Overview

Effect of Liraglutide on Glucose Profiles and Gastric Emptying in Subjects With Type 2 Diabetes

Status:
Completed
Trial end date:
2002-02-01
Target enrollment:
0
Participant gender:
All
Summary
This trial is conducted in Europe. The aim of this trial is to determine the effect of NNC 90-1170 (liraglutide) on glucose and hormonal profiles, fasting gluconeogenesis and insulin secretion in subjects with type 2 diabetes.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Novo Nordisk A/S
Treatments:
Liraglutide
Criteria
Inclusion Criteria:

- Type 2 diabetes mellitus

- Diet treated and/or subjects in monotherapy with max. 50 % of maximal dose of
sulphonylurea (SU). In addition, subjects in treatment with metformin and/or
repaglinide could be included

- Body Mass Index (BMI) maximum 35 kg/m^2

- Fasting plasma glucose 7-15 mmol/l, both inclusive

Exclusion Criteria:

- Impaired liver function

- Impaired renal function

- Anaemia

- Cardiac disease

- Uncontrolled treated/untreated hypertension

- Recurrent major hypoglycaemia as judged by the Investigator

- Known or suspected allergy to trial product or related products

- Females of child bearing potential who are pregnant, breast-feeding or have intention
of becoming pregnant or are not using adequate contraceptive measures

- Current treatment with thiazolidinediones or chronic daily use of insulin (more than 7
days) within three months in the absence of intercurrent illness

- Loss of more than 400 ml blood during the three months prior to study start

- Allergy to paracetamol