Diabetes Mellitus, Type 1
Conditions
Brief summary
This study is designed to investigate the movement of insulin NNC0363-0845 throughout the body and how it works for the treatment of type 1 diabetes mellitus. The aim of the study is to improve clinical outcomes for patients with type 1 diabetes mellitus by better controlling the blood sugar levels. Participants will get insulin NNC0363-0845 as well as insulin detemir (Levemir®). NNC0363-0845 is a new insulin molecule designed to provide blood sugar-dependent insulin action, while insulin detemir is commonly used and prescribed by doctors. Participants will get subcutaneous (under your skin) injections of insulin NNC0363-0845 (study medicine) up to 6 times daily for 3 days, and of insulin detemir up to 6 times daily for another 3 days. Which medication participants receive first and which second, insulin NNC0363-0845 or insulin detemir, is decided by chance. The study will last for about 6 weeks up to a maximum of 14 weeks. Participants will have 2 in-house visits (where participants will stay at the site for 4 nights) and 5 outpatient visits with the study doctor. Participants will have frequent contact with the study doctor during the study. During the in-house visits, two intravenous catheters (a thin tube inserted into a vein) will be inserted for blood sampling and infusions. Interested parties may not participate in the study if the study doctor believes it will affect their health negatively. Women cannot take part if they are of childbearing potential.
Interventions
DRUGNNC0363-0845
Participants will receive 0.5 nmol/kg NNC0363-0845 s.c. (subcutaneous - under the skin) every 4 hours up to 6 times daily (i.e. 3 nmol/kg/day) for 3 days The study will last for about 6 weeks up to a maximum of 14 weeks
DRUGInsulin detemir
Participants will receive 0.083 U/kg insulin detemir s.c. (subcutaneous - under the skin) every 4 hours up to 6 times daily (i.e. 0.5 U/kg/day) for 3 days The study will last for about 6 weeks up to a maximum of 14 weeks
Sponsors
Novo Nordisk A/S
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No
Inclusion criteria
Key inclusion criteria: * Male participant or female participant of non-childbearing potential. Non-child-bearing potential being defined as surgically sterilised (i.e. documented hysterectomy, bilateral salpingectomy or bilateral oophorectomy) or being postmenopausal (defined as no menses for 12 months without an alternative medical cause) prior to the day of screening. * Aged 18-64 years (both inclusive) at the time of signing informed consent. * Diagnosed with type 1 diabetes mellitus 1 year or more before screening. * Current daily basal insulin treatment greater than 0.2 and below or equal to 0.5 (I)U/kg/day. * Current total daily insulin treatment between 0.4 and 0.8 (I)U/kg/day (both inclusive). * Body mass index between 18.5-29.9 kg/m\^2 (both inclusive). * HbA1c (glycated haemoglobin) below or equal to 8.0%. Key
Exclusion criteria
* Male of reproductive age who, or whose female partner(s), is not using an adequate contraceptive method (adequate contraceptive measures as required by local regulation or practice). Adequate contraceptive measures include that the male participant uses a condom during intercourse and that the partner practices adequate contraception (risk of pregnancy must be lower than 1%). In addition, participants must not donate sperm for the duration of the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| AUCPG,0.5-2h Area under the plasma glucose-time curve at steady concentrations | From 0.5 to 2 hours after initiation of meal glucose appearance test (visit 4 day 3 and visit 5 day 3) | messured in h\*mmol/L |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| AUCPG,0-2hArea under the plasma glucose-time curve at steady concentrations | From 0 to 2 hours after initiation of meal glucose appearance test (visit 4 day 3 and visit 5 day 3) | messured in h\*mmol/L |
| AUCPG,0-4h Area under the plasma glucose-time curve at steady concentrations | From 0 to 4 hours after initiation of meal glucose appearance test (visit 4 day 3 and visit 5 day 3) | messured in h\*mmol/L |
| AUCPG,0-1h Area under the plasma glucose-time curve at steady concentrations | From 0 to 1 hour after initiation of meal glucose appearance test (visit 4 day 3 and visit 5 day 3) | messured in h\*mmol/L |
| ∆PGav,0-2h Mean change in plasma glucose at steady concentrations | From 0 to 2 hours after initiation of meal glucose appearance test (visit 4 day 3 and visit 5 day 3) | messured in mmol/L |
| Number of adverse events | From first IMP administration until 16 hours after last IMP administration (visit 4 day 3 and visit 5 day 3) | Number of events |
| ∆PGav,0-1h Mean change in plasma glucose at steady concentrations | From 0 to 1 hour after initiation of meal glucose appearance test (visit 4 day 3 and visit 5 day 3) | messured in mmol/L |
Countries
Austria
Outcome results
None listed