LivingGLP1
Study S002090

A Phase 1, Randomized, Double-Blind, Placebo- and Positive-Controlled Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Subcutaneous Injections of HRS9531 in Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT05516966
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
64
Start
2022-10-12
Primary completion
2023-05-24
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:HRS9531; DRUG:Placebo; DRUG:Dulaglutide Injection
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Incidence of Adverse Events (Safety and Tolerability) [Screening period up to Day 62]

Linked records (0)

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