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市場調查報告書
商品編碼
1279674
全球臨床試驗市場 - 2023-2030Global Clinical Trials Market - 2023-2030 |
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全球臨床試驗市場預計將實現利潤豐厚的增長,到 2022 年將達到 566.407 億美元,到 2030 年將達到 992.12 億美元。 在預測期內(2023-2030 年),臨床試驗市場預計將以 7.4% 的複合年增長率增長。
臨床試驗是一種臨床調查程序,由經過仔細驗證的指定協議監督,以解決詳細的患者護理查詢。 臨床試驗分為五個階段,每個階段都有特定的臨床試驗目的。 所有臨床試驗均受制於定義誰可以參與試驗的系統。 研發支出的增加、對新療法的需求不斷增加以及不斷變化的監管指南正在推動預測期內全球臨床試驗市場的增長。
每年,製藥行業都會生產各種具有顯著醫療效益的新藥。 藥物發現是一個昂貴且不確定的過程,許多潛在的藥物從未進入市場。 因此,公司將這些任務外包給 CRO 以降低成本。 CRO 為製藥和生物技術公司提供藥物研究外包服務。
CRO 根據所有標準和法規要求管理和完成圖像處理過程,以實現順利的圖像採集、分析、註釋和傳輸。 近年來,CRO 服務在開發新藥和治療的早期階段協助公司。 製藥公司越來越多地使用臨床研究、諮詢和實驗室 CRO 服務。
未來幾年,預計來自各個主管部門的資金增加將為全球臨床試驗市場提供有利可圖的增長機會。 例如,2023年1月,作為加拿大生物製造和生命科學戰略(BLSS)的一部分,加拿大衛生研究院(CIHR)的臨床試驗基金(CTF)啟動了中風研究、行為改變、生物統計學和臨床研究。我們計劃接受超過 3200 萬加元的共同投資,以向新一代研究人員和研究人員傳授我們的專業知識,包括我們已知的方法。
對 COVID-19 的分析包括 COVID 之前、COVID 和 COVID 之後的情景、價格動態(與 COVID 之前的情景相比,大流行期間和之後的價格變動)、供需範圍(由於供應和需求的變化還解釋了貿易限制、封鎖和後續問題)、政府舉措(政府機構為振興市場、部門和行業而採取的舉措)、製造商的戰略舉措(製造商為緩解 COVID 問題所做的努力)。
烏克蘭和俄羅斯都是國際臨床試驗活動的廣泛基地。 對烏克蘭的攻擊可能會破壞國際臨床試驗的結果,因為這兩個國家有前途的招募中心都失敗了。 軍事衝突造成的中斷對醫療保健產生了重大影響,包括臨床試驗和癌症護理。
一些專家擔心,隨著經濟持續放緩,許多國家正處於衰退的邊緣。 公司正在密切關注其影響,但生物製藥領域尤為關注。 經濟衰退將不可避免地迫使一些公司改變他們的方法。 但一些生物技術公司可能會受到更健康的結果的影響。 預計生物技術公司將尋求技術來填補資金缺口,從而提高效率、更快獲得結果並改變生物技術研究人員的工作方式。
人工智能對臨床試驗市場產生積極影響。 通過採用 AI 支持的技術,研究人員可以從過去和最近的研究中獲得見解,探索大量數據,並報告對未來研究設計的任何必要調整。 在進一步的臨床試驗中,人工智能在診斷和治療疾病方面也有很大的應用潛力。
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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