Type 2 Diabetes Mellitus Clinical Trial
Official title:
A Randomised, Double-blind, Double-dummy, Three-period Cross-over Trial to Compare Post Prandial Blood Glucose Control of BioChaperone® Combo With Humalog® Mix25 and With Simultaneous Injections of Humalog® and Lantus® in Subjects With Type 2 Diabetes
This is a two-centre, randomised, double-blind, double-dummy, 3-treatment, 3-period cross-over study using a standardised solid meal test in subjects with type 2 diabetes to investigate postprandial glucose control of BioChaperone® Combo compared with Humalog® Mix25 and with simultaneous subcutaneous injections of Humalog® and Lantus® during three separate dosing visits.
This is a two-centre, randomised, double-blind, double-dummy, 3-treatment, 3-period
cross-over study using a standardised solid meal test in subjects with type 2 diabetes to
investigate postprandial glucose control of BioChaperone® Combo compared with Humalog® Mix25
and with simultaneous subcutaneous injections of Humalog® and Lantus® during three separate
dosing visits.
Furthermore, this study aims to compare the pharmacokinetic (PK) profiles of the three
different study treatments.
During each dosing visit, subjects will be given 3 doses of IMP on three consecutive days
(Day 1, Day 2 and Day 3). Dosing on Day 2 and Day 3 will be followed by a standardised solid
meal test.
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