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A Phase 1, Multiple Ascending Dose Study to Evaluate HMS1005 in Participants With Type 2 Diabetes

2026年4月28日 更新者:Hua Medicine Limited

A Phase 1, Randomized, Placebo-Controlled, Double-Blind, Multiple- Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of HMS1005 in Participants With Type 2 Diabetes

The study is to assess the safety, pharmacokinetics, and pharmacodynamic profile of HMS1005 in patient with diabetes

研究概览

地位

招聘中

条件

研究类型

介入性

注册 (估计的)

40

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Florida
      • Miami、Florida、美国、33172
        • 招聘中
        • Clinical Pharmacology of Miami
        • 接触:
        • 首席研究员:
          • Alexander N Prezioso, MD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Males or females, of any race, between 18 and 65 years of age, inclusive.
  2. Body mass index between 18 and 38.0 kg/m2, inclusive.
  3. Females will not be pregnant or lactating, and females of childbearing potential and males will agree to use contraception as detailed in Appendix 3.
  4. T2DM, as determined by the ADA Standard Care Diagnostic Criteria 2025, and

    • are drug naïve, treated with diet and exercise, or
    • have been on a stable dose of ≤2000 mg metformin for ≥1 month, and/or
    • have been on a stable dose of other antidiabetic medications for ≥90 days.
  5. Except for findings consistent with T2DM, in good health, determined from medical history, 12-lead electrocardiogram (ECG), vital signs measurements, clinical laboratory evaluations, and physical examinations at screening and/or check in, as assessed by the Investigator (or designee).
  6. Doses of antihypertensive and lipid-lowering therapies must be stable for 30 days prior to screening and remain unchanged during the study unless necessary to protect participant safety on an emergency basis (e.g., hypertensive crisis).
  7. Glycated hemoglobin between 7.0% and 10.5%, inclusive.
  8. Fasting plasma glucose between 126 and 240 mg/dL, inclusive. Testing may be repeated once, at the discretion of the Investigator (or designee).
  9. Able to comprehend and willing to sign an ICF and to abide by the study restrictions.

Exclusion Criteria:

  1. Type 1 diabetes mellitus, maturity onset diabetes of the young, or diabetes mellitus caused by damage to the pancreas or any other condition (eg, acromegaly or Cushing's syndrome).
  2. Diabetic neuropathy, retinopathy, or nephropathy.
  3. History of acute diabetic complications such as diabetic ketoacidosis, hyperglycemic hyperosmolar syndrome, lactic acidosis, or hyperosmolar nonketotic coma within the 6 months prior to screening, or chronic metabolic acidosis.
  4. History of severe hypoglycemia, defined as severe cognitive impairment requiring external assistance for recovery within 3 months prior to dosing; or recurrent hypoglycemia (Level 2), defined as ≥2 episodes within 3 months prior to dosing; or ADA Level 3 hypoglycemia within 6 months prior to dosing.
  5. Hypoglycemia unawareness or asymptomatic hypoglycemia.
  6. Clinically significant history of liver disease (eg, hepatitis and cirrhosis) within 1 year prior to screening.
  7. Clinically significant history of renal disease. Mild to moderate chronic kidney disease is permitted.
  8. Clinically significant history of cardiovascular disease, particularly coronary artery disease, arrhythmias, atrial tachycardia, or congestive heart disease within 1 year prior to screening. Managed hypertension is permitted (defined as systolic blood pressure <160 mmHg and/or diastolic blood pressure <100 mmHg).
  9. Clinically significant history of any central nervous system or psychiatric disease, including transient ischemic attack, stroke, seizure disorder, depression, or behavioral disturbances within 1 year prior to screening.
  10. Clinically significant gastric emptying abnormality (eg, severe diabetic gastroparesis or gastric outlet obstruction) or have had gastric bypass surgery.
  11. Clinically significant or unstable history of any hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, endocrine, or psychiatric disorder, as determined by the Investigator (or designee).
  12. Known or active malignancy, except basal cell carcinoma and cutaneous squamous cell carcinoma.
  13. Any hospital admission or major surgery within 90 days prior to screening.
  14. History of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, as determined by the Investigator (or designee).
  15. Fasting C peptide < 0.81 ng/mL.
  16. Alanine aminotransferase, aspartate aminotransferase, or gamma glutamyl transferase >2 × the upper limit of normal (ULN); or total bilirubin >1.5× ULN. Testing may be repeated once, at the discretion of the Investigator (or designee).
  17. Uncontrolled hypertriglyceridemia > 500 mg/dL.
  18. Estimated glomerular filtration rate ≤ 45 mL/minutes/1.73 m2, as calculated using the 2021 Chronic Kidney Disease Epidemiology equation.
  19. Hemoglobin ≤120 g/L (male) or ≤110 g/L (female).
  20. QT interval corrected for heart rate using Fridericia's method > 450 msec.
  21. Positive hepatitis B surface antigen, hepatitis C antibody, human immunodeficiency (HIV 1 and HIV 2) antibodies and p24 antigen.
  22. Positive pregnancy test.
  23. Use of insulin, sulfonylureas, GLP-1 agonists, DPP-4 inhibitors, SGLT2 inhibitor and glinides (eg, repaglinide and nateglinide).
  24. Use of any strong or moderate cytochrome P450 (CYP) 3A4 inducers within 28 days prior to dosing or any strong or moderate CYP3A4 inhibitors within 7 days or 5 half-lives, whichever is longer, prior to dosing (Appendix 5).
  25. Use of any P glycoprotein inducers within 14 days prior to dosing or any P glycoprotein inhibitors within 5 days or 5 half-lives, whichever is longer, prior to dosing (Appendix 6).
  26. Use of any carboxylesterase 2 inhibitors within 5 days or 5 half-lives, whichever is longer, prior to dosing (Appendix 7).
  27. Participation in a clinical study involving administration of an investigational drug (new chemical entity) in the past 30 days.
  28. Positive alcohol test result, or positive urine drug screen (confirmed by repeat) at screening or check in.
  29. Current drug abuse, defined as the use of any illegal substance or misuse or excessive used of over the counter or prescription drugs; or current alcohol abuse, defined as the inability to stop or control alcohol use, despite adverse social or health consequences.
  30. Consumption of alcohol, or caffeine containing foods or beverages within 48 hours, or foods and beverages containing grapefruit or Seville oranges within 7 days prior to check in.
  31. Use of tobacco or nicotine containing products within 1 month prior to screening.
  32. Receipt or donation of > 1 unit (approximately 450 mL) of blood products within 3 months prior to screening.
  33. Poor peripheral venous access.
  34. Participants who, in the opinion of the Investigator (or designee), should not participate in this study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:顺序分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:123 mg HMS1005 (1 x 123 mg tablet) and matching placebo
active vs placebo: 6 to 2
匹配安慰剂
The investigational medicinal products (IMPs) HMS1005 ER tablets
实验性的:184.5 mg HMS1005 (1 x 184.5 mg tablet) and matching placebo
active vs placebo: 6 to 2
匹配安慰剂
The investigational medicinal products (IMPs) HMS1005 ER tablets
实验性的:369 mg HMS1005 (2 x 184.5 mg tablet) and matching placebo
active vs placebo: 6 to 2
匹配安慰剂
The investigational medicinal products (IMPs) HMS1005 ER tablets
实验性的:492 mg HMS1005 (2 x 246 mg tablet) and matching placebo
active vs placebo: 6 to 2
匹配安慰剂
The investigational medicinal products (IMPs) HMS1005 ER tablets
实验性的:246 mg HMS1005 (1 x 246 mg tablet) or placebo
active vs placebo: 6 to 2
匹配安慰剂
The investigational medicinal products (IMPs) HMS1005 ER tablets

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Incidence of adverse events
大体时间:From enrollment to the end of treatment at Day 19
incidence and severity of adverse events from Day1 to Day 19
From enrollment to the end of treatment at Day 19
Area under the plasma concentration versus time curve (AUC)
大体时间:Single-dose: Day 1-3 steady-state: Day 14-17
Measure area under the concentration-time curve from time 0 to 72 hours postdose of HM-002-1005 in plasma after single-dose and at steady-state
Single-dose: Day 1-3 steady-state: Day 14-17
Maximum observed concentration (Cmax)
大体时间:Single-dose: Day 1-3 steady-state: Day 14-17
Cmax of HM-002-1005 in plasma after single and multiple dose
Single-dose: Day 1-3 steady-state: Day 14-17
Time of the maximum observed concentration (Tmax)
大体时间:Single-dose: Day 1-3 steady-state: Day 14-17
Time of the maximum observed concentration (Tmax) of HM-002-1005
Single-dose: Day 1-3 steady-state: Day 14-17
Apparent terminal elimination half life (t1/2)
大体时间:Single-dose: Day 1-3 steady-state: Day 14-17
t1/2 of HM-002-1005 in plasma
Single-dose: Day 1-3 steady-state: Day 14-17

次要结果测量

结果测量
措施说明
大体时间
Glucose concentration
大体时间:Day -1 and 14
Measure serum glucose concentration over 24 hours after dosing
Day -1 and 14
Glucose time in range (70-180 mg/dL) %
大体时间:From Day -10 (baseline) to Day 17
Percentage of glucose time in range (70-180 mg/dL) will measured by continous glucose monitor
From Day -10 (baseline) to Day 17

其他结果措施

结果测量
措施说明
大体时间
Insulin concentration
大体时间:Day -2, -1, 13, and 14
Measure serum insulin concentration under fasting condition and postmeal
Day -2, -1, 13, and 14
C-peptide concentration
大体时间:Day -2, -1, 13, and 14
C-peptide concentration under fasting and after meal
Day -2, -1, 13, and 14
Glucagon concentration
大体时间:Day -2, -1, 13, and 14
Measure serum glucagon concentration under fasting and postmeal
Day -2, -1, 13, and 14
GLP-1 concentration
大体时间:Day -1 and Day 14
Measure postmeal GLP-1 concentration in blood
Day -1 and Day 14

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

合作者

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年12月4日

初级完成 (估计的)

2026年8月13日

研究完成 (估计的)

2026年10月13日

研究注册日期

首次提交

2026年1月20日

首先提交符合 QC 标准的

2026年4月28日

首次发布 (实际的)

2026年5月6日

研究记录更新

最后更新发布 (实际的)

2026年5月6日

上次提交的符合 QC 标准的更新

2026年4月28日

最后验证

2026年4月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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