Sputum Pharmacokinetics of TB Drugs and Bacterial Drug Resistance

Tuberculosis Clinical Trial

Official title:

Sputum Pharmacokinetics of TB Drugs and Bacterial Drug Resistance

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02534727
• Other study ID #: 150187
• Secondary ID: 15-I-0187
• Status: Completed
• Start date: January 27, 2016
• Est. completion date: December 31, 2020

Study information

• Verified date: March 2022
• Source: National Institutes of Health Clinical Center (CC)
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Background: Many people around the world get tuberculosis (TB) and non-tuberculous mycobacteria (NTM) infections. Sometimes medicine that treats these infections does not get to where the bacteria are in the lungs. Researchers want to find a way to tell if enough medicine is getting to where it is needed in the lungs. They will look at how much medicine is in your sputum (what you cough up) compared to how much is in your blood. They will also investigate a new test to quickly figure out what medicines are likely to treat TB effectively. Objective: To determine the relationship between the concentration of TB drugs in plasma and sputum over time. Eligibility: People ages 18 and older who have TB or NTM infection that is suspected to be drug resistant. They must be taking TB or NTM medicines. Design: Participants will be screened with medical history. Participants will be in the study for 2 8 days. Participants will give 3 or more sputum samples over at least 2 different days. They will cough sputum into a cup. Participants will have blood drawn 4 times a day on 2 different days.

Description:

This study will support two avenues of research, pharmacokinetics (PK) of drugs used to treat tuberculosis and resistance to those drugs that has been developed by the pathogen. Given the high inter-individual variability in TB drug exposure, therapeutic drug monitoring would be of value to adjust the drug dose in TB patients in order to improve clinical outcome and minimize toxicity. It is not practiced in most settings for reasons associated with costs but also because blood collection is an invasive procedure. Sputum on the other hand is often produced spontaneously and discarded as waste. Drug levels can be measured in sputum just as in plasma. Here we will test the hypothesis that sputum drug levels are predictive of drug concentrations in plasma and/or in specific lesion compartments such as the caseum of open cavities. We will also characterize the exposure of standard 1st and 2nd line TB drugs at one of the sites of infection, since sputum is in direct contact with cavity caseum. The subjects will contribute three or more sputum samples spontaneously produced over at least two days and four blood samples following drug administration on two different days (8 blood samples total). The data will be analyzed using population PK modeling approaches to generate concentration-time profiles and 24-hour area under the curve (AUC) of each study drug in sputum. Correlations between these values, plasma and lesion AUCs will be examined. We will draw from a recently completed TB lesion pharmacokinetic study (www.ClinicalTrials.gov #NCT00816426) to seek correlations between drug exposure in sputum and in pulmonary lesions. In addition to drug concentrations, sputum will be cultured by standard methods to isolate Mycobacterium tuberculosis (Mtb), determine the drug resistance profile, and be saved for testing a second generation of the Xpert TB XDR assay.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 215
• Est. completion date: December 31, 2020
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

• INCLUSION CRITERIA:

1. At least 18 years of age

2. Diagnosis of TB (and/or NTM for NIH clinical center subjects)

3. Ongoing signs and/or symptoms of pulmonary TB (and/or NTM at the NIH CC)

4. Suspected drug resistance (drug susceptible allowed at the NIH CC)

5. Available to provide at least 3 sputa over 2 or more days

6. Taking anti-tuberculosis medicines (or NTM meds at NIH CC) during the time sputa are provided

7. Thought likely to be Mycobacterium culture positive (including NTM infected for the NIH CC) by enrolling physician

8. GeneXpert MTB/RIF sputum TBpositive (China subjects only)

9. Likely able to produce sputum samples while on study

10. Willing to provide blood samples

11. Willing to have samples stored

EXCLUSION CRITERIA:

1. Acute liver or kidney disease

2. Conditions which compromise the subject s ability to take or absorb oral drugs

Related Conditions & MeSH terms

• Non-Tuberculosis Mycobacteria
• Tuberculosis

Locations

Country	Name	City	State
China	Henan Provincial Chest Hospital	Zhengzhou,
United States	National Institutes of Health Clinical Center, 9000 Rockville Pike	Bethesda	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)

Countries where clinical trial is conducted

United States,  China, 

References & Publications (3)

Dartois V. Drug forgiveness and interpatient pharmacokinetic variability in tuberculosis. J Infect Dis. 2011 Dec 15;204(12):1827-9. doi: 10.1093/infdis/jir662. Epub 2011 Oct 21. — View Citation

Peloquin C. Use of therapeutic drug monitoring in tuberculosis patients. Chest. 2004 Dec;126(6):1722-4. — View Citation

Wilkins JJ, Savic RM, Karlsson MO, Langdon G, McIlleron H, Pillai G, Smith PJ, Simonsson US. Population pharmacokinetics of rifampin in pulmonary tuberculosis patients, including a semimechanistic model to describe variable absorption. Antimicrob Agents Chemother. 2008 Jun;52(6):2138-48. doi: 10.1128/AAC.00461-07. Epub 2008 Apr 7. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary endpoint is the AUC (0-24) in sputum and blood.	drug-specific correlation coefficients of the AUCs for sputum and blood	0-24 hrs
Secondary	drug-specific time-concentration curves, as well as drug exposure in sputum relative to that in cavity caseum	Estimation of time-concentration curves, as well as variance components of sputum PK parameters to better inform sputum PK sampling in future studies. Additionally, the relationship between drug-specific exposures in cavity caseum, from historical data, and that in sputum will be evaluated using correlation coefficients.	Throughout

External Links

•   NIH Clinical Center Detailed Web Page