Overview

LXE408 for Treatment of Visceral Leishmaniasis in Ethiopia, a Proof of Concept Study

Status:
Recruiting
Trial end date:
2025-10-03
Target enrollment:
Participant gender:
Summary
This is a randomized, open-label, phase II, single-centre study, with one LXE408 regimen and one calibrator arm with the standard of care SSG combined with PM, to be conducted in male and female adult (≥18 years and <45 years) patients with confirmed primary visceral leishmaniasis in Ethiopia.
Phase:
Phase 2
Details
Lead Sponsor:
Drugs for Neglected Diseases
Collaborator:
Novartis Pharmaceuticals
Treatments:
Antimony Sodium Gluconate
Paromomycin