Trial reportDiabetes technology & therapeutics2026
Inhaled Technosphere Insulin Reduces Postmeal Glucose Excursion in Youth Living with Type 1 Diabetes.
Trial report in Diabetes technology & therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- AFREZZAPaediatric drugs · 2026Review
Corrections and comments
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Authors and funding
10 authors.
Funding
Abstract
objectiveTo assess postprandial glucose excursions following a meal bolus of inhaled technosphere insulin (TI) in youth with type 1 diabetes.
methodsAs part of a multicenter randomized controlled trial, 217 youth 4-17 years old with type 1 diabetes using multiple daily injections (MDI) completed an in-clinic standardized meal challenge with their first TI dose. Glucose levels were monitored for 2 h. Outcomes were compared with outcomes in MDI-using adults with T1D who received a TI (
resultsFollowing TI inhalation, the glucose excursion and glycemic metrics were similar in the pediatric cohort to those of the adult TI cohort. In contrast, compared with the adult RAA cohort, the pediatric TI cohort had a smaller glucose excursion (
conclusionsIn children with type 1 diabetes, the postmeal glucose excursion following a TI bolus was similar to the postmeal glucose excursion that occurs with TI in adults and significantly lower than the excursion that has been observed with RAA in adults. These findings are consistent with the known pharmacokinetic profile of TI.
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