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GIP/GLP-1RA as Adjunctive to Automated Insulin Delivery in Adults With Type 1 Diabetes

Study acronym: AID-JUNCT
StatusRecruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated January 26, 2026 (before its estimated June 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Minor Site contacts updated at 1 of 3 sitesv6
  2. Minor Study sites: 1 to 3
    • Collaborators: 1 to 3
    v5
  3. Minor Re-verified, no change to tracked fieldsv4
  4. Notable Trial status: Not Yet Recruiting to Recruitingv3 Show 4 more changesShow less
    • Primary and study completion dates: Dec 2025 to Jun 2026
    • Start date changed from estimate of Nov 2024 to Feb 14, 2025
    • Secondary endpoints: 47 to 8
    • Site details revised
  5. Minor Re-verified, no change to tracked fieldsv2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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Blood glucose management in type 1 diabetes (T1D) remains a challenge, with only \~30% of adults within the recommended consensus guidelines. Novel drugs like glucagon-like peptide-1 receptor agonists (GLP-1RAs) and glucose-dependent insulinotropic polypeptide (GIP)/GLP-1RAs have emerged as promising add-ons to insulin in T1D. This application has been designed to test in a prospective study whether adding a new medicine called tirzepatide (GIP/GLP-1RA) to the usual insulin therapy would make a difference for people with T1D in terms of better glucose control.
Trial Details
NCT Number NCT06630585
Lead Sponsor University of Bern
Collaborators: Kantonsspital Olten, Luzerner Kantonsspital, Clinique des Grangettes, Chêne-Bougeries
Conditions
(from sponsor)
Type 1 Diabetes (T1D)
Related terms Diabetes Mellitus, Type 1
Enrollment 42 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov