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NCT03172494Completed

A Trial Comparing Insulin Degludec/Liraglutide, Insulin Degludec, and Liraglutide in Chinese Subjects With Type 2 Diabetes Inadequately Controlled on Oral Antidiabetic Drugs (OADs)

A Trial Comparing the Efficacy and Safety of Insulin Degludec/Liraglutide, Insulin Degludec, and Liraglutide in Chinese Subjects With Type 2 Diabetes Inadequately Controlled on Oral Antidiabetic Drugs (OADs)
Novo Nordisk A/SPhase 3ClinicalTrials.govdrug
Study focus
Drug/Device/Intervention
Insulin degludec/liraglutide
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Novo Nordisk A/S
Location
Hefei,Beijing,Beijing,ChongQing,Fuzhou,Fuzhou,Guangzhou,Guangzhou,Guangzhou,Cangzhou,Shijiazhuang,Shijiazhuang,Changzhou,Huai'an,Huai'an,Nanjing,Nanjing,Nanjing,Zhenjiang,Nanchang,Changchun,Dalian,Yin, China
Timeline & enrollment
Phase
Phase 3
Start date
May 26, 2017
End date
Jul 13, 2019
Enrollment
720 participants
Primary outcome

Change in HbA1c

Summary

This trial is conducted in Asia. The aim of this trial is to confirm the efficacy of insulin
 degludec/liraglutide in controlling glycaemia in Chinese subjects with type 2 diabetes
 mellitus inadequately controlled on oral antidiabetic agents

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
NCT03172494
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT03172494 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 720 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.