drugset / Trial / NCT07600944

Comparison of the Pharmacokinetics (PK)and Pharmacodynamics (PD)Biosimilarity of Insulin Aspart Injections After Single-Dose Subcutaneous Administration to Healthy Volunteers

NCT07600944

Recruiting 44 enrolled Zhuhai United Laboratories Co., Ltd.
RandomizedCrossoverTriple-blindHealth-services research

Summary

The present study is designed to compare the pharmacokinetic, pharmacodynamic and safety characteristics of UBLIN® (test product) and NovoRapid® (reference product) in healthy male participants. The treatment consists of one single dose of the test or reference product, administered during each of the two study periods, separated by 7 days between dosing. A total of 44 participants will be enrolled in this trial and randomized in a 1:1 ratio into two groups (A/B), stratified by race (Asian, non-Asian).

Timeline

Start
2026-05-06
Primary completion
2026-08-10
Completion
2026-08-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator insulin aspart Protein / enzyme biologic 0.2 iu/kg Subcutaneous

Indications

No indication recorded.