| Purpose: |
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Although effective therapy for tuberculosis is available, TB continues to cause significant
problems worldwide, and rates of multi-drug resistant (MDR) TB cases are on the rise. A
major obstacle to the control of TB is poor adherence with lengthy (usually 6 months) and
complicated treatment regimens. Incomplete TB treatment can lead to serious consequences
such as increased severity of illness and death, prolonged infectiousness and transmission
in the community, and the development of drug resistance. The development of new treatment
strategies with more stronger drugs could lead to shorter and simpler regimens. A TB
treatment regimen that allowed treatment duration to be meaningfully decreased would have
important public health implications.
This trial will compare the effect and safety of a new oral regimen to that of the standard
regimen for the first phase of treatment for pulmonary tuberculosis.
The experimental regimen will consist of the following:
- Two months of isoniazid, rifapentine, pyrazinamide and moxifloxacin (HPZM) administered
once daily. Pyridoxine (vitamin B6) will be given with each dose of isoniazid.
The standard control intensive phase regimen will consist of the following:
- Two months of isoniazid, rifampin, pyrazinamide, and ethambutol (HRZE) administered
once daily. Pyridoxine (vitamin B6) will be given with each dose of isoniazid.
Following intensive phase therapy (the study phase), all patients will be treated with a
non-experimental continuation phase regimen.
In mice, the combination of Moxifloxacin and Rifapentine have cured the animals
significantly faster than the standard regimen and this study will be the first step to see
if the potential is also there in humans.
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| Criteria: |
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Inclusion Criteria:
- Presumptive diagnosis of sputum smear-positive pulmonary TB.
- Age: ≥18 years
- Seven (7) or fewer days of multidrug therapy for TB disease in the preceding 6
months.
- Seven (7) or fewer days of fluoroquinolone therapy in the preceding 3 months.
- Documentation of HIV infection status.
- For HIV seropositive individuals, a CD4 T lymphocyte count of greater than or equal
to 200 cells/mm3.
- Documentation of study baseline laboratory parameters done at, or ≤ 14 days prior to
screening:
- AST less than or equal to 2.5 times upper limit of normal.
- Total bilirubin level less than 2.5 times upper limit of normal.
- Creatinine level less than 2 times upper limit of normal.
- Hemoglobin level of at least 8.0 g/dl.
- Platelet count of at least 75,000 mm3.
- Potassium level of at least 3.5.
- Negative pregnancy test (women of childbearing potential).
- Karnofsky score of at least 60 (requires occasional assistance but is able to care
for most of his/her needs).
- Male or nonpregnant, nonnursing female.
- Provision of informed consent.
Exclusion Criteria:
- CD4 count < 200 cells/cu mm.
- Presence of active AIDS-related opportunistic infection (other than TB) or active
AIDS-related malignancy.
- Known intolerance to any of the study drugs.
- Concomitant disorders or conditions for which any of the study drugs is
contraindicated. These include severe hepatic damage, acute liver disease of any
cause, and acute uncontrolled gouty arthritis.
- Inability to take oral medication.
- Central nervous system TB.
- Pulmonary silicosis.
- Current or planned therapy, during study phase (intensive phase of TB treatment),
with any one or more of the following drugs: quinidine, procainamide, amiodarone,
sotalol, disopyramide, terfenadine, cisapride, erythromycin, clarithromycin,
phenothiazines, haloperidol, olanzapine, ziprasidone, tricyclic antidepressants,
chronic corticosteroids administered either orally or intravenously, chronic
fluconazole,chronic itraconazole, chronic ketoconazole, oral or intravenous
tacrolimus, oral or intravenous cyclosporine, HIV protease inhibitor, HIV
non-nucleoside reverse transcriptase inhibitor.
- Concurrent severe and/or uncontrolled medical or psychiatric condition that, in the
opinion of the investigator, could cause unacceptable safety risks or compromise
compliance with the protocol.
- Unable or unwilling to receive directly observed therapy and/or adhere with follow-up
(e.g. due to residence remote from the study site).
- Refusal of consent. |