findmyKOL
Clinical trialNCT06217302RecruitingPhase 3Interventional

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

SponsorAlessandro DoriaEnrollment150Diabetes Mellitus Type 1Diabetic NephropathiesHeart FailureKidney Failure, Chronic
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

19 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada
  • Unversity of Calgary

    Calgary, Alberta, Canada

    Ronald Sigal, MD MPH
    Recruiting
  • Alberta Diabetes Institute

    Edmonton, Alberta, Canada

    Anna Lam, MDPeter Senior, MD
    Recruiting
  • St. Paul'S Hospital

    Vancouver, British Columbia, Canada

    Adeera Levin, MDSean Barbour, MD
    Recruiting
  • Lmc Diabetes and Endocrinology

    Toronto, Ontario, Canada

    Ronnie Aronson, MD
    Recruiting
  • Toronto General Hospital

    Toronto, Ontario, Canada

    Ayodele Odutayo, MDBruce Perkins, MD MPHDavid Cherney, MDHuajing Ni, MDTaewon Yi, MDVikas S. Sridhar, MD
    Recruiting
  • Institut de Recherches Cliniques de Montréal

    Montreal, Quebec, Canada

    Nadine Taleb, MDRemi Rabasa-Lhoret, MD
    Recruiting
United States
  • Stanford University Medical Center

    Stanford, California, United States

    David Maahs, MDMarina Basina, MD
    Recruiting
  • Barbara Davis Center / University of Colorado Denver

    Aurora, Colorado, United States

    Halis Akturk, MDSarit Polsky, MD
    Recruiting
  • Adventhealth

    Orlando, Florida, United States

    Tina Thethi
    Recruiting
  • Northwestern University Feinberg School of Medicine

    Chicago, Illinois, United States

    Amisha Wallia, MD
    Recruiting
  • Joslin Diabetes Center

    Boston, Massachusetts, United States

    Alessandro Doria, MD PhD MPHElena Toschi, MDSylvia Rosas, MD
    Recruiting
  • Washington University

    St Louis, Missouri, United States

    Huda Al-Bahadili, MDJanet McGill, MDKai Jones, MDMaamoun Salam, MD
    Recruiting
  • Suny Upstate Medical University

    Syracuse, New York, United States

    Katherine McPhee, MSN, FNP-C, RNMalek El Muayed, MD, MSCIRuth Weinstock, MD
    Recruiting
  • Albert Einstein College of Medicine / Montefiore Medical Center

    The Bronx, New York, United States

    Jill Crandall, MDJustin Mathew, MDMatthew Abramowitz, MD
    Recruiting
  • Cleveland Clinic Foundation

    Cleveland, Ohio, United States

    Keren Zhou, MDLuiza Caramori, MD PhD
    Recruiting
  • Oregon Health and Science University

    Portland, Oregon, United States

    Andrew Ahmann, MDRodica Busui, MD, PhD
    Recruiting
  • University of Texas Southwestern

    Dallas, Texas, United States

    Amy Shah, MDIldiko Lingvay, MDOksana Hamidi, DO
    Recruiting
  • University of Washington

    Seattle, Washington, United States

    Ian de Boer, MDIrl Hirsch, MDKalie Tommerdahl, MDPetter Bjornstad, MD
    Recruiting
  • Providence Sacred Heart Medical Center

    Spokane, Washington, United States

    Katherine R. Tuttle, MDMichael Ryan, MDRadica Alicic, MD
    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Oct 2024
Primary completion
31 Dec 2028
Completion
31 May 2029
Last update posted
24 Mar 2026
Registered enrollment
150
Registry id
NCT06217302

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.