CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 458 enrolled
Drug / intervention
Sitagliptin +2 moredrug
Likely dose
Sitagliptin 100 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02791490
NCT02791490Phase 3Completed

A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Trial to Study the Safety and Efficacy of the Addition of Sitagliptin During Metformin Up-titration Compared With Metformin Up-titration Alone in Subjects With Type 2 Diabetes Mellitus

Merck Sharp & Dohme LLC·interventional·Posted Jun 6, 2016·Updated Feb 28, 2019

In Brief

A Phase 3 clinical trial evaluating Sitagliptin, Placebo, and 1 other intervention for Type 2 Diabetes Mellitus. Completed, enrolled 458 participants.

Detailed Summary

This trial is designed to evaluate, in adult participants with Type 2 diabetes mellitus (T2DM) and inadequate glycemic control on sub-maximal metformin mono-therapy (1000 mg/day), the effect of up-titration of metformin plus the addition of sitagliptin compared to up-titration of metformin alone on glycemic control. The primary hypothesis of this study is that up-titration of metformin to 2000 mg/day (1000 mg/twice a day) plus the addition of sitagliptin 100 mg/day provides greater reduction in hemoglobin A1C (A1C) compared to metformin up-titration alone. Another primary objective of this study is to evaluate the safety and tolerability of this treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

Phase 3CompletedFinished
2017201820192020202120222023202420252026
First PostedJun 6, 2016
Enrollment StartJun 16, 2016
Primary CompletionFeb 1, 2018
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 10.1 years ago

Interventions

Sitagliptindrug

Oral tablet, 100 mg, once daily at approximately the same time each day

Placebodrug

Oral tablet, once daily at approximately the same time each day

Metformin IRdrug

All participants will take Met-IR as background medication. Initially, they will take 1 x 500 mg tablet Met-IR b.i.d. (1000 mg/day). After randomization, all participants will be titrated to 2 x 500 mg tablets of Met-IR b.i.d. (2000 mg/day).