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Current status of selected oral peptide technologies in advanced preclinical development and in clinical trials

机译:选定的口服肽技术在高级临床前开发和临床试验中的现状

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The development of oral dosage forms that allows absorption of therapeutic peptides to the systemic circulation is one of the greatest challenges for the pharmaceutical industry. Currently, a number of technologies including either mixtures of penetration enhancers or protease inhibitors and/or nanotechnology-based products are under clinical development. Typically, these formulations are presented in the form of enteric-coated tablets or capsules. Systems undergoing preclinical investigation include further advances in nanotechnology, including intestinal microneedle patches, as well as their combination with regional delivery to the colon. This review critically examines four selected promising oral peptide technologies at preclinical stage and the twelve that have progressed to clinical trials, as indicated in www.clinicaltrials.gov. We examined these technologies under the criteria of peptide selection, formulation design, system components and excipients, intestinal mechanism of action, efficacy in man, and safety issues. The conclusion is that most of the technologies in clinical trials are incremental rather than paradigm-shifting and that even the more clinically advanced oral peptide drugs examples of oral bioavailability appear to yield oral bioavailability values of only 1-2% and are, therefore, only currently suitable for a limited range of peptides. (C) 2016 Elsevier B.V. All rights reserved.
机译:允许将治疗性肽吸收到全身循环的口服剂型的开发是制药工业的最大挑战之一。当前,包括渗透促进剂或蛋白酶抑制剂的混合物和/或基于纳米技术的产品在内的许多技术正在临床开发中。通常,这些制剂以肠溶片或胶囊形式存在。正在进行临床前研究的系统包括纳米技术的进一步发展,包括肠道微针贴片以及它们与向结肠的局部递送的结合。如www.clinicaltrials.gov所示,该综述对临床前阶段选定的四种有前途的口服肽技术以及已进行到临床试验的十二种进行了严格审查。我们在肽选择,制剂设计,系统组成和赋形剂,肠道作用机理,对人体的功效以及安全性等标准下检查了这些技术。结论是,临床试验中的大多数技术都是渐进式的,而不是范式转换,即使是临床上更先进的口服肽类药物,口服生物利用度的实例似乎也只能产生1-2%的口服生物利用度,因此,目前适用于有限范围的肽。 (C)2016 Elsevier B.V.保留所有权利。

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