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全球体内给药设备市场 - 2025 - 2033Global On-body Drug Delivery Devices Market - 2025 - 2033 |
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2024年,全球体内给药装置市场规模达405.4亿美元,预估至2033年将达827.4亿美元,2025-2033年预测期间复合年增长率为8.6%。
体内药物输送装置 (OBDD) 是一种新型医疗装置,可在皮下分配药物(特别是生物製剂),同时保持附着在患者身体上。这些设备通常经过修补并设计用于输送单株抗体等大分子,这需要精确的剂量和时间。 OBDD 的基本目标是创建一个更可预测和可控的药物传递系统,从而提高患者的依从性并减少治疗反应的变异性。这些设备可以在家中进行自我管理,从而减少了频繁去医院和针刺的需要,大大提高了慢性病患者的生活品质。
对体内给药设备的需求不断增长是预测期内推动市场的驱动因素。糖尿病和癌症等慢性病的发生率不断增加,需要持续有效的药物管理,这推动了对体内给药系统的需求不断增长。这些设备增强了自我管理能力,使患者能够在家中管理他们的治疗,从而提高对治疗方案的依从性。此外,技术进步带来了更用户友好和高效的分销系统,提高了其感知价值。
驱动程式和限制
对体内给药装置的需求不断增加
对体内药物输送装置的需求不断增长预计将成为全球体内药物输送装置市场成长的重要因素。由于慢性病盛行率上升、技术进步以及最近的推出和批准,对体内给药装置的需求不断增加。
慢性病的日益普及是推动体内给药设备需求的主要驱动力。糖尿病、心血管疾病和癌症等慢性疾病需要持续且复杂的治疗方案,而增强的药物传递系统可以有效地支持这些治疗方案。随着慢性病变得越来越频繁,对新解决方案的需求不断增长,这些解决方案允许患者在传统医疗保健环境之外自行给药。例如,根据美国心臟学会基金会的数据,高收缩压对年龄标准化 CVD 伤残调整生命年 (DALY) 的贡献最大,全世界每 10 万人中有 2,564.9 人患有高收缩压。
对体内药物输送系统不断增长的需求与提高其功能、安全性和患者依从性的技术改进密切相关。体内药物传输技术的最新进展包括开发用于精确施用生物製剂和其他药物的复杂设备。这些设备,例如可穿戴注射器和输液泵,旨在提供延长和受控的药物释放,这对于解决糖尿病和癌症等慢性疾病至关重要。最新的体内药物传输系统不仅旨在提供药物,而且还具有改善其功能的智慧功能。现在许多设备都具有剂量监测和追踪功能,可以帮助患者更有效地遵守治疗计划。
例如,2023年4月,全球医疗技术领导者美敦力公司宣布,其配备Guardian 4感测器的MiniMed 780G系统已获得FDA认证,该系统在使用SmartGuard技术时无需进行指尖采血。这一里程碑标誌着唯一一个使用膳食检测技术每 5 分钟自动调节和纠正血糖水平的系统获得认证。
严格的监管要求
严格的监管要求等因素预计将阻碍全球体内给药设备市场。控制这些设备的法规的复杂性部分源于它们被指定为组合商品,其中既有药物又有设备组件。这种双重分类要求製造商穿越复杂的监管系统网络,这些系统在不同地区(尤其是美国和欧洲)差异很大。每个地区都有自己的一套指导方针和审批流程,这可能会导致新产品推向市场的混乱和延误。
由于药物输送系统技术的快速进步,监管环境变得更加复杂。随着新技术的发展,它们经常提供新的功能,需要监管组织进行额外的监管。例如,网路药物输送系统必须满足严格的安全、效能和网路安全要求,在批准之前需要进行广泛的测试和验证。这种对上市前提交的严格要求可能会减慢创新週期,因为公司必须投入大量时间和资源来确保遵守所有相关法规。
The global on-body drug delivery devices market reached US$ 40.54 billion in 2024 and is expected to reach US$ 82.74 billion by 2033, growing at a CAGR of 8.6% during the forecast period 2025-2033.
On-body drug delivery devices (OBDDs) are novel medical devices that dispense drugs, notably biologics, subcutaneously while remaining attached to the patient's body. These devices are often patched on and designed to deliver large molecules like monoclonal antibodies, which require precise dosing and timing. The basic aim of OBDDs is to create a more predictable and controlled drug delivery system, which improves patient compliance and reduces treatment response variability. These devices enable self-administration at home, which reduces the need for frequent hospital visits and needle pricks, greatly enhancing the quality of life for patients with chronic diseases.
The increasing demand for on-body drug delivery devices is the driving factor that drives the market over the forecast period. The growing frequency of chronic diseases, such as diabetes and cancer, necessitates constant and effective medication administration, which is driving the growing demand for on-body drug delivery systems. These devices enhance self-administration, allowing patients to manage their treatments at home and therefore increasing adherence to therapy regimens. Furthermore, technological improvements have resulted in more user-friendly and efficient distribution systems, increasing their perceived value.
Market Dynamics: Drivers & Restraints
Increasing demand for on-body drug delivery devices
The increasing demand for on-body drug delivery devices is expected to be a significant factor in the growth of the global on-body drug delivery devices market. The demand for on-body drug delivery devices is increasing owing to the rising prevalence of chronic diseases, technological advancements, and recent launches and approvals.
The growing prevalence of chronic diseases is a major driver that drives the demand for on-body drug delivery devices. Chronic diseases, such as diabetes, cardiovascular diseases, and cancer, necessitate persistent and frequently sophisticated management regimens, which can be efficiently supported by enhanced drug delivery systems. As chronic diseases become more frequent, there is a growing demand for novel solutions that allow patients to self-administer medications outside of traditional healthcare settings. For instance, according to the American College of Cardiology Foundation, High systolic blood pressure contributed the most to age-standardized CVD disability-adjusted life years (DALYs), with 2,564.9 per 100,000 people worldwide.
The growing demand for on-body medication delivery systems is closely connected to technological improvements that improve their functionality, safety, and patient compliance. Recent advancements in on-body drug delivery technology include the development of sophisticated devices for administering biologics and other drugs with accuracy. These devices, such as wearable injectors and infusion pumps, are designed to deliver prolonged and controlled drug release, which is critical for addressing chronic diseases such as diabetes and cancer. The latest on-body drug delivery systems are not only designed to provide medication, but they also have smart features that improve their functionality. Many devices now have dose monitoring and tracking capabilities, which can help patients adhere to treatment plans more effectively.
For instance, in April 2023, Medtronic plc, a global leader in medical technology, announced that its MiniMed 780G system with the Guardian 4 sensor, which requires no fingersticks while using SmartGuard technology, has received FDA certification. This milestone signifies the certification of the only system that uses meal detection technology to automatically regulate and correct sugar levels every 5 minutes.
Stringent Regulatory Requirements
Factors such as stringent regulatory requirements are expected to hamper the global on-body drug delivery devices market. The complexity of regulations controlling these devices emerges partly from their designation as combination goods, which have both medication and device components. This dual classification requires manufacturers to traverse an intricate network of regulatory systems that varies greatly across locations, particularly between the United States and Europe. Each region has its own set of guidelines and approval processes, which can cause confusion and delays in introducing novel products to the market.
The regulatory landscape is further complicated by the rapid advancement of technology in drug delivery systems. As new technologies are developed, they frequently provide new functionalities that necessitate additional regulation from regulatory organizations. For instance, networked medicine delivery systems must meet stringent safety, performance, and cybersecurity requirements, necessitating extensive testing and validation prior to approval. This stringent requirement for pre-market submissions can slow down the innovation cycle since companies must devote significant time and resources to ensuring compliance with all relevant regulations.
The global on-body drug delivery devices market is segmented based on product, application, age group, end-user, and region.
Wearable Injectors segment is expected to dominate the global on-body drug delivery devices market share
The wearable injectors segment is anticipated to dominate the global on-body drug delivery devices market owing to its growing importance as a convenient and effective solution for managing chronic diseases. As healthcare shifts toward more patient-centered techniques, wearable injectors provide an easy and effective way to manage chronic conditions. These devices are designed to deliver medication subcutaneously over an extended period of time, allowing patients to self-administer their therapies while going about their regular lives. This convenience is especially compelling for people with chronic disorders like diabetes, cancer, and autoimmune diseases, which frequently necessitate daily medicine administration.
Furthermore, the design and functionality of on-body wearable injectors play a crucial role in their market dominance. These devices are often worn as skin patches, with a user-friendly interface that streamlines medicine delivery. Their water-resistant characteristics and adaptability for home usage add to their appeal, allowing patients to maintain their treatments without frequent visits to hospitals and clinics. The capacity of these devices to efficiently distribute complicated medications increases patient comfort while also lowering healthcare expenditures by reducing hospital admissions and associated charges.
Wearable injectors are also growing in popularity due to technological developments. Automated warming systems for cold pharmaceuticals and increased dosing flexibility make these devices attractive to both patients and healthcare practitioners. The spring-based injector method, which allows for exact subcutaneous injection with no effort, has acquired significant acceptance because of its ease of use. There have been recent launches and approvals in recent times. For instance, in October 2023, Apellis Pharmaceuticals, Inc. announced that the U.S. Food and Drug Administration (FDA) approved the EMPAVELI Injector. The EMPAVELI Injector is a compact, single-use, on-body device designed to enhance self-administration of EMPAVELI (pegcetacoplan), which is approved for adults with paroxysmal nocturnal hemoglobinuria (PNH).
North America is expected to hold a significant position in the global on-body drug delivery devices market share
North America will likely account for a significant share of the global on-body drug delivery devices market, owing to its advanced healthcare infrastructure, a high prevalence of chronic diseases, technological advancements, and recent launches and approvals. The increased prevalence of chronic diseases in North America has a substantial impact on the growth of the on-body drug delivery device market.
For instance, according to the National Institute of Health, common types of cardiovascular disease include coronary heart disease (CHD), stroke, hypertension, and congestive heart failure. An estimated 16.3 million Americans aged 20 and older have CHD, a prevalence of 7 percent. The prevalence for men is 8.3 percent and for women is 6.1 percent. About 7 million Americans aged 20 or older have had a stroke. Each year approximately 610,000 experience their first stroke and another 185,000 experience a recurrence. Approximately 87 percent of all strokes are ischemic of which 10 percent result from intracerebral hemorrhage and 3 percent result from subarachnoid hemorrhage. Cardiovascular disease, diabetes, and autoimmune disorders are becoming more prevalent in the population.
The regulatory environment in North America also influences the on-body drug delivery device market. The United States Food and Drug Administration (FDA) has set defined rules for approving combination items that incorporate both medications and devices. This regulatory framework promotes innovation while protecting patient safety. Companies benefit from a streamlined clearance procedure, which enables them to bring new products to market faster than in regions with more complex regulatory regulations.
The region has a strong healthcare infrastructure and a high emphasis on R&D, which encourages innovation in drug delivery technology. These developments are critical to fulfill the growing demand for effective, patient-friendly chronic disease management options. The incorporation of smart technologies is a significant technological advancement in the on-body drug delivery devices industry. Many current wearable injectors now include connection features that enable them to communicate with smartphones and other digital health systems. This connectivity enables real-time monitoring of medication adherence and patient health parameters, delivering useful information to both patients and healthcare practitioners. For instance, in May 2023, Coherus BioSciences, Inc., announced that the single-dose (6mg/0.6mL), prefilled autoinjector presentation of UDENYCA (pegfilgrastim-cbqv) is now available for commercial sale in the United States. UDENYCA is a pegfilgrastim biosimilar administered the day after chemotherapy to decrease the incidence of infection as manifested by febrile neutropenia. UDENYCA AI's streamlined design offers a simple option for in-office and at-home settings of care that administers pegfilgrastim in less than 10 seconds.
Asia Pacific is growing at the fastest pace in the global on-body drug delivery devices market
The Asia Pacific region is emerging as the fastest-growing market for on-body drug delivery devices, owing to a combination of demographic trends, increased healthcare investment, recent launches, technological advancements, and a rising number of chronic diseases. The rising prevalence of chronic diseases such as diabetes, cardiovascular disease, and respiratory ailments is a major contributor to this growth. The rising prevalence of chronic diseases increases the demand for on-body drug delivery devices.
For instance, according to the National Institute of Health, coronary heart disease prevalence rates in India have been estimated over the past several decades and have ranged from 1.6% to 7.4% in rural populations and from 1% to 13.2% in urban populations. These medical conditions necessitate continuing treatment and control, resulting in an increased demand for dependable and user-friendly medication delivery systems. The surge in chronic diseases needs innovative approaches that enable patients to successfully self-administer drugs at home, improving treatment adherence and overall health outcomes.
The major global players in the global on-body drug delivery devices market include BD, Gerresheimer AG, NOVO Engineering, West Pharmaceutical Services, Inc., Enable Injections, Stevanato Group, LTS Lohmann Therapie-Systeme AG, Coherus BioSciences, Inc., Tandem Diabetes Care, Inc, Battelle among others.
Emerging Players
Hera Health Solutions, Vensica Medical, and Bigfoot Biomedical among others
The global on-body drug delivery devices market report delivers a detailed analysis with 60+ key tables, more than 50 visually impactful figures, and 176 pages of expert insights, providing a complete view of the market landscape.
Target Audience 2024
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