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Inhaled Vancomycin Tolerability, Safety and Pharmacokinetics

2014年3月3日 更新者:Savara Inc.

Phase I, Reference-controlled, Dose Escalating Study to Examine the Pharmacokinetics and Safety of AeroVanc Inhalation Powder.

The study is carried out to evaluate the safety, tolerability and pharmacokinetics of AeroVanc inhalation powder in healthy volunteers, and in patients with cystic fibrosis.

研究概览

详细说明

The study has three main objectives:

  • To evaluate the safety, and tolerability of AeroVanc inhalation powder in healthy volunteers, and in patients with CF.
  • To determine the systemic bioavailability of vancomycin in healthy volunteers following single dose pulmonary administration of 16 mg, 32 mg, and 80 mg doses of AeroVanc in comparison with a 250 mg dose of vancomycin administered intravenously.
  • To estimate the lung sputum concentrations of vancomycin in patients with cystic fibrosis (CF) following single dose pulmonary administration of 32 mg and 80 mg doses of AeroVanc.

研究类型

介入性

注册 (实际的)

25

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

    • Queensland
      • Brisbane、Queensland、澳大利亚、4101
        • Mater Adult Hospital
    • Western Australia
      • Perth、Western Australia、澳大利亚、6009
        • Linear Clinical Research Ltd.

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 50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 Healthy Volunteers:

  1. Healthy male volunteers between 18 and 50 years of age inclusive.
  2. Able to communicate with site personnel and to understand and voluntarily sign the Informed Consent Form.
  3. Able and willing to comply with the Protocol, including availability for all scheduled study visits.
  4. Body Mass Index (BMI) of 20 to 30 kg/m2 inclusive, and weight between 60-90 kg inclusive.
  5. No clinically significant abnormalities at screening determined by medical history, physical examination, blood chemistry, hematology, urinalysis, and 12-lead ECG. Negative urine screen for drugs of abuse and negative alcohol breath test at Screening and prior to dosing.
  6. Negative human immunodeficiency virus (HIV) and Hepatitis B and Hepatitis C screening test results.
  7. Spirometry (forced expiratory volume in 1 second (FEV1)) value at screening greater than 75% of predicted age-adjusted value.

Exclusion Criteria Healthy Volunteers:

  1. A history of pulmonary or other disorder likely to influence drug absorption.
  2. Evidence or suspicion of clinically significant respiratory, renal, hepatic, central nervous system, cardiovascular or metabolic dysfunction.
  3. A history of previous allergies or sensitivity to vancomycin, or other component(s) of the study drug or reference drug.
  4. Smokers (ex-smokers who quit smoking must have a one year period of not smoking prior to the study drug administration).
  5. Respiratory tract infection within the last two weeks prior to the first study drug administration.
  6. Treatment with any prescription medication and/or over-the-counter (OTC) products including vitamins or mineral supplements within 48 hours before Investigational Product administration.
  7. Vaccination within one month before the study drug administration.
  8. Systolic blood pressure <110 mmHg or >150 mmHg inclusive or diastolic blood pressure <60 mmHg or >90 mmHg inclusive.
  9. A history of drug or alcohol abuse.
  10. Participation in a clinical study within three months on Investigational Product administration.
  11. Donation of blood or plasma within three months of Investigational Product administration.
  12. Any other condition which in the view of the Investigator is likely to interfere with the study or put the subject at risk.

Inclusion Criteria CF Patients:

  1. Able to communicate with site personnel and to understand and voluntarily sign the Informed Consent Form.
  2. Able and willing to comply with the protocol, including availability for all scheduled study visits.
  3. Have a confirmed diagnosis of cystic fibrosis (by two established methods, e.g. positive sweat chloride value ≥ 60 mEq/L, nasal potential difference test, and/or genotype with two identifiable mutations consistent with CF, accompanied by one or more clinical features consistent with the CF phenotype).
  4. Be aged ≥ 18 years old
  5. Have FEV1 >40 % of predicted
  6. Be able to perform all the techniques necessary to measure lung function
  7. No liver enzymes increased by more than twice the upper limit of normal
  8. Ability to spontaneously produce bronchial sputum daily

Inclusion Criteria CF Patients:

  1. Administration of any investigational drug or device within 28 days of Screening and within six half-lives of the investigational drug.
  2. Oral corticosteroids in doses exceeding 10 mg per day or 16 mg every other day.
  3. History of sputum culture or throat swab culture yielding B. cepacia in the previous two years.
  4. History of positive MRSA culture, or sputum culture positive for MRSA at screening.
  5. Current daily continuous oxygen supplementation or requirement for more than 2 L/min at night.
  6. A history of previous allergies or sensitivity to vancomycin, or other component(s) of the study drug.
  7. Changes in antimicrobial, bronchodilator, anti-inflammatory or corticosteroid medications within 7 days prior to Screening.
  8. Changes in physiotherapy technique or schedule within 7 days prior to Screening.
  9. History of lung transplantation.
  10. A chest X-Ray at Screening or within the previous 90 days of Screening, with abnormalities indicating a significant acute finding (e.g., lobar infiltrate and atelectasis, pneumothorax, or pleural effusion).
  11. Positive pregnancy test. All women of childbearing potential will be tested.
  12. Female of childbearing potential who is lactating or is not practicing acceptable method of birth control (e.g., hormonal or barrier methods, or intrauterine device).
  13. Findings at Screening that, in the investigator's opinion, would compromise the safety of the subject or the quality of the study data.
  14. History of severe cough/bronchospasm upon inhalation of dry powder inhalation product.
  15. Considered "terminally ill" or eligible for lung transplantation.
  16. Have had a significant episode of hemoptysis (>60 mL) in the three months prior to enrolment.

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:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Aerovanc 16 mg in healthy volunteers
Vancomycin hydrochloride dry powder for inhalation
实验性的:AeroVanc 32 mg in healthy volunteers
Vancomycin hydrochloride dry powder for inhalation
实验性的:AeroVanc 80 mg in healthy volunteers
Vancomycin hydrochloride dry powder for inhalation
有源比较器:IV vancomycin in healthy volunteers
Vancomycin hydrochloride solution for intravenous administration
实验性的:AeroVanc 32 mg in CF patients
Vancomycin hydrochloride dry powder for inhalation
实验性的:AeroVanc 80 mg in CF patients
Vancomycin hydrochloride dry powder for inhalation

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 - Number of Participants With Treatment Emergent Adverse Events (TEAEs = Adverse Events That Started During or After the First Dose of Study Drug)
大体时间:Healthy volunteers = 2 weeks; CF Patients = 1 week
Each participant was monitored regularly for Adverse Events (AEs) throughout the study. The Investigator or designee enquired about AEs by asking participants non-leading questions such as: "How do you feel?" or "Have you had any (other) medical problems since your last visit/assessment?" Additionally, several safety procedures (physical examinations, vital signs, safety laboratory tests, 12-lead ECGs, and spirometry) were conducted on participants at regular intervals. All AEs reported spontaneously by participants or in response to questioning or observation by the Investigator, including those related to safety procedures, were recorded. For each AE, the Investigator recorded the following assessments: seriousness, severity (Mild, Moderate, or Severe), and relationship to study drug (Not Related, Remote, Possible, Probable, or Highly Probable). AEs were considered drug-related if given a relationship of Possible, Probable, or Highly Probable.
Healthy volunteers = 2 weeks; CF Patients = 1 week

次要结果测量

结果测量
措施说明
大体时间
Plasma Pharmacokinetics - Elimination Half Life (t½)
大体时间:Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose

Blood samples were obtained from the healthy volunteers to evaluate systemic pharmacokinetics of vancomycin after a single dose administration of AeroVanc or a single dose of IV vancomycin.

Half-life is the time it takes for the concentration of drug to decline by 50%.

Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose
Plasma Pharmacokinetics - Time to Reach the Maximum Plasma Concentration (Tmax)
大体时间:Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose

Blood samples were obtained from the healthy volunteers to evaluate systemic pharmacokinetics of vancomycin after a single dose administration of AeroVanc or a single dose of IV vancomycin.

Tmax is the time it takes to reach the maximum plasma concentration of a drug.

Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose
Plasma Pharmacokinetics - Maximum Plasma Concentration (Cmax)
大体时间:Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose

Blood samples were obtained from the healthy volunteers to evaluate systemic pharmacokinetics of vancomycin after a single dose administration of AeroVanc or a single dose of IV vancomycin.

Cmax is the maximum observed concentration of a drug.

Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose
Plasma Pharmacokinetics - Area Under the Plasma Concentration-time Curve From Time 0 to the Time of the Last Quantifiable Concentration (AUCt)
大体时间:Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose

Blood samples were obtained from the healthy volunteers to evaluate systemic pharmacokinetics of vancomycin after a single dose administration of AeroVanc or a single dose of IV vancomycin.

AUCt is a way of expressing the total amount of drug exposure over a specified time period.

Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose
Plasma Pharmacokinetics - Area Under the Plasma Concentration-time Curve From Time 0 to Infinite Time (AUCinf)
大体时间:Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose

Blood samples were obtained from the healthy volunteers to evaluate systemic pharmacokinetics of vancomycin after a single dose administration of AeroVanc or a single dose of IV vancomycin.

AUCinf is a way of estimating the total amount of drug exposure over an infinite time period.

Pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, and 24 hours post-dose
Lung Pharmacokinetics - Maximum Sputum Concentration (Cmax)
大体时间:1, 8 and 24 hours post-dose

Sputum samples were obtained from the patients with cystic fibrosis to evaluate lung pharmacokinetics of vancomycin after a single dose administration of AeroVanc.

Cmax is the maximum observed concentration of a drug.

1, 8 and 24 hours post-dose
Lung Pharmacokinetics - Minimum Sputum Concentration (Cmin)
大体时间:1, 8 and 24 hours post-dose

Sputum samples were obtained from the patients with cystic fibrosis to evaluate lung pharmacokinetics of vancomycin after a single dose administration of AeroVanc.

Cmin is the minimum observed concentration of a drug.

1, 8 and 24 hours post-dose

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

2011年11月1日

初级完成 (实际的)

2012年3月1日

研究完成 (实际的)

2012年3月1日

研究注册日期

首次提交

2012年2月17日

首先提交符合 QC 标准的

2012年2月17日

首次发布 (估计)

2012年2月23日

研究记录更新

最后更新发布 (估计)

2014年3月31日

上次提交的符合 QC 标准的更新

2014年3月3日

最后验证

2014年3月1日

更多信息

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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