Ultra rapid lispro shows faster pharmacokinetics and reduces postprandial glucose excursions vs Humalog in patients with type 2 diabetes mellitus in a randomized, controlled cross‐over meal test early phase study
Diabetes, Obesity and Metabolism Oct 07, 2021
Leohr J, Kazda C, Liu R, et al. - According to this 2-part, randomized, double-blind Phase 1b study, when compared with Humalog, ultra rapid lispro (URLi) demonstrated accelerated insulin lispro absorption and greater postprandial glucose reduction at different meal-to-dose timings, and it was well tolerated in patients with type 2 diabetes mellitus (T2D).
When compared with Humalog, URLi increased insulin exposure within the first 30 minutes postdose by 2.2-fold and decreased time to early half-maximal drug concentration by 22.6%.
When taken before, immediately before, or after a meal, URLi resulted in better postprandial glucose lowering.
When the same meal-to-dose timing was used for both insulins, the postprandial glucose excursion over 5 hours was reduced by 29-105% with URLi for all three dose timings (-15 minutes, 0 minutes, and +15 minutes).
In patients with T2D, the pharmacokinetics and glucodynamics were maintained after 2 weeks of daily subcutaneous dosing.
During the mixed meal tolerance tests, URLi had more hypoglycemic events; both treatments had few events during the 2-week outpatient dosing period.
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