Atorvastatin to Reduce Inflammation After Tuberculosis Treatment Completion

Prior treatment

• Participant receiving any type of lipid lowering agent at the time of screening, within three months prior to screening or likely to require any lipid lowering agent in the near future.
• Known allergy or contraindications to the investigational drug or any other statins
• Evidence of drug-resistant TB
• Unable to take oral medications
• Disease complications or concomitant illnesses that may compromise safety or interpretation of trial endpoints, such as known diagnosis of chronic inflammatory condition (e.g. sarcoidosis, rheumatoid arthritis, connective tissue disorder)
• Use of immunosuppressive medications, such as TNF-alpha inhibitors or systemic or inhaled corticosteroids, within the past 2 weeks
• Use of any investigational drug in the previous 3 months
• Alcohol and substance abuse which might interfere with medication adherence during the trial

Other illness

• Acute illness

Lab values

• Diabetes as defined by point of care HbA1c≥6.5, random glucose≥200mg/dL (or 11.1mmol/L), fasting plasma glucose≥126mg/dL (or 7.0mmol/L), or the presence of any anti-diabetic agent (including traditional medicines) as a concomitant medicine

Other

• Fever (temperature \>38.0 degrees centigrade)
• Extrapulmonary TB, including pleural TB and/or large pleural effusion
• Pregnant or desiring/trying to become pregnant in the next 6 months
• Any person for whom the physician feels this study is not appropriate

• Has completed the written informed consent process prior to undergoing any pre-screening or screening evaluations and willing to undergo HIV testing
• Age 18 to 65 years with body weight from 50 kg to 90 kg
• Clinical response to TB treatment and sputum culture negative at week 16
• Completed a 24-week course of standard TB treatment (4RHZE/2RH)
• Defined as "cured" by the TB Control Program of South Africa
  • Laboratory parameters within 30 days before enrolment:
• For HIV-infected participants: receiving antiretroviral therapy for at least 12 weeks and suppressed HIV viral load within 30 days prior to enrolment
• For HIV-infected participants: CD4 counts above 350 cells/µL within 30 days prior to enrolment
• AST and ALT \<3x upper limit of normal (ULN)
• Creatinine \<2x ULN
• Hemoglobin \>7.0 g/dL
• Platelet count \>50 x109 cells/L
• Creatinine kinase \<2x ULN
• Able and willing to return to follow-up
• Willing to have samples, including DNA, stored
• Willing to consistently practice a highly reliable method of pregnancy prevention