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Completed

NCT Number: NCT06974825

A Study of BGM0504 in Chinese Patients With Type 2 Diabetes

The purpose of this study is to evaluate the efficacy and safety of BGM0504 in Chinese patients with Type 2 Diabetes.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The Third Xiangya Hospital of Central South University

Changsha, Hunan, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Have been diagnosed with type 2 diabetes mellitus (T2DM);
  • Glycosylated hemoglobin (HbA1c) at screening/baseline: 7.0% ≤ HbA1c ≤ 10%;
  • Body Mass Index (BMI): 19.5 kg/m2 ≤ BMI ≤ 35.0 kg/m2;
  • Fasting blood glucose (FPG) at screening/baseline: FPG ≤ 13.3 mmoL/L

Exclusion criteria

  • Diagnosed with non-type 2 diabetes mellitus;
  • Grade 3 hypoglycemia within 6 months prior to screening;
  • Concomitant thyroid dysfunction that cannot be controlled at a stable drug dose at screening, or clinically significant abnormalities in thyroid function test results at screening that require initiation of therapy;
  • Subjects with uncontrolled hypertension after treatment (systolic blood pressure ≥ 160 mmHg and/or diastolic blood pressure ≥ 100 mmHg at screening) or untreated blood pressure meeting the above criteria at screening;
  • Patients with a previous history or clinical evidence of acute or chronic pancreatitis;
  • Malignant tumor confirmed within 5 years prior to screening (except cured carcinoma in situ) or potential malignant tumor assessed at screening;
  • Patients with severe mental illness or language disorder at screening, unwilling or unable to fully understand and cooperate;
  • Female subjects during pregnancy or lactation.

Treatment and study plan

BGM0504 Administered SC

Drug

5 milligrams (mg) BGM0504 administered subcutaneously (SC) once a week.

Semaglutide Administered SC

Drug

Active Comparator: 1 mg Semaglutide

1 mg semaglutide administered SC once a week

Placebo Administered SC

Drug

Placebo Comparator: Placebo Placebo administered SC once a week.

Primary outcomes

  1. Change From Baseline in Hemoglobin A1c (HbA1c)

    Time frame: Week 0 to Week 12

    Change from baseline in HbA1c after 12 weeks of treatment.

Secondary outcomes

  1. Change From Baseline in Body Weight

    Time frame: Week 0 to Week 12

    Change from baseline in body weight after 12 weeks of treatment.

  2. Percentage of Participants With HbA1c Target Value of <7%

    Time frame: Week 0 to Week 12

    Percentage of Participants With HbA1c Target Value of <7% after 12 weeks of treatment.

  3. Percentage of Participants With HbA1c Target Value of <6.5%

    Time frame: Week 0 to Week 12

    Percentage of Participants With HbA1c Target Value of <5.7% after 12 weeks of treatment.

  4. Change From Baseline in Fasting Serum Glucose

    Time frame: Week 0 to Week 12

    Change from baseline in FPG after 12 weeks of treatment.

Sponsors and collaborators

Lead sponsor

BrightGene Bio-Medical Technology Co., Ltd.

Industry

Registry information

Official study title

A Randomized, Double-blind, Placebo and Positive Drug Parallel-controlled Phase IIa Clinical Study Protocol to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Characteristics of Multiple-dose BGM0504 Injection in Patients With Type 2 Diabetes Mellitus

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
May 16, 2025
Registry last updated
May 16, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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