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the Efficacy and Safety of HRS9531 Injection in Subjects With Type 2 Diabetes, Inadequately Controlled With Diet and Exercise Alone
Sponsor: Fujian Shengdi Pharmaceutical Co., Ltd.
Summary
The primary objective of this study is to evaluate the effectiveness of HRS9531 compared to placebo in controlling blood glucose levels after 24 weeks of treatment
Official title: A Multicenter, Randomized, Double-blind, Placebo- Parallel Controlled, Phase III Study to Evaluate the Efficacy and Safety of HRS9531 Injection in Subjects With Type 2 Diabetes, Inadequately Controlled With Diet and Exercise Alone
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
218
Start Date
2024-11-08
Completion Date
2026-07
Last Updated
2025-06-12
Healthy Volunteers
No
Conditions
Interventions
HRS9531 Injection
HRS9531 Injection
HRS9531 Placebo Injection
HRS9531 Placebo Injection
Locations (1)
The Second Xiangya Hospital of Central South University
Changsha, Hunan, China