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Comparison of Explorative Formulation of Insulin Degludec and Insulin Aspart Co-formulation Versus Explorative Formulation of Insulin Degludec and Insulin Aspart Separately Compared With Biphasic Insulin Aspart 30 in Male Subjects With Diabetes

Information source: Novo Nordisk A/S
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Diabetes; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2

Intervention: insulin degludec/insulin aspart 30 (Drug); insulin degludec/insulin aspart 40 (Drug); insulin degludec/insulin aspart 50 (Drug); insulin degludec (Drug); insulin aspart (Drug); biphasic insulin aspart 30 (Drug); insulin degludec/insulin aspart 40 (Drug); insulin degludec/insulin aspart 50 (Drug); biphasic insulin aspart 30 (Drug)

Phase: Phase 1

Status: Completed

Sponsored by: Novo Nordisk A/S

Official(s) and/or principal investigator(s):
Hanne Haahr, Study Director, Affiliation: Novo Nordisk A/S

Summary

This trial is conducted in Europe. The aim of this trial is to compare different ratios of explorative formulations, not similar to the proposed commercial formulation, of IDegAsp (co-formulation of insulin degludec/insulin aspart and insulin aspart) with separately injected, simultaneous doses of insulin degludec (insulin 454), and insulin aspart, compared with biphasic insulin aspart 30 in male subjects with type 1 and type 2 diabetes mellitus. Trial part 1 is a five-period cross-over trial with incomplete block-design in subjects with type 1 diabetes where each subject will be randomised to five out of the ten possible treatments. Each treatment consists of an injection of the insulin product followed by a euglycemic clamp with a washout period of 7-15 days between treatments. Trial part 2 is a three-period cross-over trial with complete blockdesign in subjects with type 2 diabetes. Each treatment consists of an injection of the insulin product followed by a euglycaemic clamp with a washout period of 7-15 days between treatments.

Clinical Details

Official title: A Randomised, Double-blind, Multiple Period Crossover Trial Comparing Insulin 454 and Insulin Aspart Premixes With Separately Injected, Simultaneous Doses of Insulin 454 and Insulin Aspart, Compared With Biphasic Insulin Aspart 30 (NovoMix® 30) in Male Subjects With Type 1 and Type 2 Diabetes Mellitus

Study design: Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Primary outcome:

Area under the insulin aspart concentration curve from 0-2 hours (for subjects with type 1 diabetes)

Maximum glucose infusion rate divided by the average glucose infusion rate (for subjects with type 2 diabetes)

Secondary outcome:

Area under the glucose infusion rate curve

Area under the serum insulin degludec concentration curve

Eligibility

Minimum age: 18 Years. Maximum age: 69 Years. Gender(s): Male.

Criteria:

Inclusion Criteria:

- The subject will be a male volunteer, who is considered to be generally healthy,

except for underlying diabetes mellitus and concomitant medical complications (e. g. hypertension) based on an assessment of medical history, physical examination and clinical laboratory data, as judged by the Investigator

- Glycosylated haemoglobin A1c (HbA1c) below or equal to 10 % based on central

laboratory results

- ADDITIONAL INCLUSION CRITERA FOR SUBJECTS WITH TYPE 1 DIABETES:

- Diagnosed with type 1 diabetes mellitus and treated with insulin for at least 12

months

- Body Mass Index (BMI) between 18. 0 and 27. 0 kg/m^2 (both inclusive)

- ADDITIONAL INCLUSION CRITERA FOR SUBJECTS WITH TYPE 2 DIABETES:

- Diagnosed with type 2 diabetes mellitus for at least 12 months

- Treated with insulin for the last 3 months prior to screening.

- Body Mass Index (BMI) between 22. 0 and 35. 0 kg/m^2 (both inclusive)

Exclusion Criteria:

- A subject with a history of significant multiple drug allergies or with a known or

suspected allergy to the trial product or any medicine chemically related to the trial product, as judged by the Investigator

- A subject who has participated in any other trials involving investigational products

within the 3 months preceding the start of dosing

Locations and Contacts

Neuss 41460, Germany
Additional Information

Clinical Trials at Novo Nordisk

Starting date: September 2006
Last updated: May 27, 2013

Page last updated: August 23, 2015

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