Diabetes Mellitus, Type 2 Clinical Trial
Official title:
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Daily Oral TAK-875 25 mg and 50 mg Compared With Placebo in Subjects With Type 2 Diabetes
The purpose of this study is to determine the efficacy and safety of TAK-875, once daily (QD), in participants with type 2 diabetes mellitus (T2DM).
TAK-875 is being developed at Takeda Global Research and Development, Inc. as an adjunct to
diet and exercise to improve glycemic control in patients with T2DM.
This study will investigate TAK-875 in participants with type 2 diabetes mellitus who have
been treated with only diet and exercise for at least 12 weeks prior to Screening, who have
taken ≤7 days of any antidiabetic agent within the 12 weeks prior to Screening, and whose
glycemic control is inadequate.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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