The purpose of this study is to evaluate the safety, tolerability, and efficacy of LX4211 versus a placebo control in subjects with type 2 diabetes mellitus.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
36
A low dose of LX4211; daily oral intake for 28 days
A high dose of LX4211; daily oral intake for 28 days
Matching placebo dosing with daily oral intake for 28 days
Lexicon Investigational Site
San Antonio, Texas, United States
Change From Baseline at Day 28 in 24-hour Urinary Glucose Excretion
To assess 24-hour urinary glucose excretion, urine was collected over a 24-hour period and evaluated for glucose concentration.
Time frame: Baseline to Day 28
Change From Baseline at Day 29 in Fasting Plasma Glucose
Time frame: Baseline to Day 29
Change From Baseline at Day 28 in Plasma HbA1c
Time frame: Baseline to Day 28
Change From Baseline at Day 28 in Plasma Fructosamine Level
Time frame: Baseline to Day 28
Change From Baseline at Day 28 in Mean Arterial Pressure
Time frame: Baseline to Day 28
Change From Baseline at Day 28 in Triglycerides
Time frame: Baseline to Day 28
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.