GLPwatch

A Research Study to See if Two Different Formulations of Oral Semaglutide Are Equally Safe and Effective in Reducing the Blood Sugar Level in Japanese People With Type 2 Diabetes

NCT07271251 · Active, not recruiting

Last updated 2026-05-28

This study is testing whether two different versions of an oral diabetes medication called semaglutide work equally well in lowering blood sugar levels in Japanese adults with type 2 diabetes.

Status Active, not recruiting Ongoing, but no longer enrolling new participants.
Phase Phase 3 Confirms effectiveness in a large group before approval.
Type Interventional (clinical trial)
Design Randomized, open-label (no blinding) treatment study
Participants 264 people Planned (estimated).
Who can join Ages 18+ · all sexes
Timeline Started 2025-12 · est. completion 2026-08
Where 15 sites · Japan

What this study is testing ClinicalTrials.gov NCT07271251 ↗

Description as written by the study sponsor.

The purpose of the study is to find out if the new tablet formulation oral semaglutide D is equally safe and effective as the approved oral semaglutide for treating Japanese people with type 2 diabetes. Participants will receive either oral semaglutide D (the treatment being tested) or oral semaglutide (the comparator); which treatment a participant gets is decided by chance. Oral semaglutide is an approved tablet (a treatment used as a comparator), while oral semaglutide D is described as the new tablet formulation being tested in this study. The study will last approximately 27 weeks.

Treatments tested

Main thing measuredChange in glycated haemoglobin (HbA1c).
SponsorNovo Nordisk A/S
Conditions studiedType 2 Diabetes
GLP-1 drugs semaglutide

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT07271251 ↗