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A Phase 1, Randomized, Open-label Study to Characterize the Pharmacokinetics, Pharmacodynamics, and Safety of Vamifeport After Multiple Oral Administration of One Immediate-release Formulation and After Single and Multiple Oral Administration of Two Prolonged-release Formulations in Healthy Adult Subjects

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A Phase 1, Randomized, Open-label Study to Characterize the Pharmacokinetics, Pharmacodynamics, and Safety of Vamifeport After Multiple Oral Administration of One Immediate-release Formulation and After Single and Multiple Oral Administration of Two Prolonged-release Formulations in Healthy Adult Subjects

Status: Active, no longer recruiting
Phase of Trial: Phase I

Latest Information Update: 21 Jan 2025

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At a glance

  • Drugs Vamifeport (Primary)
  • Indications Beta-thalassaemia; Iron overload; Myelodysplastic syndromes; Sickle cell anaemia
  • Focus Pharmacokinetics
  • Sponsors CSL Behring

    • Most Recent Events

    • 21 Jan 2025 Last checked against ClinicalTrials.gov record.
    • 15 Jan 2025 Status changed from not yet recruiting to active, no longer recruiting.
    • 17 Dec 2024 New trial record

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