Type 2 Diabetes Mellitus Clinical Trial
Official title:
A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study of Safety and Efficacy of LGD-6972 in Patients With Type 2 Diabetes Mellitus
The purpose of this study is to evaluate the change from baseline in hemoglobin A1c (HbA1c) during 12 weeks of treatment with 3 dose levels of LGD-6972 compared to placebo in subjects with Type 2 Diabetes Mellitus (T2DM)
This will be a 12-week, randomized, double-blind, placebo-controlled, 4-arm, parallel group,
multi-center study to evaluate the safety and efficacy of LGD-6972 in subjects with T2DM
inadequately controlled on metformin monotherapy (a stable [≥12 weeks], daily dose of ≥1000mg
at randomization). Subjects with T2DM will be treated with one of 3 dose levels of LGD-6972
(5 mg, 10 mg, or 15 mg) or placebo once daily (QD) for 12 weeks. Randomization will be
stratified by HbAlc ≤8.5% or >8.5% at the Placebo Lead-in Visit.
Qualified subjects who require adjustment or stabilization of their metformin dose will
participate in a run-in period of up to 12 additional weeks prior to randomization. Subjects
will have the option to participate in an oral glucose tolerance test (OGTT) at baseline and
end of treatment for assessment of exploratory endpoints.
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