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。

First-In-Human Study of Apramycin

2021年2月22日 更新者:Juvabis AG

A Phase I, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of Apramycin Administered Intravenously in Healthy Adults.

This is a first-in-human study to assess the safety, tolerability and pharmacokinetics of escalating single doses of apramycin. This trial will be conducted as a single ascending dose trial in up to 5 sequential dose cohorts (group-comparison). Each cohort will consist of 8 healthy subjects, 6 will receive apramycin and 2 placebo.

研究概览

研究类型

介入性

注册 (实际的)

40

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。

学习地点

      • Mannheim、德国
        • CRS Clinical Research Services Mannheim GmbH

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 45年 (成人)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Healthy male and female subjects of non-childbearing potential, 18-45 years of age (both inclusive), body mass index 18.0 - 29.9 kg/m2 (inclusive) and body weight from 50 to 100 kg (inclusive).
  • Glomerular filtration rate (GFR) ≥ 90 mL/min /1.73 m2.
  • Subjects with systemic hearing, with air conduction thresholds no worse than 20 decibels (dB) hearing loss for the frequencies 0.5-1-2-4-6-8 kilohertz (kHz) bilaterally and, no threshold asymmetry ≥ 20 dB at any frequency, normal (reproducibility 70% or better) transient evoked otoacoustic emissions (TEOAE).
  • From the signing of the informed consent until the last follow-up visit, subjects must be willing to avoid exposure to loud noise and Subjects must be willing to avoid excessive physical exercise within 48 h prior to dosing.
  • Normal blood pressure and pulse rate, ECG recording without clinically significant abnormalities.
  • Thyroid-stimulating hormone, free triiodothyronine and free thyroxine within the reference ranges.
  • Having had no febrile or infectious illness for at least 7 days prior to the first administration of the Investigational medicinal product (IMP) of the study.
  • Normal microscopic findings in the ears, normal tympanic membrane mobility and stapedial reflex present.

Exclusion Criteria:

  • Vegetarian or vegan.
  • Demonstrating excess in xanthine consumption.
  • More than low-risk alcohol consumption (men: ≥24 g of pure alcohol regularly per day; women: ≥12 g of pure alcohol regularly per day).
  • Any history of alcohol or drug abuse or a positive urine drug screen test. Positive alcohol breath test.
  • Consumption of xanthine-containing food or beverages within 48 h before dosing.
  • Smokers smoking more than 10 cigarettes or equivalent per day.
  • Exposure to loud noise within 3 days prior to drug administration.
  • Taking any medication on a regular basis, with the exception of solitary doses of up to 1000 mg paracetamol.
  • Use of any investigational drug product within 30 days or 5 half-lives before screening.
  • Use of aminoglycosides or other antibiotics within 3 months prior to screening.
  • Use of neuromuscular blocking agents within 1 week or 5 half-lives prior to screening.
  • Use of potentially nephrotoxic medication 2 weeks prior to the drug administration.
  • Any history of drug hypersensitivity, asthma, urticaria or other severe allergic diathesis as well as hay fever with ongoing symptoms.
  • Any history of hypersensitivity to aminoglycosides.
  • Any history or signs of acute, chronic or recurrent metabolic, renal, hepatic, pulmonary, gastrointestinal, neurological, neuromuscular disorders, endocrinological, immunological, psychiatric or cardiovascular disease, myopathies, and bleeding tendency.
  • Problems with hearing and/or balance.
  • Previous injury or surgery to the middle or inner ears, family history of hearing loss before the age of 60.
  • Genetic predisposition to aminoglycoside-driven ototoxicity.
  • Laboratory values outside the reference range that are of clinical relevance.
  • Positive test for HIV antibodies, hepatitis B-virus surface antigen, or anti-hepatitis C-virus antibodies.
  • Blood or plasma donation of 500 mL within 3 months or more than 100 mL within 30 days before signing an informed consent to this trial.
  • Judged by the investigator to have occupational noise exposure of high risk during the trial.
  • Positive test for SARS-CoV-2.

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:基础科学
  • 分配:随机化
  • 介入模型:顺序分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:Apramycin injection in escalating doses
Apramycin, solution for infusion.
30-min infusion
安慰剂比较:Placebo
Physiological saline, solution for infusion.
30-min infusion

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
Type and incidence of treatment-emergent adverse events (TEAEs) until 2 weeks after dosing.
大体时间:until 2 weeks after dosing
until 2 weeks after dosing
Type and incidence of TEAEs related to auditory and vestibular function tests.
大体时间:until 3 months after dosing
until 3 months after dosing
Number of subjects with clinically significant vital sign measurement blood pressure.
大体时间:until 2 weeks after dosing
Frequency is defined as number of subjects with clinically significant observations.
until 2 weeks after dosing
Number of subjects with clinically significant vital sign measurement pulse rate.
大体时间:until 2 weeks after dosing
Frequency is defined as number of subjects with clinically significant observations.
until 2 weeks after dosing
Number of subjects with clinically significant observation in physical examination.
大体时间:until 2 weeks after dosing
Frequency is defined as number of subjects with clinically significant observations.
until 2 weeks after dosing
Number of subjects with clinically significant changes in clinical laboratory parameters.
大体时间:until 2 weeks after dosing
Frequency is defined as number of subjects with clinically significant observations.
until 2 weeks after dosing
Number of subjects with clinically significant changes in ECG parameters.
大体时间:until 2 weeks after dosing
ECG parameters include heart rate and PQ, QT, RS. Frequency is defined as number of subjects with clinically significant observations.
until 2 weeks after dosing

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。

赞助

调查人员

  • 首席研究员:Armin Schultz, Dr.med.、CRS Clinical Research Services Mannheim GmbH

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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)

2019年9月25日

初级完成 (实际的)

2020年7月16日

研究完成 (实际的)

2020年10月16日

研究注册日期

首次提交

2019年9月12日

首先提交符合 QC 标准的

2019年9月24日

首次发布 (实际的)

2019年9月26日

研究记录更新

最后更新发布 (实际的)

2021年2月23日

上次提交的符合 QC 标准的更新

2021年2月22日

最后验证

2020年11月1日

更多信息

与本研究相关的术语

关键字

其他相关的 MeSH 术语

其他研究编号

  • JUV18-01

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