LivingGLP1
Study S001310

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

Registration

Registration
NCT06650007
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
218
Start
2024-11-08
Primary completion
2026-01-21
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:HRS9531 Injection; DRUG:HRS9531 Placebo Injection
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Change in HbA1c [from baseline to 36 weeks treatment]

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