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Fuling Yunhua Granules and Dihuang Baoyuan Granules in Adults With Type 2 Diabetes and Poor Glycemic Control Despite Lifestyle Intervention

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase II Clinical Trial to Evaluate the Efficacy and Safety of Fuling Yunhua Granules and Dihuang Baoyuan Granules in Adult Patients With Type 2 Diabetes Mellitus and Poor Glycemic Control Despite Diet and Exercise Intervention

This trial tests whether Fuling Yunhua Granules and Dihuang Baoyuan Granules, alone or in sequence, lower blood sugar in adults with type 2 diabetes whose blood sugar remains high despite diet and exercise. It will also assess their safety.

研究概览

详细说明

This is a multicenter, randomized, double-blind, placebo-controlled Phase II study. About 150 participants aged 18-70 will be randomly assigned to one of six groups: Fuling Yunhua monotherapy, Dihuang Baoyuan monotherapy, sequential low-dose, sequential high-dose, low-dose placebo, or high-dose placebo. Neither participants nor researchers will know who gets which treatment.

The trial includes a 4-week run-in period (diet and exercise only), 24 weeks of daily treatment, and a 12-week follow-up after stopping treatment. Participants whose blood sugar stays healthy may continue follow-up for up to 52 weeks after stopping treatment.

研究类型

介入性

注册 (估计的)

150

阶段

  • 阶段2

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

      • Beijing、中国
        • Peking University People's Hospital
        • 接触:

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

18年 至 70年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age 18 to 70 years (inclusive), male or female;
  2. Body weight ≥50 kg for men and ≥45 kg for women at both screening and baseline; body mass index (BMI) between 23.0 and 35.0 kg/m2 (inclusive) at both visits;
  3. Diagnosed with type 2 diabetes mellitus (T2DM) for at least 3 months according to the diagnostic criteria of the Chinese Guidelines for the Prevention and Treatment of Diabetes;
  4. Maintained diet control and exercise therapy for 3 months prior to screening, and did not receive any systemic treatment for diabetes during this period (no prior use of hypoglycemic agents, or prior use of hypoglycemic agents but no use within 3 months before screening);
  5. Glycated hemoglobin (HbA1c) ≥7.5% and <11.0% at screening (local laboratory); HbA1c ≥7.0% and <11.0% at baseline (central laboratory);
  6. Fasting plasma glucose (FPG) <13.9 mmol/L at both screening and baseline;
  7. Traditional Chinese Medicine (TCM) syndrome differentiation consistent with spleen Yin deficiency, Yin deficiency with internal heat accompanied by spleen dampness and stomach heat, and phlegm-fluid retention pattern;
  8. Able to understand the procedures and methods of this study, willing to strictly abide by the clinical research protocol to complete this study, maintain the same diet and exercise habits throughout the trial, and voluntarily sign the informed consent form (ICF).

Exclusion Criteria:

  1. History of allergic reaction to any component of the study drugs, or history of significant allergic or hypersensitivity reaction to concomitant medications specified in this trial;

  2. Non-type 2 diabetes mellitus: type 1 diabetes, gestational diabetes, or special types of diabetes (such as diabetes due to pancreatic injury, Cushing syndrome, or acromegaly);

  3. History of acute diabetic complications within 6 months before screening (diabetic ketoacidosis, hyperosmolar hyperglycemic state, or lactic acidosis), requiring treatment as diagnosed by the investigator;

  4. Personal or family history of medullary thyroid C-cell hyperplasia, focal hyperplasia, or carcinoma (including sporadic, familial, or localized multiple endocrine neoplasia [MEN] type 2A or 2B syndrome);

  5. History of acute or chronic pancreatitis, symptomatic gallbladder disease, or pancreatic injury, or other high-risk factors for pancreatitis deemed unsuitable for this trial by the investigator;

  6. History of organ transplantation, or severe autoimmune diseases in the past or present (including but not limited to rheumatoid arthritis, systemic lupus erythematosus, and vasculitis);

  7. Diagnosed with malignant tumors within 5 years before screening (except for cured basal cell carcinoma of the skin or carcinoma in situ of the cervix), or currently under evaluation for potential malignancy;

  8. Thyroid dysfunction that cannot be controlled with stable drug dosage at screening;

  9. Any disease that may cause hemolysis or red blood cell instability affecting HbA1c measurement at screening (such as hemolytic anemia or thalassemia);

  10. Severe trauma or severe acute infection that may affect glycemic control within 3 months before screening;

  11. Severe cardiovascular disease within 6 months before screening, such as heart failure (New York Heart Association [NYHA] grade III-IV), myocardial infarction, coronary artery bypass grafting or percutaneous coronary intervention, sustained and clinically significant arrhythmia (such as second- or third-degree atrioventricular block, or QTcF interval prolongation [≥450 ms in males and ≥470 ms in females]), acute coronary syndrome, transient ischemic attack, hemorrhagic stroke, or ischemic stroke, deemed unsuitable for this trial by the investigator;

  12. Diseases that may significantly affect drug absorption, distribution, metabolism and excretion within 6 months before screening: inflammatory bowel disease, peptic ulcer, history of gastrointestinal or rectal bleeding, history of major gastrointestinal surgery (such as gastrectomy, gastrointestinal anastomosis, or intestinal resection), etc.;

  13. History of major surgery (intrathoracic, intracranial, abdominal, etc.) within 6 months before screening, or planned surgery during the study that may affect study completion or compliance;

  14. Severe hypoglycemic event (Grade 3 or above) or recurrent unexplained hypoglycemic events (at least 3 episodes per month with blood glucose <3.9 mmol/L or symptomatic hypoglycemia) within 6 months before randomization;

  15. Use of drugs that may affect glucose metabolism within 2 months before screening, including growth hormone therapy, and long-term or intermittent systemic glucocorticoids (intravenous or oral administration for >2 consecutive weeks or repeated courses, excluding inhaled or topical use), etc.;

  16. Use of any immunosuppressant within 6 months before screening, or use of any drug that the investigator judges may affect trial results;

  17. Medical or non-medical weight management within 3 months before screening, including unapproved weight management drugs or products, or weight change ≥5% within 3 months before screening (based on participant self-report), or weight change ≥5% (gain or loss) between randomization and screening;

  18. Any laboratory test meets any of the following criteria at screening:

    Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > upper limit of normal (ULN) ×2.5, or total bilirubin (TBIL) > ULN ×1.5; Estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m2 calculated using the CKD-EPI formula; Fasting triglycerides (TG) >5.7 mmol/L; Fasting C-peptide <0.8 ng/mL (or 0.26 nmol/L); Hemoglobin <100 g/L;

  19. Hepatitis B surface antigen (HBsAg) positive at screening (if HBsAg positive, HBV DNA testing is required), or hepatitis C virus (HCV) antibody positive, or human immunodeficiency virus (HIV) antibody positive, or Treponema pallidum antibody positive;

  20. Blood pressure poorly controlled at screening and baseline (systolic blood pressure >160 mmHg and/or diastolic blood pressure >100 mmHg);

  21. Blood donation or massive blood loss (>400 mL) within 3 months before screening;

  22. Participated in any interventional drug clinical trial within 3 months before screening (except screening failures without treatment);

  23. Pregnant or lactating women, or men or women of childbearing potential who plan to become pregnant during the study or are unwilling to take medically recognized contraceptive measures;

  24. Known or suspected alcohol dependence (defined as >14 units of alcohol per week; 1 unit equals 357 mL beer with 5% alcohol content, 45 mL spirits with 40% alcohol content, or 147 mL wine with 12% alcohol content) or drug abuse at screening;

  25. Severe psychiatric disorder or language barrier that prevents adequate understanding and cooperation;

  26. Participants who the investigator believes have any other factors that are inappropriate for participating 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:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:Fuling Yunhua Granules Monotherapy Group

Fuling Yunhua Granules, one bag taken orally three times daily before breakfast, lunch and dinner, for 24 weeks.

Traditional Chinese herbal medicine granules, 12 g per bag, taken orally before meals.

实验性的:Dihuang Baoyuan Granules Monotherapy Group

Dihuang Baoyuan Granules, one bag taken orally three times daily before breakfast, lunch and dinner, for 24 weeks.

Traditional Chinese herbal medicine granules, 18 g per bag, taken orally before meals.

实验性的:Sequential Treatment Low-Dose Group

Participants receive Dihuang Baoyuan Granules and Fuling Yunhua Granules alternately every 4 weeks for 24 weeks: Dihuang Baoyuan Granules in weeks 1-4, 9-12 and 17-20, and Fuling Yunhua Granules in weeks 5-8, 13-16 and 21-24. One bag is taken orally twice daily, before breakfast and dinner.

Traditional Chinese herbal medicine granules, 12 g per bag, taken orally before meals.

Traditional Chinese herbal medicine granules, 18 g per bag, taken orally before meals.

实验性的:Sequential Treatment High-Dose Group

Participants receive Dihuang Baoyuan Granules and Fuling Yunhua Granules alternately every 4 weeks for 24 weeks: Dihuang Baoyuan Granules in weeks 1-4, 9-12 and 17-20, and Fuling Yunhua Granules in weeks 5-8, 13-16 and 21-24. One bag is taken orally three times daily, before breakfast, lunch and dinner.

Traditional Chinese herbal medicine granules, 12 g per bag, taken orally before meals.

Traditional Chinese herbal medicine granules, 18 g per bag, taken orally before meals.

安慰剂比较:Low-Dose Placebo Group

Participants receive placebos matching Dihuang Baoyuan Granules and Fuling Yunhua Granules, administered in the same alternating 4-week sequence and on the same schedule as the sequential treatment groups: Dihuang Baoyuan Granules matched placebo in weeks 1-4, 9-12 and 17-20, and Fuling Yunhua Granules matched placebo in weeks 5-8, 13-16 and 21-24. One bag is taken orally twice daily, before breakfast and dinner, for 24 weeks.

Matched placebo for Fuling Yunhua Granules; identical in appearance (shape, color and packaging), odor and taste, but containing no active herbal components. Granules, 12 g per bag, taken orally before meals.

Matched placebo for Dihuang Baoyuan Granules; identical in appearance (shape, color and packaging), odor and taste, but containing no active herbal components. Granules, 18 g per bag, taken orally before meals.

安慰剂比较:High-Dose Placebo Group

Participants receive placebos matching Dihuang Baoyuan Granules and Fuling Yunhua Granules, administered in the same alternating 4-week sequence and on the same schedule as the sequential treatment groups: Dihuang Baoyuan Granules matched placebo in weeks 1-4, 9-12 and 17-20, and Fuling Yunhua Granules matched placebo in weeks 5-8, 13-16 and 21-24. One bag is taken orally three times daily, before breakfast, lunch and dinner, for 24 weeks.

Matched placebo for Fuling Yunhua Granules; identical in appearance (shape, color and packaging), odor and taste, but containing no active herbal components. Granules, 12 g per bag, taken orally before meals.

Matched placebo for Dihuang Baoyuan Granules; identical in appearance (shape, color and packaging), odor and taste, but containing no active herbal components. Granules, 18 g per bag, taken orally before meals.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Change from Baseline in Glycated Hemoglobin (HbA1c) at Week 24
大体时间:Baseline and Week 24
Baseline and Week 24

次要结果测量

结果测量
大体时间
Proportion of Participants With Type 2 Diabetes Clinical Remission at 12 Weeks After Discontinuation of Study Drug (Clinical remission defined as HbA1c <6.5%)
大体时间:12 Weeks After Discontinuation of Study Drug
12 Weeks After Discontinuation of Study Drug
Change from Baseline in Glycated Hemoglobin (HbA1c) at Weeks 8, 12, 16, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 12, 16, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 12, 16, and 12 Weeks After Discontinuation of Study Drug
Proportion of Participants With HbA1c <6.5% at Weeks 8, 12, 16, and 24
大体时间:Weeks 8, 12, 16, and 24
Weeks 8, 12, 16, and 24
Proportion of Participants With HbA1c <7.0% at Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Fasting Plasma Glucose (FPG) at Weeks 4, 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 4, 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 4, 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in 2-Hour Postprandial Glucose (PPG) at Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Continuous Glucose Monitoring (CGM) Time in Range (TIR) at Week 24
大体时间:Baseline and Week 24
Baseline and Week 24
Change from Baseline in Continuous Glucose Monitoring (CGM) Time Below Range (TBR) at Week 24
大体时间:Baseline and Week 24
Baseline and Week 24
Change from Baseline in Continuous Glucose Monitoring (CGM) Time Above Range (TAR) at Week 24
大体时间:Baseline and Week 24
Baseline and Week 24
Change from Baseline in Insulin Sensitivity (HOMA-IS) at Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Beta-Cell Function (HOMA-β) at Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in C-Peptide Index (CPI) at Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Fasting Lipid Profile (Total Cholesterol [TC], LDL-C, HDL-C, Triglycerides [TG]) at Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Systolic and Diastolic Blood Pressure at Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Serum Uric Acid at Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Fasting Body Weight at Weeks 4, 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 4, 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 4, 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Waist Circumference at Weeks 4, 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 4, 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 4, 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Hip Circumference at Weeks 4, 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 4, 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 4, 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in TCM Syndrome Score and Proportion of Participants by TCM Efficacy (Cured, Markedly Effective, Effective, Ineffective) at Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 12, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Change from Baseline in Pittsburgh Sleep Quality Index (PSQI) Score at Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
大体时间:Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug
Baseline and Weeks 8, 16, 24, and 12 Weeks After Discontinuation of Study Drug

其他结果措施

结果测量
大体时间
Change from Baseline in Biomarkers (Telomere and Mitochondria) at Week 24
大体时间:Baseline and Week 24
Baseline and Week 24
Proportion of Participants Achieving Type 2 Diabetes Clinical Remission at 24, 36, and 52 Weeks After Discontinuation of Study Drug
大体时间:24, 36, and 52 Weeks After Discontinuation of Study Drug
24, 36, and 52 Weeks After Discontinuation of Study Drug

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。

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 (估计的)

2026年11月20日

初级完成 (估计的)

2028年1月15日

研究完成 (估计的)

2028年3月15日

研究注册日期

首次提交

2026年10月28日

首先提交符合 QC 标准的

2026年11月3日

首次发布 (实际的)

2026年11月5日

研究记录更新

最后更新发布 (实际的)

2026年11月5日

上次提交的符合 QC 标准的更新

2026年11月3日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • JYHS-BAII-Pro-25001

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

There is no plan to make individual participant data (IPD) available to other researchers.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

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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