ULTRA RAPID LISPRO (URLI) IMPROVES POSTPRANDIAL GLUCOSE (PPG) CONTROL AND TIME IN RANGE (TIR) IN T1D COMPARED TO LISPRO: PRONTO-T1D CONTINUOUS GLUCOSE MONITORING (CGM) SUB-STUDY

Session Type
ORAL PRESENTATION SESSION
Date
20.02.2020, Thursday
Session Time
16:40 - 18:00
Channel
Berlin
Lecture Time
17:00 - 17:10
Presenter
  • Juliana Bue-valleskey, United States of America
Authors
  • Juliana Bue-valleskey, United States of America
  • Bruce Bode, United States of America
  • Maciej MaƂecki, Poland
  • Dachuang Cao, United States of America
  • Rong Liu, United States of America
  • Thomas Hardy, United States of America

Abstract

Background and Aims

URLi is a novel prandial insulin lispro formulation developed to more closely match physiological insulin secretion. URLi was efficacious with a similar safety profile to lispro in phase 3 studies. Ambulatory glucose profiles were evaluated in 269 (22%) patients (pts) in PRONTO-T1D assigned to double-blind URLi (n=97) or lispro (n=99) given at the start of the meal, or open-label URLi (n=73) given 20 min after the meal (URLi +20). Primary endpoint was incremental AUC0-2h (iAUC) after breakfast.

Methods

Blinded CGM (Dexcom G4 Platinum) was worn for 14 days before baseline and week 26.

Results

Pts reflected main study population: mean A1C at week 26 was 7.15% - URLi, 7.12% - lispro, 7.35% - URLi+20. Compared to lispro, URLi had significantly smaller breakfast iAUC0-2h with estimated treatment difference (ETD) -28.1 mg.h/dL, p=0.048; more daytime TIR (71-180 mg/dL) ETD +43.6 min, p=0.020; and similar nighttime TIR. Time <50 mg/dL and >180 mg/dL were both numerically lower with URLi in daytime, with less time <50 mg/dL at nighttime vs. lispro: 7.0 vs. 12.6 min, p=0.023. PPG control in pts who marked meal times improved with URLi compared to lispro and URLi +20 (Figure).

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Conclusions

When injected at the start of the meal, URLi resulted in significantly better PPG control and increased daytime TIR vs. lispro without increasing time in hypoglycemia. CGM results augment findings from PRONTO-T1D.

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