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临床试验/NCT01785927
NCT01785927Unknown1 期

Clinical Trial Phase I of Antituberculosis Dry Powder Aerosols

Prince of Songkla University2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2013年2月最近更新:
适应症

试验速览

阶段
1 期
入组人数
40
试验地点
2
主要终点
Cytokine levels (Tumor Necrosis Factor-α and Interleukin-1β)

研究概览

简要总结

The inhaled route of delivery has always been associated with the considerable challenge of getting the drug to its target. The lungs are a highly complex organ designed to filter inspired air, with many different cell types contributing to their function. Furthermore, the lungs may change dramatically when afflicted by disease resulting in an internal environment that works against the drug reaching and interacting successfully with the target. For targets in the upper airways this will have lesser significance, but drug delivery to the deep lung may be impeded by changes such as mucus hyper-secretion or thickening or airway narrowing.

In order to interpret toxicology findings it is necessary to reconcile test sensitivity, background biological variation, normal responses to inhaled materials and drug or medicine-specific adverse effects. Identification of adverse end-points is an area where better control data sets might help discern true adverse effects from a normal physiological lung response. The lung responds acutely to inhalation of irritant materials by hyper-secretion of mucus, chemokine release, inflammatory cell recruitment and cough and collectively these may be characterized as non-specific irritancy.

详细描述

Four formulations of antituberculosis drug (rifampicin, isoniazid, pyrazinamide, and levofloxacin) will be administered to each patient by randomization. Each formulation will be assigned the code, such as A, B, C, or D, and the treatment sequences will be generated as ABCD (sequence 1), BCDA (sequence 2), CDAB (sequence 3) and DABC (sequence 4). On the first day of drug dosing in period I, volunteers will be randomly assigned to a sequence of treatments as indicated in a pre-printed randomization scheme, which was generated using block randomization with block sizes of 4 and 6, and the allocation ratio of 1:1. Subjects will be stratified by sex. Subjects in sequence 1 will receive treatment A during the first study period and will then cross over to receive treatment B, C, and D at the second, third and fourth periods, respectively (each after a 7-day washout period).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18-45 years
  • Body mass index 18-27 kg/m2
  • In the case of reproductive age woman, effective contraceptive will be used for at least 4 weeks prior to a screening examination until the end of study.
  • Non-lactating women
  • Patients who are willing to participate in the trial and will first sign the informed consent form.

排除标准

  • Allergic to any antituberculosis drugs or other components
  • High blood pressure (diastolic pressure > 90 mmHg)
  • Liver enzymes (AST and ALT) > 2 times of upper normal value
  • Pregnancy or lactation
  • No underlying diseases such as asthma, COPD, chronic kidney disease, diabetes mellitus, liver disease, immunocompromised deficiency, etc.
  • HBsAg positive
  • Abnormality in chest X-ray or routine laboratory tests
  • Smokers > 10 cigarette/day or smokers < 10 cigarettes/day who could not quit at least 7 days before study and throughout study (including the washout between periods)
  • Regular alcohol consumption (more than 1 time/week) or alcohol consumption within 7 days prior to the study

结局指标

主要结局

Cytokine levels (Tumor Necrosis Factor-α and Interleukin-1β)

时间窗: Two months

次要结局

  • Liver function tests (tB/dB, AST, ALT, ALP)(Two months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Teerapol Srichana

Associate Professor

Prince of Songkla University

研究点 (2)

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