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市場調査レポート
商品コード
1663324
細胞・遺伝子治療製造 - 市場考察、競合情勢、市場予測(2032年)Cell and Gene Therapy Manufacturing - Market Insights, Competitive Landscape, and Market Forecast - 2032 |
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細胞・遺伝子治療製造 - 市場考察、競合情勢、市場予測(2032年) |
出版日: 2025年02月01日
発行: DelveInsight
ページ情報: 英文 150 Pages
納期: 2~10営業日
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世界の細胞・遺伝子治療製造の市場規模は、2024年に47億4,918万米ドルであり、2032年までに98億490万米ドルに達すると予測され、2025年~2032年の予測期間にCAGRで9.50%の成長が見込まれます。
細胞・遺伝子治療製造の市場力学
がんや希少遺伝性疾患などの遺伝性疾患や慢性疾患の有病率の増加が、先進の治療法の需要を促進しており、そのため強固な製造能力が必要とされています。細胞・遺伝子治療のパイプラインは急速に拡大しており、数多くの治療法が臨床試験を経ていることから、スケーラブルで効率的な製造ソリューションの必要性が強く示されています。パートナーシップ、最先端の製造施設への投資、自動化の進行など、産業の主要企業による戦略的活動は、生産能力と効率を高めています。これらの要因を総合すると、2025年~2032年の予測期間に世界の細胞・遺伝子治療製造市場の成長は大きく促進されると予測されます。
International Agency for Research on Cancer(2024)のデータによると、2022年の世界の新規がん患者数は2,000万人と推定され、2045年までに3,260万人に増加すると予測されています。CAR-T細胞治療などの遺伝子治療は、特定のがん種を標的とすることで有望な結果を示しており、それにより、生産規模を拡大するための強固な製造プロセスに対する需要が高まっています。同様に、幹細胞ベースの治療を含む細胞治療も、がんだけでなく、侵襲性の強いがんの治療の副作用にも対処するために開発されています。結果として、がん罹患率の上昇が細胞・遺伝子治療製造市場を大きく押し上げています。
さらに、Haemophilia Foundation Australia(2024)によると、オーストラリアでは2,500人超が遺伝性出血性疾患であるフォンヴィレブランド病(VWD)と診断されていますが、多くの症例は診断されていないと考えられています。VWDに対する細胞・遺伝子治療のアプローチでは、欠陥のあるVWF遺伝子の機能的コピーを投与し、根本的な遺伝的欠陥を修正します。この戦略では、ウイルスベクターやその他のコンポーネントを適正製造規範(GMP)に準拠した施設で専門的に製造する必要があるため、先進の製造プロセスやインフラに対する需要が高まっています。世界のVWDの有病率の上昇と従来の治療法の限界は、この障害を特異的に標的とする細胞治療や遺伝子治療の開発における研究と投資の増加に拍車をかけ、市場全体を押し上げています。
さらに、主要市場企業間の戦略的活動が、細胞・遺伝子治療製造の見通しを大きく強化しています。例えば2023年10月、Creative Medical Technology Holdings, Inc.は、慢性腰痛に対するAlloStem(TM)(CELZ-201-DDT)細胞治療を用いたStemSpine(R)手技の臨床試験について、IRB(Institutional Review Board)の承認を取得しました。この承認により、同社は椎間板変性症患者30名を対象に安全性、有効性、忍容性を評価するFDA承認のフェーズ1/2試験の募集を進めることができます。このような発展は、細胞・遺伝子治療が臨床試験を通じて急速に進捗していることを裏付けるものであり、スケーラブルで効率的な製造ソリューションが必要とされています。
しかし、市場は複雑な製造プロセスや規制上のハードルなどの課題に直面しています。細胞・遺伝子治療の生産には、細胞の抽出、改変、拡大、デリバリーといった複雑な工程が含まれます。品質を維持しながらスケーラビリティと再現性を確保することは重要な問題です。患者がこれらの治療から利益を得られるようにするためには、規制上の障害を克服しなければなりません。さらに、材料と人材へのアクセスの欠如や、実証されていない技術と未成熟なプロセスが、生産規模を拡大する上での課題となっています。これらの問題に対処することは、細胞・遺伝子治療製造市場の継続的な成長にとって極めて重要です。
まとめると、細胞・遺伝子治療製造市場は、慢性疾患や遺伝性疾患の有病率の上昇によって大きく成長する見通しですが、その可能性を十分に発揮するためには、複雑な製造および規制上の課題を乗り越えなければなりません。
当レポートでは、世界の細胞・遺伝子治療製造市場について調査分析し、市場規模と予測、過去3年の製品/技術開発、市場の主要企業、利用可能な機会などの情報を提供しています。
Cell and Gene Therapy Manufacturing Market by Therapy Type (Cell Therapy [Allogenic and Autologous] and Gene Therapy [Viral Vector-Based Gene Therapy and Non-Viral Vector-Based Gene Therapy]), Manufacturing Type (In-house Manufacturing, Contract Manufacturing), Scale of Manufacturing (Clinical-Scale Manufacturing and Commercial-Scale Manufacturing), Application (Neurological, Oncological, Hematological, Ophthalmological and Others), and Geography (North America, Europe, Asia-Pacific, and Rest of the World) is expected to grow at a steady CAGR forecast till 2032 owing to the rising prevalence of genetic disorders and chronic diseases, rapid expansion of the cell and gene therapy pipeline, and increasing strategic activities among the key players across the globe.
The Cell and Gene Therapy Manufacturing market was valued at USD 4,749.18 million in 2024, growing at a CAGR of 9.50% during the forecast period from 2025 to 2032 to reach USD 9,804.90 million by 2032. The rising prevalence of genetic disorders and chronic diseases such as cancer and rare inherited conditions is driving the demand for advanced therapies, thereby increasing the need for robust manufacturing capabilities. Concurrently, the rapid expansion of the cell and gene therapy pipeline, with numerous therapies advancing through clinical trials, is accelerating the demand for scalable and efficient production solutions.
Additionally, strategic initiatives by key market players including partnerships, investments in cutting-edge manufacturing facilities, and advancements in automation technologies are significantly enhancing production capacity and operational efficiency.
Collectively, these factors are expected to substantially propel the growth of the cell and gene therapy manufacturing market globally during the forecast period from 2025 to 2032.
Cell and Gene Therapy Manufacturing Market Dynamics:
The increasing prevalence of genetic disorders and chronic diseases, such as cancer and rare inherited conditions, is driving the demand for advanced therapies, thereby necessitating robust manufacturing capabilities. The rapid expansion of the cell and gene therapy pipeline, with numerous therapies advancing through clinical trials, underscores the need for scalable and efficient production solutions. Strategic activities by key industry players including partnerships, investments in state-of-the-art manufacturing facilities, and advancements in automation are enhancing production capacity and efficiency. Collectively, these factors are anticipated to significantly propel the growth of the global cell and gene therapy manufacturing market during the forecast period from 2025 to 2032.
According to data from the International Agency for Research on Cancer (2024), the global incidence of new cancer cases was estimated at 20 million in 2022, with projections indicating an increase to 32.6 million by 2045. Gene therapies, such as CAR-T cell treatments, have demonstrated promising results in targeting specific cancer types, thereby increasing the demand for robust manufacturing processes to scale production. Similarly, cell therapies, including stem cell-based treatments, are being developed to address not only cancer but also the adverse effects of aggressive cancer treatments. Consequently, the rising incidence of cancer is significantly boosting the cell and gene therapy manufacturing market.
Additionally, data from the Haemophilia Foundation Australia (2024) indicates that over 2,500 individuals in Australia have been diagnosed with Von Willebrand Disease (VWD), an inherited bleeding disorder, though many cases are believed to be undiagnosed. Cell and gene therapy approaches for VWD involve delivering a functional copy of the defective VWF gene to correct the underlying genetic defect. This strategy necessitates specialized manufacturing of viral vectors and other components in Good Manufacturing Practice (GMP)-compliant facilities, thereby increasing the demand for advanced manufacturing processes and infrastructure. The rising prevalence of VWD globally, coupled with the limitations of conventional treatments, has spurred increased research and investment in developing cell and gene therapies specifically targeting this disorder, thus boosting the overall market.
Furthermore, strategic activities among key market players are significantly enhancing the cell and gene therapy manufacturing landscape. For instance, in October 2023, Creative Medical Technology Holdings, Inc. received Institutional Review Board (IRB) approval for its clinical trial of the StemSpine(R) procedure using AlloStem(TM) (CELZ-201-DDT) cell therapy for chronic lower back pain. This approval enables the company to proceed with recruitment for its FDA-approved Phase 1/2 trial to evaluate safety, efficacy, and tolerability in 30 participants with Degenerative Disc Disease. Such developments underscore the rapid progression of cell and gene therapies through clinical trials, necessitating scalable and efficient manufacturing solutions.
However, the market faces challenges, including complex manufacturing processes and regulatory hurdles. Producing cell and gene therapies involves intricate steps such as cell extraction, modification, expansion, and delivery. Ensuring scalability and reproducibility while maintaining product quality is a significant concern. Regulatory obstacles must be overcome to ensure that patients can benefit from these treatments. Additionally, the lack of access to materials and talent, as well as unproven technologies and immature processes, pose challenges to scaling up production. Addressing these issues is crucial for the continued growth of the cell and gene therapy manufacturing market.
In summary, while the cell and gene therapy manufacturing market is poised for significant growth driven by the rising prevalence of chronic diseases and genetic disorders, it must navigate complex manufacturing and regulatory challenges to fully realize its potential.
Cell and Gene Therapy Manufacturing Market Segment Analysis:
Cell and Gene Therapy Manufacturing Market by Therapy Type (Cell Therapy [Allogenic and Autologous] and Gene Therapy [Viral Vector-Based Gene Therapy and Non-Viral Vector-Based Gene Therapy]), Manufacturing Type (In-house Manufacturing, Contract Manufacturing), Scale of Manufacturing (Clinical-Scale Manufacturing and Commercial-Scale Manufacturing), Application (Neurological, Oncological, Hematological, Ophthalmological and Others), and Geography (North America, Europe, Asia-Pacific, and Rest of the World)
In the therapy type segment of the cell and gene therapy manufacturing market, the allogenic sub-segment of cell therapy is anticipated to hold a significant share in 2024. Allogenic cell therapy is a major driver of market growth due to its scalability, cost-effectiveness, and broad therapeutic potential. Unlike autologous therapies, which use patient-derived cells, allogenic therapies utilize donor cells that are expanded, modified, and stored for use in multiple patients. This "off-the-shelf" approach facilitates mass production, reducing the time and costs associated with personalized treatments, and thereby improving accessibility for large patient populations suffering from chronic and life-threatening diseases.
In oncology, allogenic therapies such as CAR-T cells have demonstrated promising results in treating hematological malignancies, prompting substantial investments in their development. Beyond oncology, their application is expanding into autoimmune diseases, cardiovascular disorders, and regenerative medicine. The capability to produce large-scale, standardized cell batches ensures consistent quality, which is essential for regulatory approval and broader adoption.
Technological advancements in gene-editing tools like CRISPR-Cas9 have further enhanced the potential of allogenic therapies by enabling precise cell modifications, thereby improving efficacy and reducing the risk of immune rejection. Additionally, the adoption of advanced bioprocessing and cryopreservation techniques has improved the shelf life and global distribution capabilities of these therapies, further strengthening market penetration.
Strategic activities among key market players are also fueling the growth of the cell and gene therapy manufacturing market. For example, in December 2023, the U.S. Food and Drug Administration (FDA) approved Casgevy and Lyfgenia the first cell-based gene therapy for treating sickle cell disease (SCD) in patients aged 12 years and older. These therapies target the root cause of SCD by correcting the defective hemoglobin gene, offering potential curative solutions for a condition historically managed with symptomatic treatments like transfusions or hydroxyurea.
Overall, the combination of technological advancements, expanding therapeutic applications, and supportive regulatory developments is expected to propel the allogenic cell therapy segment, thereby boosting the global cell and gene therapy manufacturing market during the forecast period from 2025 to 2032.
North America is expected to dominate the overall cell and gene therapy manufacturing market:
North America is projected to hold the largest share of the cell and gene therapy manufacturing market in 2024. This dominance can be attributed to the region's strong presence of leading biopharmaceutical companies, robust healthcare infrastructure, and favorable regulatory environment. The U.S. Food and Drug Administration (FDA) plays a pivotal role through initiatives like fast-track designations, breakthrough therapy designations, and orphan drug approvals, expediting the development and commercialization of advanced therapies. Additionally, substantial investments from both government agencies and private entities are enhancing manufacturing capabilities and fostering innovation in the region.
The increasing prevalence of chronic diseases and genetic disorders further drives market demand. According to recent data from the Centers for Disease Control and Prevention (CDC) in 2024, approximately 1 in every 5,000 boys aged 5-9 years in the United States has Duchenne or Becker muscular dystrophy (DBMD). These X-linked genetic disorders cause progressive muscle degeneration due to mutations in the dystrophin gene. Cell and gene therapies, leveraging technologies like adeno-associated virus (AAV) vectors, are being developed to deliver functional copies of the dystrophin gene, aiming to slow disease progression and improve patient outcomes. The rising research focus on DBMD underscores the growing manufacturing need for such advanced therapies.
Furthermore, hemophilia remains a significant focus area in gene therapy development. The CDC reports that approximately 33,000 males in the United States were living with hemophilia in 2024. Gene therapies like BioMarin's Roctavian for hemophilia A and CSL Behring's Hemgenix for hemophilia B have revolutionized treatment by enabling long-term clotting factor production through a single administration. This shift toward curative solutions over traditional therapies, such as frequent factor replacement, is driving the demand for large-scale manufacturing of viral vectors and other essential components.
Product approvals continue to bolster market growth. In December 2023, the FDA approved Casgevy and Lyfgenia the first cell-based gene therapy for treating sickle cell disease (SCD) in patients aged 12 years and older. These treatments target the root cause of SCD by correcting the defective hemoglobin gene, offering potential long-term remission, and reducing dependence on symptomatic management options like blood transfusions. Such regulatory milestones emphasize the region's leadership in facilitating groundbreaking therapies.
Moreover, the region benefits from a high level of patient awareness, enabling quicker adoption of novel treatments. Strategic collaborations among biopharmaceutical companies, contract manufacturing organizations (CMOs), and academic institutions further accelerate process development and scale-up capabilities. Advances in automation, bioprocessing technologies, and supply chain management are enhancing production efficiency and consistency, ensuring timely delivery to patients.
Collectively, these factors including rising disease prevalence, supportive regulatory frameworks, technological advancements, and strategic industry initiatives are expected to significantly propel the growth of the cell and gene therapy manufacturing market in North America during the forecast period from 2025 to 2032.
Cell and Gene Therapy Manufacturing Market Key Players:
Some of the key market players operating in the cell and gene therapy manufacturing market include Lonza, Catalent, Inc., Thermo Fisher Scientific, Inc., Charles River Laboratories, WuXi AppTec, Merck KGaA, Takara Bio Inc., Oxford Biomedica PLC, Genezen, FUJIFILM Holdings Corporation, Nikon Corporation, The Discovery Labs LLC, RoslinCT, JRS Pharma, FinVector, Sarepta Therapeutics, Inc., BioCentriq, Andelyn Biosciences, ElevateBio, Anemocyte Srl, and others.
Recent Developmental Activities in the Cell and Gene Therapy Manufacturing Market:
Key Takeaways From the Cell and Gene Therapy Manufacturing Market Report Study
Target Audience Who Can be Benefited From This Cell and Gene Therapy Manufacturing Market Report Study
Frequently Asked Questions for the Cell and Gene Therapy Manufacturing Market: