CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 601 enrolled
Drug / intervention
semaglutide +1 moredrug
Likely dose
semaglutide 1.0 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/NCT02207374
NCT02207374Phase 3Completed

Safety and Efficacy of Semaglutide Once Weekly in Monotherapy or in Combination With One OAD in Japanese Subjects With Type 2 Diabetes Who Are Insufficiently Controlled on Diet/Exercise Therapy or OAD Monotherapy

Novo Nordisk A/S·interventional·Posted Aug 4, 2014·Updated Jan 7, 2019

In Brief

A Phase 3 clinical trial evaluating semaglutide and DPP-4 inhibitor for Diabetes and Diabetes Mellitus, Type 2. Completed, enrolled 601 participants across 43 sites.

Detailed Summary

This trial is conducted in Asia. The aim of the trial is to investigate safety and efficacy of semaglutide once weekly in monotherapy or in combination with one OAD (oral anti-diabetic drug) in Japanese subjects with type 2 diabetes who are insufficiently controlled on diet/exercise therapy or OAD monotherapy. All subjects will continue their pre-trial treatment (diet and exercise therapy or OAD monotherapy in addition to diet and exercise therapy) during the trial.

Study Details

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

Timeline

Phase 3CompletedFinished
201520162017201820192020202120222023202420252026
First PostedAug 4, 2014
Enrollment StartAug 4, 2014
Primary CompletionFeb 27, 2016
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 11.9 years ago

Interventions

semaglutidedrug

Subject will receive either a dose of 0.5 or 1.0 mg of semaglutide once weekly (subcutaneous (s.c.) injection).Treatment duration 56 weeks.

DPP-4 inhibitordrug

Subjects will receive one DPP-4 inhibitor in addition to pre-trial OAD monotherapy, if any, for 56 weeks.