RecruitingPhase 1NCT07224399

Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of BGM1812 Injection Following Single and Multiple Subcutaneous Administration in Normal to Overweight or Obese But Otherwise Healthy Men and Women

A Phase 1, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of BGM1812 Injection Following Single and Multiple Subcutaneous Administration in Normal to Overweight or Obese But Otherwise Healthy Men and Women


Sponsor

BrightGene Bio-Medical Technology Co., Ltd.

Enrollment

60 participants

Start Date

Oct 9, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a Phase 1, single-center, double-blind, placebo-controlled, dose-escalation study. The study will evaluate the pharmacokinetics (PK), pharmacodynamic (PD), preliminary efficacy, safety and tolerability of BGM1812 following single and multiple SC administrations in normal to overweight or obese but otherwise healthy subjects.


Eligibility

Min Age: 18 YearsMax Age: 55 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called BGM1812, a drug called BGM1812, and others for people with healhty and overweight or obesity. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 55 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGBGM1812

Administered SC.

DRUGPlacebo

Administered SC.

DRUGBGM1812

Administered SC.

DRUGPlacebo

Administered SC.


Locations(1)

Pharmaron CPC, Inc

Baltimore, Maryland, United States

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NCT07224399


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