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A Phase 2, 24 Week, Randomized, Open Label, Multi-Center Study to Assess the Safety, Tolerability, and Pharmacodynamics of FBS0701 in the Treatment of Chronic Iron Overload Requiring Chelation Therapy, With a 72 Week Dosing Extension

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Trial Profile

A Phase 2, 24 Week, Randomized, Open Label, Multi-Center Study to Assess the Safety, Tolerability, and Pharmacodynamics of FBS0701 in the Treatment of Chronic Iron Overload Requiring Chelation Therapy, With a 72 Week Dosing Extension

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 27 Aug 2024

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At a glance

  • Drugs Deferitazole (Primary)
  • Indications Iron overload
  • Focus Adverse reactions; Pharmacodynamics; Therapeutic Use
  • Sponsors FerroKin BioSciences; Shire

Most Recent Events

  • 20 Oct 2014 New trial record

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