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Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of BGM0504 Tablets in Non-diabetic Overweight or Obese Adult Subjects
Sponsor: BrightGene Bio-Medical Technology Co., Ltd.
Summary
This is a Phase 1, single-center, randomized, placebo-controlled, ascending dose study. The study will evaluate the pharmacokinetics (PK), pharmacodynamic (PD), preliminary efficacy, safety and tolerability of BGM0504 following daily oral administrations in non-diabetic overweight or obese adult subjects.
Official title: 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
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
80
Start Date
2025-08-11
Completion Date
2026-05-13
Last Updated
2025-09-19
Healthy Volunteers
No
Conditions
Interventions
BGM0504
Administered orally
BGM0504
Administered orally
BGM0504
Administered orally
Placebo
Administered orally
BGM0504
Administered orally
Locations (1)
Pharmaron CPC, Inc
Baltimore, Maryland, United States