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市場調查報告書
商品編碼
1671195
基因治療的全球市場:市場規模·佔有率·趨勢,產業分析 (各治療領域·媒介類別·方法·各給藥途徑·各地區),未來預測 (2025年~2034年)Gene Therapy Market Size, Share, Trends, Industry Analysis Report: By Therapeutic Area, Vector Type, Approach, Route of Administration, and Region - Market Forecast 2025-2034 |
根據 Polaris Market Research 的最新研究,基因治療市場預計到 2034 年將達到 272.502 億美元。該報告對當前的市場動態提供了詳細的見解,並對未來的市場成長進行了分析。
基因治療涉及糾正或替換患者細胞中的不健康基因以治療或預防疾病。基因工程的快速發展以及對分子生物學認知的不斷加深,推動了基因治療從實驗階段走向實際臨床應用。研究人員和生物製藥公司正在大力投資開發安全有效的治療方法,而監管機構正在簡化審批流程,以加速基因治療市場的擴張。
由於杜氏肌肉營養不良症 (DMD)、鐮狀細胞病、血友病和囊性纖維化等遺傳疾病的盛行率不斷上升,對基因治療的需求正在迅速增加。與專注於症狀管理的傳統治療不同,基因療法從基因層面針對這些疾病的根本原因。這種有針對性的方法提高了治療效果,並有可能帶來長期甚至永久的緩解。近年來,CRISPR-Cas9 和鋅指核酸酶 (ZFN) 等基因編輯技術的顯著進步使得基因修飾更加精確和高效。
越來越多的基因療法監管部門批准正在推動基因治療市場的成長。美國食品藥物管理局 (FDA) 和歐洲藥品管理局 (EMA) 等政府機構已經認識到這些治療方法的變革潛力。這些機構加快了有前途的候選人的審批流程。 Zolgensma 治療脊髓性肌肉萎縮症 (SMA) 和 Luxturna 治療遺傳性視網膜疾病等療法取得了顯著的臨床成功,為更廣泛地應用基因為基礎的療法和程序鋪平了道路。
基於治療領域,腫瘤疾病領域將在 2024 年引領基因治療市場佔有率,因為腫瘤疾病的流行及其治療對身體和心理產生重大影響。
根據載體類型,病毒部分在基因治療市場收入佔有率中處於領先地位,因為它可以有效且有效率地將基因傳遞到針對各種癌症、單基因疾病和傳染病的目標細胞中。
北美憑藉其強大的研究基礎設施、先進的醫療保健系統、大量的臨床試驗資金以及由 FDA 領導的支持性監管框架引領基因治療市場,從而實現新型基因療法的快速開發和批准。
全球主要公司包括abeona·serapyutikku,諾華AG,火花·serapyutikusuLLC,giriado·saienshizu,布里斯托爾·maiyazu·Squibb,adobaumu·baiotekunorojizu,arunairamu·famashutikaruzu,美國的·gene·tekunorojizu,apuraido·jenetikku·tekunorojizu·團體,baiojen,urutorajenikkusu等舉出(舉行)。
The gene therapy market size is expected to reach USD 27,250.20 million by 2034, according to a new study by Polaris Market Research. The report "Gene Therapy Market Size, Share, Trends, Industry Analysis Report: By Therapeutic Area (Autoimmune Disorders, Cardiovascular Diseases, Dermatological Disorders, Hematological Disorders, Metabolic Disorders, Muscle-Related Diseases, Oncological Disorders, and Others), Vector Type, Approach, Route of Administration, and Region (North America, Europe, Asia Pacific, Latin America, and Middle East & Africa) - Market Forecast, 2025-2034" gives a detailed insight into current market dynamics and provides analysis on future market growth.
Gene therapy involves modifying or replacing unhealthy genes within a patient's cells to treat or prevent disease. Rapid advancements in genetic engineering, along with an increasing understanding of molecular biology, have propelled gene therapy from experimental stages to real-world clinical applications. Researchers and biopharmaceutical companies are investing heavily in developing safe and effective therapies, while regulatory bodies are streamlining approval processes to accelerate gene therapy market expansion.
The demand for gene therapy has surged due to the increasing prevalence of genetic disorders such as Duchenne muscular dystrophy (DMD), sickle cell disease, hemophilia, and cystic fibrosis. Unlike traditional treatment methods that primarily focus on symptom management, gene therapy targets the underlying cause of these diseases at the genetic level. This targeted approach enhances treatment efficacy and offers the potential for long-term or even permanent relief. In recent years, significant breakthroughs in gene-editing technologies, such as CRISPR-Cas9 and zinc finger nucleases (ZFNs), have enabled more precise and efficient gene modifications.
The rising number of regulatory approvals for gene-based treatments is propelling the gene therapy market growth. Government agencies such as the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have recognized the transformative potential of these therapies. They are expediting the approval process for promising candidates. Therapies such as Zolgensma for spinal muscular atrophy (SMA) and Luxturna for inherited retinal disease have demonstrated remarkable clinical success, paving the way for broader adoption of gene-based therapies or treatments.
Based on therapeutic area, the oncological disorders segment leads the gene therapy market share in 2024 due to the prevalence of significant physical and psychological impacts of the disease and its treatment.
By vector type, the viral segment leads gene therapy market revenue share due to its effective and efficient delivering genes to the targeted cells for various cancers, monogenic and infectious diseases.
North America leads the gene therapy market due to its robust research infrastructure, advanced healthcare system, significant funding for clinical trials, and a supportive regulatory framework, particularly from the FDA, which allows for rapid development and approval of new gene therapies.
A few global key market players are Abeona Therapeutic, Novartis AG, Spark Therapeutics LLC, Gilead Sciences Inc., Bristol Myers Squibb, Adverum Biotechnologies, Alnylam Pharmaceuticals, American Gene Technologies, Applied Genetic Technologies Corporation, Biogen, and Ultragenyx.
Polaris Market Research has segmented the gene therapy market report on the basis of therapeutic area, vector type, approach, route of administration, and region: