Overview

Effect of Liraglutide on Pulsatile Insulin Secretion in Subjects With Type 2 Diabetes

Status:
Completed
Trial end date:
1999-12-01
Target enrollment:
0
Participant gender:
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 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Novo Nordisk A/S
Treatments:
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