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市場調查報告書
商品編碼
1750483
基因沉默市場機會、成長動力、產業趨勢分析及 2025 - 2034 年預測Gene Silencing Market Opportunity, Growth Drivers, Industry Trend Analysis, and Forecast 2025 - 2034 |
2024年,全球基因沉默市場規模達96億美元,預計到2034年將以11.6%的複合年成長率成長,達到285億美元,這得益於全球遺傳病發病率的上升以及對下一代療法日益成長的需求。隨著越來越多的人被診斷出患有遺傳性疾病,人們對修改或抑制致病基因的治療方法的興趣也日益濃厚。醫療保健系統正致力於精準醫療,而基因沉默在這一轉變中發揮著至關重要的作用,它能夠提供傳統藥物無法實現的精準治療效果。隨著生物技術工具的改進和臨床研發管線的不斷完善,基於基因的干涉措施正迅速受到研究人員和醫療服務提供者的青睞。
該市場見證了令人矚目的技術進步,尤其是在先進基因調控方法的應用方面。 2024年,該產品領域的規模達到77億美元,預計未來將持續成長。 CRISPR-Cas9、反義寡核苷酸 (ASO) 和RNA干擾 (RNAi) 等工具已被證明在分子層面上治療遺傳疾病方面至關重要。這些技術正在為標靶治療開闢新的機遇,ASO 在罕見疾病管理中展現出良好的前景,而RNAi 則逐漸成為更廣泛治療應用的平台。
市場範圍 | |
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起始年份 | 2024 |
預測年份 | 2025-2034 |
起始值 | 96億美元 |
預測值 | 285億美元 |
複合年成長率 | 11.6% |
由於RNAi及相關技術在研究中的應用日益廣泛,因此藥物研發領域的基因沉默市場在2024年佔了51%的佔有率。製藥和生物技術公司正在利用這些工具來精確定位致病基因,並簡化藥物開發的早期階段。隨著新型療法臨床試驗在不同治療領域的擴展,對基因標靶平台的需求持續成長。
預計2034年,美國基因沉默市場規模將達111億美元。美國擁有強大的科學研究基礎設施,並在賽默飛世爾科技、安捷倫科技和Bio-Rad Laboratories等領先公司的支持下,為基因沉默治療的持續創新提供了支持。持續的研發投入和監管支持也創造了良好的成長環境。美國仍然是基因組醫學臨床進展和資金支持的中心。
默克集團 (Merck KGaA)、金斯瑞 (GenScript)、Revvity Discovery、聖克魯斯生物技術公司 (Santa Cruz Biotechnology) 和新英格蘭生物實驗室 (New England Biolabs) 等主要參與者正透過重點投資 RNAi 和 ASO 平台來鞏固其市場地位。這些公司正在透過基因編輯工具、客製化寡核苷酸合成和可擴展的遞送系統擴展其產品組合。與學術機構和生物技術新創公司建立的策略合作夥伴關係有助於他們在臨床創新領域保持領先地位。各公司投資於自動化、基於人工智慧的基因標靶篩選和增強的實驗室基礎設施,以加快研究週期。持續努力獲得監管部門的批准並開發伴隨診斷產品也是保持競爭力的關鍵。透過將產品創新與精準治療趨勢相結合,這些公司充分利用了市場對標靶基因治療日益成長的需求。
The Global Gene Silencing Market was valued at USD 9.6 billion in 2024 and is estimated to grow at a CAGR of 11.6% to reach USD 28.5 billion by 2034, driven by a rising global incidence of genetic diseases and rising demand for next-generation therapies. As more individuals are diagnosed with inherited conditions, the interest in treatments that modify or suppress disease-causing genes has accelerated. Healthcare systems are focusing on precision medicine, and gene silencing plays a crucial role in this shift, offering targeted therapeutic outcomes that conventional drugs cannot achieve. With improved biotechnological tools and stronger clinical pipelines, gene-based interventions are rapidly gaining traction among researchers and care providers.
The market has witnessed impressive technological strides, particularly with the adoption of advanced gene regulation methods. In 2024, the products segment held USD 7.7 billion, with continued expansion expected. Tools like CRISPR-Cas9, antisense oligonucleotides (ASOs), and RNA interference (RNAi) have proven vital in addressing genetic disorders at the molecular level. These technologies are unlocking new opportunities for targeted treatment, with ASOs showing promise in rare disease management and RNAi emerging as a platform for broader therapeutic applications.
Market Scope | |
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Start Year | 2024 |
Forecast Year | 2025-2034 |
Start Value | $9.6 Billion |
Forecast Value | $28.5 Billion |
CAGR | 11.6% |
Gene silencing market from the drug discovery and development segment captured 51% share in 2024 due to the growing use of RNAi and related technologies in research. Pharmaceutical and biotech companies are utilizing these tools to pinpoint disease-causing genes and streamline the early phases of drug development. The demand for gene-targeting platforms continues to grow as clinical trials for novel therapeutics expand across different therapeutic areas.
United States Gene Silencing Market is expected to reach USD 11.1 billion by 2034. The country's robust research infrastructure, backed by leading firms such as Thermo Fisher Scientific, Agilent Technologies, and Bio-Rad Laboratories, supports steady innovation in gene silencing treatments. Ongoing R&D investment and regulatory support also contribute to a favorable growth environment. The country remains a hub for clinical advancements and funding in genomic medicine.
Key players such as Merck KGaA, GenScript, Revvity Discovery, Santa Cruz Biotechnology, and New England Biolabs are strengthening their market presence through focused investments in RNAi and ASO platforms. These companies are expanding their portfolios with gene editing tools, custom oligo synthesis, and scalable delivery systems. Strategic partnerships with academic institutions and biotech startups help them stay ahead in clinical innovation. Firms invest in automation, AI-based gene target screening, and enhanced laboratory infrastructure to speed up research cycles. Continuous efforts to secure regulatory approvals and develop companion diagnostics are also central to competitiveness. By aligning product innovation with precision therapy trends, these companies capitalize on the growing need for targeted genetic treatments.