Efficacy and Bone Safety of Sotagliflozin 400 and 200 mg Versus Placebo in Participants With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control

Stopped early · Phase 3 · Has a placebo group

Conditions studied: Type 2 Diabetes Mellitus

In brief

The primary objective is to demonstrate the superiority of Sotagliflozin 400 milligrams (mg) versus placebo with respect to hemoglobin A1c (Hb1Ac) reduction in participants with type 2 diabetes (T2D) who have inadequate glycemic control on diet and exercise only or with a stable antidiabetes regimen.

Key facts

Study ID

NCT03386344

Run by

Lexicon Pharmaceuticals

People needed

376

Starts

2018-02-19

Expected to finish

2020-05-30

Last updated by the study team

2021-06-25

Who can join

Age: 55 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants with T2D managed with diet and exercise only or with a stable antidiabetes regimen (in monotherapy or combination therapy that can include oral antidiabetes medications, insulin, or glucagon-like peptide-1 agonists) for more than 12 weeks.
• Participants has given written informed consent to participate in the study in accordance with local regulations.

You may not qualify if…

• Age <55 years.
• Women who have been postmenopausal (or undergone bilateral oophorectomy) for less than 5 years.
• Type 1 diabetes mellitus.
• Body mass index (BMI) ≤20 or >45 kilogram per meter square kg/m\^2 or bodyweight that exceeds the weight limits of the DXA scanner.
• Hemoglobin A1C (HbA1c) <7.0% or HbA1c >11.0%.
• Use of a selective sodium-glucose cotransporter type 2 (SGLT2) inhibitor or thiazolidinedione within 24 months.
• Bone mineral density (BMD) T- score <-2.0 at any site (ie, lumbar spine, total hip, or femoral neck).
• History of fracture within 12 months (except for fractures of the hand/fingers, foot/toes, facial bones, and skull).
• Treatment with medications known to affect bone mass or modify the risk of fractures within 36 months (eg, bisphosphonates, selective estrogen receptor modulators, calcitonin, teriparatide, denosumab, strontium ranelate, growth hormone, aromatase inhibitors, androgen deprivation therapy, carbamazepine, phenytoin, and phenobarbital). Use of hormonal replacement that includes systemic or transdermal estrogen or testosterone is excluded unless is stable for at least 24 months prior to Screening.
• Lower extremity complications (such as skin ulcers, infection, osteomyelitis and gangrene) identified during the Screening period, and still requiring treatment at randomization.
• Uncontrolled high blood pressure, severe anemia, severe cardiovascular problems, such as heart failure, active cancer, or other conditions that the Investigator believes with result in a short life expectancy.
• Renal disease as defined by an estimated glomerular filtration rate (eGFR) <30 milliliter per minute (mL/min)/1.73 meter square (m\^2) at the Screening Visit by the 4 variable Modification of Diet in Renal Disease equation.
• The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.

Where it is running

• Investigational Site Number 8409010 — Greenbrae, California, United States
• Investigational Site Number 8409005 — Walnut Creek, California, United States
• Investigational Site Number 8409012 — Columbus, Georgia, United States
• Investigational Site Number 8409011 — Evansville, Indiana, United States
• Investigational Site Number 8409014 — Wichita, Kansas, United States
• Investigational Site Number 8409015 — Albuquerque, New Mexico, United States
• Investigational Site Number 8409002 — Chapel Hill, North Carolina, United States
• Investigational Site Number 8409001 — Wilmington, North Carolina, United States
• Investigational Site Number 8409008 — Dayton, Ohio, United States
• Investigational Site Number 8409004 — Chattanooga, Tennessee, United States
• Investigational Site Number 8409013 — Austin, Texas, United States
• Investigational Site Number 8409003 — Dallas, Texas, United States
• Investigational Site Number 8409007 — Katy, Texas, United States
• Investigational Site Number 0369003 — Fremantle, Australia
• Investigational Site Number 0369002 — Merewether, Australia
• Investigational Site Number 0369004 — Parkville, Australia
• Investigational Site Number 1249003 — Brampton, Canada
• Investigational Site Number 1249008 — Etobicoke, Canada
• Investigational Site Number 1249005 — Pointe-Claire, Canada
• Investigational Site Number 1249006 — Thornhill, Canada
• Investigational Site Number 1249004 — Thornhill, Canada
• Investigational Site Number 1249007 — Vancouver, Canada
• Investigational Site Number 1249002 — Victoriaville, Canada
• Investigational Site Number 4849001 — Aguascalientes, Mexico
• Investigational Site Number 8409009 — Escondido, California, United States

Full record on ClinicalTrials.gov

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