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市場調査レポート
商品コード
1753970
医薬品連続製造市場レポート:治療タイプ別、製剤別、用途別、エンドユーザー別、地域別、2025年~2033年Pharmaceutical Continuous Manufacturing Market Report by Therapeutics Type, Formulation, Application, End User, and Region 2025-2033 |
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医薬品連続製造市場レポート:治療タイプ別、製剤別、用途別、エンドユーザー別、地域別、2025年~2033年 |
出版日: 2025年06月02日
発行: IMARC
ページ情報: 英文 150 Pages
納期: 2~3営業日
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世界の医薬品連続製造市場規模は2024年に15億米ドルに達しました。今後、IMARC Groupは、市場は2033年までに33億米ドルに達し、2025年から2033年にかけて9.62%の成長率(CAGR)を示すと予測しています。健康への関心の高まりと研究開発活動の活発化が市場の成長を後押ししています。
ドラッグデリバリーシステムの革新
先端材料、プロセス分析技術(PAT)、標的ナノメディシンのようなドラッグデリバリーシステムにおける現代の進歩は、標的への送達、安定性、リアルタイムモニタリング、溶解性を改善した薬剤の連続生産ラインを可能にします。これらの要因が相まって、市場は加速しています。例えば、国立医学図書館が2024年5月に発表した論文では、リポソームや脂質ナノ粒子(LNP)などの技術や、スマート、キャリアベース、3Dプリントによるドラッグデリバリー法の開発に注力することで、バイオアベイラビリティが向上し、従来の限界に対処し、研究が進むと述べられています。
製造工程における規制支援
規制機関は、製品の一貫性や効率性の向上など、連続製造の利点を認めるようになってきています。これらの機関は、連続製造技術を導入するための明確な基準と規制上の道筋を示す包括的なガイドラインとプログラムを確立しました。例えば、米国食品医薬品局(FDA)は2024年5月、希少疾患治療薬の開発を促進するためのSTARTパイロットプログラムを開始しました。これは臨床試験支援と規制ガイダンスに重点を置いたもので、新製品開発の加速と生産要件の最適化によって連続製造に利益をもたらし、医薬品連続製造市場統計を増加させています。
慢性疾患の発生率の増加
心血管疾患、糖尿病、慢性呼吸器疾患などの慢性疾患が蔓延するにつれ、信頼性の高い長期的な治療に対する需要が高まっています。連続製造プロセスは、効率性と一貫した品質で高品質の医薬品を大規模に製造できるため、この需要に対応できます。これに伴い、医薬品連続製造の価格動向の採用により、製造コストと無駄が削減され、治療がより手頃な価格で受けられるようになります。例えば、2024年2月にPublic Health Researchが発表した調査によると、米国では約1億2,900万人が少なくとも1つの主要な慢性疾患を抱えています。
The global pharmaceutical continuous manufacturing market size reached USD 1.5 Billion in 2024. Looking forward, IMARC Group expects the market to reach USD 3.3 Billion by 2033, exhibiting a growth rate (CAGR) of 9.62% during 2025-2033. The rising health concerns and the increasing research and development activities are propelling the market growth.
Innovation in Drug Delivery System
Modern advances in drug delivery systems, like advanced materials, process analytical technology (PAT), and targeted nanomedicine, enable continuous production lines to produce drugs with improved targeted delivery, stability, real-time monitoring, and solubility. Collectively, these factors accelerate the market. For instance, an article published by the National Library of Medicine in May 2024 mentioned that focusing on technologies, such as liposomes and lipid nanoparticles (LNPs) and development in smart, carrier-based, and 3D-printed drug delivery methods improve bioavailability, address conventional limitations, and advance research.
Regulatory Support in Manufacturing Process
Regulatory bodies have increasingly acknowledged the benefits of continuous manufacturing, like product consistency and enhanced efficiency. These agencies established comprehensive guidelines and programs that provide clear standards and regulatory pathways for implementing continuous manufacturing technologies. For instance, in May 2024, the U.S. Food and Drug Administration (FDA) launched the START pilot program to accelerate the development of rare disease therapeutics. It focuses on clinical trial support and regulatory guidance, which benefits continuous manufacturing by accelerating novel product development and optimizing production requirements, which is increasing the pharmaceutical continuous manufacturing market statistics.
Increasing Incidence of Chronic Disease
As chronic conditions such as cardiovascular diseases, diabetes, and chronic respiratory diseases become more prevalent, there is an increased demand for reliable and long-term treatments. Continuous manufacturing processes meet this demand due to their ability to produce quality pharmaceuticals at scale with efficiency and consistent quality. In line with this, the adoption of pharmaceutical continuous manufacturing price trends reduces production costs and waste, thereby making treatments more affordable and accessible. For example, research published by Public Health Research in February 2024 showed that approximately 129 million people in the United States have at least one major chronic disease.
Small molecules dominate the pharmaceutical continuous manufacturing market
Continuous manufacturing enhances efficiency and consistency in small-molecule drugs. Vertex Pharmaceuticals introduced Suzetrigine, a small molecule drug manufactured using continuous processes, optimizing production efficiency and ensuring consistent quality for pain management.
Solid formulation currently holds most of the pharmaceutical continuous manufacturing market demand
Solid formulations, such as capsules and tablets, excel in continuous manufacturing due to improved consistency and efficiency. For example, XenoPharma's tablet production ensures uniform quality and scalable output, which is acting as another significant growth-inducing factor.
Final drug product manufacturing dominates the market
Final drug product manufacturing in continuous processes ensures efficient production with consistent quality and scalability, thereby reducing waste and enhancing overall process control. It also results in cost savings. This is bolstering the pharmaceutical continuous manufacturing market revenue.
Pharmaceutical companies hold most of the pharmaceutical continuous manufacturing market outlook
Pharmaceutical companies increasingly adopt continuous manufacturing to enhance efficiency, streamline production processes, and ensure consistent product quality. This is leading to faster and more cost-effective drug development.
North America exhibits a clear dominance, accounting for the largest pharmaceutical continuous manufacturing market share
The market research report has also provided a comprehensive analysis of all the major regional markets, which include North America (the United States and Canada); Asia Pacific (China, Japan, India, South Korea, Australia, Indonesia, and others); Europe (Germany, France, the United Kingdom, Italy, Spain, Russia, and others); Latin America (Brazil, Mexico, and others); and the Middle East and Africa. According to the report, North America accounted for the largest market share.
As per the pharmaceutical continuous manufacturing market research report, North America accounted for the largest share, driven by advanced drug delivery technologies. Moreover, regulatory bodies in the region are highly supportive of continuous manufacturing practices. The corporation with regulatory bodies encourages pharmaceutical companies to adopt continuous manufacturing solutions, thereby propelling the market growth. For instance, in May 2024, the U.S. Food and Drug Administration (FDA) introduced the START pilot program to catalyze the development of rare disease therapeutics.
The market research report has provided a comprehensive analysis of the competitive landscape. Detailed profiles of all major market pharmaceutical continuous manufacturing companies have also been provided. Some of the key players in the market include: