LivingGLP1
Study S001139

A Phase III, Multicenter, Randomized, Double Blinded, Parallel-controlled Study Comparing the Efficacy and Safety of HRS9531 Versus Placebo in Subjects With Type 2 Diabetes Mellitus Inadequately Controlled With Basal Insulin.

Registration

Registration
NCT07060456
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
TRIPLE
Status
RECRUITING
Enrollment
300
Start
2025-07-25
Primary completion
2027-02
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Type 2 Diabetes
Interventions
DRUG:HRS9531; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Change in HbA1c [from baseline to Week 40]

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