Geneva, Sept. 21 -- International Clinical Trials Registry received information related to the study (ChiCTR2600131571) titled 'A single-center, open-label, dose-escalation, single-dose phase I clinical trial to evaluate the pharmacokinetic/pharmacodynamic (PK/PD) characteristics of NovoPhase(R) in healthy Chinese male participants' on Sept. 4.
Study Type: Interventional study
Study Design:
Single arm
Primary Sponsor: West China Hospital of Sichuan University
Condition:
None
Intervention:
Group3:Dose: 3.50 U/kg (NovoRapid?/NovoLogix?) as a single subcutaneous abdominal injection.
Group2:Dose: 2.80 U/kg (NovoRapid?/NovoLogix?) as a single subcutaneous abdominal injection.
Recruitment Status: Not Recruiting
Phase: 1
Date of Fir...