Overview
A Research Study to Look at How Insulin 287 and Semaglutide Work in the Body of People With Type 2 Diabetes When Taken Alone or Together
Status:
Completed
Completed
Trial end date:
2019-10-10
2019-10-10
Target enrollment:
0
0
Participant gender:
All
All
Summary
The study will look at how insulin 287 and semaglutide work in the body, both when given alone or together. This study will look at the way insulin 287 and semaglutide reach and stay in participants' blood after injection when given alone or together. Participants will get 3 study medicines at 3 different time points: 1) a combination of semaglutide plus insulin 287, 2) insulin 287 alone and 3) semaglutide alone. The order in which participants get them is decided by chance. Participants will get all medicines as an injection under the skin in the thigh. The injections will be done by study staff. The time between injections is 6 to 9 weeks. The study will last for about 19 to 32 weeks in total.Phase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Novo Nordisk A/STreatments:
Insulin
Insulin, Globin Zinc
Criteria
Inclusion Criteria:- Male or female, aged 18-64 years (both inclusive) at the time of signing informed
consent
- Diagnosed with type 2 diabetes mellitus more than or equal to 180 days prior to the
day of screening
- Body weight between 80.0 to 120.0 kg (both inclusive)
- Glycosylated haemoglobin (HbA1c) 6.0 to 8.5% (both inclusive)
- No current and no regular previous intake of insulin. Previous insulin treatment for
short periods of time (a maximum of 14 days) is allowed, as well as insulin use during
a previous period of gestational diabetes in the past (as declared by the subject or
reported in the medical records)
- Stable daily dose(s) of the following anti-diabetic drug(s)/regimen within the past 90
days prior to the day of screening: a) Any metformin formulation (dose as documented
in the subject medical record), b) One other oral antidiabetic drug (dose as
documented in the subject medical record) is allowed, but not mandatory: Insulin
secretagogue (sulphonylureas), dipeptidyl peptidase 4 (DPP-4) inhibitor and sodium
glucose co-transporter 2 (SGLT2) inhibitor
Exclusion Criteria:
- Known or suspected hypersensitivity to trial products or related products
- Female who is pregnant, breast-feeding or intends to become pregnant or is of
child-bearing potential and not using adequate contraceptive methods
- Recurrent severe hypoglycaemia (more than 1 severe hypoglycaemic event within the past
180 days) or hypoglycaemic unawareness as judged by the investigator or
hospitalisation for diabetic ketoacidosis within the past 180 days prior to the day of
screening
- Receipt of any investigational medicinal product within 90 days before screening
- History of severe allergies to drugs or foods or a history of severe anaphylactic
reaction