Status:
COMPLETED
Safety and Tolerability of Liraglutide in Healthy Male Volunteers
Lead Sponsor:
Novo Nordisk A/S
Conditions:
Diabetes
Healthy
Eligibility:
MALE
18-45 years
Phase:
PHASE1
Brief Summary
This trial is conducted in Europe. The aim of this trial is to assess the safety and tolerability (maximum tolerated dose) after five ascending single doses of NNC 90-1170 (liraglutide).
Eligibility Criteria
Inclusion
- Male subjects of any ethnic origin
- Written informed consent obtained. (The subject must give signed informed consent before any trial-related activities. Trial-related activities are any procedures that would not have been performed during the normal management of the subject)
- Good general health based on medical history, physical and laboratory examinations, incl. ECG (electrocardiogram)
- Body mass index within the range 20-27 kg/m\^2, inclusive
Exclusion
- Any clinically significant abnormal laboratory test results or clinically significant abnormal ECG
- History of alcoholism or drug addiction; positive results in the plasma urine screens for illicit drug
- Alcohol intake within 48 hours of visit
- Hepatitis B surface antigen (HBsAg), Hepatitis C antibodies or HIV (human immunodeficiency virus) antibodies
- History of significant drug allergy or drug hypersensitivity
- Smoke 5 cigarettes or more, or the equivalent per day and is unable to refrain from smoking during the 3 days prior to the dosing day and during the confinement period
- Subjects who drink more than 8 cups of tea/coffee per day
Key Trial Info
Start Date :
March 1 1999
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 1999
Estimated Enrollment :
34 Patients enrolled
Trial Details
Trial ID
NCT01507272
Start Date
March 1 1999
End Date
December 1 1999
Last Update
January 24 2017
Active Locations (1)
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1
Novo Nordisk Investigational Site
Manchester, United Kingdom, M15 6SH