Article ID Journal Published Year Pages File Type
8528407 Clinical Therapeutics 2017 15 Pages PDF
Abstract
After 52 weeks, patients receiving canagliflozin added to background SU had sustained reductions in HbA1c and fasting plasma glucose, without increasing hypoglycemia and body weight; safety findings were generally consistent with the known safety profile of the drug. ClinicalTrials.gov identifier: NCT01032629.
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Authors
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