HbA1c changes had no clinically relevant differences across dulaglutide groups receiving sulphonylurea, biguanide, or both.
In plain wordsHbA1c changes were similar across dulaglutide regimens with sulphonylurea, biguanide, or both.
- Peptide
- Dulaglutide (Trulicity)
- Outcome
- No significant changeHbA1c change across background therapies
- Study
n: not reported in source
- Comparator
- Dulaglutide with sulphonylurea, biguanide, or both
- Analysis
- Exploratory
- Outcome group
- Glycemic control · Metabolic and weight
Source sentences
There were no clinically relevant differences in glycated haemoglobin (HbA1c) changes among the three subgroups in the dulaglutide group;
3 context sentences(design, population, supporting numbers)
The efficacy and safety of once-weekly dulaglutide 0.75 mg (dulaglutide) in Japanese patients with type 2 diabetes (T2D) were evaluated according to subgroups defined by concomitant oral hypoglycaemic agents.
This exploratory analysis included data from a randomized, open-label, phase III study that compared dulaglutide with insulin glargine (glargine) (n = 361).
The three subgroups were dulaglutide or glargine in combination with sulphonylurea (SU) alone, biguanide (BG) alone or SU and BG combined.
In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).