Tuberculosis Clinical Trial
Official title:
Pharmacokinetics of Standard First and Second Line Anti-TB Drugs in the Lung and Lesions of Subjects Elected for Resection Surgery
This study, conducted jointly by researchers at the National Masan TB Hospital, Asan and
Samsung Medical Centers in Seoul, Republic of Korea, and the Yonsei University and the NIH in
the United States, will examine why some patients with tuberculosis (TB) develop disease that
is harder to treat than most cases. TB is an infection of the lung that usually can be
successfully treated with anti-TB drugs. However, some people get a more serious kind of
disease (called multi-drug resistant TB or extensively drug-resistant TB) that is very
difficult to treat and may not be cured by the regular medicines available. This study will
try to find out if some of the common TB drugs are getting to the place where the TB bacteria
are. It will also look at how current anti-TB drugs might be used more effectively and how
better drugs might be developed.
People 20 years of age and older with hard-to-treat TB who have elected to undergo surgical
removal of part of their lung at the National Masan Tuberculosis Hospital, Masan, the Asan
Medical Center, and the Samsung Medical Center, may be eligible for this study.
Participants undergo the following procedures:
- Medical history and physical examination, including sputum sample.
- Blood tests at various times during the study.
- Drug administration. Subjects are given one dose each of five common TB drugs
rifampicin, isoniazid, pyrazinamide, kanamycin and moxifloxacin before they undergo
surgery to remove part of their lung. After surgery, some of the lung tissue and fluid
around the lungs that was removed during surgery will be examined to determine the
regions where the TB bacteria live and analyze the lung tissue itself.
- Dynamic MRI (magnetic resonance imaging) scan. This type of scan uses a magnetic field
and radio waves to produce pictures of the lung. Subjects lie very still on a table
inside the cylindrical scanner with their head on a soft cradle and their hands over
their head. Several images are obtained for less than 5 minutes at a time.
It takes 6 to 24 months of intensive combination therapy to cure tuberculosis (TB) with antibiotics that have proven activity in vitro. In contrast, many pulmonary infectious diseases can be cured following single drug treatment with similar drugs for only one to a few weeks. We hypothesize that the unusual complexity of TB lesions and the degree of sequestration of TB bacilli within these lesions may limit access of the drugs to their site of action, leading to treatment failure, long treatment duration and the emergence of drug resistance. To test the hypothesis that drug maldistribution into lesions impacts on treatment duration and failure, we propose to examine the lesion-specific penetration properties of 5 standard anti-TB drugs in the lungs of subjects selected for lung surgery. The study is designed to understand what lesion types are the most difficult to penetrate. This aspect of TB drug pharmacokinetics has been largely neglected so far, probably owing to the lack of adequate technology and the limited availability of human TB lesion samples. Fifteen patients who elect lung resection surgery will be asked to participate in the study. Consented subjects will receive 4-5 first and second line anti-TB drugs concomitantly at 1 of 5 pre-determined times prior to surgery. At the time of resection, drug levels will be measured in plasma, in uninvolved lung tissue and in lesions using standard analytical methods as well as imaging Mass Spectrometry (MS) where drug concentration gradients can be visualized across tissue sections. The major aim of this study is to determine actual concentrations and permeability coefficients of the 5 study drugs in various lesion types contained within subjects surgically removed lung tissue. Data analysis will also provide the relative exposure of each drug in plasma versus lung tissue and lesion. If conclusive, the results may be taken into consideration when selecting drug doses and dosing regimens. Additionally, images generated by standard of care (SOC) High Resolution Computed Tomography (HRCT), and Dynamic MRI for each subject will provide information regarding lesion structure and anatomy, lesional blood flow and microvascular function. Lesion-specific correlations will be established between CT radiology and drug pharmacokinetic (PK) to identify which histopathologic lesion types may be particularly difficult to sterilize and to evaluate the potential impact of drug penetration on treatment outcome. The long term goal of this study is to identify the factors behind poor lesion penetration, so that new agents can be optimized with better penetration properties to target harder-to-sterilize lesion' types. ;
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