| Literature DB >> 33356257 |
Thomas B Kjeldsen1, František Hubálek1, Tina M Tagmose1, Lone Pridal2, Hanne H F Refsgaard2, Trine Porsgaard2, Sanne Gram-Nielsen2, Lars Hovgaard1, Henrik Valore3, Martin Münzel1, Claudia U Hjørringgaard1, Claus Bekker Jeppesen2, Valentina Manfè2, Thomas Hoeg-Jensen1, Svend Ludvigsen1, Peter Kresten Nielsen1, Inger Lautrup-Larsen1, Carsten E Stidsen2, Erik M Wulff2, Patrick W Garibay1, János T Kodra1, Erica Nishimura2, Peter Madsen1.
Abstract
Recently, the first basal oral insulin (OI338) was shown to provide similar treatment outcomes to insulin glargine in a phase 2a clinical trial. Here, we report the engineering of a novel class of basal oral insulin analogues of which OI338, 10, in this publication, was successfully tested in the phase 2a clinical trial. We found that the introduction of two insulin substitutions, A14E and B25H, was needed to provide increased stability toward proteolysis. Ultralong pharmacokinetic profiles were obtained by attaching an albumin-binding side chain derived from octadecanedioic (C18) or icosanedioic acid (C20) to the lysine in position B29. Crucial for obtaining the ultralong PK profile was also a significant reduction of insulin receptor affinity. Oral bioavailability in dogs indicated that C18-based analogues were superior to C20-based analogues. These studies led to the identification of the two clinical candidates OI338 and OI320 (10 and 24, respectively).Entities:
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Year: 2020 PMID: 33356257 DOI: 10.1021/acs.jmedchem.0c01576
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446