SeMaglutide and Albuminuria Reduction Trial in Obese Individuals Without Diabetes
NCT04889183 · Completed
Last updated 2026-05-28This clinical trial is testing whether the medication semaglutide can reduce kidney-related protein loss in obese adults who do not have diabetes.
What this study is testing ClinicalTrials.gov NCT04889183 ↗
Description as written by the study sponsor.
Study to assess the effects of weekly subcutaneous administration of the GLP1-RA semaglutide 2.4mg on kidney function parameters in obese/overweight individuals at high risk of CKD progression.
Treatments tested
- Semaglutide Drug
Patients will be treated for 24 weeks with semaglutide 3.0 mlg/ml s.c. once weekly. The starting dose of semaglutide will be 0.24 mg per week subcutaneous injection with increasing doses at 4, 8, 12, and 16 weeks to 0.5, 1,0, 1.7 and 2.4 mg.
- Placebo Drug
Patients will receive a matching placebo sc. once weekly during the treatment period of 24 weeks.
| Main thing measured | Change from baseline to week 24 in urinary albumin:creatinine ratio (UACR) |
|---|---|
| Sponsor | University Medical Center Groningen |
| Conditions studied | Obesity, Albuminuria |
| GLP-1 drugs | semaglutide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT04889183 ↗