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市場調査レポート
商品コード
1422775
RNA治療薬の世界市場:タイプ別、製品別、適応症別、エンドユーザー別、地域別、機会、予測、2017年~2031年RNA Therapeutics Market Assessment, By Type, By Product, By Indication, By End-user, By Region, Opportunities and Forecast, 2017-2031F |
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カスタマイズ可能
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RNA治療薬の世界市場:タイプ別、製品別、適応症別、エンドユーザー別、地域別、機会、予測、2017年~2031年 |
出版日: 2024年02月12日
発行: Market Xcel - Markets and Data
ページ情報: 英文 227 Pages
納期: 3~5営業日
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世界のRNA治療薬の市場規模は、2023年に101億米ドルと評価され、2031年には273億3,000万米ドルに達すると予測されており、2024年から2031年までの予測期間のCAGRは13.25%になるとみられています。世界のRNA治療薬市場に影響を与える要因としては、RNA技術の進歩、研究資金の増強、慢性疾患の罹患率の上昇、個別化医療の需要、以前は不治の病であった病態の治療におけるRNAベースの薬剤の有効性、規制当局の支援や製薬企業間の提携の大きな影響などが挙げられ、これらすべてが市場拡大に寄与しています。
複数の極めて重要な要因が世界のRNA治療薬市場に大きな影響を与えており、それぞれが市場の拡大と進展に重要な役割を果たしています。主に、RNA技術の継続的な進歩が市場成長の礎となっています。メッセンジャーRNA(mRNA)、低分子干渉RNA(siRNA)、アンチセンスオリゴヌクレオチド、および関連技術における絶え間ない技術革新は、治療アプローチの精度と有効性を一貫して強化しています。これらの進歩は、薬物の安定性、標的の正確さ、最適化されたデリバリー方法に関する歴史的課題に対処するものです。研究資金の増強は、もう一つの促進要因です。資金援助の急増は、RNAを中心とした先進的な研究を推進し、ブレークスルーを早め、発見を世界のRNA治療薬市場における実行可能な臨床応用に結びつける。資金援助の増加は、より深い探求を可能にし、イノベーションを促進し、RNA発見の実用的な治療への転換を促進します。
さらに、慢性疾患の増加により、効果的な治療法の必要性が高まっており、RNAベースの介入の適応性とシームレスに連携することで、世界のRNA治療薬市場を大きく牽引しています。RNA治療薬は、これまで克服できなかった病態に対処する有望な可能性を提供し、従来の薬物療法では不十分なシナリオに希望を与えます。個別化医療に対する需要が急増していることも、市場の拡大をさらに後押ししています。RNAベースの医薬品は、個々の遺伝子プロファイルを活用することで、患者の個別のニーズをより正確に満たすカスタマイズされた治療法を構築し、オーダーメイドのソリューションを提供します。さらに、規制当局の後押しや製薬企業間の提携の影響力は依然として極めて大きいです。有利な規制環境と戦略的パートナーシップは、研究開発・商業化を促進する環境を作り出し、最終的に世界のRNA治療薬市場の成長を後押しします。
当レポートでは、世界のRNA治療薬市場について調査し、市場の概要とともに、タイプ別、製品別、適応症別、エンドユーザー別、地域別動向、および市場に参入する企業のプロファイルなどを提供しています。
Global RNA therapeutics market size was valued at USD 10.1 billion in 2023, which is expected to reach USD 27.33 billion in 2031, with a CAGR of 13.25% for the forecast period between 2024 and 2031F. Factors impacting the global RNA therapeutics market include progress in RNA technology, augmented research funding, heightened incidence of chronic diseases, demand for personalized medicine, effectiveness of RNA-based drugs in treating previously incurable conditions, and the substantial influence of regulatory support and collaborations among pharmaceutical firms, all contributing to market expansion.
Multiple pivotal factors significantly impact global RNA therapeutics market, each wielding a crucial role in its expansion and progression. Primarily, ongoing advancements in RNA technology serve as the cornerstone for market growth. Continuous innovations in messenger RNA (mRNA), small interfering RNA (siRNA), antisense oligonucleotides, and related techniques consistently bolster the precision and effectiveness of therapeutic approaches. These strides address historical challenges concerning drug stability, target accuracy, and optimized delivery methods. Augmented research funding represents another fundamental catalyst. The surge in financial support drives progressive RNA-centered studies, hastening breakthroughs and translating discoveries into viable clinical applications in the global RNA therapeutics market. The increased funding allows for deeper exploration, fostering innovation and expediting the conversion of RNA discoveries into practical therapies.
Additionally, the escalation in chronic diseases intensifies the need for effective treatments, aligning seamlessly with the adaptability of RNA-based interventions significantly driving the global RNA therapeutics market. RNA therapeutics offer promising potential in addressing previously insurmountable conditions, providing hope in scenarios where traditional medications fall short. The burgeoning demand for personalized medicine further fuels market expansion. RNA-based drugs present tailored solutions, leveraging individual genetic profiles to craft customized treatments that more precisely meet patients' distinct needs. Moreover, the significant influence of regulatory backing and collaborations among pharmaceutical firms remains pivotal. Favorable regulatory environments, coupled with strategic partnerships, create an environment conducive to research, development, and commercialization, ultimately propelling the growth of global RNA therapeutics market.
Progress in RNA Technology
Advancements in RNA technology are the primary catalyst driving the global RNA therapeutics market. These technological strides, encompass messenger RNA (mRNA), small interfering RNA (siRNA), antisense oligonucleotides, and other RNA-based methods, fueling the creation of inventive therapeutic remedies. They improve drug stability, target precision, and delivery systems, effectively tackling persistent challenges in precision medicine. Moreover, refined manufacturing processes and increased scalability fortify the practicality of RNA-based therapies, rendering them more attainable for large-scale manufacturing and commercial viability. The precision in gene expression manipulation via RNA interventions unlocks new avenues for addressing previously untreatable diseases, instilling hope in conditions lacking viable treatment options. The continuous evolution of RNA technology amplifies therapeutic potential and garners substantial investments, collaborations, and research endeavors, driving forward the growth and expansion of global RNA therapeutics market.
Augmented Research Funding
Increased funding for research plays a crucial role in propelling the global RNA therapeutics market. This boost in financial support infuses vital resources into pioneering RNA-centered studies, hastening breakthroughs and pushing discoveries toward practical clinical applications. It cultivates an environment ideal for experimenting, exploring, and validating various RNA-based therapeutic methods. Moreover, heightened funding draws in top-tier talent, sparks collaborative initiatives, and streamlines the transition of promising RNA technologies from lab settings to clinical trials. Consequently, this amplifies market growth potential and fosters the prospect of groundbreaking medical interventions.
For example, Flanders Innovation & Entrepreneurship (VLAIO) granted Flamingo Therapeutics a research grant of USD 1.9 million (EUR 1.7 million) in June 2023. The grant amounts to 60% of the project's total budget of USD 3.2 million (EUR 2.9 million). The award money will go towards expanding Flamingo Therapeutics' RNA-targeting oncology portfolio. It includes preclinical work on the company's long non-coding RNA (LncRNA) program targeting MALAT-1 and translational research for its lead clinical program, Danvatirsen, which is now in phase II trials for head and neck squamous cell carcinoma.
Government Initiatives
Governments worldwide are leading various initiatives that substantially elevate the global RNA therapeutics market. These initiatives encompass a range of strategies, including allocating research grants, establishing supportive regulatory frameworks, and fostering collaborations between public and private entities. Additionally, incentives like financial rewards, tax credits, and streamlined approval procedures reinforce progress in RNA-based advancements. Moreover, public health programs focusing on precision medicine and addressing previously untreatable conditions align with RNA therapeutics, stimulating increased government funding. The concerted effort fosters an environment conducive to research, development, and commercialization, significantly propelling notable growth in global RNA therapeutics market. For example, the Canada First Research Excellence Fund (CFREF) at Concordia University in Montreal would receive USD 1.4 billion in funding for 11 large-scale research activities, according to an announcement made a Minister of Innovation, Science, and Industry, in April 2023. The best programmes in their fields are given CFREF funding following a highly competitive process. To begin DNA to RNA, an Inclusive Canadian Approach to Genomic-based RNA treatments (D2R), a first-of-its-kind international research project focused on the creation and delivery of more inclusive genomic-based RNA treatments, McGill has been awarded a historic USD 165 million CFREF grant.
Treatment of Rare Genetic Disorders
RNA therapeutics significantly drive the expansion of global RNA therapeutics market by being instrumental in treating rare genetic disorders. These conditions, often resistant to conventional treatments, discover promise in RNA-based interventions capable of pinpointing precise genetic irregularities. As RNA therapies prove their efficacy in managing these once untreatable disorders, enthusiasm and investment escalate, fueling market growth. This specific application highlights RNA therapeutics' potential in meeting unaddressed medical demands, propelling both research initiatives and market progress. For instance, in October 2023, Novo Nordisk (NOVOb.CO) announced on Monday that FDA in the United States has approved its treatment for a rare kidney-affecting genetic disorder. It is approved for use in patients of nine years of age and older with a form of primary hyperoxaluria and generally intact kidney function to administer the once-monthly injection, which will be marketed under the brand name Rivfloza. RNA interference technology, or RNAi, is used in the therapy to assist lower urinary oxalate levels by silencing or neutralizing genes that contribute to illness.
Extensive use of RNAi Therapeutics
The global RNA therapeutics market experiences significant demand, particularly in RNA interference (RNAi) therapies. The interest arises from RNAi's distinct ability to target specific genes, impeding disease progression. RNAi's precision in controlling gene expression renders it an appealing option for treating diverse conditions like cancers, genetic disorders, and viral infections. As ongoing research continues to affirm RNAi's therapeutic potential and its effectiveness in both preclinical and clinical settings as the demand intensifies. The growing enthusiasm originates from RNAi's potential to address unmet medical needs, fostering a robust market propelled by the quest for innovative and precise therapeutic resolutions. For example, the industry-leading RNAi therapeutics company Alnylam Pharmaceuticals, Inc. announced in July 2023 that it has entered into a strategic agreement with Roche to develop and commercialize zilebesiran, the company's investigational RNAi therapeutic currently in Phase 2 development, for the treatment of hypertension. Through the agreement, Alnylam's P5x25 approach can move closer to its ambitious development ambition of upending the global paradigm of hypertension therapy.
Future Market Scenario
The forthcoming prospects of global RNA therapeutics market project significant expansion. The upsurge is driven by key elements such as ongoing progress in RNA technology. The fast-growing class of medications known as "RNA therapeutics" will enable personalized therapy, expedite the time it takes for solutions to reach the clinic, and end using the term "undruggable." Many more RNA medications are being developed, and the first ones have been approved. Other elements such as augmented investment in research and development, the escalating prevalence of chronic ailments, broader utilization of personalized medicine, and the potential of RNA-based remedies for formerly untreatable conditions will play a major role. Moreover, partnerships between pharmaceutical firms and favorable regulatory structures add impetus to this expected growth. The market's expansion pivots on the growing need for inventive therapeutic options, signaling a promising and resilient future for RNA-based interventions in tackling unmet medical challenges.
Key Players Landscape and Outlook
Major biotech companies worldwide are joining forces to establish an impactful alliance in the global RNA therapeutics market. The joint venture serves a dual purpose: advancing innovation and assuming regulatory roles. Together, these firms aim to combine their knowledge, resources, and research efforts to propel the development of innovative RNA-based therapies. Concurrently, their objective involves setting industry standards and guidelines to maintain quality and endorse the safety and effectiveness of RNA therapeutic solutions. The collaborative alliance signifies a crucial stride towards a cohesive strategy, driving progress and ensuring adherence to standards in the rapidly evolving domain of RNA therapeutics.
For instance, the Alliance for mRNA Medicines (AMM) was established in November 2023 by 31 biotechnology, biopharma, and life science businesses as well as academic institutions at the vanguard of mRNA and next generation encoding RNA medicines and vaccine development. Before legislative and regulatory agencies in North America, Europe, and Asia, AMM was the first and only scientific and policy organization exclusively dedicated to developing and advocating for global mRNA innovation and the sector's main policy objectives.
All segments will be provided for all regions and countries covered
Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work