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Single Dose Crossover Comparative Bioavailability Study of Deferiprone 600 mg Delayed Release Tablets Versus Deferiprone Oral Solution in Healthy Male and Female Volunteers Following a 1200 mg Dose

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Single Dose Crossover Comparative Bioavailability Study of Deferiprone 600 mg Delayed Release Tablets Versus Deferiprone Oral Solution in Healthy Male and Female Volunteers Following a 1200 mg Dose

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 06 Nov 2021

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At a glance

  • Drugs Deferiprone (Primary) ; Deferiprone
  • Indications Iron overload; Pantothenate kinase-associated neurodegeneration
  • Focus Pharmacokinetics
  • Sponsors ApoPharma

    • Most Recent Events

    • 14 Jul 2015 Status changed from recruiting to completed as reported byClinicalTrials.gov record.
    • 26 May 2015 Status changed from not yet recruiting to recruiting as reported by ClinicalTrials.gov record.
    • 15 May 2015 New trial record

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