Skip to content

A Trial Investigating the Effect of NN1250 in Young and Elderly Subjects With Type 1 Diabetes

A Trial Investigating the Pharmacodynamic and Pharmacokinetic Properties of NN1250 in Young and Geriatric Subjects With Type 1 Diabetes

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00964418
Enrollment
27
Registered
2009-08-25
Start date
2009-08-31
Completion date
2009-11-30
Last updated
2017-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes, Diabetes Mellitus, Type 1

Brief summary

This trial is conducted in Europe. The aim of this clinical trial is to investigate the blood glucose lowering effect of NN1250 (insulin degludec) in young and elderly subjects with type 1 diabetes.

Interventions

DRUGinsulin degludec

0.4 U/kg body weight injected s.c. (subcutaneously) once daily for 6 days

DRUGinsulin glargine

0.4 U/kg body weight injected s.c. (subcutaneously) once daily for 6 days

Sponsors

Novo Nordisk A/S
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Male or female aged 18-35 years (both inclusive) (young group) or at least 65 years (geriatric group) * Type 1 diabetes mellitus (as diagnosed clinically) for at least 12 months * Body mass index 18.0-28.0 kg/m\^2 (both inclusive)

Exclusion criteria

* Subject who has donated any blood or plasma in the past month or more than 500 mL within 3 months prior to screening * 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

Design outcomes

Primary

MeasureTime frame
Area under the glucose infusion rate curve during one dosing interval at steady state (for NN1250)0-24 hours (derived on treatment day 6)

Secondary

MeasureTime frame
Area under the NN1250 concentration-time curve during one dosing interval at steady state0-24 hours (derived on treatment day 6)

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026