1. Safety of single-dose bedaquiline combined with rifampicin for leprosy post-exposure prophylaxis: A Phase 2 randomized non-inferiority trial in the Comoros Islands
- Author
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de Jong, Bouke Catherine, Nourdine, Said, Bergeman, Auke Thomas, Salim, Zahara, Grillone, Silahi Halifa, Braet, Sofie Marijke, Wirdane Abdou, Mohamed, Snijders, Rian, Ronse, Maya, Hoof, Carolien, Tsoumanis, Achilleas, Ortuño-Gutiérrez, Nimer, der Werf, Christian van, Piubello, Alberto, Mzembaba, Aboubacar, Assoumani, Younoussa, and Hasker, Epco
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Drug therapy ,Testing ,Physiological aspects ,Research ,Dosage and administration ,Prophylaxis -- Research ,Combination drug therapy -- Physiological aspects -- Testing ,Pharmacological research ,Rifampin -- Dosage and administration -- Physiological aspects -- Testing ,Bedaquiline -- Dosage and administration -- Physiological aspects -- Testing ,Leprosy -- Drug therapy -- Physiological aspects ,Pharmacology, Experimental ,Drug therapy, Combination -- Physiological aspects -- Testing - Abstract
Author(s): Bouke Catherine de Jong 1,*, Said Nourdine 2, Auke Thomas Bergeman 3, Zahara Salim 2, Silahi Halifa Grillone 2, Sofie Marijke Braet 1, Mohamed Wirdane Abdou 2, Rian Snijders [...], 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) 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.
- Published
- 2024
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