Clinical Trial

Study Comparing Several Drugs to Understand Which Work Against Cutaneous Leishmaniasis (CL)

Not Yet Recruiting Phase 3
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Summary
MAMS4CL comprises a clinical trial with three embedded sub-studies designed to comprehensively evaluate the administered treatments and assess the impact of CL treatment on patients and the healthcare system. The multi-centre multi-arm multi-stage phase 3 clinical trial is designed to rigorously evaluate a total of 4 alternative treatment options for systemic CL against Sodium Stibugluconate (SSG) as the standard of care. The trial comprises two seamlessly linked stages. In stage 1, all four investigational arms will be evaluated against the control arm for efficacy to inform the selection of the arms, based on a pre-defined efficacy threshold that will advance to stage 2, in addition to the control arm. After stage 2, the experimental interventions will be compared with SSG similar to a standard superiority trial for efficacy. The general study design in stage 1 and stage 2 will be identical; only the number of investigational arms may differ. Patients will be randomized into the respective treatment arms at the recruitment sites of Arba Minch hospital, Boru Meda hospital and ALERT hospital in Ethiopia. Individuals will be hospitalized during the entire course of their treatment. As different arms have different treatment duration, patient hospitalization period and visit schedules will differ between arms. In total, the study will last 180 days for each participant.
Trial Details
NCT Number NCT07463040
Lead Sponsor Institute of Tropical Medicine, Belgium
Collaborators: London School of Hygiene and Tropical Medicine, Uppsala University, University of Stellenbosch, Armauer Hansen Research Institute, Ethiopia, Wollo University, Arba Minch University
Conditions Cutaneous Leihmaniasis
Enrollment 900 participants
Start Date 2027-01-01
Primary Completion 2029-03-01 (estimated)
Study Completion 2029-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-03-10