LivingGLP1
Study S000223

A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ASC47 Injection, for Subcutaneous Use in Combination With Semaglutide in Participants With Obesity

Registration

Registration
NCT06972992
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
TRIPLE
Status
COMPLETED
Enrollment
28
Start
2025-04-18
Primary completion
2025-09-22
Lead sponsor
Ascletis Pharma (China) Co., Limited
Conditions
Chronic Weight Management
Interventions
DRUG:ASC47 +Semaglutide; DRUG:Placebo+Semaglutide
Results posted
FALSE

Registered primary outcomes

  • Adverse events [up to 71 days]

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