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市場調査レポート
商品コード
1279674
臨床試験の世界市場- 2023-2030年Global Clinical Trials Market - 2023-2030 |
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カスタマイズ可能
適宜更新あり
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臨床試験の世界市場- 2023-2030年 |
出版日: 2023年05月26日
発行: DataM Intelligence
ページ情報: 英文 195 Pages
納期: 即日から翌営業日
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臨床試験の世界市場は、2022年に566億4,070万米ドルに達し、2030年には992億1,200万米ドルに達することで有利な成長が予測されています。臨床試験市場は、予測期間中(2023-2030年)に7.4%のCAGRで成長すると予想されています。
臨床試験は、詳細な患者ケアの問い合わせに対応するために慎重に検証された指定されたプロトコルによって監督される臨床調査の手法です。臨床試験は5つのフェーズに分けられ、各フェーズには臨床試験における特定の意図があります。すべての臨床試験は、どのような人々がその試験に参加できるかを定義するシステムに委ねられています。研究開発費の増加、新しい治療薬へのニーズの高まり、規制ガイドラインの進化が、予測期間中の世界臨床試験市場の成長を後押ししています。
毎年、製薬業界では、医学的に大きなメリットをもたらすさまざまな新薬が生み出されています。新薬の開拓はコストと不確実性の高いプロセスであり、多くの潜在的な医薬品が市場に出回ることはありません。その結果、企業はコストを削減するために、これらの業務をCROに委託しています。CROは、製薬会社やバイオテクノロジー企業に対して、製薬研究のアウトソーシングサービスを提供しています。
CROは、画像取得、解析、アノテーション、転送をスムーズに行うため、すべての規格と規制要件に従って画像処理プロセスを管理し、完了します。近年、CROのサービスは、新薬や治療法の開発の初期段階にある企業を支援しています。製薬会社は、臨床研究、コンサルタント、ラボのCROサービスをますます利用するようになっています。
様々な当局からの資金提供の増加は、今後数年間、世界の臨床試験市場に有利な成長機会をもたらすと予想されます。例えば、2023年1月、カナダの生物製造・生命科学戦略(BLSS)の一環として、カナダ保健研究所(CIHR)の臨床試験基金(CTF)は、脳卒中研究、行動変化、生物統計学、臨床研究の既知のアプローチなどの専門知識を新しい世代の研究者や治験責任者に指導するために32Mカナダドル以上の共同投資を受け入れる予定です。
COVID-19の分析には、Pre-COVIDシナリオ、COVIDシナリオ、Post-COVIDシナリオがあり、価格力学(パンデミック時およびパンデミック後の価格変動とCOVID前のシナリオとの比較)、需給スペクトル(取引制限、ロックダウンおよびその後の問題による需要と供給のシフト)、政府の取り組み(政府機関による市場、セクター、産業の活性化に関する取り組み)、メーカーの戦略的取り組み(COVID問題を軽減するためのメーカーの取り組み)についても解説しています。
ウクライナとロシアは、ともに国際的な臨床試験活動の広範な拠点です。ウクライナへの攻撃は、両国の有望な採用拠点の失敗により、国際的な臨床試験の成果に力不足をもたらす可能性があります。軍事的対立による混乱は、臨床試験やがん医療を含むヘルスケアに大きな影響を与えます。
景気低迷が続く中、多くの国が景気後退の危機に瀕していると、複数の専門家が懸念しています。各企業はその影響を注視していますが、バイオファーマの領域では特にその影響を懸念しています。景気後退によって、複数の企業がアプローチを変更することは避けられないと予想されます。しかし、一部のバイオテクノロジー企業には、より健全な結果をもたらすような影響を与える可能性があります。バイオテクノロジー企業は、資金不足を補うためにテクノロジーに目を向けると予想され、その結果、効率性の向上、成果の迅速化、バイオテクノロジー研究者の仕事の仕方の転換が期待されます。
人工知能は臨床試験市場にポジティブな影響を及ぼします。AI対応技術を採用することで、治験責任医師は過去や最近の試験から理解を深め、膨大なデータを調査し、将来の試験デザインに必要な調整を報告することができます。さらなる臨床試験において、AIは障害の診断や治療への応用にも多大な可能性を持っています。
The global clinical trials market reached USD 56,640.7 million in 2022 and is projected to witness lucrative growth by reaching up to USD 99,212.0 million by 2030. The clinical trials market is expected to exhibit a CAGR of 7.4% during the forecast period (2023-2030).
Clinical trials are a methodology of clinical investigation that is overseen by a designated protocol that is carefully verified to respond to a detailed patient care query. Clinical trials are bifurcated into five phases, with every phase carrying a specific intent within the clinical trial. Every trial confers to a system that defines what sorts of people may partake in the study. The increasing R&D spending, growing need for new therapeutics, and evolving regulatory guidelines are driving the global clinical trials market growth during the forecast period.
Every year, the pharmaceutical industry creates a variety of new drugs that provide significant medical advantages. Developing new medicines is a costly and uncertain process, and many potential drugs never make it to market as a result, in order to save money, companies outsource these tasks to CROs. CROs provide pharmaceutical and biotechnology industries with outsourced pharmaceutical research services.
The CROs manage and complete the imaging process in accordance with all standards and regulatory requirements, ensuring smooth image acquisition, analysis, annotation, and transfer. In recent years, CRO services have helped companies in the early stages of developing novel medicines and therapies. Pharmaceutical firms are increasingly using clinical research, consultancy, and laboratory CRO services.
The growing funding from various authorities is expected to provide the global clinical trials market with lucrative growth opportunities in the upcoming years. For instance, in January 2023, as part of Canada's Biomanufacturing and Life Sciences Strategy (BLSS), the Canadian Institutes of Health Research (CIHR) Clinical Trials Fund (CTF) is expected to be accepting a joint investment of more than CAD 32 M to instruct a fresh generation of researchers and investigators in expertise as stroke research, behavioral change, biostatistics, and the known approach of clinical research.
The COVID-19 analysis includes Pre-COVID Scenario, COVID Scenario, and Post-COVID Scenario along with pricing dynamics (including pricing change during and post-pandemic comparing it to pre-COVID scenarios), demand-supply spectrum (shift in demand and supply owing to trading restrictions, lockdown, and subsequent issues), government initiatives (initiatives to revive market, sector or industry by government bodies) and manufacturers strategic initiatives (what manufacturers did to mitigate the COVID issues will be covered here).
Ukraine and Russia are both extensive bases for international clinical trial activity. The attack on Ukraine may cause an underpowering of global clinical trial outcomes with the failure of prospective recruitment locations for both nations. The turmoil and disorder induced by military confrontation have a significant influence over healthcare including clinical trials and cancer care.
As the economic slump persists, multiple specialists are concerned that many countries are on the cusp of a recession. While every enterprise is overseeing the possible fallout, those in the biopharma domain may be especially anxious regarding the outcomes. The recession is expected inevitably cause multiple firms to alter their approach. Nonetheless, it could influence a few biotechs for sounder outcomes. It is anticipated that biotechs' will look towards technology to compensate for funding shortcuts, that are expected to result in improved efficiencies, quicker results, and a shift in the way biotech researchers work.
Artificial intelligence has a positive impact on the clinical trials market as employing AI-enabled technologies, the investigators can analyze and yield understanding from prior and recent trials, research huge data, and report the needed adjustment in prospective trial designs. In further clinical trials, AI has a tremendous possibility in the diagnosis of disorders and treatment applications as well.
The global clinical trials market is segmented based on phase, design, indication, service, and region.
The phase III segment is estimated to hold about 47.1% of the global clinical trials market by 2030. For instance, in May 2022, the last patient is projected to begin treatment in June 2022, according to Lipidor AB (publ), which reports that half of the patients have already been enrolled in the Phase III research of the AKP02 skin spray for mild to moderate psoriasis. In the third quarter of 2022, top-line results from the Phase III investigation are anticipated.
In December 2022, by showing a statistically significant decrease in HbA1c (a measure of average blood sugar) with Jardiance (empagliflozin) compared with placebo for children and adolescents aged 10-17 years with type 2 diabetes, the DINAMO phase III clinical trial fulfilled its primary aim.
The increasing government initiatives for research drive the market in the European region and are estimated to hold around 27.7% of the total global market by 2030. For instance, in January 2022, the European Commission (EC), the Heads of Medicines Agencies, and the European Medicines Agency introduced an initiative to transform how clinical trials are initiated, developed, and run, directed to Accelerating Clinical Trials in the EU (ACT EU).
The goal is to further expand the EU as a focal point for clinical research, advance the development of high-quality, safe, and effective medicines, and better incorporate clinical research in the European health system. Creating the application of the Clinical Trials Regulation and the takeoff of the Clinical Trials Information Systems in January 2022, ACT EU will support the European environment for clinical trials while maintaining data robustness, a high level of protection of trial participants, and the transparency that EU citizens expect.
The major global players in the market include: Iqvia Holdings Inc. (Q2 Solutions), Parexel International Corporation, Charles River Laboratories International, Inc., Syneos Health, Inc., WuXi AppTec Co., Ltd. (WuXi Clinical), ICON plc, Thermo Fisher Scientific (Pharmaceutical Product Development LLC), Azelix, Pharmaron Beijing Co., Ltd., and Celerion among others.
The global clinical trials market report would provide approximately 53 tables, 54 figures, and 195 Pages.
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