技術、應用、最終用戶和地區分類的全球分析Pharmacogenomics Market Forecasts to 2030 - Global Analysis By Distribution Channel, Technology, Application, End User and By Geography |
根據 Stratistics MRC 的數據,2023 年全球藥物基因組學市場規模為 166.6 億美元,預計預測期內複合年成長率為 11.1%,到 2030 年將達到 348.1 億美元。
透過分析影響個體對特定藥物反應的人類遺傳變異來開發藥物的研究稱為藥物基因組學。這種方法對於精準醫學至關重要,可以根據遺傳標記提供個人化治療計畫。改善患者治療效果、減少副作用、提高藥物療效並提供更具成本效益的醫療保健至關重要。
根據美國癌症研究所2020年9月發布的資料,預計2020年美國將有1,806,590人新診斷出癌症,606,520人將死於癌症。
個人化醫療的普及
個人化醫療是一種根據個人的遺傳、基因組和臨床特徵量身訂做醫療照護的方法。透過客製化醫療介入措施,我們的目標是最大限度地提高治療效果、最大限度地減少副作用並改善患者的治療結果。隨著患者和醫療保健提供者越來越意識到藥物基因組學的潛在益處,對基因檢測和個體化治療計劃的需求正在增加。此外,製藥公司也投資基於基因組資料的標靶治療。患者需求、臨床相關性和產業創新的融合正在推動藥物基因組學市場的成長。
成本壁壘
成本障礙是藥物基因體學市場的主要抑制因素。基因檢測和藥物基因組學服務價格昂貴,使得許多患者和醫療系統無法獲得這些服務。 核酸定序、資料分析和解釋的高成本可能會限制藥物基因組學的採用,特別是在資源有限的環境中。這些經濟負擔導致無法平等地獲得個人化醫療的好處,並加劇了醫療保健差距。
基因檢測技術的進展
基因檢測的進步可以透過降低成本、提高可及性和擴大檢測的可用性來刺激成長。隨著科技的進步,基因檢測變得更加可用、更便宜且更準確。此外,方便用戶使用的家庭檢測套組和行動健康應用程式的開發使患者和醫療保健專業人員的測試過程變得更加容易。此外,這些發展不僅簡化了個體遺傳資訊的可用性,而且還促進將藥物基因組資料涵蓋標準治療方案。基因檢測的廣泛普及使得藥物基因組學市場佔有率的擴大和個人化醫療的廣泛採用成為可能。
資料隱私和安全
遺傳資訊高度敏感,處理不當或詐欺存取該資料可能會導致隱私侵犯、資訊盜竊和歧視。由於擔心潛在的濫用,患者可能不願意接受基因檢測或共用資料。此外,保護遺傳資訊的法律規範不斷發展,可能為醫療保健提供者和製藥公司帶來合規挑戰。因此,導致市場成長下降。
COVID-19 的爆發對市場產生了多方面的影響。一方面,它加速了數位醫療的普及,包括遠端醫療和遠端監控,可以透過促進資料共用和患者諮詢來補充藥物基因組學。大流行的緊迫性也導致醫療保健和製藥領域的研究和投資增加,這可能會刺激藥物基因組學的進步。然而,也有負面影響。許多醫療保健資源和研究工作都針對 COVID-19,這可能會減緩藥物基因組學計劃的進展。由於封鎖和安全問題,藥物基因組治療的臨床試驗可能會被推遲或中斷。
DNA定序部分預計將成為預測期內最大的部分
預計DNA定序部分將佔最大佔有率。 DNA定序涉及確定個體基因組中 DNA 鹼基的確切順序。透過分析遺傳變異,研究人員和醫療保健提供者可以識別與藥物反應和疾病感受性相關的特定基因和遺傳標記。這些資訊允許治療方法客製化,並確保為患者提供最有效和最安全的治療方法選擇。此外,次世代定序等DNA測序技術的進步使得基因組資料的獲取速度更快、更具成本效益,推動了這一領域的成長,並增加了藥物基因組學在醫療保健領域的潛在應用。
醫院和診所領域預計在預測期內複合年成長率最高。
預計醫院和診所部門在預測期內將出現良好的成長。醫療機構利用藥物基因組學測試來定製藥物治療計劃,並確保藥物對個別患者有效且安全。藥物基因組學幫助臨床醫生確定最合適的藥物治療和給藥,最大限度地減少副作用並最佳化患者的治療結果。此外,它還可以幫助選擇從癌症到心血管疾病等多種疾病的治療方法。隨著個人化醫療需求的增加,醫院和診所必須將藥物基因組學涵蓋日常臨床實踐,透過提供個體化、資料主導的治療計劃來徹底改變醫療保健。
在估計期間,亞太地區佔據最大的市場佔有率。亞太地區是藥物基因體學的重要且快速成長的市場。該地區面臨著癌症、心血管疾病和糖尿病等慢性疾病日益沉重的負擔,推動了對個人化醫療和藥物基因組學解決方案的需求。中國、日本和韓國等亞太地區國家正在大力投資基因組學研究,在了解影響藥物反應和疾病的遺傳因素方面取得了重大進展。
預計北美在預測期內將實現盈利成長。北美擁有先進的醫療保健系統,包括成熟的醫院、研究機構和製藥公司,為藥物基因組學的發展提供了堅實的基礎。美國FDA 等監管機構正在積極認知到藥物基因組學在藥物開發、核准和標籤中的重要性,這正在加速採用。此外,北美製藥公司正在藥物基因組學方面投入巨資,從而開發了許多個體化治療方法。該地區處於藥物基因組學研究的前沿,在基因組研究、臨床試驗和標靶治療開發方面進行了大量投資。
According to Stratistics MRC, the Global Pharmacogenomics Market is accounted for $16.66 billion in 2023 and is expected to reach $34.81 billion by 2030 growing at a CAGR of 11.1% during the forecast period. The study of developing drugs by analysing genetic variations in humans that affect an individual's response to a particular drug is known as pharmacogenomics. This approach is vital for precision medicine, offering personalised treatment plans based on genetic markers. It is essential to improving patient outcomes, reducing adverse drug reactions, enhancing medication efficacy, and providing more cost-effective healthcare.
According to data published by National Cancer Institute in September 2020, stated that an estimated 1,806,590 new cases of cancer will be diagnosed in the U.S. and 606,520 people will die from the disease in 2020.
Increasing adoption of personalized medicine
Personalised medicine is an approach that tailors medical treatments to an individual's genetic, genomic, and clinical characteristics. It aims to maximise treatment effectiveness, minimise side effects, and improve patient outcomes by customising healthcare interventions. As patients and healthcare providers become more aware of the potential benefits of pharmacogenomics, the demand for genetic testing and personalised treatment plans is on the rise. Furthermore, pharmaceutical companies are also investing in targeted therapies based on genomic data. This convergence of patient demand, clinical relevance, and industry innovation is propelling the growth of the pharmacogenomics market.
Cost barriers
Cost barriers pose a significant restraint on the Pharmacogenomics market. Genetic testing and pharmacogenomic services can be expensive, making them inaccessible to many patients and healthcare systems. The high costs of DNA sequencing, data analysis, and interpretation can limit the adoption of pharmacogenomics, especially in resource-constrained environments. This financial burden can result in unequal access to the benefits of personalised medicine, exacerbating healthcare disparities.
Advancements in genetic testing technologies
Developments in genetic testing can spur growth by lowering the cost, increasing accessibility, and expanding the availability of testing. Genetic testing is getting easier to obtain, less expensive, and more accurate as technology advances. Furthermore, the process is made easier for patients and healthcare professionals by the creation of user-friendly at-home testing kits and mobile health applications. Moreover, these developments not only simplify genetic information availability for individuals but also make it easier to incorporate pharmacogenomic data into standard therapeutic procedures. Growing pharmacogenomics market share and wider adoption of personalised medicine are made possible by the increasing prevalence of genetic testing.
Data privacy and security
Genetic information is highly sensitive, and the mishandling or unauthorised access to this data could lead to privacy breaches, identity theft, or discrimination. Patients may be hesitant to undergo genetic testing or share their data, fearing potential misuse. Furthermore, regulatory frameworks for safeguarding genetic information are continually evolving and can create compliance challenges for healthcare providers and pharmaceutical companies. Hence, it will lead to a decrease in market growth.
The COVID-19 pandemic has had a multifaceted impact on the market. On one hand, it accelerated the adoption of digital health, including telehealth and remote monitoring, which can complement pharmacogenomics by facilitating data sharing and patient consultations. The urgency of the pandemic also led to increased research and investment in healthcare and pharmaceuticals, potentially driving advancements in pharmacogenomics. However, there were negative effects as well. Many healthcare resources and research efforts were redirected toward COVID-19, potentially slowing the progress of pharmacogenomics projects. Clinical trials for pharmacogenomic therapies may have been delayed or disrupted due to lockdowns and safety concerns.
The DNA Sequencing segment is expected to be the largest during the forecast period
The DNA Sequencing segment is estimated to hold the largest share. DNA sequencing involves determining the precise order of DNA bases in an individual's genome. By analysing genetic variations, researchers and healthcare providers can identify specific genes and genetic markers relevant to drug response and disease susceptibility. This information enables the customization of medical treatments, ensuring the most effective and safe therapeutic options for patients. In addition, advances in DNA sequencing technologies, such as next-generation sequencing, have made it faster and more cost-effective to obtain genomic data, driving the growth of this segment and expanding the potential applications of pharmacogenomics in healthcare.
The Hospitals & Clinics segment is expected to have the highest CAGR during the forecast period
The Hospitals & Clinics segment is anticipated to have lucrative growth during the forecast period. The healthcare facilities utilise pharmacogenomic testing to customise drug treatment plans, ensuring that medications are both effective and safe for individual patients. Pharmacogenomics can help clinicians identify the most suitable drug therapies and dosages, minimising adverse reactions and optimising patient outcomes. Furthermore, it aids in the selection of treatments for various medical conditions, from cancer to cardiovascular diseases. As the demand for personalised medicine grows, hospitals and clinics are essential in integrating pharmacogenomics into routine clinical practice, revolutionising healthcare by providing individualised, data-driven treatment plans.
Asia Pacific commanded the largest market share during the extrapolated period. The Asia-Pacific region is a significant and rapidly growing market for pharmacogenomics. The region faces a rising burden of chronic diseases, including cancer, cardiovascular diseases, and diabetes, which has led to a growing demand for personalised medicine and pharmacogenomic solutions. Countries in the Asia-Pacific region, such as China, Japan, and South Korea, have made substantial investments in genomics research, leading to significant advancements in understanding genetic factors influencing drug responses and diseases.
North America is expected to witness profitable growth over the projection period. North America boasts advanced healthcare systems, including well-established hospitals, research institutions, and pharmaceutical companies, providing a solid foundation for the growth of pharmacogenomics. Regulatory agencies, such as the FDA in the United States, have been proactive in recognising the importance of pharmacogenomics in drug development, approval, and labelling, which accelerates its adoption. Furthermore, North American pharmaceutical companies have heavily invested in pharmacogenomics, resulting in the development of numerous personalised therapies. The region is at the forefront of pharmacogenomic research, with substantial investments in genomic studies, clinical trials, and the development of targeted therapies.
Some of the key players in the Pharmacogenomics Market include Novartis AG, Ferndale Pharma Group, Inc., Mylan N.V., F. Hoffmann-La Roche Ltd, Takeda Pharmaceutical Company Limited, Pfizer Inc., AstraZeneca, Merck & Co., Inc., Eli Lilly and Company, Sun Pharmaceutical Industries Ltd., Lupin, NATCO Pharma Limited, Teva Pharmaceutical Industries Ltd, AbbVie Inc., Boehringer Ingelheim International GmbH, Abbott, Bayer AG, Thermo Fisher Scientific, Inc., Admera Health and Agilent Technologies.
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