市場調查報告書
商品編碼
1463320
全球臨床試驗用品市場規模、佔有率、成長分析,依階段(第一階段、第二階段)、應用(製藥和生物製藥以及合約研究組織 (CRO))- 2024-2031 年產業預測Global Clinical Trial Supplies Market Size, Share, Growth Analysis, By Phase(Phase I, Phase II), By Application(Pharmaceutical and Biopharmaceutical, and Contract Research Organizations (CROs)) - Industry Forecast 2024-2031 |
2022年,全球臨床試驗用品市場規模為29億美元,預計將從2023年的30.9億美元成長到2031年的51.1億美元,預測期間(2024-2031年)複合年成長率為6.5%。
在全球化趨勢不斷增強、臨床試驗活動激增以及生物製劑和生物相似藥測試不斷升級的推動下,全球臨床試驗用品市場經歷了顯著成長。生技製藥公司採用供應鏈管理系統來降低與研發相關的高成本,同時提高營運效率。值得注意的是,臨床試驗用品佔研發總支出的很大一部分。此外,試驗中的生物製品和溫度敏感藥物的日益普及促使對臨床試驗設施的需求增加。目前,大約 38% 的藥物表現出溫度敏感性,其中 35% 的後期藥物被歸類為生物製劑。與傳統藥物相比,生物製劑的不良反應發生率較低,因此對生物製劑的需求不斷增加。已開發經濟體和發展中經濟體對生物相似藥的需求增加進一步推動了市場成長。由於成本較低且病患招募流程簡化,臨床試驗主要在發展中經濟體進行。亞太、拉丁美洲、中東歐、中東等地區為生物製藥公司提供了相當大的經濟優勢。新加坡和中國政府撥款促進生物醫學研究,而拉丁美洲則因語言障礙的減少而受益於簡化的患者招募。此外,發展中經濟體的多樣化疾病狀況有利於針對罕見疾病的臨床試驗。
The global clinical trial supplies market size was valued at USD 2.9 billion in 2022 and is poised to grow from USD 3.09 billion in 2023 to USD 5.11 billion by 2031, growing at a CAGR of 6.5% in the forecast period (2024-2031).
The global market for clinical trial supplies has experienced remarkable growth, fueled by the increasing trend of globalization, a surge in clinical trial activities, and the escalating testing of biologics and biosimilar drugs. Biopharmaceutical companies have adopted supply chain management systems to mitigate the high costs associated with research and development while enhancing operational efficiency. Notably, clinical trial supplies constitute a significant portion of the total R&D expenditure. Furthermore, the growing prevalence of biologics and temperature-sensitive drugs under trial has led to an uptick in demand for clinical trial facilities. Presently, approximately 38% of pharmaceutical drugs exhibit temperature sensitivity, with 35% of late-phase pharmaceutical drugs being categorized as biologics. The rising demand for biologics stems from their lower incidence of adverse effects compared to traditional drugs. Market growth is further propelled by the heightened demand for biosimilars across developed and developing economies. Clinical trials predominantly take place in developing economies due to lower costs and simplified patient recruitment processes. Regions such as Asia Pacific, Latin America, Central & Eastern Europe, and the Middle East offer considerable economic advantages to biopharmaceutical companies. Governments in Singapore and China allocate funds to foster biomedical research, while Latin America benefits from simplified patient recruitment owing to reduced language barriers. Moreover, the diverse disease landscape in developing economies facilitates clinical trials focusing on rare diseases.
Top-down and bottom-up approaches were used to estimate and validate the size of the global clinical trial supplies market and to estimate the size of various other dependent submarkets. The research methodology used to estimate the market size includes the following details: The key players in the market were identified through secondary research, and their market shares in the respective regions were determined through primary and secondary research. This entire procedure includes the study of the annual and financial reports of the top market players and extensive interviews for key insights from industry leaders such as CEOs, VPs, directors, and marketing executives. All percentage shares split, and breakdowns were determined using secondary sources and verified through Primary sources. All possible parameters that affect the markets covered in this research study have been accounted for, viewed in extensive detail, verified through primary research, and analyzed to get the final quantitative and qualitative data.
Global Clinical Trial Supplies Market Segmental Analysis
The global clinical trial supplies market is segmented based on phase, application, and region. By phase, the market is segmented into phase I, phase II, phase III, and phase IV. By application, the market is segmented into pharmaceutical and biopharmaceutical, and contract research organizations (CROs). By region, the market is segmented into North America, Europe, Asia Pacific, Middle East and Africa, and Latin America.
Drivers of the Global Clinical Trial Supplies Market
An essential catalyst for the global clinical trial supplies market is the rising need for specialized drug products, particularly biologics. These intricate therapeutic agents demand specific clinical trial supplies to uphold their safety, effectiveness, and stability throughout the trial process. Biologics, distinguished by their complex molecular structure derived from living organisms, serve as vital treatments for a spectrum of ailments. Given their unique characteristics, biologics necessitate specialized clinical trial provisions, including precise refrigeration, tailored packaging materials, and sophisticated temperature monitoring systems. The escalating demand for biologics, fueled by their proven efficacy and reduced adverse effects compared to conventional therapies, is propelling the requirement for specialized clinical trial supplies.
Restraints in the Global Clinical Trial Supplies Market
A significant obstacle facing the global clinical trial supplies market is the exorbitant cost associated with conducting clinical trials. The expenses incurred in conducting these trials have witnessed a substantial increase in recent times, posing a restraint on market expansion. Furthermore, challenges abound in patient recruitment due to the intricacies involved, alongside stringent regulatory requirements that must be adhered to throughout the trial process. These complexities not only impede the growth of the market but also pose barriers for small and mid-sized companies seeking entry, thereby constraining the overall progression of the clinical trial supplies market.
Market Trends of the Global Clinical Trial Supplies Market
An emerging trend in the global clinical trial supplies market is the integration of blockchain technology. This technology presents a decentralized and transparent system capable of tracking and managing the clinical trial supply chain effectively, from production to patient delivery. By enabling real-time tracking of supplies, blockchain technology enhances operational efficiency, minimizes errors, and strengthens data security. As such, its adoption within the clinical trial supplies market is anticipated to rise significantly in the foreseeable future.