LivingGLP1
Study S003354

A Phase 1, Double-Blind, Parallel-arm, Placebo-Controlled, Multiple-dose Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of BGM0504 Injection Administered Subcutaneously in Non-diabetic Overweight or Obese Adult Subjects

Registration

Registration
NCT06714955
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
30
Start
2024-10-21
Primary completion
2025-01-21
Lead sponsor
BrightGene Bio-Medical Technology Co., Ltd.
Conditions
Non-diabetic Overweight or Obese
Interventions
DRUG:Experimental: 10 mg BGM0504 10 milligrams (mg) BGM0504 administered subcutaneously (SC) once a week.; DRUG:Experimental: 15 mg BGM0504 15 mg BGM0504 administered SC once a week.; DRUG:Placebo Comparator: Placebo Placebo administered subcutaneously (SC) once a week.
Results posted
FALSE

Registered primary outcomes

  • Number of treatment adverse events [10 weeks]

Linked records (0)

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