This is a Phase 1, double-blind, parallel-arm ,placebo-controlled study. The study will evaluate the pharmacokinetics (PK), pharmacodynamic (PD), safety and tolerability of BGM0504 following multiple subcutaneous (SC) administrations in non-diabetic overweight or obese adult subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
30
Drug: BGM0504 Administered SC
Drug: BGM0504 Administered SC
Drug: Placebo Administered SC
Pharmaron CPC, Inc
Baltimore, Maryland, United States
Number of treatment adverse events
The relationship of each adverse event tothe investigational product was assessed by the investigator
Time frame: 10 weeks
Pharmacokinetic endpoint: Concentration of BGM0504 in plasma
Time frame: 10 weeks
Change in fasting weight at week 10
Time frame: 10 weeks
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