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Metformin as adjunctive therapy in combination with multidrug treatment for multibacillary leprosy: A protocol for a randomized double-blind, controlled Phase 2 trial in Indonesia (MetLep Trial) [version 2; peer review: 2 approved]

Authors :
Dian E. Hasvitasari
Nelly Imbiri
Nico Tarino
Dwi R. Fajrianti
Stephen L. Walker
Fitri Wulandari
Raph L. Hamers
Nindya N. Utami
Annemieke Geluk
Marlous L. Grijsen
Duc H. Du
Hardyanto Soebono
Khairunnisa Puspatriani
Ronald B. Geskus
Reinout van Crevel
Evelyne Kestelyn
Hana Krismawati
Mutia Rahardjani
Sri V. Muchtar
Syamsiah .
Margareta Oktaviani
Source :
Wellcome Open Research, Vol 8 (2024)
Publication Year :
2024
Publisher :
Wellcome, 2024.

Abstract

Background The clinical management of leprosy is complicated by leprosy reactions (LR) causing irreversible nerve damage and disabilities. LR often require long-term use of corticosteroids causing serious side effects. Adjunct host-directed therapy (HDT) is a potentially attractive strategy in leprosy to prevent LR and associated immunopathology, modulate immunological memory that protects against recurrence, and thereby reduce nerve damage, disability and corticosteroid-associated morbidities. Metformin, a well-tolerated, safe and cheap anti-hyperglycaemic drug, is repurposed as HDT in auto-immune and infectious diseases, like tuberculosis (TB). Metformin use in people with diabetes is associated with reduced risks of TB-infection, progression to active TB, treatment failure and TB-mortality. Given the similarities both mycobacteria share, we hypothesize that among persons with multibacillary (MB) leprosy, adjunctive metformin may prevent/mitigate LR. Methods We will perform a double-blind controlled proof-of-concept trial in which people with newly diagnosed multibacillary leprosy will be randomized (1:1) to metformin hydrochloride 1000mg extended release once daily versus placebo for 24 weeks in addition to standard-of-care WHO MB multidrug therapy (MDT) during 48 weeks. We aim to enrol 166 participants aged between 18 and 65 years, across five clinical sites in two leprosy endemic areas in Indonesia. Primary outcomes are the proportion of participants experiencing a LR and the frequency of (serious) adverse events. Secondary outcomes are the severity and time to first LR, the cumulative corticosteroid usage, and quality of life. The total study follow-up is 48 weeks. Discussion LR signify the most important cause of irreversible nerve damage leading to anatomical deformities and disabilities, imposing a social and financial burden on those affected. Our study aims to evaluate the efficacy, tolerability and safety of adjunct metformin added to MDT in persons with multibacillary leprosy, and explore its effects on clinical and immunological outcomes. ClinicalTrials.gov registration NCT05243654 (17/02/2022)

Details

Language :
English
ISSN :
2398502X
Volume :
8
Database :
Directory of Open Access Journals
Journal :
Wellcome Open Research
Publication Type :
Academic Journal
Accession number :
edsdoj.64427f2e37bc440388b375cb5d04e8ac
Document Type :
article
Full Text :
https://doi.org/10.12688/wellcomeopenres.19455.2