The Innovation Paradox in Emerging Pharmaceutical Markets: Barriers and Opportunities for Sustainable Development.

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Frederico Severino Martins, Sivacharan Kollipara, Praveen Sivadasu, Mingming Yu, Patricia Severino, Eliana Souto
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Abstract

Emerging pharmaceutical markets like Brazil, India, and China have seen significant growth due to rising medication demand, expanding middle-class access, and government support. However, this growth often focuses on cost-driven strategies like generic drug production rather than innovation. Challenges such as fragmented regulatory systems, limited infrastructure, low R&D budgets, and dependence on imported active pharmaceutical ingredients (APIs) limit global competitiveness in drug innovation. R&D investment in these markets rarely exceeds 5% of revenue, compared to 20% in established markets, widening the innovation gap. Advanced technologies such as physiologically based pharmacokinetic (PBPK) modeling, artificial intelligence (AI), and virtual bioequivalence studies present opportunities to overcome these barriers. These tools streamline drug development, lower costs, and improve regulatory processes. For instance, a case study on generic donepezil showed that a $150,000 investment in PBPK modeling software could yield returns of 113.7% when clinical studies are required and 1,120% if a biowaiver is granted. These results demonstrate the financial and operational advantages of adopting innovative technologies, enabling faster market entry and scalability across portfolios. By embracing advanced tools, companies in emerging markets can align with global regulatory trends, enhance sustainability through resource efficiency, and improve access to affordable medicines. This approach bridges the gap between economic growth and technological leadership, fostering global competitiveness and contributing to public health advancements.

新兴医药市场的创新悖论:可持续发展的障碍与机遇。
巴西、印度和中国等新兴制药市场由于药品需求上升、中产阶级获得机会扩大以及政府支持而出现了显著增长。然而,这种增长往往侧重于成本驱动型战略,如仿制药生产,而不是创新。监管体系分散、基础设施有限、研发预算低以及对进口活性药物成分(api)的依赖等挑战限制了药物创新的全球竞争力。这些市场的研发投资很少超过收入的5%,而成熟市场的这一比例为20%,这加大了创新差距。基于生理的药代动力学(PBPK)建模、人工智能(AI)和虚拟生物等效性研究等先进技术为克服这些障碍提供了机会。这些工具简化了药物开发、降低了成本并改进了监管程序。例如,对仿制药donepezil的案例研究表明,在PBPK建模软件上投资15万美元,当需要进行临床研究时,回报率为113.7%,如果获得生物豁免,回报率为1120%。这些结果证明了采用创新技术的财务和运营优势,能够更快地进入市场并实现跨投资组合的可扩展性。通过采用先进的工具,新兴市场的公司可以与全球监管趋势保持一致,通过资源效率提高可持续性,并改善可负担药品的可及性。这种做法弥合了经济增长和技术领先之间的差距,促进了全球竞争力,并促进了公共卫生进步。
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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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