Pharmacokinetics of Insulin Detemir in Healthy Volunteers From Taiwan
NCT ID: NCT01497587
Last Updated: 2017-01-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
20 participants
INTERVENTIONAL
2005-08-31
2005-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Insulin detemir
insulin detemir
Single dose, 0.5 U/kg, administered s.c. (under the skin)
Interventions
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insulin detemir
Single dose, 0.5 U/kg, administered s.c. (under the skin)
Eligibility Criteria
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Inclusion Criteria
* Body mass index (BMI) between 18 and 27 kg/m\^2, inclusive
* Fasting plasma glucose maximum 6.1 mmol/l
* Non-smoker or smoking maximum 5 cigarettes per day or the equivalent
Exclusion Criteria
* Subject with a history of alcohol or drug dependence
* Subject with a first-degree relative with diabetes mellitus
18 Years
55 Years
MALE
No
Sponsors
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Novo Nordisk A/S
INDUSTRY
Responsible Party
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Principal Investigators
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Global Clinical Registry (GCR, 1452)
Role: STUDY_DIRECTOR
Novo Nordisk A/S
Locations
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Novo Nordisk Investigational Site
Taipei, , Taiwan
Countries
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References
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Kwok C-F, Tsai T-H, Lim S-H, Vaz J, Ho L-T. The Pharmacokinetic Profile of Insulin Detemir in Healthy Male Taiwanese and Caucasian Subjects. ASEAN Federation of Endocrine Societies (AFES); Country: Malaysia City: Kuala Lumpur
Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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NN304-3023
Identifier Type: -
Identifier Source: org_study_id
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