TBTC Study 27/28 PK: Moxifloxacin Pharmacokinetics During TB Treatment

Inclusion Criteria: For Healthy Volunteers: Provision of informed consent for the study. Age > 18 years. Willingness to be available for 2 weeks of DOT. Willingness to be admitted to a GCRC or hospital on two occasions. Women of child-bearing potential must agree to practice an adequate method of birth control. Barrier methods of contraception or abstinence from sexual activity are satisfactory methods. Willingness to have HIV testing done if documented results are not available. (A prior negative result must be obtained within one year and consists of a negative HIV ELISA. A positive result must be both a positive HIV ELISA and Western Blot, or a plasma HIV PCR RNA level greater than 5000 copies/ml). Laboratory screening (if not already available) within 30 days of the first PK admission: Serum potassium within normal limits Hematocrit > 35% Absolute neutrophil count > 1000 /mm3 AST < 3 times the upper limit of normal Bilirubin < 2 times the upper limit of normal Creatinine < 2 times the upper limit of normal Eligible and enrolled for medical health care sponsored by the United States federal government (such as the Veterans Administration enrollment Priority 1 through 7, VHA Directive 2003-003). For Patients with Tuberculosis Enrolled in TBTC Study 27 or Study 28: Any patient enrolled in TBTC Study 27 or Study 28 receiving a daily (5-7 days per week) regimen. Provision of informed consent for the study. Willingness to be admitted to a GCRC or hospital on one occasion. Exclusion Criteria: For Healthy Volunteers: Karnofsky score less than 90 Pregnancy or breast-feeding. (A negative pregnancy test is required for women of childbearing potential within 14 days before the first dose of moxifloxacin.) Known allergy to any fluoroquinolone or rifamycin antibiotic Current or planned therapy during the study with drugs having unacceptable interactions with rifampin History of prolonged QT syndrome or current or planned therapy with quinidine, procainamide, amiodarone, sotalol, or ziprasidone during period of administration of moxifloxacin and for one week after treatment For Patients with Tuberculosis Enrolled in TBTC Study 27 or Study 28: Severe anemia as defined by a hematocrit less than 25% (most recent value, measured within 30 days of the PK study). History of severe liver disease classified as Child Pugh Class C.