Overview
Effect of Liraglutide on Pulsatile Insulin Secretion in Subjects With Type 2 Diabetes
Status:
Completed
Completed
Trial end date:
1999-12-01
1999-12-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This trial is conducted in Europe. The aim of this trial is to assess the effect of NNC 90-1170 (liraglutide) on pulsatile insulin secretion and insulin secretion after a standard meal in subjects with type 2 diabetes.Phase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Novo Nordisk A/STreatments:
Liraglutide
Criteria
Inclusion Criteria:- Diagnosed with type 2 diabetes, either newly diagnosed with at least two months of
diet treatment, or in current OHA (oral hypoglycaemic agent) treatment with stable
dose for at least six months
- BMI (Body Mass Index) between 24 and 35 kg/m^2 (both inclusive)
- Fasting plasma glucose between 6 and 15 mmol/l (both inclusive)
- Anti-GAD (glutamic acid decarboxylase) negative
Exclusion Criteria:
- Known or suspected allergy to trial product or related products
- Receipt of any investigational drug within three months prior to this trial
- Recurrent severe hypoglycaemia as judged by the investigator
- Cardiac disease or any clinically significant abnormal ECG (electrocardiogram)
- Use of any drug (except oral hypoglycaemic agents (OHAs)) which in the investigator's
opinion could interfere
- with the blood glucose level (i.e., insulin, systemic corticosteroids, thiazides)
- Liver or renal disease