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Study 8 of 57Semaglutide literaturePubMed · RCT · Phase 32026

Insulin, Semaglutide and Dapagliflozin in Adults With Type 1 Diabetes: Design and Methods of Triple Therapy for Type 1 Diabetes (TTT1)-An International Phase 3 Clinical Trial.

This trial investigates the effects of adding semaglutide and dapagliflozin to insulin therapy in adults with Type 1 Diabetes, aiming to improve glycaemic control while addressing insulin-induced weight gain.

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Where it sits

this study against the rest of the semaglutide corpus
13
Preclinical
34
Observational
2
Open-label
2
Randomised · this one
6
Reviews

Summary and findings

This study evaluates the efficacy and safety of adding semaglutide and dapagliflozin to insulin therapy in overweight and obese adults with Type 1 Diabetes (T1D) and HbA1c levels between 7.5% and 11.0%. Participants are randomized to receive either triple therapy (semaglutide, dapagliflozin, and insulin) or dual therapy (semaglutide and insulin) over a 26-week period. The study aims to assess changes in HbA1c and safety outcomes.

How much of this paper we could read: full text read (0.70). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Not reported in abstract.Phase 32026

Abstract

The authors’ words, as PubMed supplied them

<h4>Aims</h4>Attaining target glycaemia can be a challenge in Type 1 Diabetes (T1D) due to insulin-induced weight gain. Adjunct therapy with modern glucose-lowering agents developed for type 2 diabetes (T2D) has great potential but may be insufficiently efficacious and carries risks of hypoglycaemia and ketosis. We designed the first Phase 3 clinical trial to assess the efficacy and safety of adding a Glucagon-Like Peptide 1 receptor agonist (GLP-1RA) and a Sodium-Glucose Co-transporter (SGLT2) Inhibitor to insulin therapy in overweight and obese adults with T1D and glycaemia above target (HbA1c 7.5%-11.0% inclusive) (NCT03899402).<h4>Materials and methods</h4>In Period 1, participants are randomized 2:1 (open label) for 26 weeks to semaglutide and insulin (uptitrated to 1.0 mg weekly) or standard insulin therapy. In Period 2, those randomized to semaglutide and insulin in Period 1 are further randomized (double-blind) for 26 weeks to dapagliflozin (10 mg daily) or placebo, in addition to semaglutide. The primary objective is to compare change in HbA1c on 'triple therapy' (dapagliflozin, semaglutide and insulin) with 'dual therapy' (placebo, semaglutide and insulin). Secondary objectives include comparisons of triple therapy with standard insulin therapy and dual therapy (semaglutide and insulin) with standard insulin therapy. Safety outcomes include hypoglycaemia and ketosis. A sample size recalculation during the trial based on analysis of masked data revised the original recruitment target from 114 to 82 participants.<h4>Conclusion</h4>The TTT1 trial will provide clinically useful information on combination adjunct therapy in the treatment of T1D.

Background

This paper addresses the clinical question of how a combination therapy of insulin, semaglutide, and dapagliflozin may affect adults with type 1 diabetes. Previous studies have focused on individual components of this therapy, but the combination's effects are less understood. This study is significant as it seeks to explore a novel approach to managing type 1 diabetes.

Methods

The study is designed as a Phase 3 clinical trial involving adults with type 1 diabetes. Specific details regarding the population size, dosing regimen, duration, and outcome measures are not reported in the abstract.

Results

Not reported in abstract.

Interpretation

Due to the lack of reported results, it is not possible to compare this study's findings to prior literature or assess the clinical significance of the proposed therapy. Without specific data, the implications for practice remain unclear.

Key findings

  • Not reported in abstract.

Limitations

  • Not reported in abstract.

Elsewhere in the Semaglutide corpus

DSemaglutide and Suicidality in Adults with Overweight or Obesity: A Bayesian Meta-Analysis of Randomized Trialsbiorxiv-preprint · Completed suicide: pooled OR 1.56 (95% CrI 0.55–4.67), P(OR > 1) = 80.6%, n=17,086 semaglutide vs 15,304 placebo.reviewBWeight loss with a lower dose compounded semaglutide and behavioral weight management program: A real-world matched retrospective cohort studybiorxiv-preprint · At 16 weeks, NMGP users lost 8.3% of their baseline weight.HumanBSide effects of lower dose compounded semaglutide paired with a behavioral management program: A real-world retrospective studybiorxiv-preprint · 34% lower relative odds of reporting GI side effects by week 16, p=0.001, n=2,481 per group.HumanBA study on risk factors for the progression from T2DM to end-stage renal disease based on Mendelian randomization and logistic regression analysis.Renal failure · 2026 · n=875 · AUC of the logistic regression-based nomogram was 0.88 (95% CI: 0.85-0.91).HumanBFeasibility and acceptability of an everyday patient-centered discussion model for primary care: An exploratory, single-center study in the VA primary care setting.PEC innovation · 2026 · n=23 · Mean SDM-Q-9 score was 90.9 out of 100.HumanBOral Health Outcomes with GLP1 Receptor Agonists Compared with Other Metabolic Interventionsbiorxiv-preprint · 2026 · 8.69% of GLP-1 users developed at least one newly documented oral-health condition.Human