The Third Xiangya Hospital of Central South University
Changsha, Hunan, China
NCT Number: NCT06974825
The purpose of this study is to evaluate the efficacy and safety of BGM0504 in Chinese patients with Type 2 Diabetes.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
Changsha, Hunan, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
5 milligrams (mg) BGM0504 administered subcutaneously (SC) once a week.
Active Comparator: 1 mg Semaglutide
1 mg semaglutide administered SC once a week
Placebo Comparator: Placebo Placebo administered SC once a week.
Time frame: Week 0 to Week 12
Change from baseline in HbA1c after 12 weeks of treatment.
Time frame: Week 0 to Week 12
Change from baseline in body weight after 12 weeks of treatment.
Time frame: Week 0 to Week 12
Percentage of Participants With HbA1c Target Value of <7% after 12 weeks of treatment.
Time frame: Week 0 to Week 12
Percentage of Participants With HbA1c Target Value of <5.7% after 12 weeks of treatment.
Time frame: Week 0 to Week 12
Change from baseline in FPG after 12 weeks of treatment.
BrightGene Bio-Medical Technology Co., Ltd.
Industry
A Randomized, Double-blind, Placebo and Positive Drug Parallel-controlled Phase IIa Clinical Study Protocol to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Characteristics of Multiple-dose BGM0504 Injection in Patients With Type 2 Diabetes Mellitus
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.
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