RecruitingPhase 3NCT06217302

Sotagliflozin to Slow Kidney Function Decline in Persons With Type 1 Diabetes and Diabetic Kidney Disease

Effectiveness and Safety of Sotagliflozin in Slowing Kidney Function Decline in Persons With Type 1 Diabetes and Moderate to Severe Diabetic Kidney Disease


Sponsor

Alessandro Doria

Enrollment

150 participants

Start Date

Oct 31, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Powerful new drugs that can prevent or delay end stage kidney disease (ESKD) - so called sodium-glucose cotransporter-2 inhibitors (SGLT2i) - are now available for patients with type 2 diabetes. Whether these drugs have similar effects in patients with type 1 diabetes (T1D) remains unknown because of the few studies in this population, due to concerns about the increase in risk of diabetic ketoacidosis (DKA, a serious, potentially fatal acute complication of diabetes due to the accumulation of substances called ketone bodies) observed with SGLT2i therapy in T1D. One of the few T1D studies conducted to date showed that implementing an enhanced DKA prevention plan can reduce the risk of DKA associated with the SGLT2i sotagliflozin (SOTA) to very low levels. In the present study, a similar DKA prevention program will be used to carry-out a 3-year trial to test the kidney benefit of SOTA in 150 persons with T1D and moderate to advanced DKD. After a 2-month period, during which diabetes care will be standardized and education on monitoring and minimizing DKA implemented, eligible study subjects will be randomly assigned (50/50) to take one tablet of SOTA (200 mg) or a similarly looking inactive tablet (placebo) every day for 3 years followed by 2-months without treatment. Neither the participants nor the study staff will know whether a person was assigned to taking SOTA or the inactive tablet. Kidney function at the end of the study will be compared between the two treatment groups to see whether SOTA prevented kidney function loss in those treated with this drug as compared to those who took the inactive tablet. The DKA prevention program will include participant education, close follow-up with study staff, continuous glucose monitoring, and systematic ketone body self-monitoring with a meter provided by the study. If successful, this study will provide efficacy and safety data that could be used to seek FDA approval of SOTA for the prevention of kidney function decline in patients with T1D and DKD.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying whether sotagliflozin, a drug that lowers blood sugar and has shown heart and kidney benefits, can slow the decline of kidney function in people with type 1 diabetes who have chronic kidney disease. **You may be eligible if...** - You have type 1 diabetes - You have chronic kidney disease (reduced kidney function) - You are 18 or older - Your kidney function meets the study's minimum threshold **You may NOT be eligible if...** - You are on dialysis or have very advanced kidney failure - You have a history of diabetic ketoacidosis (a dangerous complication of type 1 diabetes) that is not well controlled - You are pregnant or planning to become pregnant - You have other major medical conditions that would make participation unsafe Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSotagliflozin

Oral sotagliflozin (200 mg per day)

DRUGPlacebo

Inactive tablets identical to sotagliflozin tablets


Locations(19)

Stanford University Medical Center

Stanford, California, United States

Barbara Davis Center / University of Colorado Denver

Aurora, Colorado, United States

AdventHealth

Orlando, Florida, United States

Northwestern University Feinberg School of Medicine

Chicago, Illinois, United States

Joslin Diabetes Center

Boston, Massachusetts, United States

Washington University

St Louis, Missouri, United States

SUNY Upstate Medical University

Syracuse, New York, United States

Albert Einstein College of Medicine / Montefiore Medical Center

The Bronx, New York, United States

Cleveland Clinic Foundation

Cleveland, Ohio, United States

Oregon Health and Science University

Portland, Oregon, United States

University of Texas Southwestern

Dallas, Texas, United States

University of Washington

Seattle, Washington, United States

Providence Sacred Heart Medical Center

Spokane, Washington, United States

Unversity of Calgary

Calgary, Alberta, Canada

Alberta Diabetes Institute

Edmonton, Alberta, Canada

St. Paul's Hospital

Vancouver, British Columbia, Canada

LMC Diabetes and Endocrinology

Toronto, Ontario, Canada

Toronto General Hospital

Toronto, Ontario, Canada

Institut de Recherches Cliniques de Montréal

Montreal, Quebec, Canada

View Full Details on ClinicalTrials.gov

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NCT06217302


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