ADO09, a co-formulation of pramlintide and insulin A21G, lowers body weight versus insulin lispro in type 1 diabetes.
AIM: To study safety, efficacy and weight loss with ADO09, a co-formulation of insulin A21G and pramlintide, in type 1 diabetes.
Evidence label explains the kind of source behind this article (for example peer-reviewed literature vs community video). It is not medical advice.
Key takeaways
- AIM: To study safety, efficacy and weight loss with ADO09, a co-formulation of insulin A21G and pramlintide, in type 1 diabetes.
- MATERIALS AND METHODS: A randomized, two-arm ambulatory 16-week study compared ADO09 with insulin lispro in 80 participants with type 1 diabetes.
- We compared changes of weight, glycated haemoglobin, glycaemic patterns during continuous glucose monitoring, and insulin doses at baseline and at the end of treatment.
What the research looked at
AIM: To study safety, efficacy and weight loss with ADO09, a co-formulation of insulin A21G and pramlintide, in type 1 diabetes.
MATERIALS AND METHODS: A randomized, two-arm ambulatory 16-week study compared ADO09 with insulin lispro in 80 participants with type 1 diabetes.
We compared changes of weight, glycated haemoglobin, glycaemic patterns during continuous glucose monitoring, and insulin doses at baseline and at the end of treatment.
RESULTS: A significant and continuing weight loss, the primary endpoint, was observed with ADO09 compared with lispro as prandial insulin.
In the whole group, the weight loss with ADO09 relative to lispro was 2.1 kg.
What it reported
Glycaemic control was relatively good (7.7% mean glycated haemoglobin) in both groups and did not change during treatment.
Prandial insulin doses were reduced by 21% in the ADO09 group, whereas basal insulin dosage was not modified.
Gastrointestinal symptoms were more frequent with ADO09, but no clear difference in hypoglycaemia was observed.
CONCLUSIONS: These results extend previous observations on the efficacy and safety of this insulin/pramlintide co-formulation.
They show a beneficial effect on weight, using less mealtime insulin and without increased hypoglycaemia.
What it means for the Type 1 community
This is pubmed indexed literature and is shared for information, not as medical advice. One study is a data point, not a verdict, so read it alongside the broader body of evidence and your own care team's guidance.
Evidence label
Source: Diabetes, obesity & metabolism. Evidence type: PubMed indexed literature. Type1Cure is an information and intelligence hub, not a medical advice service. This article summarizes published research and does not provide diagnosis, treatment, or personal medical guidance. Always talk to your own care team before changing anything about your Type 1 diabetes management.
Type1Cure is an information and intelligence hub, not a medical advice service. This article summarizes published research and does not provide diagnosis, treatment, or personal medical guidance. Always talk to your own care team before changing anything about your Type 1 diabetes management.
Related reading
More evidence-labeled coverage across the Type1Cure library.
- Peptide TherapiesHybrid Insulin Peptides: A New Target for Type 1 Diabetes ResearchPubMed indexed literature
- Peptide TherapiesAmylin: A Hormone Therapy Moving Beyond InsulinPubMed indexed literature
- Peptide TherapiesGLP-1 Drugs in Type 1 Diabetes: Learning from Daily Injections to Weekly OptionsPubMed indexed literature
- Peptide TherapiesNew Nanoparticle Approach Shows Promise for Preventing Type 1 Diabetes in Early ResearchPubMed indexed literature
- Peptide TherapiesCould Exercise Before Islet Transplant Improve Outcomes? New Rat Study Suggests YesPubMed indexed literature
- Peptide TherapiesAmylin: A Hormone-Based Approach to Blood Sugar Control in Type 1 DiabetesPubMed indexed literature