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Study details
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A Study to Test Whether Vicadrostat in Combination With Empagliflozin Helps People With Chronic Kidney Disease

Boehringer Ingelheim
NCT IDNCT06926660ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

416

Study length

about 1.5 years

Ages

18+

Locations

37 sites in AL, CA, FL +16

About this study

This trial is testing whether a treatment combining vicadrostat and empagliflozin helps people with chronic kidney disease. This treatment will be compared to a placebo combined with empagliflozin for some participants. It lasts about 4.5 months, during which doctors monitor kidney function and check for any side effects.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Empagliflozin
  • 2.Take Placebo matching vicadrostat
  • 3.Take Vicadrostat
PhasePhase 2
DrugEmpagliflozin
Routeoral
Primary goalAbsolute change in estimated glomerular filtration rate (eGFR) (mL/min/1.73m2) from baseline to Week 14 and week 16

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low12%
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

empagliflozin (SGLT2 inhibitor; increases glucose excretion in urine)

Drug routes

oral (Oral Tablet)

Endpoints

Primary: Absolute change in estimated glomerular filtration rate (eGFR) (mL/min/1.73m2) from baseline to Week 14 and week 16

Secondary: Absolute change in estimated glomerular filtration rate (eGFR) (mL/min/1.73m2) from baseline to Week 12, Absolute change in systolic blood pressure (SBP) (mmHg) from baseline to Week 12, Relative change (ratio) in Urine Albumin Creatinine Ratio (UACR) from baseline to Week 6

Body systems

Renal