Compares a higher rifampicin dose with standard dosing in pulmonary tuberculosis

Trial details

Who runs it

Radboud University Medical Center

Trial code

NCT06057519

Record updated

21 January 2026

Original description

The goal of this clinical trial is to compare an optimized dose (1800 mg) of rifampicin to standard dose (450 mg if patient <50 kg and 600 mg if patient >50kg) of rifampicin in tuberculosis patients.Read full original descriptionShow less

Pragmatic Trial on the Safety and Tolerability of an Optimized Dose of Rifampicin in Tuberculosis Patients

The goal of this clinical trial is to compare an optimized dose (1800 mg) of rifampicin to standard dose (450 mg if patient <50 kg and 600 mg if patient >50kg) of rifampicin in tuberculosis patients.

The main questions it aims to answer are:

* To compare the incidence of hepatotoxicity occurs in the optimized dose vs standard dose arm * To compare any adverse events occur in the optimized dose vs standard dose arm * To compare final treatment outcome at the end of treatment according to WHO definitions of cure in the optimized dose regimen versus the standard dose regimen. * To compare two and three months culture conversion rates in the optimized dose regimen versus the standard dose regimen. * To describe and compare the steady-state plasma pharmacokinetics of the optimized dose regimen versus the standard dose regimen.

Participants will be given an optimized dose of 1800 mg of rifampicin daily. Researchers will compare the optimized and standard dose to see if more hepatotoxicity occurs.

Inclusion: The patient has provided informed consent for study participation prior to all trial-related procedures; The patient has a diagnosis of pulmonary tuberculosis according to the local diagnostic criteria; The patient is aged 18 years or older at the day of informed consent; No known allergic reactions or toxicity to rifampicin in the past; Female patients of childbearing potential must have a negative serum pregnancy test, and consent to practice an effective method of birth control during the study. And they should not be lactating during the trial (female participants of childbearing potential only). Effective birth control for female patients has to include two methods, including methods that the patient's sexual partner(s) use. At least one must be a barrier method. Female patients are considered not to be of childbearing potential if they are post-menopausal with no menses for the last 12 months, or surgically sterile (this condition is fulfilled by bilateral oophorectomy, hysterectomy, and by tubal ligation which is done at least 12 months prior to enrolment); The patient will be compliant to the study schedule, in the discretion of the investigator.

Exclusion: Poor general condition or comorbidities where delay in treatment cannot be tolerated or death within three months is likely. Or if there is concurrent treatment that may interfere; The participant has a known or suspected, current alcohol or drug or amphetamine abuse, that is, in the opinion of the investigator, sufficient to compromise the safety or cooperation of the patient; The patient has a known allergy or intolerance, or concomitant disorders or conditions for which rifamycins or other standard TB treatment drugs are contraindicated; The patient has had treatment with any other investigational drug within 1 month prior to enrolment, or enrolment into other clinical (intervention) trials is planned in the upcoming 6 months; Previous anti-TB treatment: the patient ended a previous TB treatment (episode) within last 3 months; The patient has tuberculosis which is assessed to receive high dose rifampicin according to the local standard of care; Patient infected with a rifampicin-resistant strain of M. tuberculosis; Known allergy or intolerance for rifamycins; Acute or severe or life-threatening liver disease induced by drugs in the past; The patient has a chronic disorder such as liver disease or renal disease; Laboratory: at screening one or more of the following abnormalities were observed for the patient in screening laboratory:; Serum amino aspartate transferase (AST) and/or serum alanine aminotransferase (ALT) activity >3x the upper limit of normal; Serum total bilirubin level >2.5 times the upper limit of normal; Creatinine clearance (CrCl) level lower than 30 mls/min; The patient started current TB treatment more than 4 weeks ago; The patient has TB meningitis; The patient is in a coma; Circumstances that raise doubt about free, uncoerced consent to study participation (e.g. in a prisoner or mentally handicapped person); The patient is not able to give consent personally; The patient is pregnant or breast-feeding; The patient has icterus.

ClinicalTrials.gov NCT06057519