Clinical trial

Trial of Semaglutide for Diabetic Kidney Disease in Type 1 Diabetes

Recruiting now · Phase 2 · 2 countries · Registry ID NCT05822609

Recruiting nowPhase 2Interventional

What this study is about

The primary objective of this study is to determine the effects of semaglutide on change in albuminuria from baseline to 26 weeks in type 1 diabetes. The secondary objective is to determine the effects of semaglutide on change in kidney parameters (including kidney oxygenation and function) measured by MRI from baseline to 26 weeks in type 1 diabetes. Other objectives are to determine the glycemic effects and safety of semaglutide in type 1 diabetes.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to Not listed
SexAll
Healthy volunteersNot accepted
ConditionDiabetic Kidney Disease, Type 1 Diabetes

Full registry criteria

Inclusion Criteria: * Adults (≥18 years) with type 1 diabetes * Diabetes duration of ≥5 years * Persistent urine albumin-to-creatinine ratio (UACR) ≥ 30 mg/g, on the most recent two measurements within the prior 3 years * Estimated glomerular filtration rate ≥ 20 mL/min/1.73m2 * Stable doses of drugs altering blood pressure (e.g., Angiotensin-converting enzyme inhibitor) required for at least 4 weeks prior to randomization, and requested for the duration of the trial * Stable doses of lipid-lowering medications required for at least 4 weeks prior to randomization, and requested for the duration of the trial * Adequate contraceptive method for females of child-bearing potential Exclusion Criteria: * HbA1c \>9%, recent diabetic ketoacidosis, hyperosmolar hyperglycemic state or severe illness requiring hospitalization in past 30 days * Other causes of diabetes mellitus, including type 2 diabetes and maturity-onset diabetes of the young (MODY) * Chronic kidney disease unrelated to diabetes * Personal or family history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia syndrome type 2 (MEN 2) or thyroid nodule palpated by endocrinologist at screening * Personal history of pancreatitis * Current/planned pregnancy or nursing * Uncontrolled thyroid disease or hypertension (Systolic blood pressure \[SBP\] ≥ 160 mm Hg or diastolic blood pressure \[DBP\] ≥ 100 mm Hg despite treatment) * Proliferative retinopathy with treatment in the past 6 months * Uncontrolled or potentially unstable diabetic retinopathy or maculopathy, verified by fundus examination with pupil dilation unless performed using a digital fundus photography camera specified for non-dilated examination * More than 2 severe hypoglycemic episodes (requiring glucagon and/or assistance from another person) in the past 6 months * Frequent hypoglycemia during the last two weeks of the study run-in phase (time below range \[\<70 mg/dL\] ≥4%) * Pramlintide and the use of glycemia treatments not approved for type 1 diabetes by the FDA, e.g., metformin, SGT-2 inhibitor, GLP-1 receptor agonist, closed loop insulin delivery using unapproved algorithms * Significant systemic conditions or treatment such as cancer or immunomodulators * Known liver disease other than non-alcoholic fatty liver disease (NAFLD) or aspartate aminotransferase (AST) or alanine aminotransferase (ALT) \>100 IU/L, history of severe gastrointestinal disease (e.g., gastroparesis) or gallstones * Body mass index \<20 kg/m2 * Known or suspected allergy/sensitivity to semaglutide or its excipients * Pregnant, breast feeding, or the intention of becoming pregnant * The receipt of any investigational drug within 3 months prior to this trial * Previously randomized in this trial

Treatments and study arms

Semaglutide

Drug

1.0 mg

Placebo

Other

Placebo

Primary outcomes

Change in urine albumin excretionBaseline to 26 weeks

Measured as mean of multiple urine albumin-creatinine ratio measurements in spot urine

Study locations

4 locations were listed when this page was built. The first 40 are shown.

Toronto General Hospital, University Health Network🇨🇦 Toronto, Ontario, Canada
Vesta LaiContact
Cheng XuContact
David Cherney, MD CM PhDPrincipal Investigator
University of Colorado Anschutz Medical Campus🇺🇸 Aurora, Colorado, United States
Madeline Harbour, BAContact
Carissa Birznieks, BSContact
Jessica Kendrick, MDPrincipal Investigator
University of Washington🇺🇸 Seattle, Washington, United States
Jesica D BaranContact
Dori Khakpour, RDN CDEContact
Irl Hirsch, MDPrincipal Investigator
Providence Sacred Heart Medical Center🇺🇸 Spokane, Washington, United States
Nicole Maser, MSN RNContact
Susan Hood, PhD CCRCContact
Katherine Tuttle, MDPrincipal Investigator