LivingGLP1
Study S000782

To Explore the Safety, Tolerability, and Pharmacokinetics/Pharmacodynamics of Multiple Doses of HRS-7535 in Obese Subjects

Registration

Registration
NCT06621316
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1; PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
74
Start
2024-10-30
Primary completion
2025-07-14
Lead sponsor
Shandong Suncadia Medicine Co., Ltd.
Conditions
Overweight or Obesity
Interventions
DRUG:HRS-7535 Tablet; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Number of Adverse Events [24 weeks]

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