Investigation on Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Doses of a Long-acting GLP-1 Analogue in Healthy Male Subjects and Male Subjects With Type 2 Diabetes

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Novo Nordisk A/S
ClinicalTrials.gov Identifier:
NCT01686945
First received: September 13, 2012
Last updated: April 15, 2013
Last verified: April 2013

September 13, 2012
April 15, 2013
September 2012
April 2013   (final data collection date for primary outcome measure)
Number of treatment emergent adverse events (TEAEs) recorded [ Time Frame: From the time of first dosing and until completion of the post treatment follow-up visits (Day 90 to 104) ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01686945 on ClinicalTrials.gov Archive Site
  • Area under the plasma concentration curve over the dosing interval (0-24 hours) [ Time Frame: After the last 3 daily doses for semaglutide and carrier ] [ Designated as safety issue: No ]
  • Change from baseline in fasting plasma glucose (FPG) [ Time Frame: Week 0, week 10 (Day 69) ] [ Designated as safety issue: No ]
  • Change from baseline in C-peptide [ Time Frame: Week 0, week 10 (Day 69) ] [ Designated as safety issue: No ]
  • Change from baseline in insulin [ Time Frame: Week 0, week 10 (Day 69) ] [ Designated as safety issue: No ]
  • Change from baseline in glucagon [ Time Frame: Week 0, week 10 (Day 69) ] [ Designated as safety issue: No ]
  • Change from baseline in glycosylated haemoglobin type A1c (HbA1c) [ Time Frame: Week 0, week 10 (Day 69) ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Investigation on Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Doses of a Long-acting GLP-1 Analogue in Healthy Male Subjects and Male Subjects With Type 2 Diabetes
Investigation on Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Doses of a Long-acting GLP-1 Analogue in Healthy Male Subjects and Male Subjects With Type 2 Diabetes

This trial is conducted in Europe. The aim of the trial is to investigate safety, tolerability, pharmacokinetics (the exposure of the trial drug in the body), and pharmacodynamics (the effect of the investigated drug on the body) of multiple doses of a long-acting GLP-1 analogue (oral semaglutide) and a carrier in healthy male subjects and male subjects with type 2 diabetes (T2D).

Not Provided
Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
  • Diabetes
  • Diabetes Mellitus, Type 2
  • Healthy
  • Drug: semaglutide
    Start doses of 5 mg and 10 mg with end dose of 20 mg. For oral administration.
  • Drug: semaglutide
    Start doses of 5 mg and 10 mg with end doses of either 20 mg or 40 mg. For oral administration.
  • Drug: semaglutide
    Start doses of 5 mg and 10 mg with end doses of either 20 mg, 40 mg or 60 mg. For oral administration.
  • Drug: placebo
    Placebo semaglutide. For oral administration.
  • Drug: placebo
    Placebo semaglutide with carrier. For oral administration.
  • Experimental: Healthy - 20 mg
    Interventions:
    • Drug: semaglutide
    • Drug: placebo
    • Drug: placebo
  • Experimental: Healthy - 40 mg
    Interventions:
    • Drug: semaglutide
    • Drug: placebo
    • Drug: placebo
  • Experimental: Healthy - 60 mg
    Interventions:
    • Drug: semaglutide
    • Drug: placebo
    • Drug: placebo
  • Experimental: T2D - 20/40/60 mg
    Interventions:
    • Drug: semaglutide
    • Drug: placebo
    • Drug: placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
107
April 2013
April 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male subject, who is considered to be generally healthy, based on the medical history, physical examination, and the results of vital signs, electrocardiogram (ECG) and laboratory safety tests performed during the screening visit, as judged by the investigator. This also applies to subjects with T2D, except for the underlying diabetes with or without associated hyperlipidaemia and/or hypertension
  • Body mass index (BMI): a) Healthy subjects: above or equal to 20 and below 30 kg/m^2. b) Subjects with T2D: BMI above or equal to 20 and below or equal to 37 kg/m^2
  • Glycosylated haemoglobin (HbA1c): a) Healthy subjects: below 6.0%. b) Subjects with T2D: between 6.5 and 9.0% (both inclusive)
  • Additional inclusion criterion only for subjects with T2D: Male subjects with T2D (diagnosed within the past 10 years) treated with diet and exercise and/or who have been on stable doses of metformin for at least 12 weeks prior to Visit 3 (Day -1 or 0) and for whom no changes in treatment are planned for the trial period

Exclusion Criteria:

  • History of, or presence of, cancer, diabetes (only for healthy subjects) or any clinically significant cardiovascular (only for healthy subjects), respiratory, metabolic, renal, hepatic, gastro-intestinal (GI), endocrinological (except diabetes in subjects with T2D), haematological, dermatological, venereal, neurological, psychiatric diseases or other major disorders, as judged by the investigator
  • Blood pressure in supine position at the screening examination above: a) 140 mmHg systolic and/or above 90 mmHg diastolic for healthy subjects. b) 160 mmHg systolic and/or above 95 mmHg diastolic for subjects with T2D
  • Use of prescription or non-prescription medicinal products (except routine vitamins) within three weeks preceding the dosing. Occasional use of paracetamol or acetylsalicylic acid is permitted. a. For subjects with T2D: Any other current diabetes treatment apart from metformin (e.g. treatment with incretin mimetics, Dipeptidyl Peptidase-IV (DPP-IV) inhibitors, insulin secretagogues, insulin or thiazolidinediones (TZDs)). Use of blood lipidregulating agents, as well as blood pressure regulating, and thrombo-embolic agents is allowed
  • Exclusion criteria only for subjects with T2D:
  • Proliferative retinopathy or maculopathy requiring acute treatment as determined by funduscopy/fundus photography and judged by the investigator. If subject presents a medical certificate for funduscopy/fundus photography performed within last 3 months this can substitute the funduscopy/fundus photography at screening
  • Nephropathy stages 3 to 5, i.e. estimated glomerular filtration rate (eGFR) below 60. The eGFRshould be determined using the Modification of Diet in Renal Disease 4-variable method encompassing creatinine, age, gender, and race
  • Diabetic peripheral neuropathy using the 10 g Semmes-Weinstein monofilament examination at the great toe or plantar aspect of the fifth metatarsal
  • Clinically significant active cardiovascular disease including history of myocardial infarction and/or heart failure (New York Heart Association (NYHA) class III and IV1) at the discretion of the investigator
Male
18 Years to 64 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT01686945
NN9924-3991, 2012-000361-20, U1111-1127-4408
No
Novo Nordisk A/S
Novo Nordisk A/S
Not Provided
Study Director: Charlotte Granhall Novo Nordisk A/S
Novo Nordisk A/S
April 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP