LivingGLP1
Study S003240

A Phase 1, Double-Blind, Randomized, Ascending-Dose, Placebo-Controlled, Multiple-dose Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of BGM0504 Tablets Orally Administered in Non-diabetic Overweight or Obese Adult Subjects

Registration

Registration
NCT07166081
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
RECRUITING
Enrollment
80
Start
2025-08-11
Primary completion
2026-01-12
Lead sponsor
BrightGene Bio-Medical Technology Co., Ltd.
Conditions
Non-diabetic Overweight or Obese
Interventions
DRUG:BGM0504; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • Number of treatment adverse events [11 weeks]

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