Efficacy and Safety of Levofloxacin for the Treatment of MDR-TB
Information source: Boston University
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Tuberculosis, Multidrug-Resistant
Intervention: Levofloxacin (Drug); Optimized background regimen (OBR) (Drug)
Phase: Phase 2
Status: Recruiting
Sponsored by: Boston University Official(s) and/or principal investigator(s): Charles R Horsburgh, MD, Principal Investigator, Affiliation: Boston University
Overall contact: Biljana Bazdar-Vinovrski, PharmD, Phone: 617-638-5887, Email: bbazdarv@bu.edu
Summary
Multi-drug-resistant tuberculosis (MDR-TB) affects nearly 600,000 persons each year around
the world. This type of tuberculosis is very difficult to treat, and many patients die from
it. Drugs of the fluoroquinolone class are very important for treating MDR-TB, but the best
dose of one of the most effective fluoroquinolones, levofloxacin, is not known. This
application proposes a study to determine the best dose of levofloxacin to use in treating
MDR-TB. 100 patients will receive their usual treatment, plus levofloxacin at one of four
doses. The study will be performed in Peru and in South Africa, where MDR-TB is common.
Clinical Details
Official title: Prospective, Randomized, Blinded Phase II Pharmacokinetic/Pharmacodynamic Study of the Efficacy and Tolerability of Levofloxacin in Combination With Optimized Background Regimen for the Treatment of MDR-TB
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: Efficacy
Secondary outcome: Safety
Detailed description:
MDR-TB is a growing threat to international health. A recent report from WHO estimated that
over 440,000 new cases of MDR-TB occurred in 127 countries in 2008, causing 150,000 deaths;
this represents a 55% increase in the number of cases since 2000. Current treatment regimens
have only a 58-67% success rate, and as many as 20% of those who fail to respond to
treatment die of tuberculosis; those who do not die become chronic carriers and spread
MDR-TB to others.
Fluoroquinolones (FQ) are an essential part of regimens for the treatment of MDR-TB;
substantially better outcomes have consistently been seen in patients with MDR-TB who are
treated with FQ, and newer FQ (levofloxacin, gatifloxacin and moxifloxacin) are the most
potent antituberculosis agents available for MDR-TB treatment. However, gatifloxacin has
been taken off the market because of dysglycemic reactions and moxifloxacin produces marked
QT prolongation, increasing risk of fatal arrhythmia. In contrast, QT studies of
levofloxacin have found minimal prolongation at doses up to 20mg/kg. Levofloxacin is
currently given for TB at doses of 11-14 mg/kg/day and has been well tolerated at doses up
to 20 mg/kg. Although the efficacy of levofloxacin increases as exposure increases both in
animal studies of TB and in human studies of gram-negative bacteria, its efficacy at higher
doses against TB in humans has not been studied. Thus, determination of the most efficacious
and well-tolerated dose of levofloxacin is an important research priority. In this Phase 2
study, we will determine the levofloxacin dose and exposure that achieve the greatest
reduction in mycobacterial burden with acceptable tolerability by studying 100 adults with
smear- and culture-positive pulmonary MDR-TB at sites in Peru and South Africa. Levofloxacin
will be administered with an optimized background regimen (OBR) to address the following
Specific
Aims:
Specific Aim 1: To determine the levofloxacin AUC/MIC that provides the shortest time to
sputum culture conversion in solid medium.
Specific Aim 2: To determine the highest levofloxacin AUC that is both safe and associated
with fewer than 25% of patients discontinuing or reducing their dose of levofloxacin.
Specific Aim 3: To develop a dosing algorithm to achieve the levofloxacin AUC associated
with maximal efficacy and acceptable safety/tolerability.
This clinical trial will increase our ability to cure MDR-TB and prevent the emergence of
resistance to new TB drug classes by optimizing dosing and improving the effectiveness of an
existing antimycobacterial agent, using a novel and versatile study design which more
rapidly and efficiently identifies advances in this critical area. Construction of an
algorithm to predict the optimal levofloxacin dose will allow more effective use of
levofloxacin, particularly in areas with limited resources, where the burden of MDR-TB is
the greatest.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
1. Patients with smear-positive, culture positive* pulmonary TB
2. Sputum contains isoniazid* and rifampin-resistant, Ofloxacin-susceptible MTB, all by
MTBDR-sl
3. Previously treated or newly diagnosed with tuberculosis
4. Willingness to have HIV testing performed, if HIV serostatus is not known or if the
last documented negative HIV test was more than 3 months prior to enrollment.
5. Age ≥ 18 years.
6. Weight > 40 Kg
7. Karnofsky score of > 60 (see section 18. 1)
8. Willingness by the patient to attend scheduled follow-up visits and undergo study
assessments.
9. Women with child-bearing potential must agree to use birth control if you are having
sex with men while participating in this study and for three months afterward.
10. Laboratory parameters (performed within 14 days prior to enrollment):
- Estimated Serum creatinine clearance should be <50, using nomogram78
- Hemoglobin concentration ≥ 9. 0 g/dL
- Platelet count of ≥ 80,000/mm3
- Absolute neutrophil count (ANC) > 1000/ mm3
- Negative pregnancy test (for women of childbearing potential) within 14 days of
enrollment
- HIV viral load and CD4 count if HIV infected (within 3 months)
- Serum ALT and total bilirubin <3 times upper limit of normal
11. Able to provide informed consent
Note: *Subjects may be enrolled on the basis of a presumption that they will be culture
positive at either screening or baseline if they are smear-positive, but they will be
excluded from the analysis if cultures are subsequently negative. This will not be deemed
a protocol violation. Similarly, subjects with rifampin susceptibility on a DNA-based test
may be enrolled on the basis of a presumption that they will also be INH-resistant, but
they will be excluded from the analysis if the isolate is subsequently shown to be
INH-susceptible. This will also not be deemed a protocol violation.
Exclusion Criteria:
1. Currently breast-feeding or pregnant.
2. Known allergy or intolerance to or toxicity from fluoroquinolones or other
medications utilized in this study.
3. In the judgment of the physician the patient is not expected to survive for 6 months
4. Anticipated surgical intervention for the treatment of pulmonary tuberculosis
5. Participation in another investigational drug trial within the past 30 days
6. Concurrent use of known QT-prolonging drugs: a list of such medications can be found
at http://www. azcert. org/medical-pros/drug-lists/printable-drug-list. cfm
7. Poorly controlled diabetes
8. Known g-6-phosphate dehydrogenase deficiency
9. Use of quinolone for 7 days within past 30 days
10. QTc interval greater than 450 msec for men or greater than 470 msec for women
Locations and Contacts
Biljana Bazdar-Vinovrski, PharmD, Phone: 617-638-5887, Email: bbazdarv@bu.edu
Partners in Health, Lima, Peru; Recruiting Leonid Lecca, MD, Email: Llecca_SES@pih.org Leonid Lecca, MD, Principal Investigator
University of Cayetana Heredia, Lima, Peru; Recruiting Carlos Zamudio, MD, Email: carlos.zamudio@upch.pe Eduardo Gotuzzo, MD, Principal Investigator
Stellenbosch University, Capetown, South Africa; Recruiting Jeannine DuBois, MD, Email: dr.jeannine@task.org.za Ramonde F Patientia, MD, Principal Investigator
Additional Information
Starting date: January 2015
Last updated: February 4, 2015
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