LivingGLP1
Study S003371

A Single-Center, Single-Dose, Randomized, Open-Label, Single-Period, Parallel Bioequivalence Study of BGM0504 Injection in Overweight/Obese Participants

Registration

Registration
NCT07382908
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
RECRUITING
Enrollment
144
Start
2025-12-23
Primary completion
2026-02-12
Lead sponsor
BrightGene Bio-Medical Technology Co., Ltd.
Conditions
Overweight/Obesity
Interventions
DRUG:BGM0504 Injection multi-dose pen; DRUG:BGM0504 Injection single-dose pen
Results posted
FALSE

Registered primary outcomes

  • Peak Plasma Concentration (Cmax) [0 to 672 hours]
  • Area under the plasma concentration versus time curve (AUC)0-t [0 to 672 hours]

Linked records (0)

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