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市場調査レポート
商品コード
1090214
RNA治療薬の世界市場:成長機会Global RNA Therapeutics Growth Opportunities |
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RNA治療薬の世界市場:成長機会 |
出版日: 2022年05月31日
発行: Frost & Sullivan
ページ情報: 英文 51 Pages
納期: 即日から翌営業日
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核酸系治療法における科学の進歩は、世界のバイオ医薬品業界に大きな影響を与えています。RNA(リボ核酸)治療薬市場は、「治療不可能」な経路を標的とすることから、著しい臨床的な進歩を遂げることが期待されています。技術的な優位性と、競争力を高めるためにRNA治療薬の臨床的に優れたポートフォリオを構築する必要性の高まりは、RNA治療薬業界のステークホルダー間の戦略的パートナーシップを促進すると予想されます。
当レポートでは、世界のRNA治療薬市場について調査分析し、戦略的必須要因、促進要因、抑制要因、主要動向、収益予測、競合環境、成長機会等に関する情報を提供しています。
Future Growth Potential Driven by Co-Development Programs and Robust Clinical Trials for Diverse Disease Areas
Scientific advancements in nucleic acid-based therapies have significantly impacted the global biopharmaceutical industry. The ribonucleic acid (RNA) therapeutics market is expected to witness remarkable clinical progress as therapies target "undruggable" pathways. Technologically advanced platforms are integrated into RNA therapeutics bioprocessing to overcome stability issues. Technological advantages, coupled with the growing need to build clinically superior portfolios in RNA therapeutics for a competitive edge, are anticipated to drive strategic partnerships among stakeholders in the RNA therapeutics industry.
Spurred by the COVID-19 pandemic, biopharmaceutical companies are likely to prioritize microRNA, small interfering RNA, and antisense oligonucleotides as promising therapeutic modalities during the forecast period. Midsize and large companies have ramped up the production of starting materials and the final formulation of RNA therapeutics, which is likely to propel stakeholders to seek synergistic partnerships. In the industry's transition to personalized therapeutics, RNA developers are capitalizing on the high precision of RNA to treat untapped chronic disease areas such as cystic fibrosis, solid tumors, and spinal muscular atrophy. They engage in co-development programs to improve the stability profile of RNA therapeutics by optimizing drug delivery carriers, such as lipid nanoparticles.
Scaling up the production of starting materials, including plasmid DNA, oligonucleotides, and delivery materials, to ensure continuous manufacturing is anticipated to reduce the operational timeframe of RNA therapeutics production. Technology transfer and the outsourcing of crucial operations to contract development and manufacturing organizations (CDMO) catalyze the development of cost-effective and efficient models for RNA therapeutics.
This Frost & Sullivan research service provides an overview of the global RNA therapeutics industry from 2021 to 2027, including emerging trends, growth drivers, and growth opportunities.
The research service highlights the following: