生物仿制药:新兴的生物医学领域

Anshi Mehra, Hemanreet Kaur, Anoor Fatima, A. Noor, Khushi Gupta, A. Shukla, Keshwanand Tripathi, Amit Joshi
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引用次数: 1

摘要

生物仿制药是生物制剂领域的新兴药品,是医药工业快速发展的领域。它是原始研究基础药物的非专利替代品。由于生物制剂是由多种产品生产的,更常见的是包括从人类、动物、微生物中提取的细胞,这些细胞在表型上各不相同,因此它们与原始产品“相似但不相同”。作为一种新产品,它在市场上产生了一些挑战,包括监管准则、生产效率、质量管理和安全因素等。这些产品的质量以及其有效性和降低的成本使它们越来越受欢迎。由于生物类似药在市场上的应用越来越广泛,提高其疗效的研究仍在不断进行。一些国家已经制定了这些生物类似药的生产和临床使用的单独规范,包括加拿大、日本、韩国和美利坚合众国等。越多的生物制剂因为更好的创新而吸引知名科学家的注意,它获得的市场批准就越少。为了改善这种情况,美国国会通过了2009年生物制剂价格竞争和创新法案,美国食品药品监督管理局允许“简化途径”批准,印度是最适合的生产地区,也准备了某些指导方针,称为“类似生物制剂指南草案”,该指南于2012年6月由波士顿生物技术部门宣布。随着技术/分析方法的进步和生物类似药开发新靶点的出现,生物类似药的监管环境不断发展。随着这些努力的出现,生物仿制药正试图包围市场。生物仿制药的苛刻部门揭示了纳米药物的挑战性门户,这也表明,随着这些生物仿制药之后生物技术的进步,我们正在朝着其他新的生物衍生产品前进。
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Biosimilars: Novel Emerging Field of Biomedicine
A biosimilar is the new emerging drug product of the sector of Biologics that comes under speedily evolving area of pharmaceutical industry. It is the generic substitute for original research-based drugs. Since the Biologics are produced by a variety of products more commonly including cells extracted from humans, animals, microorganisms which varies phenotypically therefore they are “similar but not same” to the original product. Being a new product, it produces several challenges in the market including its regulation guidelines, production efficiency, quality management, and safety factors etc. The quality of these products along with its effectiveness and reduced costs are making them more and more popular. Different research is still being going on for enhancing the efficacy of biosimilars due to its more and more usage in the market. Several countries have developed their separate norms for the production and clinical usage of these biosimilars constituting Canada, Japan, Korea, and United States of America etc. The more biologics grab the attention of the eminent scientists for better innovations, the less marketing approval it gets. To enhance such a situation U S Congress passed the Biologics Price Competition and Innovation act 2009 and US FDA allowed “abbreviated pathway” for their approval and India being the most suited manufacturing area has also prepared certain guidelines stated as “Draft Guidelines on Similar Biologics” which were announced in June 2012, by Department of Biotechnology at Boston bio. The regulatory environment for biosimilars continues to evolve, both in recognition of advances in technology/ analytical methods and the availability of new targets for biosimilar development. With the advent of such efforts biosimilars are trying to surround the market. The demanding sector of biosimilars reveals the challenging gateway towards the nanomedicines also which shows that with the advancing biotechnology after these biosimilars, we are heading towards other newly biologically derived products.           
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