Precision Rifampin Trial for Personalized Dosing

PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

October 1, 2025

Primary Completion Date

December 30, 2027

Study Completion Date

June 1, 2028

Conditions
Tuberculosis
Interventions
DIAGNOSTIC_TEST

urine spectrophotometry for rifampin absorbance

All participants will received conventional weight-based TB therapy, standard of care for active TB disease. After enrollment, participants will be randomized to early Day 14 or delayed Day 21 dose modification of rifampin informed by urine spectrophotometry where absorbance is determined above or below a threshold. Below a threshold, single tablets of rifampin are added to conventional fixed drug combination standard of care, above a threshold, no additional rifampin is added. Dose adjustment of rifampin may be up to \~30mg/kg and will be continued through day-56.

All Listed Sponsors
collaborator

Rutgers University

OTHER

collaborator

Haydom Lutheran Hospital

OTHER

lead

University of Virginia

OTHER