The fourth controlled release society workshop on oral peptide administration.

IF 4.4
Frontiers in drug delivery Pub Date : 2026-06-01 eCollection Date: 2026-01-01 DOI:10.3389/fddev.2026.1860678
David J Brayden, Stephen T Buckley, Andrew L Lewis
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引用次数: 0

Abstract

The Controlled Release Society (CRS, www.controlledrelease.org) held its fourth iteration of research and development in oral peptide administration on 14 July 2025 in Philadelphia (United States), entitled "Recent advances in oral peptide delivery: from molecule to market." The previous versions were held in 2008, 2014, and 2023 (online), so it is a topic of continuing interest to drug delivery scientists as several oral peptide products have been released in the market over the period despite the enormous technical and commercial challenges involved. The workshop was co-sponsored by Frontiers in Drug Delivery, Novo Nordisk, Johnson and Johnson, Merck, Protagonist Therapeutics, Quotient Sciences, Genentech (Roche), and Bristol-Myers Squibb. It consisted of nine talks and two roundtable sessions. The overall aim of the workshop was to provide an update on the current clinical oral peptide programmes, address mechanistic progress on permeation enhancers, and evaluate the limitations of preclinical bioassays and animal models.

第四届控释学会口服肽类药物研讨会。
控制释放学会(CRS, www.controlledrelease.org)于2025年7月14日在费城(美国)举行了口服肽给药的第四次研究和开发,题为“口服肽给药的最新进展:从分子到市场”。之前的版本分别于2008年、2014年和2023年(在线)举行,因此这是药物输送科学家持续感兴趣的话题,因为在此期间,尽管存在巨大的技术和商业挑战,但仍有几种口服肽产品在市场上发布。该研讨会由药物输送前沿、诺和诺德、强生、默克、主角治疗、商科、基因泰克(罗氏)和百时美施贵宝共同主办。会议包括九场会谈和两场圆桌会议。研讨会的总体目标是提供当前临床口服肽方案的最新进展,解决渗透增强剂的机制进展,并评估临床前生物测定和动物模型的局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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