Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT07166081
PHASE1

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.

View on ClinicalTrials.gov

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

Interventions

DRUG

BGM0504

Administered orally

DRUG

BGM0504

Administered orally

DRUG

BGM0504

Administered orally

DRUG

Placebo

Administered orally

DRUG

BGM0504

Administered orally

Locations (1)

Pharmaron CPC, Inc

Baltimore, Maryland, United States