# The Bring BPaL2Me Trial - Comparing Nurse-Led RR-TB Treatment in Primary Care to Physician-Led, Hospital-Based RR-TB Treatment: A Cluster Randomized, Non-Inferiority Trial

> **NIH NIH R01** · JOHNS HOPKINS UNIVERSITY · 2024 · $775,426

## Abstract

In South Africa (SA), Mycobacterium tuberculosis (TB) is managed within primary care clinics (PCCs), where
nurses treat drug-susceptible TB and TB/HIV coinfection with treatment outcomes rivaling the best in the world.
A PCC management strategy offers a more convenient, patient-centered, differentiated model of care that
integrates TB and HIV treatment within the same setting. A diagnosis of rifampicin-resistant TB (RR-TB),
however, upends this model, requiring referral to a hospital-based, physician-led outpatient treatment center.
Hospital-based, physician-led models add significant patient-associated costs, with estimates suggesting 81% of
RR-TB patients experience catastrophic costs even in a decentralized outpatient model. There is hope, however,
to move RR-TB care into PCCs and in many settings this involves nurse-led management. The BringBPaL2Me
Trial is a multi-principal investigator, multi-site, cluster randomized, non-inferiority trial (CR-NIT), to compare
nurse-led RR-TB treatment in PCCs to standard of care physician-led RR-TB treatment at district hospitals in
the provinces of KwaZulu-Natal (KZN), Gauteng (GP) and Eastern Cape (EC), SA. Clusters include 10 PCCs
affiliated with 5 decentralized outpatient programs at RR-TB district hospitals (n=50 clusters). We estimate the
need to screen 3,800 RR-TB positive patients to enroll 2,944, or 64 RR-TB participants per PCC cluster. We
estimate 60-70% will be HIV co-infected. The interclass correlation is 0.024 based on our prior CRT enrolling
3,000 patients in KZN and EC. The non-inferiority margin is set at 5% with the assumption of 90% treatment
success in the physician-led arm. Treatment will include either a 6-month RR-TB regimen (i.e., bedaquiline,
pretomanid, linezolid and moxifloxacin, or BPaLM) or fluroquinolone-resistant TB (i.e., BPaL) regimen. The
BringBPaL2Me primary aim is to conduct a 5-year, analyst and clinical safety review committee blinded, multi-
site, CR-NIT to evaluate 1) treatment outcome; 2) safety; and 3) patient associated catastrophic costs with the
following hypotheses: 1) Outpatient nurse-led treatment in PCCs will be non-inferior to outpatient physician-led
treatment at hospital-based outpatient sites among RR-TB patients, regardless of HIV co-infection, as
determined by a successful treatment outcome [H1]; 2) The proportion of severe adverse events (SAEs) identified
will not significantly differ by blinded, independent review [H2]; 3) Patient associated catastrophic costs (i.e.,
costs 20% or more of household income) will be lower in nurse-led treatment [H3]. Our secondary aims include:
1) time to event analysis for a) RR-TB treatment initiation; b) smear/culture conversion; and, as applicable, c)
HIV treatment initiation; d) HIV viral suppression; and e) AE and SAE symptom resolution; 2) characterization
of provider adherence to guidelines for: a) dosing requirements; b) RR-TB dosing changes based on AE and SAE
events; and c) AE and SAE adjuvant medication man...

## Key facts

- **NIH application ID:** 10807079
- **Project number:** 5R01AI177135-02
- **Recipient organization:** JOHNS HOPKINS UNIVERSITY
- **Principal Investigator:** Denise Evans
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $775,426
- **Award type:** 5
- **Project period:** 2023-03-10 → 2028-02-29

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10807079

## Citation

> US National Institutes of Health, RePORTER application 10807079, The Bring BPaL2Me Trial - Comparing Nurse-Led RR-TB Treatment in Primary Care to Physician-Led, Hospital-Based RR-TB Treatment: A Cluster Randomized, Non-Inferiority Trial (5R01AI177135-02). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10807079. Licensed CC0.

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