SHR-3167
DrugSHR-3167 Injection.
NCT Number: NCT07018453
The purpose of this study is to evaluate the glycemic control and safety of SHR-3167 and Insulin Degludec in type 2 diabetic participants treated with basal insulin with or without oral antidiabetic drugs.
This study is active but is not currently recruiting participants.
Notify Me18 year–65 year
All sexes
Interventional
Phase 2
The First Affiliated Hospital of Chongqing Medical University, Chongqing, Chongqing Municipality, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
SHR-3167 Injection.
Insulin Degludec Injection.
Time frame: 16 weeks.
Time frame: 16 weeks.
Time frame: 16 weeks.
Time frame: 16 weeks.
Jiangsu HengRui Medicine Co., Ltd.
Industry
A Randomized, Open-label, Treat-to-target, Parallel-Controlled Phase II Clinical Study Investigating the Efficacy and Safety of SHR-3167 and Insulin Degludec in Type 2 Diabetic Subjects Treated With Basal Insulin With or Without Oral Antidiabetic Drugs
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06208189
Diabetes Mellitus, Diabetes Mellitus, Type 2
Albuquerque, New Mexico, United States
View Trial DetailsNCT07228117
Autoimmune Diseases, Diabetes Mellitus
Little Rock, Arkansas, United States
View Trial DetailsNCT06848244
Binge Eating, Binge-Eating Disorder
Chapel Hill, North Carolina, United States
View Trial DetailsNCT07775664
Arterial Occlusive Diseases, Arteriosclerosis
Shanghai, Shanghai Municipality, China
View Trial Details