LivingGLP1
Study S002321

Efficacy and Safety of Once Weekly Semaglutide in Adults With Obesity and Inadequately Controlled Type 1 Diabetes Using Hybrid Closed-Loop System.

Registration

Registration
NCT05537233
Acronym
ADJUST-T1D
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
115
Start
2023-04-11
Primary completion
2024-08-06
Lead sponsor
Viral N. Shah
Conditions
Type 1 Diabetes; Obesity
Interventions
DRUG:Semaglutide; DRUG:Placebo
Results posted
TRUE
Individual participant data sharing
NO

Registered primary outcomes

  • Proportion of Adults With T1D Achieving Composite Outcome (CGM-measured Time in Range (TIR)>70% With Time Below Range (TBR) of <4% and Reduction in Body Weight by 5%) at 26 Weeks in the Semaglutide Group Compared to Placebo Group [26 weeks]

Linked records (2)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R00457772866-LB: Semaglutide Use Along with Neural Network Fully Closed-Loop Systems Improves Time in Range (TIR) to 87% in Adults with Type 1 diabetes: In Silico Study
Dayu Lv, Diabetes
2026Randomized trialDOIcites ClinicalTrials.gov:NCT05537233
R0017153Semaglutide in Adults with Type 1 Diabetes and Obesity.
Shah VN, NEJM evidence
2025Randomized trialPMID 40550013DOIcites ClinicalTrials.gov:NCT05537233; registry reference DERIVED:40550013