drugset / Trial / NCT01958671

A Study of the Efficacy and Safety of Ertugliflozin Monotherapy in the Treatment of Participants With Type 2 Diabetes Mellitus and Inadequate Glycemic Control Despite Diet and Exercise (MK-8835-003, VERTIS MONO)

NCT01958671 ↗

Phase 3 Completed 461 enrolled Merck Sharp & Dohme LLC Pfizer · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

This trial will evaluate the efficacy and safety of ertugliflozin monotherapy in the treatment of participants with type 2 diabetes mellitus (T2DM) and inadequate glycemic control on diet and exercise. This trial consists of a run-in period of 3 to 11 weeks, a 26-week placebo-controlled treatment period (Phase A), and a 26-week active treatment period (Phase B). The primary hypotheses of the trial are that at Week 26, the mean reduction from baseline in hemoglobin A1c (A1C) for 15 mg ertugliflozin is greater than that for placebo and the mean reduction from baseline in A1C for 5 mg ertugliflozin is greater than that for placebo.

Timeline

Start
2013-10-09
Primary completion
2016-07-28
Completion
2016-07-28

Outcome

Met primary endpoint

registry analysis (superiority or other test); Ertugliflozin 5 mg vs Placebo; p <0.001; Difference in least squares means -0.99 (95% CI -1.22 to -0.76) NCT01958671 ↗

registry analysis (superiority or other test); Ertugliflozin 15 mg vs Placebo; p <0.001; Difference in least squares means -1.16 (95% CI -1.39 to -0.93) NCT01958671 ↗

release “A 26-week investigational study (VERTIS Mono), which evaluated ertugliflozin as monotherapy, met its primary endpoint” merck.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ertugliflozin Unknown 5 mg Oral
Subject Ertugliflozin Unknown 15 mg Oral
Background Glimepiride Small molecule — —
Background Metformin Small molecule 1000 mg —