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
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