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Clinical Trial Summary

This Phase 2, multi-center, double-blind, randomized, placebo-controlled, parallel group, add-on study of MLR 1023 in adults with uncontrolled T2DM on metformin anti diabetic monotherapy is designed to evaluate the efficacy and safety of MLR 1023 in combination with metformin in subjects with uncontrolled T2DM.


Clinical Trial Description

Medical management of T2DM involves diet, exercise, weight management, and pharmacotherapy. Pharmacological agents, such as metformin, α-glucosidase inhibitors, orlistat, and thiazolidinediones, have been shown to decrease incident diabetes. Metformin has the strongest evidence base and demonstrated long-term safety as pharmacological therapy for diabetes treatment. The American Diabetes association position statement on diabetes care recommends that if Hemoglobin A1C (HbA1C) targets are not achieved after approximately 3 months of metformin anti-diabetic monotherapy, a combination of metformin and one of several oral treatment options should be considered.

In this study, subjects with a diagnosis of T2DM who are not adequately controlled (HbA1C between 7.0% and 10.0%, inclusive) and started metformin therapy at least 3 months prior to Screening will be recruited into the study. Subjects will continue taking metformin for the duration of the study and once daily oral MLR 1023 or placebo will be added to metformin.

The efficacious dose-level range of MLR 1023 in diabetic subjects is anticipated to be between 25 and 100 mg. Therefore, the efficacy, safety, and tolerability of 25 mg and 50 mg doses in addition to the 100 mg dose that was shown to be effective in the Phase 2a proof of concept study will be assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03279263
Study type Interventional
Source Melior Pharmaceuticals
Contact
Status Active, not recruiting
Phase Phase 2
Start date September 1, 2017
Completion date September 2019

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