Expired Study
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San Antonio, Texas 78209


This protocol is intended to compare the effects of both a solid (tablet) and liquid oral dosage form of LX4211 in subjects with type 2 diabetes mellitus.


Inclusion Criteria: - Adults aged 18 to 65 years of age - Males and females of non-childbearing potential - Diagnosis of type 2 diabetes mellitus for at least 6 months prior to screening - Fasting plasma glucose ≤240 mg/dL - Body mass index <42 kg/sq m - HbA1c of 7-11% - C-peptide of ≥1.0 ng/mL - Ability to provide written informed consent Exclusion Criteria: - History of type 1 diabetes mellitus, diabetic ketoacidosis, hyperosmolar nonketonic syndrome, incontinence, or nocturia - Current use of any blood glucose-lowering agent other than metformin - Exposure to insulin, thiazide, or loop diuretics within 4 weeks prior to screening - History of HIV, Hepatitis B, or Hepatitis C - Surgery within 6 months of screening - Donation or loss of >400 mL of blood or blood product within 8 weeks prior to start of study - Use of proteins or antibodies within 12 weeks prior to screening. (Flu shots are allowed.) - Exposure to any investigational agent or participation in an investigational trial within 30 days of the start of the study - History of drug or alcohol abuse within 12 months prior to screening.



Primary Contact:

Study Director
Joel P. Freiman, MD, MPH
Lexicon Pharmaceuticals, Inc.

Backup Contact:


Location Contact:

San Antonio, Texas 78209
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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