drugset / Trial / NCT05184868

AT247, NovoLog® and Fiasp® Administered Via Continuous Subcutaneous Infusion in Glucose Clamp Study

NCT05184868

Phase 1 Completed 24 enrolled Arecor Limited
RandomizedCrossoverQuadruple-blindTreatment

Summary

Phase 1 randomized, double-blind, three period, crossover study comparing the pharmacodynamic, pharmacokinetic, safety and tolerability profiles for Arecor ultra-rapid insulin aspart (AT247), NovoLog® and Fiasp® in participants with type 1 diabetes mellitus (T1DM) during continuous subcutaneous infusion (CSII)

Timeline

Start
2022-01-03
Primary completion
2022-09-09
Completion
2022-09-09

Drugs

EvaluationDrugModalityDoseRoute
Subject AT247 Protein / enzyme biologic 0.02 iu/kg Subcutaneous
Subject AT247 Protein / enzyme biologic 0.15 iu/kg Subcutaneous
Subject insulin aspart Protein / enzyme biologic 0.02 iu/kg Subcutaneous
Subject insulin aspart Protein / enzyme biologic 0.15 iu/kg Subcutaneous