Completed

NNC 90-1170 Impact on Weight and Appetite in Obese Type 2 Diabetes Patients

Study Aim

This phase 2 study aims to evaluate the impact of NNC 90-1170 on weight change in obese individuals with type 2 diabetes.

What is being tested

liraglutide

+ placebo

Drug

Who is being recruted

Diabetes Mellitus+3

+ Diabetes Mellitus, Type 2

+ Endocrine System Diseases

Over 18 Years

+14 Eligibility Criteria

See all eligibility criteria

How is the trial designed

Treatment Study

Placebo-ControlledPhase 2

Interventional

Study Start: June 2001

See protocol details

Summary

Principal SponsorNovo Nordisk A/S

Last updated: January 28, 2026

Sourced from a government-validated database.Claim as a partner

Study start date: June 1, 2001

Actual date on which the first participant was enrolled.

This trial is conducted in Europe. The aim of the trial is to investigate the effect of NNC 90-1170 (liraglutide) on weight and appetite in obese subjects with type 2 diabetes treated with diet and/or sulphonylurea or repaglinide.

Official TitleNNC 90-1170 Mechanism of Action: A Single-centre, Randomised, Double-blind, Parallel-group, Placebo-controlled Trial Evaluating the Effect of NNC 90-1170 on Weight and Appetite in Obese Subjects With Type 2 Diabetes

NCT01508949

Principal SponsorNovo Nordisk A/S

Last updated: January 28, 2026

Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

35 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.

Conditions

Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Diabetes MellitusDiabetes Mellitus, Type 2Endocrine System DiseasesMetabolic DiseasesNutritional and Metabolic DiseasesGlucose Metabolism Disorders

Criteria

7 inclusion criteria required to participate

Type 2 diabetes mellitus

Diet treated and/or subjects in monotherapy with sulphonylurea or repaglinide

HbA1c for diet treated subjects 6.5-12%, both inclusive

HbA1c for sulphonylurea or repaglinide treated subjects maximum 10%

Show More Criteria

7 exclusion criteria prevent from participating

Impaired liver function

Impaired renal function

Cardiac problems

Uncontrolled treated/untreated hypertension

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.

Treatment Groups

Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Experimental

Group II

Placebo

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Novo Nordisk Investigational Site

Frederiksberg C, DenmarkOpen Novo Nordisk Investigational Site in Google Maps

CompletedOne Study Center