Isoniazid alone for 6 or 9 months, or an isoniazid–rifamycin combination for 2 or 3 months |
Recommended by WHO and CDC; considered equivalent though not compared directly in clinical trials |
– |
Individuals with diagnosed LTBI at risk of reactivation in endemic countries, all individuals with diagnosed LTBI in the USA |
32–34 |
Rifampicin for 4 months |
Recommended by the American Thoracic Society in 2000; higher completion rate than and comparable safety to 9-month isoniazid |
– |
Children diagnosed with LTBI |
194 |
Various second-line drugs and duration |
Evaluated in observational studies |
– |
Household contacts (children and/or adults) of patients infected with MDR M. tuberculosis
|
195 |
Levofloxacin versus placebo control for 6 months |
Placebo-controlled trial |
TB-CHAMP |
Children household contacts of patients infected with MDR M. tuberculosis
|
36 |
Levofloxacin versus placebo for 6 months |
Placebo-controlled trial |
VQUIN MDR |
Household contacts of all ages of individuals who are infected with rifampicin-resistant or MDR M. tuberculosis
|
38 |
Delamanid versus isoniazid for 6 months |
Placebo-controlled trial |
PHOENIx MDR-TB |
High risk (individuals positive for HIV-1 or individuals without HIV-1 positivity that are immunosuppressed, and children under 5 years old) household contacts of individuals who are infected with MDR M. tuberculosis
|
NCT03568383 |