LivingGLP1
Study S000738

A Multi-center, Randomized, Double-blind, Placebo- Parallel Controlled, Phase II Study to Evaluate the Efficacy and Safety of HRS9531 Injection in Type 2 Diabetes Subjects

Registration

Registration
NCT05966272
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
199
Start
2023-08-12
Primary completion
2024-09-24
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Type 2 Diabetes
Interventions
DRUG:HRS9531 injection; DRUG:HRS9531 injection Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Change From Baseline in HbA1c after 20 weeks of treatment [Week 0 to Week 20]

Linked records (0)

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