BENITIONSClinical Trial Intelligence

TBTC Study 29: Rifapentine During Intensive Phase Tuberculosis (TB) Treatment

Phase 2 Completed NCT00694629

ConditionPulmonary Tuberculosis
PhasePhase 2
SponsorCenters for Disease Control and Prevention
StatusCompleted
Enrollment334 participants
Interventionsrifapentine, rifapentine 10 mg/kg, rifapentine 15 mg/kg, rifapentine 20 mg/kg
Start dateDec, 2008
Completion dateJun, 2013
Results postedJul 23, 2026

Summary

This Phase 2, multicenter, open-label clinical trial evaluated the antimicrobial activity and safety of rifapentine-containing regimens during the intensive phase of pulmonary tuberculosis treatment. Participants were randomized to receive either a standard rifampin-based regimen (RHZE) or a rifapentine-substituted regimen (PHZE). An extension study evaluated higher daily doses of rifapentine (10, 15, and 20 mg/kg). The primary endpoint was sputum culture conversion at 8 weeks. Secondary outcomes included time to culture conversion, safety, and treatment discontinuation.

Participants With Negative Sputum Culture at 8 Weeks

8 weeks. · participants

Standard Intensive-Phase TB Treatment: Rifampin (10 mg/kg) + Isoniazid + Pyrazinamide + Ethambutol52 participants
lRifapentine 10 mg/kg TB Treatment (PHZE): Isoniazid + Pyrazinamide + Ethambutol62 participants
Rifapentine 15 mg/kg TB Treatment (PHZE): Isoniazid + Pyrazinamide + Ethambutol59 participants
Rifapentine 20 mg/kg TB Treatment (PHZE): Isoniazid + Pyrazinamide + Ethambutol54 participants

Participants Who Discontinued Treatment During Intensive Phase

8 weeks · participants

Standard Intensive-Phase TB Treatment: Rifampin (10 mg/kg) + Isoniazid + Pyrazinamide + Ethambutol11 participants
lRifapentine 10 mg/kg TB Treatment (PHZE): Isoniazid + Pyrazinamide + Ethambutol5 participants
Rifapentine 15 mg/kg TB Treatment (PHZE): Isoniazid + Pyrazinamide + Ethambutol5 participants
Rifapentine 20 mg/kg TB Treatment (PHZE): Isoniazid + Pyrazinamide + Ethambutol9 participants

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