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Sodium-glucose cotransporter 2 (SGLT2) inhibitor

Empagliflozin for Polycystic Kidney Disease

Phase 2
Recruiting
Led By Michel B Chonchol, MD
Research Sponsored by University of Colorado, Denver
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Autosomal Dominant Polycystic Kidney Disease (ADPKD) as defined by modified Pei-Ravine Criteria
Age 18-50 yrs
Must not have
Current use of tolvaptan or other V2 receptor antagonist
Current use of loop diuretic
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, check-in visit (3 months), post-testing (12 months)

Summary

This trial tests empagliflozin, a drug that helps remove excess sugar through urine, in patients with ADPKD who suffer from kidney cysts and eventual kidney failure. The drug may help reduce kidney damage and improve heart health by blocking a protein that reabsorbs sugar. Empagliflozin has been shown to slow the progression of diabetic kidney disease.

Who is the study for?
This trial is for adults aged 18-50 with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and moderately reduced kidney function, but not diabetes or heart failure. Participants should have stable kidney health without recent infections and must not be pregnant, using certain diuretics, or have contraindications to MRI scans.
What is being tested?
The study tests the safety of Empagliflozin in ADPKD patients over a year. It's a double-blind trial where half the participants will receive Empagliflozin and the other half a placebo, neither group knowing which they're getting to ensure unbiased results.
What are the potential side effects?
Potential side effects of Empagliflozin may include urinary tract infections, dehydration leading to low blood pressure, ketoacidosis (a serious condition related to diabetes), genital yeast infections, increased cholesterol levels, and allergic reactions.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have been diagnosed with ADPKD according to specific criteria.
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I am between 18 and 50 years old.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I am currently taking tolvaptan or a similar medication.
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I am currently taking medication to help remove excess fluid from my body.
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I currently have a urinary tract or genital infection.
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I have heart failure with a low heart pumping rate.
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I have leg pain when walking, skin infections, or ulcers on my legs.
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I have been diagnosed with diabetes.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, check-in visit (3 months), post-testing (12 months)
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, check-in visit (3 months), post-testing (12 months) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Adverse Events
Returned Number of Tablets
Subject Drop Out Rate
Secondary study objectives
Aortic Pulse Wave Velocity (aPWV)
Height-Adjusted Total kidney volume
Tumor Markers
+1 more

Side effects data

From 2021 Phase 3 trial • 5988 Patients • NCT03057951
15%
Cardiac failure
7%
Hypertension
7%
Hypotension
7%
Urinary tract infection
6%
Renal impairment
6%
Hyperkalaemia
6%
Fall
5%
Atrial fibrillation
5%
Diabetes mellitus
4%
Hyperuricaemia
4%
Anaemia
3%
Acute kidney injury
3%
Pneumonia
2%
COVID-19
2%
Death
2%
Acute myocardial infarction
2%
Cardiac failure congestive
1%
Basal cell carcinoma
1%
Cardiac failure chronic
1%
Cellulitis
1%
Syncope
1%
Chronic kidney disease
1%
COVID-19 pneumonia
1%
Ischaemic stroke
1%
Coronary artery disease
1%
Chronic obstructive pulmonary disease
1%
Myocardial infarction
1%
Sepsis
1%
Transient ischaemic attack
1%
Angina unstable
1%
Cerebrovascular accident
1%
Angina pectoris
1%
Ventricular tachycardia
100%
80%
60%
40%
20%
0%
Study treatment Arm
Placebo
10 mg Empagliflozin

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: ExperimentalExperimental Treatment1 Intervention
Empagliflozin
Group II: Placebo comparatorPlacebo Group1 Intervention
Placebo
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Empagliflozin
2017
Completed Phase 4
~181750

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Polycystic Kidney Disease (PKD) include AMPK activators like metformin and salsalate, which downregulate mTOR and CFTR pathways to slow cyst growth. SGLT2 inhibitors, such as empagliflozin, reduce glucose reabsorption in the kidneys, potentially benefiting kidney function and slowing disease progression. These mechanisms are crucial for PKD patients as they offer strategies to manage and slow the progression of the disease.
Sodium-glucose cotransporter 2 inhibition suppresses HIF-1α-mediated metabolic switch from lipid oxidation to glycolysis in kidney tubule cells of diabetic mice.Renal Effects of Incretin-Based Diabetes Therapies: Pre-clinical Predictions and Clinical Trial Outcomes.

Find a Location

Who is running the clinical trial?

University of MarylandOTHER
168 Previous Clinical Trials
304,891 Total Patients Enrolled
University of Colorado, DenverLead Sponsor
1,803 Previous Clinical Trials
2,822,073 Total Patients Enrolled
Michel B Chonchol, MDPrincipal InvestigatorUniversity of Colorado, Denver
1 Previous Clinical Trials
61 Total Patients Enrolled

Media Library

Empagliflozin (Sodium-glucose cotransporter 2 (SGLT2) inhibitor) Clinical Trial Eligibility Overview. Trial Name: NCT05510115 — Phase 2
Polycystic Kidney Disease Research Study Groups: Experimental, Placebo comparator
Polycystic Kidney Disease Clinical Trial 2023: Empagliflozin Highlights & Side Effects. Trial Name: NCT05510115 — Phase 2
Empagliflozin (Sodium-glucose cotransporter 2 (SGLT2) inhibitor) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05510115 — Phase 2
~20 spots leftby Mar 2026