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Study details
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A Research Study Comparing How Well Different Doses of the Medicine NNC0519-0130 Can Reduce Kidney Damage in People Living With Chronic Kidney Disease

Novo Nordisk A/S
NCT IDNCT06717698ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

465

Study length

about 1.8 years

Ages

18+

Locations

18 sites in CA, CO, FL +8

About this study

Researchers are testing how well different doses of a new medicine called NNC0519-0130 can reduce kidney damage in people with chronic kidney disease. Participants will receive either NNC0519-0130, semaglutide (a medicine that doctors can already prescribe), or a placebo. The trial will last for up to 43 weeks.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take NNC0519-0130
  • 2.Take Placebo
  • 3.Take Semaglutide
PhasePhase 2
DrugSemaglutide
Routeoral
Primary goalChange in urinary albumin-to-creatinine ratio (UACR) at week 12

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low15%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

semaglutide (GLP-1 agonist; stimulates insulin release)

Drug routes

oral (Oral Tablet)

Endpoints

Primary: Change in urinary albumin-to-creatinine ratio (UACR) at week 12, Change in urinary albumin-to-creatinine ratio (UACR) at week 24, Change in urinary albumin-to-creatinine ratio (UACR) at week 36

Secondary: Change in diastolic blood pressure, Change in estimated glomerular filtration rate (eGFR) (creatinine and cystatin C-based Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI] 2021), Change in estimated glomerular filtration rate (eGFR) (creatinine-based CKD-EPI 2021), Change in glycated haemoglobin (HbA1c), Change in systolic blood pressure, Change in waist circumference, Number of treatment emergent adverse events (TEAEs), Relative change in body weight

Body systems

Renal