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Completed

NCT Number: NCT02212067

A Trial Investigating the Effects of Semaglutide on ß-cell Function in Subjects With Type 2 Diabetes

This trial is conducted in Europe. The aim of the trial is to investigate the effects of semaglutide on ß-cell function in subjects with type 2 diabetes.

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Key information

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Novo Nordisk Investigational Site

Neuss, 41460, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 18-64 years (both inclusive) at the time of signing the informed consent
  • For subjects with type 2 diabetes:
  • Male and female subjects diagnosed with type 2 diabetes
  • Treated with diet and exercise and/or metformin monotherapy. Metformin dose should be unchanged in a period of 30 days prior to screening
  • Body Mass Index (BMI) between 20.0-35.0 kg/m^2 (both inclusive)
  • Glycosylated haemoglobin (HbA1c) between 6.5-9.0 % (both inclusive)
  • For healthy control group for graded glucose infusion:
  • Healthy male and female subjects
  • BMI between 24.0-32.0 kg/m^2 (both inclusive)
  • HbA1c less than 6.5 %

Exclusion criteria

  • Female who is pregnant, breast-feeding or intends to become pregnant or is of child bearing potential and not using an adequate contraceptive method. Women of child bearing potential must use an effective method of birth control for the duration of the trial and for subjects with type 2 diabetes for 5 weeks following the last dose of semaglutide. Only highly effective methods of birth control are accepted (i.e. one that results in less than 1% per year failure rate when used consistently and correctly such as implants, injectables, combined oral contraceptives, some intrauterine devices), or sexual abstinence or vasectomised partner
  • Any clinically significant disease history, in the opinion of the investigator, or systemic or organ disease including: cardiac, pulmonary, gastrointestinal, hepatic, neurologic, renal, genitourinary and endocrine, dermatologic or hematologic
  • Use of any prescription or non-prescription medication which could interfere with trial pharmacokinetic or pharmacodynamic results, as judged by the investigator or specifically: a) current treatment with systemic (oral or i.v.) corticosteroids, non-selective betablockers, b) thyroid hormones are not allowed unless the use of these have been stable during the past 2 month prior to screening
  • History of drug/chemical substance abuse within 1 year prior to screening, or a positive result in the urine drug test
  • History of alcohol abuse within 1 year prior to screening, or a positive result in the alcohol breath test
  • Smoker (defined as a subject who is smoking more than 5 cigarettes or the equivalent per day)
  • Not able or willing to refrain from smoking and use of nicotine gum or transdermal nicotine patches during the inpatient period

Treatment and study plan

semaglutide

Drug

Administered subcutaneously (s.c., under the skin) once weekly for 12 weeks.

Placebo

Drug

Administered subcutaneously (s.c., under the skin) once weekly for 12 weeks.

Primary outcomes

  1. Area under the serum insulin concentration time curve from 0 to 10 minutes after a 25 g glucose bolus i.v. infusion (IVGTT,intravenous glucose tolerance test) over 2 minutes

    Time frame: Day -1, day 86

  2. Area under the serum insulin concentration time curve from 10-120 minutes after a 25 g glucose bolus i.v. infusion (IVGTT).

    Time frame: Day -1, day 86

Secondary outcomes

  1. Area under the insulin secretion rate (ISR)-time curve within 0 to 10 min after i.v. glucose challenge

    Time frame: Day -1, day 86

  2. Area under the ISR-time curve within 10 to 120 min after i.v. glucose challenge

    Time frame: Day -1, day 86

  3. 24-hour plasma glucose, glucagon, serum insulin, and C-peptide measured as total AUC0-24h during a test day with 3 standardised meals

    Time frame: Day -1, day 85

  4. Area under the insulin secretion rate (ISR)-time curve within 0 to 10 min after i.v. arginine application; ISR will be derived from the C-peptide concentration profile

    Time frame: Day -1, day 86

  5. Area under the ISR curve over the 5-12 mmol/L (90-216 mg/dL) glucose interval; ISR will be derived from the C-peptide concentration profile

    Time frame: Day -1, day 87

  6. Slope of the ISR vs. glucose curve (dose-response relationship)

    Time frame: Day -1, day 87

Sponsors and collaborators

Lead sponsor

Novo Nordisk A/S

Industry

Registry information

Official study title

A Single-centre, Randomised, Double-blind, Multiple-dose, Placebo-controlled, Parallel-group Trial Investigating the Effects of Semaglutide on ß-cell Function in Subjects With Type 2 Diabetes

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Aug 8, 2014
Registry last updated
Mar 7, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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