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Phase 1 Study on the Safety, Tolerability, and Pharmacokinetics of JST-018 in Healthy Adults

2026年8月3日 更新者:Just-Evotec Biologics

Phase 1, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of JST-018 in Healthy Adults

The goal of this clinical trial is to learn if a single dose of the study drug, JST-018, is safe and tolerable when administered by injection into the arm or thigh muscle of healthy men and women aged 18 to 55. The main questions it aims to answer are:

  • Is a single administration of JST-018 safe?
  • What is the concentration of the JST-018 in the blood over time?
  • Do antibodies to JST-018 develop following a dose of JST-018? Researchers will compare JST-018 to Placebo to see if there are any differences in the safety and tolerability of a single dose at different dose levels.

Participants will be confined to the clinic for the first 3 days. They will receive an injection on the second day, and then return for 9 more visits over the period of 1 year for:

  • Physical exam with vital signs
  • Electro-cardiogram (ECG)
  • Bood collection for clinical labs and research samples
  • Urine sample
  • Assessment of potential adverse effects and medications taken

研究概览

详细说明

This is a Phase 1, first-in-human (FIH), randomized, double-blind, placebo-controlled, single ascending dose (SAD) study to assess the safety, tolerability, and PK of a single dose of JST-018 administered IM to healthy participants.

The study will be comprised of a minimum of 3 cohorts (Cohorts A, B, and C, with 12 participants per cohort), each evaluating a single dose of JST-018 administered IM. In each cohort, 2 sentinel participants will be randomized 1:1 such that one participant receives JST-018 and 1 participant receives placebo. Following a favorable blinded safety review committee (SRC) review of sentinel safety data collected through Day 8, the remainder of the cohort (10 non-sentinel participants) will be randomized 4:1 to JST-018 or placebo, and will be dosed.

All safety data for all participants in the current cohort through Day 8 will be reviewed by the SRC in a blinded fashion for each dose cohort before escalating to the next dose cohort (for escalation from Cohort A to Cohort B and escalation from Cohort B to Cohort C); A recommendation on whether to implement Cohort D (along with a recommended dose of JST-018 to be evaluated in Cohort D) may be provided by the SRC following review of blinded safety data from Cohorts A, B, and C.

研究类型

介入性

注册 (估计的)

48

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

    • Nevada
      • Las Vegas、Nevada、美国、89113
        • 招聘中
        • PPD Las Vegas Clinical Research Unit
        • 接触:
          • 电话号码:(877) 362-2608

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:

  1. Healthy men or women 18 to 55 years of age
  2. BMI between 18 and 32 kg/m2
  3. Negative serum pregnancy test
  4. Use of highly effective birth control method(s) for a minimum of 60 days prior to consent and is willing to continue use for at least 12 months, or abstinence
  5. In good general health as determined by medical history, exams and tests

Exclusion Criteria:

  1. Acute illness or fever (≥100.4°F) within 7 days prior to dosing
  2. Any history of receiving treatment, vaccine, or monoclonal antibodies (mAbs) against smallpox, monkeypox, or other orthopox viruses.
  3. Receipt of any vaccine within 30 days prior to Screening, planned receipt of any vaccine prior to Day 1, or planned receipt of any vaccines before 45 days post-injection.
  4. Any medical condition for which IM injections would be contraindicated in the opinion of the investigator (eg, bleeding disorders, anticoagulant therapy, and severe thrombocytopenia)
  5. History of congenital or acquired immunodeficiency syndrome, , including positive human immunodeficiency virus (HIV-1/-2) antibody result
  6. Prior solid organ or bone marrow transplant
  7. Clinically significant corneal or lens abnormality as determined by history, clinical examination, or diagnostic imaging. Including, but not limited to:

    • Corrected vision of less (worse) than 20/40
    • History of any clinically significant history of eye trauma, in the opinion of the investigator
    • History of cataracts or current cataracts
    • Lens opacity greater than NC2, C2, or P0 as determined by the Lens Opacities Classification System (LOCS) III
    • History of uveitis (including acute)
    • Use of ocular or inhaled prescription steroids within 1 year prior to Screening nasal steroids are permissible). A single short course (ie, less than 14 days) of systemic steroid therapy is allowed provided it is concluded more than 6 months prior to Screening.
    • History of diabetes
  8. Use of immunosuppressive agents, anticoagulants, or antiarrhythmics within 1 year prior to Screening. Nasal steroid use is permissible.
  9. Upper arms and thighs are with insufficient muscular tissue for IM injections or is obscured by tattoos or rash
  10. Use of any medications started within 30 days prior to Day -1, including prescription medications, nutritional supplements, and over-the-counter medications

    • Vitamin supplements are allowed
    • Recommended doses of acetaminophen are allowed, except for 24 hours prior to dosing
    • Recommended doses of non-steroidal anti-inflammatory drugs (NSAIDs) (eg, aspirin, ibuprofen) are also allowed, except for 7 days prior to dosing
  11. Positive hepatitis B surface antigen, hepatitis B core antigen, or hepatitis C antibody
  12. Positive urine drug test or cotinine (indicating active current smoking) at Screening or Day -1, positive alcohol breath test at Screening or on Day -1, or suspected/known drug abuse and/or alcohol use disorder
  13. Smoking or has used nicotine or nicotine-containing products (eg, snuff, nicotine patch, nicotine chewing gum, mock cigarettes, or inhalers) within 3 months before study drug dosing
  14. Dosing in any clinical research study evaluating another investigational drug or therapy within 30 days or at least 5 half-lives (whichever is longer) of receiving the investigational drug prior to Screening
  15. Progressive, unstable, or uncontrolled medical conditions that have required medical attention or changes to medication for medical reasons within 90 days prior to consent
  16. History of allergic reactions or hypersensitivity reactions to other therapeutic antibodies or immunoglobulins
  17. Receipt of any mAbs in the 12 months prior to Screening
  18. High blood pressure
  19. Women who are either pregnant or breast-feeding
  20. Vulnerable individuals (eg, military recruits, persons in compulsory detention, those with limited legal capacity)
  21. Receipt of immunoglobulins or any blood products within 90 days prior to consent or planned receipt during the study period
  22. Donation or loss of >500 mL of blood within 30 days or plasma within 7 days of Day 1; any planned donation of blood or plasma during the study period
  23. History of any malignant neoplasm within the last 5 years, with the exception of adequately treated localized or in situ non-melanoma carcinoma of the skin or the cervix
  24. Strenuous activity or contact sports within 48 hours before study drug dosing and through Day 8

26. History of relevant drug and/or food allergies

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:预防
  • 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
有源比较器:JST-018 Investigational Product
Monoclonal antibodies
安慰剂比较:JST-017 Placebo
安慰剂比较

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 and tolerability of of JST-018 administered intramuscularly (IM)
大体时间:From injection to Day 7
Incidence of solicited local (injection site) and systemic AEs post-injection through Day 7 (with the inpatient and outpatient participant diaries being collected on Day 3 and Day 8, respectively)
From injection to Day 7
Safety and tolerability of of JST-018 administered IM
大体时间:From injection to final visit at Week 48
Incidence of unsolicited AEs through end of study (EOS)
From injection to final visit at Week 48
Safety and tolerability of of JST-018 administered IM
大体时间:From injection to final visit at Week 48
Incidence of SAEs, medically attended AEs (MAAEs), and AEs of special interest (AESIs)
From injection to final visit at Week 48
Safety and tolerability of of JST-018 administered IM
大体时间:From injection to final visit at Week 48
Incidence of Clinically Significant Changes in Laboratory Values
From injection to final visit at Week 48
Safety and tolerability of JST-018 administered as IM
大体时间:From injection to final visit at Week 48
Incidence of Clinically Significant Changes in Vital Sign Measurements
From injection to final visit at Week 48
Safety and tolerability of JST-018 administered as IM
大体时间:From injection to final visit at Week 48
Incidence of Clinically Significant Changes in ECG results
From injection to final visit at Week 48

次要结果测量

结果测量
措施说明
大体时间
Pharmacokinetic Cmax of JST-018
大体时间:From enrollment to the end of study at 48 weeks
Maximum observed concentration (Cmax)
From enrollment to the end of study at 48 weeks
Pharmacokinetic Tmax of JST-018
大体时间:Time Frame: From enrollment to the end of study at 48 weeks
Time to reach maximum observed concentration (Tmax)
Time Frame: From enrollment to the end of study at 48 weeks
Pharmacokinetic Tlast of JST-018
大体时间:From enrollment to the end of study at 48 weeks
The timepoint with the last quantifiable concentration (Tlast)
From enrollment to the end of study at 48 weeks
Pharmacokinetic AUC0-t of JST-018
大体时间:From enrollment to the end of study at 48 weeks
Area under the concentration versus time curve (AUC) from time 0 to the timepoint with the last quantifiable concentration (AUC0-t)
From enrollment to the end of study at 48 weeks
Pharmacokinetic AUC0-inf of JST-018
大体时间:From enrollment to the end of study at 48 weeks
AUC from time 0 extrapolated to infinity (AUC0-inf)
From enrollment to the end of study at 48 weeks
Pharmacokinetic t1/2 of JST-018
大体时间:From enrollment to the end of study at 48 weeks
Terminal elimination half-life (t1/2)
From enrollment to the end of study at 48 weeks
Pharmacokinetic CL/F of JST-018
大体时间:From enrollment to the end of study at 48 weeks
Apparent clearance after IM administration (CL/F)
From enrollment to the end of study at 48 weeks
Pharmacokinetic Vz/F of JST-018
大体时间:From enrollment to the end of study at 48 weeks
Apparent volume of distribution after IM administration (Vz/F)
From enrollment to the end of study at 48 weeks
Evaluation the effect of anti-drug antibodies (ADA)
大体时间:From enrollment to the end of study at 48 weeks
Effect of ADAs on pharmacokinetics of JST-018
From enrollment to the end of study at 48 weeks
Evaluate if and to what extent ADAs develop following a single dose of JST-018
大体时间:From enrollment to the end of study at 48 weeks
Proportion of participants with pre-existing ADAs and those who develop ADAs (treatment boosted and treatment induced) to JST-018
From enrollment to the end of study at 48 weeks

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 (实际的)

2026年6月23日

初级完成 (估计的)

2026年11月9日

研究完成 (估计的)

2027年10月4日

研究注册日期

首次提交

2026年5月7日

首先提交符合 QC 标准的

2026年5月14日

首次发布 (实际的)

2026年5月19日

研究记录更新

最后更新发布 (实际的)

2026年8月5日

上次提交的符合 QC 标准的更新

2026年8月3日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • DDF4-CL101
  • MCDC No. W15QKN-16-9-1002 (其他标识符:US Department of War)

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

This is a study in healthy volunteers. Individual participant data is not meaningful.

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

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