A Trial to Investigate Post Prandial Blood Glucose Control With Fast-acting Human Insulin HinsBet® Compared to Insulin Lispro (Humalog®) and Regular Human Insulin (Huminsulin® Normal) After Ingestion of a Standardized Meal in Subjects With T1DM

• Status: Completed
• Trial end date: 2016-08-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a 2 centres, randomised, double blind, three-treatment, three-period cross-over trial in subjects with type 1 diabetes mellitus.

Each subject will be administered individualised single subcutaneous doses of BioChaperone Human Insulin (HinsBet®), insulin lispro (Humalog®) and regular human insulin (Huminsulin® Normal) immediately before ingesting a standardised mixed meal.

Following trial drug administration, PK and PD assessments will be carried until 6 hours after start of the standardized test meal.

The total trial duration for an individual subject will be up to 11 weeks.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Adocia
• Treatments: Insulin; Insulin Lispro; Insulin, Globin Zinc

Criteria

Inclusion Criteria:

• Male or female subject aged 18-64 years (both inclusive).

• Type 1 diabetes mellitus (as diagnosed clinically) >= 12 months.

• Treated with multiple daily insulin injections or CSII >= 12 months.

• Current total daily insulin treatment < 1.2 (I)U/kg/day.

• Current total daily bolus insulin treatment < 0.7 (I)U/kg/day.

• BMI 18.5-28.0 kg/m^2 (both inclusive).

• HbA1c <= 9.0 % by local laboratory analysis

• Fasting C-peptide <= 0.30 nmol/L.

Exclusion Criteria:

• Known or suspected hypersensitivity to IMPs or related products.

• Type 2 diabetes mellitus.

• Previous participation in this trial. Participation is defined as randomised.

• Participation in any clinical trial within 3 months prior to this trial.

• Clinically significant abnormal haematology, coagulation, biochemistry, lipids, or urinalysis screening tests, as judged by the Investigator considering the underlying disease.

• Presence of clinically significant acute gastrointestinal symptoms (e.g. nausea, vomiting, heartburn or diarrhoea), as judged by the Investigator.

• Known slowing of gastric emptying and or gastrointestinal surgery that in the opinion of the Investigator might change gastrointestinal motility and food absorption.

• Unusual meal habits and special diet requirements or unwillingness to eat the food provided in the trial.

• Females of childbearing potential who are pregnant, breast-feeding or intend to become pregnant or are not using highly effective contraceptive methods