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

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-75
SponsorAlessandro Doria

About this trial

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 criteria

Qualifiers

Type1 diabetes (T1D) continuously treated with insulin within one year from diagnosis.

Duration of T1D ≥ 8 years;

eGFR based on serum creatinine and cystatin c (2021 serum creatinine-cystatin C CKD-EPI equation) between 20 and 60 ml/min/1.73 m2 at screening (with the option of a second eGFR measurement within 4 weeks from the first one if the eGFR was in the range of >60 to ≤65 or ≥16 to <20 ml/min/1.73 m2);

a. First morning void urinary albumin creatinine ratio (UACR) ≥200 mg/g at Screening or on repeat measurement within 4 weeks from the first one, or b. First morning void urinary UACR ≥100 mg/g at Screening or on repeat measurement within 4 weeks and at least one uACR >=30 in the previous 2 years while treated with RASB at a stable dose;

Disqualifiers

Type 2 diabetes or monogenic forms of diabetes or diabetes secondary to pancreatic disease;

Use of automated insulin delivery devices that are not approved by health regulatory agencies, or used in ways that do not align with manufacturer recommendations;

Use of any SGLT inhibitor in the previous 2 months;

Use of dual medication RASB therapy (spironolactone, eplerenone, finerenone are allowed in combination with RASB therapy);

Trial design

Treatments tested in this trial

  • Sotagliflozin
  • Placebo

Treatment groups

150 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Alessandro Doria

Lead sponsor

Joslin Diabetes Center

Sponsor institution

Canadian Institutes of Health Research (CIHR)

Collaborator

The Kidney Foundation of Canada

Collaborator

The Cleveland Clinic

Collaborator

University of Michigan

Collaborator

University of Colorado, Denver

Collaborator

Northwestern University

Collaborator

Washington University School of Medicine

Collaborator

State University of New York - Upstate Medical University

Collaborator

Providence Medical Research Center

Collaborator

Stanford University

Collaborator

Montefiore Medical Center

Collaborator

University of Toronto

Collaborator

University Health Network, Toronto

Collaborator

University of Calgary

Collaborator

University of Alberta

Collaborator

University of British Columbia

Collaborator

Institut de Recherches Cliniques de Montreal

Collaborator

LMC Diabetes & Endocrinology Ltd.

Collaborator

Joslin Diabetes Center

Collaborator

Lexicon Pharmaceuticals

Collaborator

DexCom, Inc.

Collaborator

University of Washington

Collaborator

Breakthrough T1D

Collaborator

AdventHealth

Collaborator