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A Randomized, Open-label, Phase II, Single-centre Study to Evaluate the Efficacy, Safety and Pharmacokinetics of LXE408 in Patients With Primary Visceral Leishmaniasis in Ethiopia

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Trial Profile

A Randomized, Open-label, Phase II, Single-centre Study to Evaluate the Efficacy, Safety and Pharmacokinetics of LXE408 in Patients With Primary Visceral Leishmaniasis in Ethiopia

Status: Not yet recruiting
Phase of Trial: Phase II

Latest Information Update: 11 Nov 2024

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At a glance

  • Drugs LXE 408 (Primary) ; Paromomycin; Sodium stibogluconate; Sodium stibogluconate
  • Indications Visceral leishmaniasis
  • Focus Proof of concept; Therapeutic Use

Most Recent Events

  • 05 Apr 2024 Planned End Date changed from 30 Sep 2025 to 3 Oct 2025.
  • 05 Apr 2024 Planned primary completion date changed from 30 Sep 2025 to 30 Jun 2025.
  • 27 Feb 2024 Planned End Date changed from 31 Jul 2025 to 30 Sep 2025.

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