Safety of single-dose bedaquiline combined with rifampicin for leprosy post-exposure prophylaxis: A Phase 2 randomized non-inferiority trial in the Comoros Islands.

Autor: de Jong BC; Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium., Nourdine S; National Tuberculosis and Leprosy control Program, Moroni, Union of the Comoros., Bergeman AT; Heart Centre, Department of Cardiology, Amsterdam UMC location AMC, University of Amsterdam, Amsterdam, the Netherlands., Salim Z; National Tuberculosis and Leprosy control Program, Moroni, Union of the Comoros., Grillone SH; National Tuberculosis and Leprosy control Program, Moroni, Union of the Comoros., Braet SM; Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium., Wirdane Abdou M; National Tuberculosis and Leprosy control Program, Moroni, Union of the Comoros., Snijders R; Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium., Ronse M; Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium., Hoof C; Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium., Tsoumanis A; Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium., Ortuño-Gutiérrez N; Damien Foundation, Brussels, Belgium., der Werf CV; Heart Centre, Department of Cardiology, Amsterdam UMC location AMC, University of Amsterdam, Amsterdam, the Netherlands., Piubello A; Damien Foundation, Brussels, Belgium., Mzembaba A; National Tuberculosis and Leprosy control Program, Moroni, Union of the Comoros., Assoumani Y; National Tuberculosis and Leprosy control Program, Moroni, Union of the Comoros.; Damien Foundation, Brussels, Belgium., Hasker E; Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium.
Jazyk: angličtina
Zdroj: PLoS medicine [PLoS Med] 2024 Oct 21; Vol. 21 (10), pp. e1004453. Date of Electronic Publication: 2024 Oct 21 (Print Publication: 2024).
DOI: 10.1371/journal.pmed.1004453
Abstrakt: Background: To reduce leprosy risk in contacts of patients with leprosy by around 50%, the World Health Organization (WHO) recommends leprosy post-exposure prophylaxis (PEP) using single-dose rifampicin (SDR). Results from a cluster randomized trial in the Comoros and Madagascar suggest that PEP with a double dose of rifampicin led to a similar reduction in incident leprosy, prompting the need for stronger PEP. The objective of this Phase 2 trial was to assess safety of a bedaquiline-enhanced PEP regimen (intervention arm, bedaquiline 800 mg with rifampicin 600 mg, BE-PEP), relative to the WHO recommended PEP with rifampicin 600 mg alone (control arm, SDR-PEP).
Methods and Findings: From July 2022 to January 2023, consenting participants were screened for eligibility, including a heart rate-corrected QT interval (QTc) <450 ms and liver enzyme tests (ALT/AST) below 3× the upper limit of normal (ULN), before they were individually randomized 1:1 in an open-label design. Recruitment was sequential, by age group. Pediatric dosages were weight adjusted. Follow-up was done at day 1 post-dose (including ECG) and day 14 (including ALT/AST), with repeat of ALT/AST on the last follow-up at day 30 in case of elevation on day 14. The primary outcome was non-inferiority of BE-PEP based on a <10 ms difference in QTc 24 h after treatment administration, both unadjusted and adjusted for baseline QTc. Of 408 screened participants, 313 were enrolled, starting with 187 adults, then 38 children aged 13 to 17 years, and finally 88 children aged 5 to 12 years, of whom 310 (99%) completed all visits. Across all ages, the mean QTc change on BE-PEP was from 393 ms to 396 ms, not significantly different from the change from 392 ms to 394 ms on SDR-PEP (difference between arms 1.8 ms, 95% CI -1.8, 5.3, p = 0.41). No individual's QTc increased by >50 ms or exceeded 450 ms after PEP administration. Per protocol, all children were analyzed together, with no significant difference in mean QTc increase for BE-PEP compared to SDR-PEP, although non-inferiority of BE-PEP in children was not demonstrated in unadjusted analysis, as the upper limit of the 95% CI of 10.4 ms exceeded the predefined margin of 10 ms. Adjusting for baseline QTc, the regression coefficient and 95% CI (3.3; -1.4, 8.0) met the 10 ms non-inferiority margin. No significant differences in ALT or AST levels were noted between the intervention and control arms, although a limitation of the study was false elevation of ALT/AST during adult recruitment due to a technical error. In both study arms, one serious adverse event was reported, both considered unlikely related to the study drugs. Dizziness, nausea, headache, and diarrhea among adults, and headaches in children, were nonsignificantly more frequently observed in the BE-PEP group.
Conclusions: In this study, we observed that safety of single-dose bedaquiline 800 mg in combination with rifampicin is comparable to rifampicin alone, although non-inferiority of QTc changes was demonstrated in children only after adjusting for the baseline QTc measurements. A Phase 3 cluster randomized efficacy trial is currently ongoing in the Comoros.
Trial Registration: ClinicalTrials.gov NCT05406479.
Competing Interests: The trial was funded by Janssen Pharmaceuticals, manufacturer of bedaquiline used in the study, awarded to the Institute of Tropical Medicine, Principal Investigator EH, as an investigator-initiated collaboration. Financial support included the expenses related to training for and conduct of the trial, laboratory analyses, data analysis, and trial monitoring. The role of Janssen Pharmaceuticals was limited to support for regulatory duties and to deliver the study product. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. This does not alter our adherence to PLoS policies. The authors declare to have no other conflicts relevant to this trial.
(Copyright: © 2024 de Jong et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
Databáze: MEDLINE
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