此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

A Phase I Study of HLX109 in Healthy Participants

2026年11月6日 更新者:Shanghai Henlius Biotech

A Randomized, Double-Blind, Single Ascending Dose, Phase I Clinical Study to Evaluate Safety, Tolerability and Pharmacokinetic Profiles of HLX109 in Healthy Participants

This study is a randomized, double-Blind, single ascending dose, phase I clinical study to evaluate safety, tolerability and pharmacokinetic profiles of HLX109 in healthy participants

研究概览

详细说明

This first-in-human clinical trial of HLX109 is a randomized, double-blind, placebo-controlled, single ascending dose phase Ia clinical study to evaluate the safety, tolerability, and pharmacokinetic characteristics of HLX109 in healthy adult participants. Each participant is expected to participate in the study for 112 days. The first 28 days constitute the screening period, followed by a study drug administration and an 84-day follow-up period.

研究类型

介入性

注册 (估计的)

64

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

    • Anhui
      • Hefei、Anhui、中国
        • The Second Affiliated Hospital of Anhui Medical University
        • 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 55年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Voluntarily participates in the clinical study, with a full understanding of the study procedures; provides written informed consent by signing and dating the informed consent form (ICF); and is willing and able to comply with all protocol-specified requirements and follow-up visits.
  2. Adult male or female, aged 18 (inclusive) to 55 years (inclusive) at the time of ICF signing.
  3. Body mass index (BMI) between 18.5 (inclusive) and 28.0 (exclusive) kg/m2 at screening.
  4. No clinically significant abnormalities in medical history or clinical evaluations (including physical examination, clinical laboratory assessments, diagnostic imaging, vital signs, and 12-lead ECG) at screening. At the investigator's discretion, screening assessments may be repeated to confirm eligibility, provided that all assessments are completed within the defined screening window.
  5. A female participant must be of no childbearing potential, postmenopausal, or premenopausal with one of the following records: hysterectomy, tubal ligation, or bilateral salpingectomy. The heterosexual partners of all participants and the participants must agree to take contraceptive measures during the treatment period and at least 3 months after the last dose of IMP. (Appendix 2.)
  6. Prior to randomization, complete all age-appropriate vaccinations according to current immunization guidelines.

Exclusion Criteria:

  1. Pregnant or lactating women.

  2. With sunburn, scar tissue, tattoos (more than 25% of body area), open sores, or branding at screening that, in the opinion of the investigator, would interfere with the assessment of adverse skin reactions.

  3. History of clinically significant hypersensitivity or allergic reactions to two or more medications, or known hypersensitivity to IMP or any of its excipients, or a history of anaphylaxis. Additionally, individuals with a history of multiple and/or severe allergic manifestations (including food allergies) are excluded. (Note: Prospective participants with seasonal allergic rhinitis/allergies are eligible for enrollment, provided they are currently asymptomatic or their symptoms are well-controlled).

  4. History of venous thromboembolic events and/or has a first-degree relative with an idiopathic venous thromboembolic event.

  5. History or evidence of substance or alcohol abuse, defined as follows:

    • A history of substance abuse within 1 year prior to screening, or a positive urine drug screen at the screening.
    • A history of alcohol abuse within 6 months prior to screening, or a positive breath alcohol test at the screening.
  6. History of the following diseases with a clear diagnosis within 6 months prior to screening: cardiovascular diseases, hematological diseases, respiratory diseases, gastrointestinal diseases, hepatic impairment, renal impairment (e.g. glomerular filtration rate less than 75 mL/min/1.73m²), endocrine, metabolic, neurological, psychiatric, dermatological, musculoskeletal, or immunological disorders. Participants will also be excluded if they present with any other concurrent medical condition that, in the judgment of the investigator, may confound the interpretation of the study data or compromise participant safety.

  7. History of hemorrhagic diathesis (including but not limited to non-traumatic bleeding) within 6 months before screening or diagnosed diseases that increase hemorrhagic diathesis.

  8. Malignancy or increased risk of malignancy prior to screening: suspected and/or diagnosed with any malignancy (except for basal cell carcinoma, squamous cell carcinoma of skin in situ, or cervical carcinoma in situ occurring within 5 years prior to screening with no evidence of recurrence after treatment).

  9. Major surgery (including procedures under general anesthesia) within 3 months prior to screening or organ transplantation prior to screening. Or still in the state of disease, trauma, or incomplete recovery after surgery at screening (significant changes in organ function, or significantly limited ability to live and work compared with that before disease, trauma, or surgery, or requiring continuous rehabilitation treatment), or planning to undergo surgery during the study.

  10. Chronic or recurrent infection at screening, systemic or local severe infection requiring hospitalization or intravenous injection of antibiotics within 1 month before screening, or history of acute infection within 14 days before screening.

  11. Any severe herpes infection at any time prior to before screening, but not limited to, disseminated herpes (ever), herpes encephalitis (ever), recurrent herpes zoster (defined as 2 episodes within 2 years prior to Screening), or ophthalmic herpes (ever).

  12. Any condition requires medication and/or other treatments at screening.

  13. Evidence of active or prior tuberculosis (TB) infection on lung imaging during the screening period.

  14. Abnormalities in 12-lead ECG at screening or admission, such as corrected QT (QTc) interval > 450 ms in males and > 470 ms in females (Fridericia's method).

  15. Abnormal results of the following Laboratory assessments at screening or admission:

    • Hemoglobin > 1.1 × upper limit of normal (ULN), or Hemoglobin < 0.9× lower limit of normal (LLN)
    • Platelet count > 1.1 ×ULN, or Platelet count < 0.9× LLN
    • Neutrophil count < 1.5 × 109/L.
    • Alkaline phosphatase (ALP) > 1.5 × ULN, or total bilirubin (TBIL) > 1.5 × ULN, or alanine aminotransferase (ALT) > 1.5 × ULN, or aspartate aminotransferase (AST) > 1.5 × ULN, or AST/ALT between 1-1.5 × ULN (inclusive) and considered clinically significant by the investigator, or blood amylase > 1 × ULN.
    • International normalized ratio (INR) > 1.5.
    • Blood thyroid-stimulating hormone (TSH) < 1×LLN, or TSH > 1 ×ULN.
    • Estimated glomerular filtration rate (eGFR) < 75mL/min/1.73 m2, or urine protein qualitative≥2+
    • Positive interferon-γ release assay.
    • Positive serology for Human Immunodeficiency Virus (HIV) antibody, Hepatitis B Virus surface antigen (HBsAg), or Hepatitis C Virus (HCV) antibody; or a positive treponemal test for syphilis.
  16. Have participated in a clinical study of other investigational products before screening, with an interval between this study and the previous study being too short: within 1 month before the first dose of this study or within 5 half-lives of the previous investigational product (whichever is longer). Or plan to participate in clinical studies of other investigational products before completing all scheduled assessments in this clinical study. Participants who violate the restrictions on concomitant medications (Appendix 6) should be excluded.

  17. Have participated in surgical or device clinical studies within 3 months prior to screening, or are currently participating in other surgical or device clinical studies, or plan to participate in other surgical or device clinical studies during this study.

  18. Receipt of any vaccine within 14 days prior to randomization or planned receipt of any vaccine during the study.

  19. Unable to follow the lifestyle restrictions (Appendix 3) during the study.

  20. Prescription and over the counter (OTC) drugs, herbal medicines, vitamins, minerals, or oral iron supplements (Appendix 3) not approved by the investigator during the study.

  21. Unable or unwilling to undergo repeated venipuncture due to poor tolerance or difficulty in finding a vein, or with a history of fear of blood or needles.

  22. Donated whole blood or blood components (more than 400 mL) or lost a large amount of blood (more than 400 mL) within 2 months prior to IMP administration , or plan to donate whole blood or blood components during the study.

  23. The participant has a hierarchical or dependent relationship with the investigator or the study site (including employees and their immediate family members), or has any other condition that, as determined by the investigator, renders the participants unsuitable for participation or places their rights and well-being at risk.

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:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:HLX109

Dose Escalation

HLX109: A mg, SC, single dose

HLX109: B mg, SC, single dose

HLX109: C mg, SC, single dose

HLX109: D mg, SC, single dose

HLX109: E mg, SC, single dose

HLX109: F mg, SC, single dose

HLX109: G mg, SC, single dose

安慰剂比较:Placebo

Dose Escalation

Placebo: A mg, SC, single dose

HLX109: B mg, SC, single dose

HLX109: C mg, SC, single dose

HLX109: D mg, SC, single dose

HLX109: E mg, SC, single dose

HLX109: F mg, SC, single dose

HLX109: G mg, SC, single dose

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
Safety: number and percentage of participants with adverse events (AEs) assessed by CTCAE v6.0
大体时间:Up to approximately 84 days
Up to approximately 84 days
Safety: number and percentage of participants with serious adverse events (SAEs) assessed by CTCAE v6.0
大体时间:Up to approximately 84 days
Up to approximately 84 days
Safety: number and percentage of participants with adverse events of special interest (AESIs) assessed by CTCAE v6.0
大体时间:Up to approximately 84 days
Up to approximately 84 days
Safety: number and percentage of participants with laboratory abnormalities
大体时间:Up to approximately 84 days

Following parameters were analyzed for laboratory examination: hematology (hemoglobin, hematocrit, red blood cell count, platelet count, white blood cell count, total neutrophils, eosinophils, monocytes, basophils, lymphocytes); chemistry (blood urea nitrogen, creatinine, glucose, calcium, sodium, potassium, chloride, total bicarbonate, aspartate aminotransferase, alanine aminotransferase, total bilirubin, alkaline phosphatase, uric acid, albumin, total protein); urinalysis (decimal logarithm of reciprocal of hydrogen ion activity [pH], glucose, protein, blood, ketones, nitrites, leukocyte esterase, microscopy[if urine tested positive for blood, protein, nitrites or leukocyte esterase]. Laboratory abnormalities were assessed based on values outside the reference range and/or judged clinically significant by the investigator according to NCI CTCAE Version 6.0.

Up to approximately 84 days
Safety: number and percentage of participants with notable 12-Lead electrocardiogram (ECG) values
大体时间:Up to approximately 84 days

Criteria for notable ECG values were as follow: corrected QT interval by Fredericia formula (QTcF) in msec new(newly occurring post-baseline value) > 500, or increase from baseline >60.

Up to approximately 84 days
Safety: number and percentage of participants with clinically notable vital signs
大体时间:Up to approximately 84 days

Criteria for notable vital signs: Pulse rate <40 beats per minute (bpm) to >120 bpm, Diastolic blood pressure < 50 millimeter of mercury (mmHg), systolic blood pressure < 90 mmHg.

Up to approximately 84 days

次要结果测量

结果测量
大体时间
PK: peak concentration (Cmax)
大体时间:Up to approximately 84 days
Up to approximately 84 days
PK: area under the concentration-time curve (AUC0-t, AUC0-inf)
大体时间:Up to approximately 84 days
Up to approximately 84 days
PK: time to peak concentration (Tmax)
大体时间:Up to approximately 84 days
Up to approximately 84 days
PK: terminal elimination half-life (t1/2)
大体时间:Up to approximately 84 days
Up to approximately 84 days
PK: apparent clearance (CL/F)
大体时间:Up to approximately 84 days
Up to approximately 84 days
PK: apparent volume of distribution (Vz/F)
大体时间:Up to approximately 84 days
Up to approximately 84 days
PK: mean residence time (MRT)
大体时间:Up to approximately 84 days
Up to approximately 84 days
PK: percentage of extrapolated AUC (%AUCex)
大体时间:Up to approximately 84 days
Up to approximately 84 days
Immunogenicity: incidence of anti-drug antibody (ADA) against HLX109 and recombinant human hyaluronidase.
大体时间:Up to approximately 84 days
Up to approximately 84 days
Immunogenicity: incidence of neutralizing antibody (NAb) against HLX109 and recombinant human hyaluronidase.
大体时间:Up to approximately 84 days
Up to approximately 84 days
Exploratory: serum free/total soluble IL-1RAP (sIL-1RAP) levels
大体时间:Up to approximately 84 days
Up to approximately 84 days
Exploratory: ex vivo stimulated cytokine release levels in whole peripheral blood
大体时间:Up to approximately 84 days
Up to approximately 84 days
Exploratory: IL-1RAP receptor occupancy (RO)
大体时间:Up to approximately 84 days
Up to approximately 84 days

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18日

初级完成 (估计的)

2027年9月20日

研究完成 (估计的)

2027年11月20日

研究注册日期

首次提交

2026年10月18日

首先提交符合 QC 标准的

2026年11月6日

首次发布 (实际的)

2026年11月13日

研究记录更新

最后更新发布 (实际的)

2026年11月13日

上次提交的符合 QC 标准的更新

2026年11月6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

  • HLX109-FIH101

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

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

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.

订阅