An in-depth analysis of the continuous glucose monitoring data from the phase 2b trial DIAGNODE-2 with Diamyd Medical AB (publ) sheds new light on the importance of residual beta cell function in individuals recently diagnosed with Type 1 Diabetes. Most notably, the results show highly statistically significant and positive associations between residual beta cell function measured as stimulated C-peptide and reduction of the number and severity of hyperglycemic events, in other words episodes of high blood glucose levels, as well as improvments in glucose control during meal time. The results lend further support to the clinical relevance of therapeutically preserving C-peptide in Type 1 Diabetes, one of the two primary endpoints in the ongoing Phase 3 trial DIAGNODE-3. The updated analysis, performed in collaboration with the digital decision support company OneTwo Analytics, dissects all the continous glucose monitoring (CGM) data from DIAGNODE-2 into a large number of established and novel metrics describing glycemic control including mean glucose features, hyperglycemic features, hypoglycemic features and meal related features.

These metrics convey information relevant to both the health and quality of life of the patient. The preliminary results show a statistically highly significant positive association between residual beta cell function measured as stimulated C-peptide and several of these CGM metrics. The most substantial impact, with p-values below 0.0001, is seen on reducing the number and severity of hyperglycemic events, (episodes of high blood glucose levels), as well as improvments in glucose control during meal times for patients with recently diagnosed type 1 diabetes.

The results also show a significant protective effect of endogenous insulin production on several hypoglycemic measures, (episodes of below normal blood glucose levels). The preliminary analyses also provide more detailed support to the previously published effect of Diamyd on improving glycemic control in individuals carrying the HLA DR3-DQ2 haplotype, emphaszing the importance of therapeutically preserving C-peptide. As previously published in Diabetes Care in 2021, a significant effect of Diamyd in the Phase 2b trial DIAGNODE-2 on preserving endogenous insulin production measured as stimulated C-peptide was seen in the prespecified genetic subgroup of individuals that carried the HLA DR3-DQ2 haplotype.

A follow-up publication published in JCEM in 2022 showed a significant effect of Diamyd on 1) improving time spent in the optimal glucose range (time in range, TIR), 2) reducing time spent in hyperglycemia (high blood glucose levels) and 3) reduced glucose fluctuations. Also, an updated meta-analysis published in Diabetes, Obesity and Metabolism in 2022, based on the comprehensive data package comprising four placebo controlled clinical trials with Diamyd, showed a clear correlation between preserved C-peptide and improved HbA1c, a measure of the average blood glucose levels over the span of 2-3 months. The most comprehensive meta-analysis to date, recently published in The Lancet Diabetes & Endocrinology in 2023, encompassing data from approximately 2,700 newly diagnosed type 1 diabetes patients who participated in 21 trials evaluating disease-modifying therapies including Diamyd, underscores the significance of preserved C-peptide.

The study's results indicated that preserving C-peptide in T1D patients led to a significant improvement in metabolic outcomes. The findings support the use of C-peptide as a surrogate endpoint in clinical trials and confirm the potential of beta cell preserving interventions as effective adjuncts to insulin therapy in managing new-onset type 1 diabetes. Beyond these findings on therapeutically preserved C-peptide that can be seen directly in clinical trials conducted on individuals with recent-onset T1D, there is also substantial evidence that preserved endogenous insulin production significantly reduce the incidence of diabetes-related complications such as diabetic ketoacidosis, severe hypoglycemia retinopathy, neuropathy, and nephropathy.

CGM technology, compared to traditional blood sugar testing methods, such as finger-pricking, offers real-time glucose level monitoring through a small, under-the-skin sensor. This sensor continuously tracks glucose concentrations, providing comprehensive data that is wirelessly transmitted to a receiver or a smartphone application. The continuous nature of this monitoring is invaluable in identifying glucose trends and patterns, enabling individuals with diabetes to make more informed decisions about diet, exercise, and medication in real time.