LivingGLP1
Study S000874

A Phase I Study of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Multiple Doses of HRS9531 Tablets in Healthy Subjects

Registration

Registration
NCT06435676
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
TRIPLE
Status
COMPLETED
Enrollment
72
Start
2024-06-04
Primary completion
2024-10-08
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Overweight or Obesity; Type 2 Diabetes
Interventions
DRUG:HRS9531; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • SAD Stage: Number of Adverse Events [36 days]
  • MAD Stage: Number of Adverse Events [63 days]

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