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A Phase 1 Study of GZC8072 Tablets Following a Single Dose in Healthy Study Participants and Multiple Doses in Obese/Overweight Study Participants

2026年8月21日 更新者:Gan & Lee Pharmaceuticals.

A Phase 1 Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetic Profile of Single Doses of GZC8072 Tablets in Healthy Adult Participants and to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Profile of Multiple Doses in Participants With Overweight or Obesity

This trial is conducted in China. This study plans to include 2 parts, i.e., a single-dose study and a multiple-dose study:

The single-dose study will be conducted in healthy adult participants to evaluate the safety, tolerability, and pharmacokinetic profile of single doses of GZC8072 Tablets; The multiple-dose study will be conducted in obese or overweight study participants to evaluate the safety, tolerability, pharmacokinetic and pharmacodynamic profiles of multiple doses of GZC8072 Tablets.

研究概览

研究类型

介入性

注册 (估计的)

112

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

      • Beijing、中国
        • Beijing Shijitan 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

  • 成人

接受健康志愿者

是的

描述

Inclusion Criteria:

SAD:

  1. Provide written informed consent, fully understand the purpose and stipulated procedures of this study, and be willing to participate.
  2. Male or female, aged 18-55 years (inclusive) at the time of signing the ICF.
  3. Body mass index (BMI) at screening is 19.0-28.0 kg/m² (inclusive); and weight is ≥ 54.0 kg for males and ≥ 50.0 kg for females.
  4. Participants must agree to take reliable contraceptive measures for themselves and their partners during the study and within 3 months after administration, and not donate sperm or eggs (egg cells, oocytes) for assisted reproductive purposes.

MAD:

  1. Provide written informed consent, fully understand the purpose and stipulated procedures of this study, and be willing to participate.
  2. Male or female, aged 18-55 years (inclusive) at the time of signing the ICF.
  3. At screening, the body mass index (BMI) is 24 kg/m2 to 35 kg/m2 (inclusive).
  4. Participants must agree to take reliable contraceptive measures for themselves and their partners during the study and within 3 months after the last dose, and not donate sperm or eggs (egg cells, oocytes) for assisted reproductive purposes.

Exclusion Criteria:

SAD:

  1. History of allergic diathesis, or allergic diseases such as bronchial asthma, urticaria, or eczema (except for mild seasonal allergies) prior to screening, or known or suspected allergy, intolerance, or hypersensitivity to GLP-1RA drugs, SNAC, C10 or other excipients of the investigational medicinal product (IMP) at screening.
  2. Participants with a previous or existing history of cardiovascular system, digestive system, respiratory system, urinary system, blood system, nervous system, psychiatric disorders, endocrine diseases (except obesity or overweight), malignant tumors and other diseases that are judged by the investigator to have an impact on the evaluation of the results of this study.
  3. Hemorrhage tendency (including but not limited to non-traumatic hemorrhage) within 6 months before screening, or presence of diseases with increased hemorrhage tendency that are clearly diagnosed.
  4. History of hypoglycemia (including symptomatic hypoglycemia) within 3 months prior to screening.
  5. History of acute or chronic pancreatitis, symptomatic gallbladder disease, pancreatic surgery or trauma before screening; high-risk cholelithiasis (such as sand-like stones, gallbladder and bile duct stones ≤ 5 mm in diameter) during screening; newly diagnosed cholecystitis at screening.
  6. Presence of reflux esophagitis at screening, functional dyspepsia, constipation, irritable bowel syndrome, intestinal obstruction, abnormal gastric emptying (e.g., pyloric obstruction), or active peptic ulcer.
  7. History or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2 prior to screening, or presence of suspected and/or diagnosed malignancy at screening, or history of malignancy prior to screening.
  8. Participants who have any clinically significant abnormalities in 12-lead ECG, vital signs (blood pressure, respiration, pulse and body temperature), physical examinations, imaging procedures or laboratory tests (hematology, urinalysis, blood biochemistry and coagulation) at screening or predose as judged by the investigator to be unsuitable for participation in this study, or whose laboratory test items at screening or predose meet any of the following criteria:

    1. eGFR < 90 mL/min/1.73 m2 (eGFR should be estimated using the CKD-EPI formula);
    2. Abnormal fasting plasma glucose (FPG) (FPG ≥ 6.1 mmol/L, or < 3.9 mmol/L);
    3. Hemoglobin A1c (HbA1c) ≥ 6.5%;
    4. Calcitonin ≥ 20 pg/mL;
    5. Those who are positive for four tests for infectious diseases.
  9. Major surgery within 6 months prior to screening, or scheduled surgery or hospitalization during the study.
  10. Participants who have received any vaccine within 1 month before screening, or plan to receive any vaccine during the study.
  11. Use of prescription or over-the-counter drugs, herbal medicines, traditional Chinese medicines, local traditional medicines, vitamins, minerals, or oral iron supplements within 2 weeks prior to IMP administration, or consumption of any food or beverage containing caffeine, xanthine, or potentially affecting study results (e.g., coffee, tea, cola, grapefruit or pomelo juice, dragon fruit, mango), or inability to comply with the above dietary restrictions during the study.
  12. Participation in other interventional clinical trials before screening (within the past 3 months or within 5 half-lives after administration of the investigational drug, whichever is longer). Or plan to participate in another clinical study of an IMP, surgery, or device before completing all scheduled assessments in the clinical study.
  13. Those who have donated blood or blood products (> 100 mL) or lost a large volume of blood (> 400 mL) within 2 months prior to screening or have planned to donate blood or blood products during the study.
  14. History of drug abuse prior to screening; or positive results for drug abuse on D-1.
  15. Hisory of alcohol abuse within 3 months prior to screening, defined as an average intake of more than 14 units per week (1 standard unit = 360 mL of beer or 150 mL of 12% wine or 45 mL of 40% spirits); or use of any alcohol-containing products 48 hours before dosing and throughout the study; or abnormal results for breath alcohol test on D-1.
  16. Female participants who are pregnant or lactating, or have a positive human chorionic gonadotropin (β-HCG) pregnancy test at screening.
  17. Participants who are allergic to any food or have specific dietary requirements and cannot adhere to a standardized diet.
  18. Unwillingness to undergo repeated venipuncture due to poor tolerance or difficult venous access, or participant experiences needle or blood phobia.
  19. Any condition that, in the investigator's opinion, renders the participant unsuitable for participation in this study, including potential compromise of the participant's rights.

MAD:

  1. History of allergic diathesis, or allergic diseases such as bronchial asthma, urticaria, or eczema (except for mild seasonal allergies) prior to screening, or known or suspected allergy, intolerance, or hypersensitivity to GLP-1RA drugs, SNAC, C10 or other excipients of the investigational medicinal product (IMP) at screening.
  2. Participants with one of the following prior or existing medical history or conditions:

    1. Participants with cardiovascular system, digestive system, respiratory system, urinary system, blood system, nervous system, psychiatric disorders, endocrine diseases (except obesity or overweight), malignant tumors and other diseases that are judged by the investigator to have an impact on the evaluation of the results of this study.
    2. Diseases that increase the risk to participants, such as hypoglycemia, acute or chronic pancreatitis, history of pancreatic surgery or trauma, and history of symptomatic gallbladder disease; cholelithiasis with a high risk of acute biliary pancreatitis at screening (such as sand-like stones, and gallbladder and bile duct stones ≤ 5 mm in diameter); newly diagnosed cholecystitis at screening;
    3. History or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2;
    4. Participants with clinically significant digestive system diseases who are judged unsuitable for the study by the investigator, such as history of active peptic ulcer or hemorrhage, inflammatory bowel disease, abnormal gastric emptying (such as gastroparesis or pyloric stenosis, gastric outlet obstruction), continuous use of drugs affecting gastrointestinal motility for ≥ 1 week (including but not limited to domperidone, mosapride, macrolides), and acute hemorrhoidal attacks within the past three months;
    5. Participants with severe infection or unexplained infection within 4 weeks before screening.
  3. Participants with a weight change > 5.0% within 12 weeks prior to screening.
  4. Participants who have any clinically significant abnormalities in 12-lead ECG, vital signs (blood pressure, respiration, pulse and body temperature), physical examinations, imaging procedures or laboratory tests (hematology, urinalysis, blood biochemistry and coagulation) at screening or predose as judged by the investigator to be unsuitable for participation in this study, or whose laboratory test items at screening, on D-2 or D-1 meet any of the following criteria:

    1. eGFR <90 mL/min/1.73 m2;
    2. Hemoglobin A1c (HbA1c) ≥ 6.5%;
    3. FPG ≥ 7.0 mmol/L;
    4. Two-hour venous plasma glucose > 11.1 mmol/L after a 75 g oral glucose tolerance test (OGTT);
    5. Calcitonin ≥ 20 pg/mL;
    6. Those who are positive for four tests for infectious diseases.
  5. Those who have undergone bariatric surgery (except for acupuncture weight loss, liposuction, and abdominoplasty performed more than 1 year before screening), those who have had major surgery within 6 months prior to screening, or those who schedule to have surgery or hospitalization during the study.
  6. Participants who have received any vaccine within 1 month before screening, or plan to receive any vaccine during the study.
  7. Use of any prescription drugs, over-the-counter drugs or Chinese herbal medicines within 2 weeks prior to screening; or use of any GLP-1R agonists or drugs with the same mechanism of action as GLP-1R agonists [such as GLP-1R/glucagon receptor (GCGR) agonists or glucose-dependent insulinotropic polypeptide receptor (GIPR)/GLP-1R agonists or GIPR/GLP-1R/GCGR agonists) within 6 months prior to screening; or use of any weight loss drugs within 6 months prior to screening or use of concomitant medications from the screening period to before the first dose.
  8. Participation in other interventional clinical trials before screening (within the past 3 months or within 5 half-lives after administration of the investigational drug, whichever is longer). Or plan to participate in another clinical study of an IMP, surgery, or device before completing all scheduled assessments in the clinical study.
  9. Those who have donated blood or blood products (> 100 mL) or lost a large volume of blood (> 400 mL) within 2 months prior to screening or have planned to donate blood or blood products during the study.
  10. History of drug abuse within 1 year prior to screening; or positive results for drug abuse on D-2.
  11. History of alcohol abuse within 3 months prior to screening, defined as an average intake of more than 14 units per week (1 standard unit = 360 mL of beer or 150 mL of 12% wine or 45 mL of 40% spirits); or use of any alcohol-containing products 48 hours before dosing and throughout the study; or abnormal results for breath alcohol test on D-2.
  12. Female participants who are pregnant or lactating, or have a positive human chorionic gonadotropin (β-HCG) pregnancy test at screening.
  13. Participants who are allergic to any food or have specific dietary requirements and cannot adhere to a standardized diet.
  14. Unwillingness to undergo repeated venipuncture due to poor tolerance or difficult venous access, or participant experiences needle or blood phobia.
  15. Any condition that, in the investigator's opinion, renders the participant unsuitable for participation in this study, including potential compromise of the participant's rights.

    -

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:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:安慰剂
每位参与者接受单次口服剂量 (SAD) 或多次口服剂量 (MAD) 匹配的安慰剂。
口服药物
实验性的:GZC8072 Tablets
Each participant receives either a single oral dose (SAD) or multiple oral doses (MAD) of GZC8072 Tablets
Oral drug

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Incidence of adverse events and serious adverse events
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
mmunogenicity: including anti-drug antibodies and neutralizing antibodies to GZC8072.
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57

次要结果测量

结果测量
大体时间
Cmax
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
AUC0-t
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
AUC0-inf
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
Tmax
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
λ
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
t1/2
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
CL/F
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
Vd
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
Cmin(ss)
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
Cmax(ss)
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
Cav(ss)
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
AUC0-τ
大体时间:SAD:Baseline to Day36 MAD:Baseline to Day57
SAD:Baseline to Day36 MAD:Baseline to Day57
Fasting weight
大体时间:MAD:Baseline to Day57
MAD:Baseline to Day57
body mass index (BMI)
大体时间:MAD:Baseline to Day57
MAD:Baseline to Day57
waist circumference
大体时间:MAD:Baseline to Day57
MAD:Baseline to Day57
FPG
大体时间:MAD:Baseline to Day57
MAD:Baseline to Day57
fasting insulin
大体时间:MAD:Baseline to Day57
MAD:Baseline to Day57

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9月4日

初级完成 (估计的)

2027年8月18日

研究完成 (估计的)

2027年8月18日

研究注册日期

首次提交

2026年8月21日

首先提交符合 QC 标准的

2026年8月21日

首次发布 (实际的)

2026年8月25日

研究记录更新

最后更新发布 (实际的)

2026年8月25日

上次提交的符合 QC 标准的更新

2026年8月21日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

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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