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Clinical Trial Details

Trial ID: L6641
Source ID: NCT01538511
Associated Drug: Biphasic Insulin Aspart 70
Title: Insulin Profile of Biphasic Insulin Aspart 70 to That of Biphasic Insulin Aspart 30 in Healthy Volunteers
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Diabetes|Diabetes Mellitus, Type 2
Interventions: DRUG: biphasic insulin aspart 70|DRUG: biphasic insulin aspart 30
Outcome Measures: Primary: Area under the plasma insulin concentration curve from 0 to 24 hours | Secondary: Area under the concentration curve of plasma insulin from 0 to 4 hours after meals|Maximum plasma insulin concentration observed from 0 to 4 hours after meals|Time to reach the maximum plasma insulin concentration from 0 to 4 hours after meals|The 24-hour plasma insulin profile deviances in Japanese type 2 diabetic subjects|Pre-meal plasma glucose concentration before meals|Postprandial plasma glucose (PPPG) excursion from 0 to 4 hours after meals|The maximum plasma glucose concentration observed from 0 to 4 hours after meals|The time to reach the maximum plasma glucose concentration of observed from 0 to 4 hours after meals|Average of plasma glucose concentration from 0 to 24 hours|The area under the plasma C-peptide concentration curve from 0 to 24 hours derived from the 24-hour plasma C-peptide profile|Frequency of hypoglycaemic episodes|Frequency of adverse events
Sponsor/Collaborators: Sponsor: Novo Nordisk A/S
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 59
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2006-06-05
Completion Date: 2007-03-13
Results First Posted:
Last Update Posted: 2017-10-06
Locations: Novo Nordisk Investigational Site, Tokyo, 1000005, Japan
URL: https://clinicaltrials.gov/show/NCT01538511