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ABSTRACT: Background
Accumulating data indicate that higher rifampicin doses are more effective and shorten tuberculosis (TB) treatment duration. This study evaluated the safety, tolerability, pharmacokinetics, and 7- and 14-day early bactericidal activity (EBA) of increasing doses of rifampicin. Here we report the results of the final cohorts of PanACEA HIGHRIF1, a dose escalation study in treatment-naive adult smear-positive patients with TB.Methods
Patients received, in consecutive cohorts, 40 or 50 mg·kg-1 rifampicin once daily in monotherapy (day 1-7), supplemented with standard dose isoniazid, pyrazinamide and ethambutol between days 8 and 14.Results
In the 40 mg·kg-1 cohort (n=15), 13 patients experienced a total of 36 adverse events during monoth
SUBMITTER: Te Brake LHM
PROVIDER: S-EPMC8411896 | biostudies-literature | 2021 Jul
REPOSITORIES: biostudies-literature