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 Study of NHL907 in Healthy Adult Participants

2026年6月8日 更新者:NeuHyll AUS Pty Ltd

A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study to Assess Safety, Tolerability, and Pharmacokinetics of NHL907 Combination Drug Following Multiple Oral Doses in Healthy Adult Participants

The goal of this study is to evaluate the safety, tolerability and pharmacokinetics of NHL907 when administered as multiple oral doses in healthy adult participants.

研究概览

地位

招聘中

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

    • South Australia
      • Adelaide、South Australia、澳大利亚、5000
        • 招聘中
        • CMAX Clinical Research Pty Ltd
        • 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:

  1. Healthy adult male and female participants aged between 18 and 60 years of age, inclusive.
  2. Has a body mass index (BMI) between ≥ 18 and ≤ 32 kg/m2 inclusive, with body weight ≥ 50 kg at Screening.
  3. Able and willing to understand and sign the informed consent form, communicate meaningfully with study personnel, and comply with all study restrictions, procedures, laboratory tests, and other study requirements.
  4. In good health, determined by the Investigator on the basis of medical history, physical examination, vital signs, Screening laboratory results, Screening ECG, and mental status.
  5. Participants of non-childbearing potential should be congenitally or surgically sterile or in a menopausal state as confirmed by follicle-stimulating hormone (FSH) concentrations (≥ 40 IU/L at Screening).
  6. Female participants with childbearing potential must agree to use accepted contraceptive regimens from time of Screening, during the study, and for at least 60 days after end of study.
  7. Male participants with the potential to father a child must agree to abstain from sperm donation and to use accepted contraceptive regimens from Screening, during the study, and for at least 90 days after end of study.
  8. Participants should agree to refrain from donating blood for at least 30 days after end of study.

Exclusion Criteria:

If an individual meets any of the following criteria, they will be ineligible for this study:

  1. History or evidence of clinically significant disorders and deemed not suitable to participants in the study by the Principal Investigator or delegate.
  2. History or presence of any gastrointestinal (GI) disease (except for Gilbert's syndrome or cholecystectomy) or condition that could compromise the participant safety and/or absorption of the study drug, including irritable bowel disease, known untreated helicobacter pylori infection, abnormal gastric emptying, dyspepsia, GI ulcers, GI bleeding, or GI surgeries within 6 months before Screening.
  3. Have a known hypersensitivity to any component of the IP formulation or related derivatives of each component.
  4. Have abnormalities in resting vital signs at Screening, on Day -1, or on Day 1 prior to dosing.
  5. History of or ongoing cardiac abnormalities as assessed during Screening, including abnormal and clinically relevant ECG changes, considered by the Investigator.
  6. History of smoking in the past 90 days before Screening which is defined as more than the equivalent of 5 cigarettes weekly (including alternative nicotine products such as cigars, e-cigarettes, chewing tobacco, etc.); and /or have a positive urine test for cotinine at Screening or Baseline, or unable to abstain from smoking starting from at least 3 days before Screening, or Day -1 / check-in until end of study.
  7. History of illicit or prescription drug abuse or addiction within 1 year of Screening, or positive urine drug screen at Screening or Baseline. Participants who used a THC / CBD product within 30 days before Screening and added a deterrent from any use before that are excluded.
  8. History of alcohol abuse (unless fully recovered with no use of alcohol within the 12 months prior to Screening), which is defined as exceeding an average weekly intake of 21 standard drinks for males or 14 standard drinks for females (1 standard drink is equivalent to 5 ounces [150 mL] of wine or 12 ounces [360 mL] of beer or 1.5 ounces [45 mL] of hard liquor); or positive alcohol breath test at Screening or Baseline; incapable to refrain from consuming alcohol starting from at least 48 h prior to Day 1 / check-in until end of study.
  9. Has participated in any interventional trial or drug investigation or device investigation (including placebo) within 30 days, or 5 half-lives of the IP, whichever is longer, prior to Screening or has the intention to participate in another trial during the present study.
  10. Have received vaccines within 14 days and within 60 days for live-attenuated vaccines before screening.
  11. Have any medical condition(s) screened by the Investigator and determined to be ineligible or have any acute illness within 7 days prior to Day 1 will be excluded or may be considered for the next cohort if still within their screening window.
  12. Have clinical safety laboratory parameters at Screening (serum chemistry and lipid panel, hematology, coagulation, and urinalysis) that are outside the normal limits and are considered clinically significant in the opinion of the Investigator and the Sponsor's MM (e.g., LFTs / bilirubin ≥ 1.5 ULN and eGFR ≤ 60 ml/min/1.73 m2). Participants with elevated unconjugated bilirubin (Gilbert's syndrome) are not excluded.
  13. History of suicidal ideations or suicide attempts, including current instances of either case or any "yes" response to C-SSRS at screening.
  14. The participant is pregnant, lactating, or planning to become pregnant within 6 months of being discharged from the trial.
  15. Use of any prescription medicine within 2 weeks, or over the counter (OTC) medicine, herbal remedy, or nutritional supplement, or within 5 half-lives of any drugs, whichever is longer prior to dosing, except for vitamins and occasional use of paracetamol / acetaminophen (≤ 2 g/day; no more than 3 consecutive days) which will be reviewed by the PI and the Sponsor's MM for determination of acceptability.
  16. Have undergone surgery within 90 days before Screening, or have surgery planned during the study period or within 90 days after the last dose or has previously undergone any surgery that may affect drug absorption, distribution, metabolism, or excretion during the study.
  17. Blood donation or loss of ≥ 450 mL of blood within 90 days before dosing or receiving a blood transfusion within 90 days before dosing. Platelet/Plasma donation is prohibited within 30 days before Screening and until at least 30 days after study completion.
  18. Positive hepatitis B virus (HBsAg), hepatitis B core antibody (HBcAb), hepatitis C virus (HCV-Ab), human immunodeficiency virus (HIV-1 and HIV-2), or syphilis at Screening.
  19. History of malignancy, with the exception of non-melanoma skin cancer or curatively treated cancer that has not been in full remission for ≥ 5 years, without evidence of recurrence.
  20. Have any special dietary requirements that may include CYP2D6 inhibitors, e.g., grapefruit, bitter citrus products, tonic water, or any other requirement that would prevent compliance with study standardized meals.
  21. History of dysphagia or difficulty swallowing tablets / capsules.
  22. Unable or unwilling to comply with the lifestyle guidelines and evaluations detailed in this protocol, for the duration of the study or have a situation or condition that, in the opinion of the Investigator, may interfere with participation in the study.
  23. Participants who cannot perform venous blood sampling (i.e., poor venous access or vasovagal response to injection).
  24. Any other circumstances or laboratory abnormalities that, in the Investigator's judgement, may result in an unacceptable increase in risk to the participant, or impair the participant's ability to participate in and complete the study, or could preclude the evaluation of the participant's response.
  25. Have any clinically significant abnormality on physical examination at Screening, on Day -1, or on Day 1 prior to dosing which in the opinion of the Investigator would exclude them from the study.
  26. History of a severe allergic reaction to any drug or multiple food / drug allergies.
  27. Heavy caffeine drinker (> 5 cups or glasses of caffeinated beverages, e.g., coffee, tea, cola per day).
  28. Have any condition which, in the judgement of the Investigator, would prevent the participant from completing the study or complying with study procedures and requirements.

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:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:NHL907 Dose 1
Investigational product NHL907
实验性的:NHL907 Dose 2
Investigational product NHL907
实验性的:NHL907 Dose 3
Investigational product NHL907
实验性的:NHL907 Dose 4
Investigational product NHL907
实验性的:NHL907 Dose 5
Investigational product NHL907
实验性的:NHL907 Dose 6
Investigational product NHL907
实验性的:NHL907 Dose 7
Investigational product NHL907
实验性的:NHL907 Dose 8
Investigational product NHL907
安慰剂比较:Placebo Dose 1
Placebo for Dose 1
NHL907 matching placebo
安慰剂比较:Placebo Dose 2
Placebo for Dose 2
NHL907 matching placebo
安慰剂比较:Placebo Dose 3
Placebo for Dose 3
NHL907 matching placebo
安慰剂比较:Placebo Dose 4
Placebo for Dose 4
NHL907 matching placebo
安慰剂比较:Placebo Dose 5
Placebo for Dose 5
NHL907 matching placebo
安慰剂比较:Placebo Dose 6
Placebo for Dose 6
NHL907 matching placebo
安慰剂比较:Placebo Dose 7
Placebo for Dose 7
NHL907 matching placebo
安慰剂比较:Placebo Dose 8
Placebo for Dose 8
NHL907 matching placebo

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Number of Participants with Treatment Emergent Adverse Events
大体时间:Baseline to 7 days after the last dose (Day 14)
Baseline to 7 days after the last dose (Day 14)

次要结果测量

结果测量
大体时间
Cmax: Maximum observed plasma concentration
大体时间:Day 1, Day 7
Day 1, Day 7
Tmax: Time of occurrence of Cmax
大体时间:Day 1, Day 7
Day 1, Day 7
AUC0-24: Area under the concentration-time curve from 0 to 24 hours
大体时间:Day 1, Day 7
Day 1, Day 7
AUC0-inf: Area under the concentration-time curve from 0 to infinity
大体时间:Day 1, Day 7
Day 1, Day 7
Cmax/dose: Cmax normalized by dose
大体时间:Day 1, Day 7
Day 1, Day 7
CL/F: Apparent total clearance
大体时间:Day 1, Day 7
Day 1, Day 7
Vz/F: Apparent volume of distribution
大体时间:Day 1, Day 7
Day 1, Day 7
AUC0-24/dose: AUC0-24 normalized by dose
大体时间:Day 1, Day 7
Day 1, Day 7
AUC0-inf/dose: AUC0-inf normalized by dose
大体时间:Day 1, Day 7
Day 1, Day 7
t1/2: Apparent terminal elimination half-life
大体时间:Day 1, Day 7
Day 1, Day 7
Ctrough: Trough plasma concentration
大体时间:Day 4-7
Day 4-7
RA Cmax: Observed accumulation ratio based on Cmax
大体时间:Day 7 to Day 1
Day 7 to Day 1

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5月12日

初级完成 (估计的)

2027年2月1日

研究完成 (估计的)

2027年4月1日

研究注册日期

首次提交

2026年4月29日

首先提交符合 QC 标准的

2026年5月5日

首次发布 (实际的)

2026年5月12日

研究记录更新

最后更新发布 (实际的)

2026年6月10日

上次提交的符合 QC 标准的更新

2026年6月8日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • NHL907-101

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

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