Targeting Beta Cell Dysfunction With Liraglutide or Golimumab in Longstanding T1D
Part of paid clinical trials in Idaho Falls, Idaho.
- Sponsor
- Carla Greenbaum, MD
- Study ID
- NCT03632759
- Phase
- EARLY_PHASE1
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 50 Years
- Healthy Volunteers
- Not accepted
Interventions
- Liraglutide — DRUGParticipants will receive subcutaneous (SC) liraglutide for 8 weeks
- Golimumab — DRUGParticipants will receive subcutaneous (SC) golimumab for 8 weeks
Study Details
The purpose of this study is to determine whether 8 weeks of Liraglutide or Golimumab can transiently improve beta cell function in patients with longstanding Type 1 diabetes (T1D) who secrete proinsulin and little/no C-peptide.
Key Dates
- Start date
- Aug 15, 2018
- Status verified
- Jan 2022
- Primary completion
- Nov 9, 2021
- Completion
- Nov 9, 2021
Study Design
- Enrollment
- 16 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: LiraglutideParticipants will receive subcutaneous (SC) liraglutide for 8 weeks
- Experimental: GolimumabParticipants will receive subcutaneous (SC) golimumab for 8 weeks
Primary Outcome Measure
Proportion of individuals with peak MMTT stimulated C-peptide >0.017 pmol/mL. [ Time Frame: 0-to-8 weeks ]
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Rocky Mountain Diabetes and Osteoporosis Center | Idaho Falls | Idaho | 83404 | - |
| Benaroya Research Institute | Seattle | Washington | 98101 | - |
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