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CompletedNCT05373212

A Trial Investigating the Dose Linearity and Safety of BC Combo THDB0207 in Subjects With Type 2 Diabetes

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Adocia · Industry
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Not accepted

Summary

This is a randomised, double-blind, four-period crossover euglycaemic clamp trial in subjects with type 2 diabetes. Each subject will be randomly allocated to one of four treatment sequences. Each sequence will comprise 3 different single doses of BC Combo THDB0207 (Low dose, Medium dose, and High dose) and one single dose of Humalog® Mix25. Subjects will come to the clinical trial centre in a fasted state in the morning of each dosing day and stay at the clinical trial centre until the 30-hour clamp procedures have been terminated.

Detailed description

Subjects will attend the study site in the morning in a fasted state and will be connected to an automated glucose clamp device. Prior to dose administration plasma glucose will be stabilised at a target level of 100 mg/dL by means of an intravenous infusion of glucose or insulin. IMP administration will be done by an unblinded person by means of subcutaneous injections in the abdominal wall. Following each dosing a euglycaemic glucose clamp procedure will be carried out for up to 30 hours. The pharmacodynamic assessment will be based on the time course of glucose infusion rate (GIR) and plasma glucose. Plasma insulin concentrations will be measured using a specific validated bioanalytical method differentiating concentrations of insulin glargine, of its main metabolites insulin-glargine-M1 and insulin-glargine-M2, and of insulin lispro. Pharmacokinetic assessments will be based on total insulin concentration (insulin glargine + insulin glargine-M1 + insulin glargine-M2 + insulin lispro), on insulin glargine concentration (insulin glargine + insulin glargine-M1 + insulin glargine-M2), or on insulin lispro concentration.

Conditions

Interventions

TypeNameDescription
DRUGEuglycemic clamp with BC Combo THDB0207Administration of a single dose of BC Combo THDB0207 during an euglycemic clamp procedure.
DRUGEuglycemic clamp with Humalog® Mix25Administration of a single dose of Humalog® Mix25 during an euglycemic clamp procedure.

Timeline

Start date
2022-05-12
Primary completion
2023-01-02
Completion
2023-01-02
First posted
2022-05-13
Last updated
2023-09-15

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT05373212. Inclusion in this directory is not an endorsement.

A Trial Investigating the Dose Linearity and Safety of BC Combo THDB0207 in Subjects With Type 2 Diabetes (NCT05373212) · Clinical Trials Directory