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NCT03061214Completed

Efficacy and Safety of Semaglutide Once-weekly Versus Sitagliptin Once-daily as add-on to Metformin in Subjects With Type 2 Diabetes (SUSTAIN - CHINA MRCT)

Efficacy and Safety of Semaglutide Once-weekly Versus Sitagliptin Once-daily as add-on to Metformin in Subjects With Type 2 Diabetes. A 30-week Randomised, Double-blind, Double-dummy, Active-controlled, Parallel-group, Multi-centre and Multi-national Trial
Novo Nordisk A/SPhase 3ClinicalTrials.govdrug
Study focus
Drug/Device/Intervention
Semaglutide 0.5 mg
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Novo Nordisk A/S
Location
Aparecida de Goiania,Porto Alegre,São Paulo,Hefei,Hefei,Beijing,Beijing,Beijing,Beijing,Beijing,ChongQing,Fuzhou,Guangzhou,Guangzhou,Guangzhou,Zhuhai,Guiyang,Qiqihar,Chenzhou,Changzhou,Nanjing,Nanjing, Brazil,China,China,South Korea,South Africa,Taiwan,Ukraine
Timeline & enrollment
Phase
Phase 3
Start date
Aug 28, 2017
End date
Apr 15, 2019
Enrollment
868 participants
Primary outcome

Change in HbA1c

Summary

This trial is conducted in Africa, Asia, Europe and South America. The aim of the trial is to
 compare the effect of once-weekly dosing of two dose levels of semaglutide versus sitagliptin
 100 mg once-daily on glycaemic control after 30 weeks of treatment. Subjects will remain on
 their stable pre-trial metformin.

ICD-10 classifications
Type 2 diabetes mellitusType 2 diabetes mellitus with other specified complicationsType 2 diabetes mellitus with unspecified complicationsType 2 diabetes mellitus without complicationsType 2 diabetes mellitus with multiple complications
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT03061214
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT03061214 through Pure Global AI's free database. This Phase 3 trial is sponsored by Novo Nordisk A/S and is currently Completed. The study focuses on Diabetes,Diabetes Mellitus, Type 2. Target enrollment is 868 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.