RecruitingPhase 2Phase 3NCT06441006

Program for Rifampicin-Resistant Disease With Stratified Medicine for Tuberculosis

Program for Rifampicin-Resistant Disease With Stratified Medicine for Tuberculosis (PRISM-TB)


Sponsor

University of California, San Francisco

Enrollment

400 participants

Start Date

Oct 3, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

PRISM-TB is an international, seamless, multicenter, open-label, randomized, controlled, pragmatic, stratified medicine, treatment shortening, multi-arm multi-stage (MAMS), noninferiority Phase 2/3 clinical trial for fluoroquinolone-susceptible multidrug-resistant/rifampin-resistant pulmonary tuberculosis (FQ-S MDR/RR-TB). In Stage 1, participants will be randomized among one of three treatment arms (one control and two experimental). Following the interim analysis (at the end of Stage 1) based on DOOR outcome comparisons and the entirety of the data, one of the four possible experimental strategies will be identified and continue into Stage 2. In Stage 2, participants will be randomized among one of two treatment arms (one control and one experimental). The trial objective is to identify, among participants with fluoroquinolone-susceptible multidrug-resistant/rifampicin-resistant tuberculosis (FQ-S MDR/RR-TB), the preferred BPaLM strategy of 13 or 17 weeks for participants stratified to receive shorter treatment and 17 or 24 weeks for participants stratified to receive longer treatment, as defined by a prespecified stratification algorithm, and to evaluate whether this BPaLM strategy has noninferior efficacy to the control strategy at Week 73.


Eligibility

Min Age: 14 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Bedaquiline, a drug called Control Arm FQ-S MDR/RR-TB regimen, designed according to latest international guidelines, and others for people with tuberculosis, mdr, tuberculosis, multidrug-resistant, and other related conditions. The study is currently recruiting participants at 6 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGBedaquiline

Frequency: daily Route of administration: oral

DRUGLinezolid

Frequency: daily Route of administration: oral

DRUGPretomanid

Frequency: daily Route of administration: oral

DRUGMoxifloxacin

Frequency: daily Route of administration: oral

DRUGControl Arm FQ-S MDR/RR-TB regimen, designed according to latest international guidelines

The local SOC regimen consistent with preferred regimen(s) in international guidelines. In most cases this will be 24 weeks of bedaquiline, pretomanid, linezolid, and moxifloxacin (6BPaLM). Doses and durations of each component may change based on the latest international guidelines and the local SOC.


Locations(6)

National Center for Communicable Diseases

Ulaanbaatar, Mongolia

Institute of Chest Diseases

Kotri, Pakistan

Hospital Nacional Sergio E. Bernales

Lima, Peru

Policlínico SES

Lima, Peru

Mulago National Referral Hospital

Kampala, Uganda

Hanoi Lung Hospital

Hanoi, Vietnam

View Full Details on ClinicalTrials.gov

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NCT06441006


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