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市場調査レポート
商品コード
1703280
RNA療法の臨床試験市場- 世界の産業規模、シェア、動向、機会、予測、モダリティ別、フェーズ別、治療分野別、地域別、競合別、2020-2030年予測RNA Therapy Clinical Trials Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Modality, By Phase, By Therapeutic Areas, By Region and Competition, 2020-2030F |
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RNA療法の臨床試験市場- 世界の産業規模、シェア、動向、機会、予測、モダリティ別、フェーズ別、治療分野別、地域別、競合別、2020-2030年予測 |
出版日: 2025年04月11日
発行: TechSci Research
ページ情報: 英文 184 Pages
納期: 2~3営業日
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RNA療法の臨床試験の世界市場規模は2024年に28億7,000万米ドル、2030年には40億1,000万米ドルに達し、予測期間中のCAGRは5.73%で拡大すると予測されています。
市場概要 | |
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予測期間 | 2026-2030 |
市場規模:2024年 | 28億7,000万米ドル |
市場規模:2030年 | 40億1,000万米ドル |
CAGR:2025年~2030年 | 5.73% |
急成長セグメント | 希少疾患 |
最大市場 | 北米 |
RNA治療は、遺伝子発現を標的とすることで、さまざまな疾患を治療する画期的なアプローチを提供する、医学研究の最先端領域です。メッセンジャーRNA(mRNA)、small interfering RNA(siRNA)、アンチセンス・オリゴヌクレオチド(ASO)などのリボ核酸(RNA)分子を活用するRNAベース療法は、遺伝子活性を制御する精密主導型の手法を提供します。このアプローチは、遺伝性疾患、感染症、がん、そして現在有効な治療法がない希少疾患への対応に大きな期待が寄せられています。
従来の医薬品とは異なり、RNA療法は遺伝子レベルで作用するため、より的を絞った個別化治療が可能となります。世界の臨床試験の急増は、RNA科学の進歩と、ヘルスケアの展望を再定義したmRNAワクチンなどのRNAベースの製品開発の成功を反映しています。学術機関、製薬会社、研究機関の協力によって実施されるこれらの臨床試験は、規制当局の承認に先立ってこれらの革新的な治療法の安全性と有効性を評価する上で極めて重要です。
RNA技術革新の加速
送達メカニズムの複雑さ
個別化医療と精密医療の進展
Global RNA Therapy Clinical Trials Market was valued at USD 2.87 billion in 2024 and is projected to reach USD 4.01 billion by 2030, expanding at a CAGR of 5.73% during the forecast period.
Market Overview | |
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Forecast Period | 2026-2030 |
Market Size 2024 | USD 2.87 Billion |
Market Size 2030 | USD 4.01 Billion |
CAGR 2025-2030 | 5.73% |
Fastest Growing Segment | Rare Diseases |
Largest Market | North America |
RNA therapy represents a cutting-edge domain in medical research, offering a transformative approach to treating a wide range of diseases by targeting gene expression. Leveraging ribonucleic acid (RNA) molecules such as messenger RNA (mRNA), small interfering RNA (siRNA), and antisense oligonucleotides (ASOs), RNA-based therapies provide a precision-driven method to regulate gene activity. This approach holds significant promise in addressing genetic disorders, infectious diseases, cancer, and rare conditions that currently lack effective treatment options.
Unlike conventional pharmaceuticals, RNA therapies operate at the genetic level, enabling more targeted and personalized treatment solutions. The surge in clinical trials globally reflects both advancements in RNA science and the successful development of RNA-based products, such as mRNA vaccines, which have redefined the healthcare landscape. These clinical trials, conducted through collaborations between academic institutions, pharmaceutical companies, and research organizations, are pivotal in evaluating the safety and efficacy of these innovative therapies prior to regulatory approval.
Key Market Drivers
Accelerated Innovation in RNA Technology
The market's growth is largely fueled by rapid technological advancements in RNA science, reshaping the future of medicine and therapeutic development. A critical area of progress is the refinement of RNA synthesis techniques, which now enable the creation of highly specific and efficient RNA molecules customized to target particular genes or disease pathways.
For instance, in May 2022, Moderna and the nonprofit research organization IAVI announced the initiation of Phase I clinical trials for an experimental mRNA-based HIV vaccine (mRNA-1644), with initial screenings in Rwanda and South Africa.
Further innovations in RNA modification have enhanced molecular stability, reducing degradation and improving biodistribution, which extends the therapeutic effect and reduces dosing frequency-key factors in improving patient compliance. Delivery technologies have also evolved significantly, with lipid nanoparticles and polymer-based carriers protecting RNA during systemic circulation and facilitating precise cellular uptake.
Additionally, combination RNA therapies-which integrate multiple RNA modalities or pair RNA treatments with other therapeutic strategies-are under exploration, offering synergistic potential for more comprehensive disease management.
Key Market Challenges
Complexities in Delivery Mechanisms
A major challenge within the RNA therapy clinical trials market is the effective delivery of RNA molecules to specific cells or tissues. Due to their inherent fragility, RNA molecules are susceptible to enzymatic degradation and immune system activation, limiting their therapeutic utility if not adequately protected and directed.
Moreover, RNA molecules typically exhibit short biological half-lives, requiring repeated administrations to maintain therapeutic levels. Efficient delivery systems are essential to ensure therapeutic RNA reaches the intended cellular targets while minimizing systemic exposure and off-target effects.
To overcome these barriers, researchers have developed advanced delivery platforms-most notably lipid nanoparticle formulations-that encapsulate RNA, shielding it from degradation and enhancing cellular uptake. These systems can be engineered for targeted delivery, ensuring better therapeutic outcomes and minimizing toxicity.
However, challenges remain, particularly in achieving consistent delivery across varied patient profiles and disease states, making delivery optimization a key area of ongoing research and development.
Key Market Trends
Advancing Personalized and Precision Medicine
The shift toward personalized and precision medicine is a transformative trend shaping the RNA therapy clinical trials landscape. This approach leverages individual genetic and molecular profiles to tailor therapeutic interventions, significantly improving treatment outcomes and minimizing adverse effects.
In RNA therapy, personalized medicine involves designing RNA-based therapies that target patient-specific mutations or gene expressions. This enables highly focused treatment strategies, especially for rare or complex conditions.
Precision medicine goes a step further by using genetic profiling and advanced diagnostics to predict how patients will respond to specific RNA therapies. This data-driven approach enhances treatment efficacy, optimizes resource allocation in clinical trials, and supports the development of more targeted RNA-based drug candidates.
IQVIA Inc.
ICON Plc
Laboratory Corporation of America Holdings
Charles River Laboratories International, Inc.
PAREXEL International Corp.
Syneos Health
Medpace Holdings, Inc.
Novotech Inc.
PPD Inc.
Veristat, LLC.
In this report, the Global RNA Therapy Clinical Trials Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:
RNA interference
Antisense therapy Messenger RNA
Oligonucleotide
Non-antisense
Non-RNAi
Phase I
Phase II
Phase III
Phase IV
Rare Diseases
Anti-infective
Anticancer
Neurological
Alimentary/Metabolic
Musculoskeletal
Cardiovascular Respiratory
Sensory
Others
North America
Europe
Asia-Pacific
South America
Middle East & Africa
Company Profiles: Detailed analysis of the major companies present in the Global RNA Therapy Clinical Trials Market.
Global RNA Therapy Clinical Trials Market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report:
Detailed analysis and profiling of additional market players (up to five).