Trial Profile

A Randomized, Multicentre, Observer-blind Phase II Study to Evaluate the Efficacy, Safety and Pharmacokinetics (PK) of Two LXE408 Regimens and Miltefosine as an Active Control in Patients With Localized Cutaneous Leishmaniasis in the Region of the Americas (AMR).

Status: Not yet recruiting

Phase of Trial: Phase II

Latest Information Update: 08 Jun 2025

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