drugset / Trial / NCT06492226

Study to Demonstrate Pharmacokinetic and Pharmacodynamic Similarity Between NKF-INS(A), US-NovoLog®, and EU-NovoRapid®

NCT06492226 ↗

Phase 1 Completed 54 enrolled Xentria, Inc.
RandomizedCrossoverDouble-blindOther

Summary

Single-dose, double-blind, randomized, three-period, three-treatment, six-sequence, crossover study to demonstrate pharmacokinetic and pharmacodynamic similarity between NKF-INS(A), US-NovoLog®, and EU-NovoRapid®

Timeline

Start
2024-07-30
Primary completion
2024-10-31
Completion
2024-10-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator EU-NovoRapid® Unknown 0.3 iu/kg Subcutaneous
Subject NKF-INS(A) Unknown 0.3 iu/kg Subcutaneous
Comparator US-NovoLog® Unknown 0.3 iu/kg Subcutaneous

Indications

No indication recorded.